renegadetribune--2020-12-15--Combats That Never End

Combats That Never End

By Donald Alexander Mackenzie From Wonder Tales from Scottish Myth and Legend [ 1917 ] There are two mountains that overlook the Spey valley , one to the east and one to the west , and a fairy king dwells on each of them .
They are both sons of Beira .
One fairy king is white , and has great fame as an archer ; he has a silver bow and arrows of gold , and once a day he shoots an arrow across the strath .
The other fairy king is black as the raven , and on @ @ @ @ @ @ @ spot .
He has no weapon , but is yet terrible in battle , because he can make himself invisible at will .
When he does so , nothing remains in sight except the red spot .
He has great strength , and when he goes against his enemies he seizes them unawares and throws them to the ground .
No matter how well they are armed , his enemies tremble when the invisible fairy comes against them .
All they see is a red spot moving about in the air .
Now @ @ @ @ @ @ @ bride whose name is Face-of-Light .
It is a great joy to her to wander among the mountains where herds of deer crop the green herbage , and through the strath where cornfields rustle in soft winds and fragrant flowers bloom fair to see .
The black fairy has no bride , and is jealous of the white fairy because his days are filled with joy by the beauty of Face-of-Light .
These two fairies have ever been enemies .
The black fairy keeps out of sight of the famous archer , fearing @ @ @ @ @ @ @ evening when the twilight shadows were lengthening and deepening across the strath , Face of Light tripped merrily over the grassy banks , gathering wild flowers .
Silence had fallen on the world ; no bird sang and no wind whispered , the lochs were asleep , and the shrunken river made scarcely a sound louder than the sigh of a sleeping babe ; it was no longer bright when Face-of-Light turned away from it .
The black fairy looked out from his mountain home .
He knew that the white fairy had @ @ @ @ @ @ @ watched Face-of-Light gathering wild flowers .
Nearer and nearer she came to his dwelling , and he crept into a deep forest which conceals the entrance to his mountain , and waited to seize her .
Face-of-Light , never dreaming of her peril , tripped towards the edge of the forest ; and , seeing many flowers growing beneath the trees , went in to pluck them .
She made the forest bright with her beauty , and the flowers grew fairer as she drew near them .
Suddenly a great black hand @ @ @ @ @ @ @ of bushes .
The hand seized her , and she shrieked in terror and struggled to escape .
The white fairy heard her cries , which pierced the air like the keen long whistle of the curlew , leapt up , and looked forth from his mountain top .
In a moment he knew what had happened .
Face-of-Light had been seized by his enemy , the black fairy , who was dragging her to a dark dungeon in the middle of his mountain .
The white fairy was unable to go to @ @ @ @ @ @ @ his dark enemy , he could not pass the utmost limits of his mountain house , and having already shot a golden arrow that day , he could not shoot another until a new day had dawned .
Night came on , and the black fairy climbed to the top of his mountain , where he danced with joy because be had taken captive the bride of his enemy .
The white fairy was stricken with sorrow , and when he heard the cries of Face-of-Light coming from the dungeon , he fell @ @ @ @ @ @ @ long Face-of-Light sobbed and wept , while the black fairy danced on the mountain top and sang songs of triumph .
He danced so fast that he raised a wind which swept down the strath and shook the trees from sleep , so that they moaned and sighed all night long .
The cries of Face-of-Light were heard by human beings , and those who were awakened said one to another : “ Listen to the hag of night .
How terrible are her cries !
” Not until the dawn began to @ @ @ @ @ @ @ his swoon .
Just when the first shaft of grey light pierced the eastern sky , he opened his eyes .
Then he remembered his sorrow and wept softly .
His tears fell as dew on the flowers and the grass .
Weeping , he climbed his mountain , and then wandered round about the crest of it .
His heart was heavy for the loss of Face-of-Light , and when he listened he heard her moaning in her dark prison .
The black fairy had ceased to dance .
He stood upright @ @ @ @ @ @ @ house , and shouted to his enemy : “ Ha !
Face-of-Light is my prisoner.
” Then suddenly he was silent .
He saw the white fairy stringing his silver bow and then drawing from his shining quiver a bright golden arrow .
“ Ha !
” cried the black fairy , “ would you dare shoot at me ?
” “ Set free Face-of-Light , or I shall shoot , ” the white fairy made answer .
His face was white as snow and hard as ice .
The black fairy laughed @ @ @ @ @ @ @ , and then , just as the white fairy raised his bow to take aim , his enemy vanished from sight .
No part of him could be seen but the great red spot on his left breast , which seemed to float in the air .
For a moment the white fairy , gazing eastward , looked with wonder at the red spot which grew brighter and brighter .
His bow was bent , and his golden arrow was held ready for flight .
The sound of defiant laughter came down the @ @ @ @ @ @ @ invisible , danced with joy on his mountain top .
To and fro swayed the red spot , and the white fairy thought he would shoot at it .
His aim was true and his arm was strong .
Straight from the bow flew the bright golden arrow .
It darted through the air with lightning speed and struck the red spot , which , be it known , was the heart of the black fairy .
A shriek rang out across the strath .
It was the death shriek of the black @ @ @ @ @ @ @ bare rock and died .
His life-blood streamed forth , and the whole eastern sky was covered with it .
In the midst of the redness gleamed the bright golden arrow of the white fairy .
No sooner was the black fairy slain than Face-of-Light was set free .
The doors of her dungeon flew open , and she came forth in all her beauty .
When she did so , the mountains and the strath were made bright , the river sparkled in the light , and the lochs flashed like burnished @ @ @ @ @ @ @ glad when Face-of-Light was set free from her dark prison .
The slumbering flowers opened their eyes to gaze upon her , and the birds broke forth in merry song , while the white fairy smiled and danced with joy .
The black fairy lay dead and invisible on his mountain top until evening came on .
Then Beira came to visit him .
When she found that her son had been slain , she took from her wallet a pot of healing balsam and rubbed it on his wound .
Then she @ @ @ @ @ @ @ on his lips .
When she did this , he came to life , and began once again to plot evil against the white fairy and his beautiful bride .
This story , which used to be told in Strathspey , is the story of the struggle between darkness and light .
The black fairy is night , which begins to , make itself invisible at dawn , and the red spot on his left breast is the red light of morning .
The golden arrow of the white fairy is the golden @ @ @ @ @ @ @ eastern heaven as the sun rises in morning splendour .
Face-of-Light is the spirit of the River Spey , which is bright in daytime and lost to sight in the darkness of night .
When the story-teller says that Face-of-Light leaves the river , he means that its brightness leaves it when the shadows of night are falling .
A different story is told in the Ness valley .
There are two mountains on either side of Loch Ness , and on each is a Fooar , or giant .
These sons of @ @ @ @ @ @ @ daylight and the other loves darkness .
Every morning at dawn one Fooar flings across Loch Ness a white boulder .
When the boulder goes through the air the sky becomes bright .
Every evening the other Fooar flings across Loch Ness a black boulder , and the sky grows dark .
The rivals can throw their boulders only once in every twenty-four hours .
When the white boulder is flung , it strikes the night Fooar , and he falls down in a swoon .
He does not recover until evening , @ @ @ @ @ @ @ turn , flings his black boulder , and strikes down his rival , who then lies unconscious until the dawn .
When the giant of day grasps his white boulder and raises it on high , his red hand can be seen in the sky , and the red hand of the giant of night is often seen at evening .
Sometimes the giants turn round the boulders to adjust them for throwing .
Then the gold rings on their fingers and the golden armlets on their arms flash athwart the sky in @ @ @

By Donald Alexander Mackenzie
From Wonder Tales from Scottish Myth and Legend [1917]
There are two mountains that overlook the Spey valley, one to the east and one to the west, and a fairy king dwells on each of them. They are both sons of Beira. One fairy king is white, and has great fame as an archer; he has a silver bow and arrows of gold, and once a day he shoots an arrow across the strath. The other fairy king is black as the raven, and on his left breast there is a red spot. He has no weapon, but is yet terrible in battle, because he can make himself invisible at will. When he does so, nothing remains in sight except the red spot. He has great strength, and when he goes against his enemies he seizes them unawares and throws them to the ground. No matter how well they are armed, his enemies tremble when the invisible fairy comes against them. All they see is a red spot moving about in the air.
Now, the white fairy has a fair bride whose name is Face-of-Light. It is a great joy to her to wander among the mountains where herds of deer crop the green herbage, and through the strath where cornfields rustle in soft winds and fragrant flowers bloom fair to see. The black fairy has no bride, and is jealous of the white fairy because his days are filled with joy by the beauty of Face-of-Light. These two fairies have ever been enemies. The black fairy keeps out of sight of the famous archer, fearing his arrows of gold.
One summer evening when the twilight shadows were lengthening and deepening across the strath, Face of Light tripped merrily over the grassy banks, gathering wild flowers. Silence had fallen on the world; no bird sang and no wind whispered, the lochs were asleep, and the shrunken river made scarcely a sound louder than the sigh of a sleeping babe; it was no longer bright when Face-of-Light turned away from it.
The black fairy looked out from his mountain home. He knew that the white fairy had lain down to rest, and he watched Face-of-Light gathering wild flowers. Nearer and nearer she came to his dwelling, and he crept into a deep forest which conceals the entrance to his mountain, and waited to seize her. Face-of-Light, never dreaming of her peril, tripped towards the edge of the forest; and, seeing many flowers growing beneath the trees, went in to pluck them. She made the forest bright with her beauty, and the flowers grew fairer as she drew near them.
Suddenly a great black hand was thrust out from a thick clump of bushes. The hand seized her, and she shrieked in terror and struggled to escape. The white fairy heard her cries, which pierced the air like the keen long whistle of the curlew, leapt up, and looked forth from his mountain top. In a moment he knew what had happened. Face-of-Light had been seized by his enemy, the black fairy, who was dragging her to a dark dungeon in the middle of his mountain. The white fairy was unable to go to her rescue for two reasons. Like his dark enemy, he could not pass the utmost limits of his mountain house, and having already shot a golden arrow that day, he could not shoot another until a new day had dawned.
Night came on, and the black fairy climbed to the top of his mountain, where he danced with joy because be had taken captive the bride of his enemy. The white fairy was stricken with sorrow, and when he heard the cries of Face-of-Light coming from the dungeon, he fell down in a swoon.
All night long Face-of-Light sobbed and wept, while the black fairy danced on the mountain top and sang songs of triumph. He danced so fast that he raised a wind which swept down the strath and shook the trees from sleep, so that they moaned and sighed all night long. The cries of Face-of-Light were heard by human beings, and those who were awakened said one to another: “Listen to the hag of night. How terrible are her cries!”
Not until the dawn began to break did the white fairy recover from his swoon. Just when the first shaft of grey light pierced the eastern sky, he opened his eyes. Then he remembered his sorrow and wept softly. His tears fell as dew on the flowers and the grass.
Weeping, he climbed his mountain, and then wandered round about the crest of it. His heart was heavy for the loss of Face-of-Light, and when he listened he heard her moaning in her dark prison. The black fairy had ceased to dance. He stood upright on the highest point of his mountain house, and shouted to his enemy: “Ha! Face-of-Light is my prisoner.” Then suddenly he was silent. He saw the white fairy stringing his silver bow and then drawing from his shining quiver a bright golden arrow.
“Ha!” cried the black fairy, “would you dare shoot at me?”
“Set free Face-of-Light, or I shall shoot,” the white fairy made answer. His face was white as snow and hard as ice.
The black fairy laughed, and willed himself to become invisible, and then, just as the white fairy raised his bow to take aim, his enemy vanished from sight. No part of him could be seen but the great red spot on his left breast, which seemed to float in the air.
For a moment the white fairy, gazing eastward, looked with wonder at the red spot which grew brighter and brighter. His bow was bent, and his golden arrow was held ready for flight.
The sound of defiant laughter came down the wind as the black fairy, now invisible, danced with joy on his mountain top.
To and fro swayed the red spot, and the white fairy thought he would shoot at it. His aim was true and his arm was strong. Straight from the bow flew the bright golden arrow. It darted through the air with lightning speed and struck the red spot, which, be it known, was the heart of the black fairy. A shriek rang out across the strath. It was the death shriek of the black fairy, who fell down on the bare rock and died. His life-blood streamed forth, and the whole eastern sky was covered with it. In the midst of the redness gleamed the bright golden arrow of the white fairy.
No sooner was the black fairy slain than Face-of-Light was set free. The doors of her dungeon flew open, and she came forth in all her beauty. When she did so, the mountains and the strath were made bright, the river sparkled in the light, and the lochs flashed like burnished silver. All the land was made glad when Face-of-Light was set free from her dark prison. The slumbering flowers opened their eyes to gaze upon her, and the birds broke forth in merry song, while the white fairy smiled and danced with joy.
The black fairy lay dead and invisible on his mountain top until evening came on. Then Beira came to visit him. When she found that her son had been slain, she took from her wallet a pot of healing balsam and rubbed it on his wound. Then she rubbed the balsam on his eyes and on his lips. When she did this, he came to life, and began once again to plot evil against the white fairy and his beautiful bride.
This story, which used to be told in Strathspey, is the story of the struggle between darkness and light. The black fairy is night, which begins to, make itself invisible at dawn, and the red spot on his left breast is the red light of morning. The golden arrow of the white fairy is the golden shaft of sunlight that darts across the eastern heaven as the sun rises in morning splendour. Face-of-Light is the spirit of the River Spey, which is bright in daytime and lost to sight in the darkness of night. When the story-teller says that Face-of-Light leaves the river, he means that its brightness leaves it when the shadows of night are falling.
A different story is told in the Ness valley. There are two mountains on either side of Loch Ness, and on each is a Fooar, or giant. These sons of Beira are rivals. One loves the daylight and the other loves darkness.
Every morning at dawn one Fooar flings across Loch Ness a white boulder. When the boulder goes through the air the sky becomes bright. Every evening the other Fooar flings across Loch Ness a black boulder, and the sky grows dark.
The rivals can throw their boulders only once in every twenty-four hours. When the white boulder is flung, it strikes the night Fooar, and he falls down in a swoon. He does not recover until evening, and then he rises and, in turn, flings his black boulder, and strikes down his rival, who then lies unconscious until the dawn. When the giant of day grasps his white boulder and raises it on high, his red hand can be seen in the sky, and the red hand of the giant of night is often seen at evening. Sometimes the giants turn round the boulders to adjust them for throwing. Then the gold rings on their fingers and the golden armlets on their arms flash athwart the sky in bright splendour.
Share now!
Author: Thanks for being a reader of this site. Your contributions make this all possible. You can send support to: Kyle Hunt, PO Box 1052, Sorrento FL 32776. Bitcoin address: 1AfppjYZddJzc2C15PXKMsnyBPjPJQezwA . CashApp: Thanks for being a reader of this site. Your contributions make this all possible. You can send support to: Kyle Hunt, PO Box 1052, Sorrento FL 32776. Bitcoin address: 1AfppjYZddJzc2C15PXKMsnyBPjPJQezwA . CashApp: https://cash.app/$thekylehunt


renegadetribune--2020-12-15--Ben Klassen: A Short History of the Jews – Masters of Deceit

This is a reading of chapters 6 through 9 of Ben Klassen ’ s 1973 book Nature ’ s Eternal @ @ @ @ @ preservation of the White race , it clearly identifies the enemy .

This is a reading of chapters 6 through 9 of Ben Klassen's 1973 book Nature's Eternal Religion. While promoting the preservation of the White race, it clearly identifies the enemy.


renegadetribune--2020-12-15--Gypsy Crusader is a Non-White Agent Sent to Make Our Cause Look Bad

Gypsy Crusader came on the scene not too long ago and has since blown up in apparent popularity .
I must assure you that I do not write this article out of jealousy or anything of the sort , as I would love it if our cause was being promoted in a big way , but this is certainly not what Gypsy Crusader ( Paul Miller ) is all about .
Gypsy Crusader is a non-White man who dresses up in various costumes ( joker , riddler , punisher ) and goes on Omegle to shock random people , most @ @ @ @ @ @ @ jokes ” .
This is the same thing that Brandon Martinez ( another non-White ) and CatBoyKami are doing as supposed activism .
None of this actually helps educate people regarding our cause .
If you would like to see more of what this fool is doing , here are a couple of compilation videos that are still up on jewtube , which should tell you all you really need to know about this loser and his many characters .
It seems Gypsy Crusader and CatBoyKami even “ found each other ” on @ @ @ @ @ @ @ the same CatBoy who went on a date with Nick Fuentes and was recently hailed as a great hero for “ naming the jew ” at a Trump rally .
He also likes to groom children and suck on black dildos .
Some Youtubers have put together videos detailing the origins and rise of Gypsy Crusader , but most of them take the line that he really believes everything he is saying now .
Supposedly he was at a Proud Boys rally and was jumped by Antifa .
Then BLM doxxed him and @ @ @ @ @ @ @ the self-proclaimed “ Nazi King ” and “ King of the Day of the Rope ” you see before you .
Here he is , before his transformation , telling OANN all about what happened with the Antifa altercation .
How would getting beaten up and harassed really turn someone ( especially a non-White ) into a jewy character played by a jewish actor in a jewish hollywood movie that is intended to make White people look like evil terrorists ?
Adding further absurdity to this all , the love interest in the @ @ @ @ @ @ @ freaking based !
I mean , Andrew Anglin told me White women are the devil , so why not just make out with your Black neighbor ?
Perhaps the biggest absurdity here is that this man actually claims to be White .
Here is a video , by a content creator I do not endorse , showing how the Gypsy claims to be White ( even though he is NOT ) and says jews should be allowed into a White ethno-state , so as to avoid purity spiraling .
When his videos are @ @ @ @ @ @ @ massive number of views , and even on his Bitchute channel , the view counts are extremely high .
Most comments seem to be very supportive .
Are people really this dumb or is he being astro-turfed ?
Now some people might claim that I am just “ infighting ” again , but this is impossible , because Paul Miller is not “ in ” my group or cause .
He is an obvious agent sent in to make us look bad and steer things in an unproductive direction .
Look at all @ @ @ @ @ @ @ him .
You really think this clown crusader would still be allowed on PayPal if he was legitimate ?
I should not need to even spell it all out for regular readers , as I hope you have enough discernment to be able to see right through Gypsy Crusader , but hopefully this article will help stop this clown from becoming even more popular .
Gypsy Crusader and those like him need to be nipped in the bud .

Gypsy Crusader came on the scene not too long ago and has since blown up in apparent popularity. I must assure you that I do not write this article out of jealousy or anything of the sort, as I would love it if our cause was being promoted in a big way, but this is certainly not what Gypsy Crusader (Paul Miller) is all about. Gypsy Crusader is a non-White man who dresses up in various costumes (joker, riddler, punisher) and goes on Omegle to shock random people, most children, with incendiary and offensive “jokes”. This is the same thing that Brandon Martinez (another non-White) and CatBoyKami are doing as supposed activism. None of this actually helps educate people regarding our cause.
https://www.youtube.com/watch?v=0KUClag7CoM
If you would like to see more of what this fool is doing, here are a couple of compilation videos that are still up on jewtube, which should tell you all you really need to know about this loser and his many characters.
https://www.youtube.com/watch?v=SMDtVfoMBz8
https://www.youtube.com/watch?v=4dc5Nb7tE5Q
It seems Gypsy Crusader and CatBoyKami even “found each other” on Omegle.
https://www.youtube.com/watch?v=JaR0d6Err7Y
Yes, that’s the same CatBoy who went on a date with Nick Fuentes and was recently hailed as a great hero for “naming the jew” at a Trump rally. He also likes to groom children and suck on black dildos.
What a role model!
Some Youtubers have put together videos detailing the origins and rise of Gypsy Crusader, but most of them take the line that he really believes everything he is saying now. Supposedly he was at a Proud Boys rally and was jumped by Antifa. Then BLM doxxed him and harassed his parents, turning him into the self-proclaimed “Nazi King” and “King of the Day of the Rope” you see before you. Here he is, before his transformation, telling OANN all about what happened with the Antifa altercation.
https://www.youtube.com/watch?v=xonZGhGA0y0
How would getting beaten up and harassed really turn someone (especially a non-White) into a jewy character played by a jewish actor in a jewish hollywood movie that is intended to make White people look like evil terrorists? Adding further absurdity to this all, the love interest in the movie is a Black woman!
https://www.youtube.com/watch?v=eGLF8FsabxI
So freaking based! I mean, Andrew Anglin told me White women are the devil, so why not just make out with your Black neighbor?
Perhaps the biggest absurdity here is that this man actually claims to be White. Here is a video, by a content creator I do not endorse, showing how the Gypsy claims to be White (even though he is NOT) and says jews should be allowed into a White ethno-state, so as to avoid purity spiraling.
WorldTruth Link
When his videos are up on jewtube, he gets a massive number of views, and even on his Bitchute channel, the view counts are extremely high. Most comments seem to be very supportive. Are people really this dumb or is he being astro-turfed?
Now some people might claim that I am just “infighting” again, but this is impossible, because Paul Miller is not “in” my group or cause. He is an obvious agent sent in to make us look bad and steer things in an unproductive direction.
Look at all the ways you can still financially support him.
You really think this clown crusader would still be allowed on PayPal if he was legitimate?
I should not need to even spell it all out for regular readers, as I hope you have enough discernment to be able to see right through Gypsy Crusader, but hopefully this article will help stop this clown from becoming even more popular. Gypsy Crusader and those like him need to be nipped in the bud.
Share now!
Author: Kyle Hunt Kyle is the publisher of the Renegade Tribune and the founder of Kyle is the publisher of the Renegade Tribune and the founder of Renegade Broadcasting , where he hosts The Solar Storm . He also organized the 2014 White Man March and created the film adaptation of Hellstorm . You can send support to: Kyle Hunt, PO Box 1052, Sorrento FL 32776. Bitcoin address: 1AfppjYZddJzc2C15PXKMsnyBPjPJQezwA


renegadetribune--2020-12-16--The Scam Has Been Confirmed: PCR Does Not Detect SARS-CoV-2

Unoﬃcial English translation of ‘ Frauds and falsehoods in the medical field ’ originally published on www.dsalud.com The genetic sequences used in PCRs to detect suspected SARS-CoV-2 and to diagnose cases of illness and death attributed to Covid-19 are present in dozens of sequences of the human genome itself and in those of about a hundred microbes .
And that includes the initiators or primers , the most extensive fragments taken at random from their supposed “ genome ” and even the so-called “ target genes ” allegedly specific to the “ new coronavirus ” .
The test is worthless @ @ @ @ @ @ @ so far should be scientifically invalidated and communicated to those aﬀected ; and if they are deceased , to their relatives .
Stephen Bustin , one of the world ’ s leading experts on PCR , in fact says that under certain conditions anyone can test positive !
We have been warning you since March : you can not have specific tests for a virus without knowing the components of the virus you are trying to detect .
And the components can not be known without having previously isolated/purified that virus .
Since @ @ @ @ @ @ @ no one has isolated SARS-CoV-2 and , more importantly , that it can never be isolated for the reasons we explained last month ( read the report “ Can you prove that there are pathogenic viruses ?
” on our website –www.dsalud.com- ) .
And in the present report we are going to oﬀer new data that show that RT-PCR does not detect the so called SARS-CoV-2 as it is known , but fragments of human RNA and those of numerous microbes .
We have already explained the numerous problems that RT-PCR poses @ @ @ @ @ @ @ as the WHO or the CDC and by prestigious international experts such as Dr. Stephen Bustin who considers both the arbitrariness of establishing criteria for results and the choice of the number of cycles to be nonsense because they can lead to anyone testing positive .
In this report we are going to add the results of a particular research we have done from the data published on the alleged SARS-CoV-2 and on the protocols endorsed by the WHO for the use of RT-PCR as well as the data corresponding to the rest @ @ @ @ @ @ @ And the conclusions are extremely serious : none of the seven “ human coronaviruses ” have actually been and all the sequences of the primers of their respective PCRs as well as those of a large number of fragments of their supposed genomes are found in diﬀerent areas of the human genome and in genomes of bacteria and archaea , such as these : Shwanella marina JCM , Dialister succinatiphilus , Lactobacillus porcine , Lactobacillus manihotivorans , Leptospira sarikeiensis , Bizionia echini , Sanguibacteroides justesenil , Bacteroides massiliensis , Lacinutrix venerupis , Moraxella @ @ @ @ @ @ @ , Acetobacterium puteale , Chryseobacterium hispanicum , Paenibacillius koleovorans , Tamiana fuccidanivorans , Fontibacillua panacisegetis , Ru bacter ruber , Skemania piniformis , Chryseobacterium shigense , Caloramator peoteoclasticus , Cellulosilyticum ruminicola , Nitrosopumilius evryensis and a long list of others .
We are going to explain step by step the research that has led us to such an unusual conclusion .
HAVE ANY HUMAN CORONAVIRUSES BEEN ISOLATED ?
During the first half of April , when the first research we conducted indicated that SARS-CoV-2 had not been isolated and since those who claimed @ @ @ @ @ @ @ “ isolates ” of previous “ human coronaviruses ” , we began to do a thorough review of those claimed isolates .
Specifically , we reviewed the alleged isolation work of suspected human coronaviruses 229E ( said to have been isolated in 1965 ) , OC43 ( in 1967 ) , SARS-CoV ( in 2003 ) , NL63 ( in 2004 ) , HKU1 ( in 2005 ) and MERSCoV ( in 2012 ) .
And these have been the results : : Dorothy Hamre and John Procknow .
A new virus isolated @ @ @ @ @ @ @ of the Society for Experimental Biology and Medicine , 121 : 1:190-193 .
January 1 , 1966 .
Since the authors refer to other articles to explain the method of isolation – which they call Complement Fixation – we consulted a reference article for that method : that of Janet W. Hartley et al .
Complement Fixation and tissue culture assay for mouse leukaemia viruses PNAS , 53 ( 5 ) :931-938 , May 1965 .
This is a procedure already in disuse that uses the antigen-antibody reaction to detect either one or @ @ @ @ @ @ @ are dealing with , the aim was to detect the antigens of the supposed new virus but , as we have already explained , specific antibodies are needed which can not be obtained the first time a virus is detected .
: Paul Lee .
Molecular epidemiology of human coronavirus OC43 in Hong Kong .
Thesis for the Department of Microbiology , University of Hong Kong , August 2007 .
The HKU Scholars Hub .
What was considered to be viral RNA was extracted from cultures without any proof that the The tool @ @ @ @ @ @ @ reagents , inhibitors and contaminants but what it can not do is determine where the extracted RNA comes from .
there are no controls .
It is then amplified by PCR and sequenced assuming ( ! )
that it is genetic information of a virus .
Finally , the author speculates about mutations , recombinations , genotypes , molecular evolution , strains and other jargon that conveys the idea -unproven- that a “ virus ” is being worked with .
J. S. M. Peiris and others .
Coronavirus as a possible cause of @ @ @ @ @ @ @ April 2003 .
There is no mention of purification in the article .
There is not even any mention of filtration or centrifugation .
It is only stated that “ the viruses were isolated in fetal monkey liver cells from nasopharyngeal aspirates and lung biopsies of two patients ” .
There are no controls .
The only mention is of a “ cytopathic eﬀect ” that is attributed to a virus and that PCR was done for known viruses and retroviruses without obtaining results .
Finally , RT-PCR was done with “ random @ @ @ @ @ @ @ unknown origin ” is detected to which “ a weak homology with the coronaviridiae family ” is found .
Then they designed primers for that sequence and when testing 44 samples from SARS patients only 22 were positive .
Lia van der Hock and others .
Identification of a new human coronavirus .
Nature Medicine , 10 , 4 April 2004 .
The authors state that “ the identification of unknown pathogens using molecular biology tools is diﬃcult because the target sequence is not known so that PCR-specific initiators can not be designed @ @ @ @ @ @ @ tool they developed themselves called VIDISCA which , they claim , does not require prior knowledge of the sequence !
Is that possible ?
Let ’ s see how it works : first the culture is prepared and it is assumed that a virus is present due to the evidence of “ cytopathic eﬀect ” .
The novelty introduced by this method is that “ restriction enzymes ” are added , enzymes that cut the nucleic acid molecules at certain locations and always by the same length .
In this way , if @ @ @ @ @ @ @ observe many fragments of DNA or RNA that are the same or very similar , they deduce that it comes from a virus , since the host genome would present random cuts , while the virus genome presents a large number of copies that are the same due to the replication of the virus .
And is such a deduction correct ?
Of course not !
This assumption ( which adds to the previous assumption that there is a virus ) does not take into account that there are “ virus-like particles ” @ @ @ @ @ @ @ endogenous retroviruses ” , “ exosomes ” , “ extracellular ” particles and even mitochondrial DNA .
In denial , there are a multitude of particles that possess the same reproductive characteristics in large quantities as “ viruses ” and by producing large numbers of identical copies when cut by enzymes as recognised in an article on the VIDISCA technique entitled Enhanced bioinformatic proSling of VIDISCA libraries for virus detection and Discovery .
It was published in volume 263 of Virus Research on April 2 , 2019 , and its authors-Cormac M. Kinsella @ @ @ @ @ @ @ expected in the VIDISCA insert from the host background nucleic acid , i.e.
, high copy numbers as in mitochondrial DNA .
Patrick C. Y .
Woo and others .
Characterisation and Complete Genome Sequence of a Novel Coronavirus , Coronavirus HKU1 , from Patients with Pneumonia .
Journal of Virology , 79 , 2 , January 2005 .
The article , incredibly , begins with these words : “ Despite extensive research in patients with respiratory tract infections , no microbiological cause has been identified in a significant .
RNA is extracted @ @ @ @ @ @ @ with coronavirus genes is used .
For the sequencing they use two protein databases organised in families , domains and functional sites -PFAM and INterProScan- combined with two computer programs that carry out “ predictions ” on how nucleotides should be combined .
The text adds : “ The sequences were manually assembled and edited to produce a final sequence of the viral genome ” .
again there are no controls .
: Ali Moh Zaki and others .
Isolation of a Novel Coronavirus from a Man with Pneumonia in Saudi Arabia .
@ @ @ @ @ @ @ 367:19 , November 2012 .
The genetic material is extracted and sputum sample with a tool called High Puré Viral Nucleic Acid Kit and then tested with diﬀerent PCRs for various known microorganisms .
There is no mention of purification and there are no controls .
In short , what had been done with the first coronaviruses -and with many other supposed viruses– is – any “ cytopathic eﬀect ” was attributed to the presence of a virus only – and then either some proteins are obtained which without any test are considered @ @ @ @ @ @ @ “ antigens ” are detected in cultures it is interpreted as “ isolation ” , or fragments of nucleic acids are extracted assuming that they belong to a virus .
We already explained in the article published in the previous issue of the magazine that according to Dr. Stefan Lanka the so-called “ cytopathic eﬀect ” is actually an eﬀect caused by the conditions of the culture itself .
This is recognised for example in the article Antibiotic-induced release of small extracellular vesicles ( exosomes ) with surface-associated DNA published on August 15 @ @ @ @ @ @ @ and signed by Andrea Németh and others ( https : //www.ncbi.nlm.nih.gov/pmc/articles/PMC5557920/pdf/41598_2017_Article_8392.pdf It explains that certain substances -such as antibiotics- added to in vitro experiments can stress the cell cultures so that they generate new sequences that had not been previously detected .
This had already been noticed by none other than Dr. Barbara McClintock in 1983 during her Nobel Prize lecture , as can be seen at https : //www.nobelprize.org/uploads/2018/06/mcclintock-lecture.pdf In essence , NOT ONE OF THE SEVEN SUPPOSED HUMAN CORONAVIRUS HAS REALLY BEEN ISOLATED .
The only thing that has been diﬀerent @ @ @ @ @ @ @ techniques that were becoming progressively more sophisticated which , in this case , has implied not a greater accuracy but a greater capacity for deception and self-deception that has culminated in the virtual manufacture of the SARS-CoV-2 .
And the obvious consequence of the lack of evidence of its isolation is that such “ coronaviruses ” can not be held responsible for any disease .
Moreover , all tests – of whatever kind – based on the presumed components of these “ viruses ” ( nucleic acids or proteins ) are completely disqualified @ @ @ @ @ @ @ more as “ diagnostics ” of diseases .
In the previous issue we already collected the answers given by the authors of several articles that supposedly described the isolation of SARS-CoV-2 in which they acknowledged that they had not “ purified ” which implicitly means acknowledging that the virus was not isolated .
And now we are going to add one more piece of evidence : the responses given by diﬀerent authorities – political and health – from various countries about the purification and isolation of SARS-CoV-2 .
James McCumiskey -author of the @ @ @ @ @ @ @ Paradigm– tells us that the National Virus Reference Laboratory of Ireland requested information about it from the University of Dublin and the latter responded that “ it has no records that could provide an answer to their request ” .
The director of legal services of the laboratory insisted on his request to the university and the university responded as follows : “ The position of the university is that material of academic debate can not be subject to the Freedom of Information Act ” .
It follows from the NVR ’ s @ @ @ @ @ @ @ or purified it .
They only acknowledge having “ detected SARS-CoV-2 RNA in diagnostic samples.
” On June 22 , a group of experts sent a consultation in similar terms to British Prime Minister Boris Johnson .
The letter was signed by Dr. Kevin Corbett , Piers Corbyn – professor at Imperial College London - , the engineer and independent researcher – who we interviewed in the journal at the time – David Crowe , Dr. Andrew Kaufman , the Edinburgh professor of biology Roger Watson and the biologist and chemist David Rasnick @ @ @ @ @ @ @ have not received a reply !
Another similar request – in this case to the National Research Council of Canada – received the following response : “ We have not been able to carry out a complete search of the NRC ’ s records so we regret to inform you that no records have been identified that respond to your request.
” We will add that two journalists have been sending similar requests – under the Freedom of Information Act – to various institutions in Canada , New Zealand , Australia , Germany @ @ @ @ @ @ @ States , and as of September 5 , twelve institutions have responded , all indicating the same thing : that they have no record of work describing the isolation of the virus that is supposed to cause Covid-19 .
The details and the answers can be seen at LOOKING FOR THE ORIGIN OF THE FALSE GENOME The question we asked ourselves then was : if the sequences that have been published do not belong – as claimed- to new viruses , where do they come from ?
And to try to answer that @ @ @ @ @ @ @ search with a computer program called Basic Local Alignment Search Tool ( BLAST ) , a sequence alignment search tool that allows us to compare a given sequence with all the sequences stored in the National Institutes of Health of the United States ( it is public and can be consulted at https : //blast.ncbi.nlm.nih.gov/Blast.cgi .
We explain step by step what we did so that our readers can repeat the search for themselves and check the results .
First we collected all the initiators of the PCRs described in the protocols hosted @ @ @ @ @ @ @ which were these : • China CDC protocol : uses ORF1ab and N genes as target .
• Protocol of the Pasteur Institute ( France ) : uses two fragments of the RdRP ( which is supposed to be SARS.CoV-2 specific ) .
• United States CDC protocol : uses three fragments of the N gene .
• Protocol of the National Institute of Infectious Diseases of Japan : it is the only one that has as target the S gene together with other genes supposedly shared with other coronaviruses .
• Charite @ @ @ @ @ @ @ E , N and RdRP genes .
• National Institute of Health Thailand protocol : uses the N gene .
We then introduced the sequence of the primers – the one that indicates the beginning of the sequence to be detected ( forward ) and the one that indicates the final ( reverse ) – into the BLAST so that it could search for them in two databases : a collection of microbe genomes and the one corresponding to the human genome .
THE SEQUENCES OF THE SO-CALLED SARS-COV-2 ARE FOUND BOTH IN @ @ @ @ @ @ @ ’ s see in detail the procedure taking as an example the initiators of the French protocol .
Once on the BLAST website , we chose Microbes to search the microbial genome databases and moved to the next page .
Then a form appeared in which we entered the sequence of the forward initiator of the French protocol -that is ATGAGCTTAGTCCTGTG- , we selected the option Highly similar sequences and pressed the BLAST key .
Just a few seconds later the results appeared -we took a screenshot ( image 1 ) – and @ @ @ @ @ @ @ -particularly bacteria and archaea- with a coincidence of between 77 % and 100 % with an identity percentage of 100 % .
We then returned to the home page and that second time we chose Human to search the human genome , we repeated the same operation and after a few seconds the result appeared which we screen captured again ( image 2 ) .
And it turns out that the sequence entered coincides with 74 sequences of the human genome , with a coincidence of between 66 % and 100 % and @ @ @ @ @ @ @ .
And that indicates that the sequence of that initial PCR primer that is supposed to be specific to SARS-CoV-2 actually corresponds to 74 fragments of the human genome and a hundred microbial fragments as well !
We then decided to repeat the operation but with the final or reverse primer – which is CTCCCTTTGTGTGTGT – and the results were similar .
Since these were very short sequences -about twenty genetic letters or nucleotides- we decided to try again but with the target sequence defined by these two primers , i.e .
the @ @ @ @ @ @ @ is between the initial primer and the final primer .
Obviously , for this we needed the sequence that is oﬃcially claimed to be the “ SARS-CoV-2 genome ” and although thousands of laboratories claim to have isolated and sequenced it -a false claim as we have explained in previous reports- we decided to go to the National Centre for Biotechnology Information website : https : //www.ncbi.nlm.nih.gov/nuccore/NC_045512.2 ?
report=genbank & to=29903 .
Once there , we located the “ target sequence ” , a fragment of 108 nucleotides located between positions 12,690 and @ @ @ @ @ @ @ which is this one : With this we repeated the steps previously described and the results were again surprising since there appeared again a hundred microbe sequences with a percentage of a match of 100 % and four sequences of the human genome with an identity percentage between 83 % and 95 % .
The matches were therefore lower but the important thing is that we continue to find fragments of the supposed “ target sequence ” of SARS-CoV-2 both in microbes and in our own genome .
Truly astonished we took a @ @ @ @ @ @ @ considered at that time as the most specific of SARS-CoV-2 , the E gene that is supposed to generate the envelope proteins and is located between positions 26,245 and 26,472 : We repeated with it the steps already described and the result was even more surprising because despite its length another hundred microbe sequences appeared with a percentage of identity of 100 % and 10 sequences of the human genome with a percentage of identity between 80 % and 100 % .
And similar results were obtained with a fragment chosen at random @ @ @ @ @ @ @ say corresponds to the proteins of the SARS-CoV-2 nucleocapsid .
We finally decided to test with the S gene which is said to generate the structural “ spike ” proteins that are key to entry into the cell and was subsequently considered to be the most specific SARS-CoV-2 gene .
Since it is a gene whose sequence is much longer – 3821 nucleotides between positions 21,563 and 25,384 – we tested with two fragments chosen at random within that gene and the first – TTGGCAAAATTCAAGACTCACTTTC – resulted in another hundred microbe sequences and @ @ @ @ @ @ @ the second – CTTGCTGCTACTAAATGCAGAGTGT – a hundred microbial sequences and 90 of the human genome .
Finally we decided to test with the initiators of the Japan Protocol , the only one that includes target sequences of the S gene and , the reader will have already guessed , the results were once again similar : a hundred microbe sequences and 93 sequences of the human genome with an identity percentage between 94.12 % and 100 % !
The consequence of all that we have just explained is clear and immediate : THERE @ @ @ @ @ @ @ antigen tests nor RT-PCR .
And we included those based on the supposed gene that codes for the S1 or spike protein .
And that means that ALL THE NUMBERS OF “ CASES ” , “ INFECTED ” , “ SICK ” , “ Asymptomatic ” OR “ DEAD DUE TO COVID-19 ” AND ALL “ POSITIVES ” ARE FALSE POSITIVES , something that should be communicated immediately to those aﬀected and those responsible should be held accountable .
We end by adding that even the WHO itself does not really believe in @ @ @ @ @ @ @ published last September 11 as a laboratory guide for SARS-CoV-2 entitled Diagnostic tests for SARS-CoV-2 – it is available at https : //apps.who.int/iris/rest/bitstreams/1302661/ retrieve – and it literally says on page 5 : “ Whenever possible , suspected active infection should be tested with a nucleic acid amplification test ( NAAT ) such as RT-PCR .
NAAT tests should target the SARS-CoV-2 genome but since there is no known global circulation of SARS-CoV-1 a Sarbecovirus sequence ( presumed to include at least five human and animal coronaviruses including SARS-CoV-1 and SARS-Cov-2 ) is @ @ @ @ @ @ @ is , WHO agrees to use to detect SARS-CoV-2 .
That is not all because the manual later states , “ An optimal diagnosis consists of a NAAT test with at least two genome-independent targets of the SARS-CoV-2 ; however , in areas where transmission is widespread , The WHO manual states , “ One or more negative results do not necessarily rule out SARS-CoV-2 infection .
There are a number of factors that can produce a negative result in an infected individual including poor quality of the sample , late collection of @ @ @ @ @ @ @ technical reasons inherent in the test , such as mutation of the virus or inhibition of PCR.
” What are the judges waiting for to act on their own initiative ?
the author publicly thanks Juan Pedro Aparicio Alcaraz for his patient and meticulous collaborative work in the search for scientific articles and for his tedious work with the BLAST .

By GMI Reporter
Unoﬃcial English translation of ‘Frauds and falsehoods in the medical field’ originally published on www.dsalud.com
The genetic sequences used in PCRs to detect suspected SARS-CoV-2 and to diagnose cases of illness and death attributed to Covid-19 are present in dozens of sequences of the human genome itself and in those of about a hundred microbes. And that includes the initiators or primers, the most extensive fragments taken at random from their supposed “genome” and even the so-called “target genes” allegedly specific to the “new coronavirus”. The test is worthless and all “positive” results obtained so far should be scientifically invalidated and communicated to those aﬀected; and if they are deceased, to their relatives. Stephen Bustin, one of the world’s leading experts on PCR, in fact says that under certain conditions anyone can test positive!
We have been warning you since March: you cannot have specific tests for a virus without knowing the components of the virus you are trying to detect. And the components cannot be known without having previously isolated/purified that virus. Since then we continue to accumulate evidence that no one has isolated SARS-CoV-2 and, more importantly, that it can never be isolated for the reasons we explained last month (read the report “Can you prove that there are pathogenic viruses?” on our website –www.dsalud.com-). And in the present report we are going to oﬀer new data that show that RT-PCR does not detect the so called SARS-CoV-2 as it is known, but fragments of human RNA and those of numerous microbes.
We have already explained the numerous problems that RT-PCR poses, recognised by organisations or governments such as the WHO or the CDC and by prestigious international experts such as Dr. Stephen Bustin who considers both the arbitrariness of establishing criteria for results and the choice of the number of cycles to be nonsense because they can lead to anyone testing positive.
In this report we are going to add the results of a particular research we have done from the data published on the alleged SARS-CoV-2 and on the protocols endorsed by the WHO for the use of RT-PCR as well as the data corresponding to the rest of the “human coronaviruses”. And the conclusions are extremely serious: none of the seven “human coronaviruses” have actually been isolated and all the sequences of the primers of their respective PCRs as well as those of a large number of fragments of their supposed genomes are found in diﬀerent areas of the human genome and in genomes of bacteria and archaea, such as these: Shwanella marina JCM, Dialister succinatiphilus, Lactobacillus porcine, Lactobacillus manihotivorans, Leptospira sarikeiensis, Bizionia echini, Sanguibacteroides justesenil, Bacteroides massiliensis, Lacinutrix venerupis, Moraxella bovis, Leptospira saintgironsiae, Winogradskyella undariae, Acetobacterium puteale, Chryseobacterium hispanicum, Paenibacillius koleovorans, Tamiana fuccidanivorans, Fontibacillua panacisegetis, Ru bacter ruber , Skemania piniformis, Chryseobacterium shigense, Caloramator peoteoclasticus, Cellulosilyticum ruminicola, Nitrosopumilius evryensis and a long list of others.
We are going to explain step by step the research that has led us to such an unusual conclusion.
HAVE ANY HUMAN CORONAVIRUSES BEEN ISOLATED?
During the first half of April, when the first research we conducted indicated that SARS-CoV-2 had not been isolated and since those who claimed to have done so were relying on “isolates” of previous “human coronaviruses”, we began to do a thorough review of those claimed isolates. Specifically, we reviewed the alleged isolation work of suspected human coronaviruses 229E (said to have been isolated in 1965), OC43 (in 1967), SARS-CoV (in 2003), NL63 (in 2004), HKU1 (in 2005) and MERSCoV (in 2012). And these have been the results:
Coronavirus 229E.
Reference article : Dorothy Hamre and John Procknow. A new virus isolated from the human respiratory Tract. Proceedings of the Society for Experimental Biology and Medicine, 121: 1:190-193. January 1, 1966.
Since the authors refer to other articles to explain the method of isolation – which they call Complement Fixation – we consulted a reference article for that method: that of Janet W. Hartley et al. Complement Fixation and tissue culture assay for mouse leukaemia viruses PNAS, 53(5):931-938, May 1965. This is a procedure already in disuse that uses the antigen-antibody reaction to detect either one or the other. In the case we are dealing with, the aim was to detect the antigens of the supposed new virus but, as we have already explained, specific antibodies are needed which cannot be obtained the first time a virus is detected.
Coronavirus OC43.
Reference article : Paul Lee. Molecular epidemiology of human coronavirus OC43 in Hong Kong. Thesis for the Department of Microbiology, University of Hong Kong, August 2007. The HKU Scholars Hub.
What was considered to be viral RNA was extracted from cultures without any proof that the RNA belongs to a virus. The tool used – a QIAamp kit – removes reagents, inhibitors and contaminants but what it cannot do is determine where the extracted RNA comes from. And there are no controls. It is then amplified by PCR and sequenced assuming (!) that it is genetic information of a virus. Finally, the author speculates about mutations, recombinations, genotypes, molecular evolution, strains and other jargon that conveys the idea -unproven- that a “virus” is being worked with.
SARS-CoV Coronavirus.
Reference article: J. S. M. Peiris and others. Coronavirus as a possible cause of SARS. Lancet 361: 1319-25, April 2003.
There is no mention of purification in the article. There is not even any mention of filtration or centrifugation. It is only stated that “the viruses were isolated in fetal monkey liver cells from nasopharyngeal aspirates and lung biopsies of two patients”. There are no controls . The only mention is of a “cytopathic eﬀect” that is attributed to a virus and that PCR was done for known viruses and retroviruses without obtaining results. Finally, RT-PCR was done with “random initiators” and a sequence “of unknown origin” is detected to which “a weak homology with the coronaviridiae family” is found. Then they designed primers for that sequence and when testing 44 samples from SARS patients only 22 were positive.
Coronavirus NL63.
Reference article: Lia van der Hock and others. Identification of a new human coronavirus. Nature Medicine, 10, 4 April 2004.
The authors state that “the identification of unknown pathogens using molecular biology tools is diﬃcult because the target sequence is not known so that PCR-specific initiators cannot be designed”.
What they used is a tool they developed themselves called VIDISCA which, they claim, does not require prior knowledge of the sequence! Is that possible? Let’s see how it works: first the culture is prepared and it is assumed that a virus is present due to the evidence of “cytopathic eﬀect”. The novelty introduced by this method is that “restriction enzymes” are added, enzymes that cut the nucleic acid molecules at certain locations and always by the same length. In this way, if after the action of these enzymes they observe many fragments of DNA or RNA that are the same or very similar, they deduce that it comes from a virus, since the host genome would present random cuts, while the virus genome presents a large number of copies that are the same due to the replication of the virus. And is such a deduction correct? Of course not! This assumption (which adds to the previous assumption that there is a virus) does not take into account that there are “virus-like particles”, “retrovirus-like particles”, “endogenous retroviruses”, “exosomes”, “extracellular” particles and even mitochondrial DNA. In denial, there are a multitude of particles that possess the same reproductive characteristics in large quantities as “viruses” and therefore can falsify results by producing large numbers of identical copies when cut by enzymes as recognised in an article on the VIDISCA technique entitled Enhanced bioinformatic proSling of VIDISCA libraries for virus detection and Discovery. It was published in volume 263 of Virus Research on April 2, 2019, and its authors-Cormac M. Kinsella et al.-recognise that “no redundancy is expected in the VIDISCA insert from the host background nucleic acid except in the case of ‘virus-like’ characteristics , i.e., high copy numbers as in mitochondrial DNA.
Coronavirus HKU1.
Reference article: Patrick C. Y. Woo and others. Characterisation and Complete Genome Sequence of a Novel Coronavirus, Coronavirus HKU1, from Patients with Pneumonia. Journal of Virology, 79, 2, January 2005.
The article, incredibly, begins with these words: “Despite extensive research in patients with respiratory tract infections, no microbiological cause has been identified in a significant proportion of patients . RNA is extracted from non-purified cultures.” And a PCR with coronavirus genes is used. For the sequencing they use two protein databases organised in families, domains and functional sites -PFAM and INterProScan- combined with two computer programs that carry out “predictions” on how nucleotides should be combined. The text adds: “The sequences were manually assembled and edited to produce a final sequence of the viral genome”. And once again there are no controls.
MERS-CoV Coronavirus.
Reference article : Ali Moh Zaki and others. Isolation of a Novel Coronavirus from a Man with Pneumonia in Saudi Arabia. The New England Journal of Medicine, 367:19, November 2012.
The genetic material is extracted directly from the culture supernatant and sputum sample with a tool called High Puré Viral Nucleic Acid Kit and then tested with diﬀerent PCRs for various known microorganisms. There is no mention of purification and there are no controls.
In short, what had been done with the first coronaviruses -and with many other supposed viruses– is to cultivate supposedly infected tissues – any “cytopathic eﬀect” was attributed to the presence of a virus only – and then either some proteins are obtained which without any test are considered “virus antigens” and when these “antigens” are detected in cultures it is interpreted as “isolation”, or fragments of nucleic acids are extracted assuming that they belong to a virus.
We already explained in the article published in the previous issue of the magazine that according to Dr. Stefan Lanka the so-called “cytopathic eﬀect” is actually an eﬀect caused by the conditions of the culture itself. This is recognised for example in the article Antibiotic-induced release of small extracellular vesicles (exosomes) with surface-associated DNA published on August 15, 2017 on the website of Nature and signed by Andrea Németh and others
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557920/pdf/41598_2017_Article_8392.pdf It explains that certain substances -such as antibiotics- added to in vitro experiments can stress the cell cultures so that they generate new sequences that had not been previously detected. This had already been noticed by none other than Dr. Barbara McClintock in 1983 during her Nobel Prize lecture, as can be seen at https://www.nobelprize.org/uploads/2018/06/mcclintock-lecture.pdf
In essence, NOT ONE OF THE SEVEN SUPPOSED HUMAN CORONAVIRUS HAS REALLY BEEN ISOLATED. The only thing that has been diﬀerent between them are the laboratory procedures and techniques that were becoming progressively more sophisticated which, in this case, has implied not a greater accuracy but a greater capacity for deception and self-deception that has culminated in the virtual manufacture of the SARS-CoV-2.
And the obvious consequence of the lack of evidence of its isolation is that such “coronaviruses” cannot be held responsible for any disease. Moreover, all tests – of whatever kind – based on the presumed components of these “viruses” (nucleic acids or proteins) are completely disqualified as “infection tests” and even more as “diagnostics” of diseases.
MORE UNANSWERED REQUESTS
In the previous issue we already collected the answers given by the authors of several articles that supposedly described the isolation of SARS-CoV-2 in which they acknowledged that they had not “purified” which implicitly means acknowledging that the virus was not isolated. And now we are going to add one more piece of evidence: the responses given by diﬀerent authorities – political and health – from various countries about the purification and isolation of SARS-CoV-2.
James McCumiskey -author of the book The Latest Conspiracy: The Biomedical Paradigm– tells us that the National Virus Reference Laboratory of Ireland requested information about it from the University of Dublin and the latter responded that “it has no records that could provide an answer to their request”. The director of legal services of the laboratory insisted on his request to the university and the university responded as follows: “The position of the university is that material of academic debate cannot be subject to the Freedom of Information Act”. It follows from the NVR’s request that they have not cultivated SARS-CoV-2 or purified it. They only acknowledge having “detected SARS-CoV-2 RNA in diagnostic samples.”
On June 22, a group of experts sent a consultation in similar terms to British Prime Minister Boris Johnson. The letter was signed by Dr. Kevin Corbett, Piers Corbyn – professor at Imperial College London -, the engineer and independent researcher – who we interviewed in the journal at the time – David Crowe, Dr. Andrew Kaufman, the Edinburgh professor of biology Roger Watson and the biologist and chemist David Rasnick – and to this day they still have not received a reply!
Another similar request – in this case to the National Research Council of Canada – received the following response: “We have not been able to carry out a complete search of the NRC’s records so we regret to inform you that no records have been identified that respond to your request.”
We will add that two journalists have been sending similar requests – under the Freedom of Information Act – to various institutions in Canada, New Zealand, Australia, Germany, the United Kingdom and the United States, and as of September 5, twelve institutions have responded, all indicating the same thing: that they have no record of work describing the isolation of the virus that is supposed to cause Covid-19. The details and the answers can be seen at
https://www.fluoridefreepeel.ca/u-k-dept-of-health-and-social-care-has-no-record-of-covid-19-virus-isolation/
LOOKING FOR THE ORIGIN OF THE FALSE GENOME
The question we asked ourselves then was: if the sequences that have been published do not belong – as claimed- to new viruses, where do they come from? And to try to answer that question we decided to carry out a search with a computer program called Basic Local Alignment Search Tool (BLAST), a sequence alignment search tool that allows us to compare a given sequence with all the sequences stored in the National Institutes of Health of the United States (it is public and can be consulted at https://blast.ncbi.nlm.nih.gov/Blast.cgi. We explain step by step what we did so that our readers can repeat the search for themselves and check the results.
First we collected all the initiators of the PCRs described in the protocols hosted on the WHO website at the time which were these:
China CDC protocol: uses ORF1ab and N genes as target.
Protocol of the Pasteur Institute (France): uses two fragments of the RdRP (which is supposed to be SARS.CoV-2 specific).
United States CDC protocol: uses three fragments of the N gene.
Protocol of the National Institute of Infectious Diseases of Japan: it is the only one that has as target the S gene together with other genes supposedly shared with other coronaviruses.
Charite Protocol (Germany): uses the E, N and RdRP genes.
Hong Kong University Protocol: uses ORF1b-nsp14 and N gene.
National Institute of Health Thailand protocol: uses the N gene.
We then introduced the sequence of the primers – the one that indicates the beginning of the sequence to be detected (forward) and the one that indicates the final (reverse) – into the BLAST so that it could search for them in two databases: a collection of microbe genomes and the one corresponding to the human genome.
THE SEQUENCES OF THE SO-CALLED SARS-COV-2 ARE FOUND BOTH IN HUMANS AND IN NUMEROUS MICROBES!
Let’s see in detail the procedure taking as an example the initiators of the French protocol. Once on the BLAST website, we chose Microbes to search the microbial genome databases and moved to the next page. Then a form appeared in which we entered the sequence of the forward initiator of the French protocol -that is ATGAGCTTAGTCCTGTG-, we selected the option Highly similar sequences and pressed the BLAST key. Just a few seconds later the results appeared -we took a screenshot (image 1)– and we were shown 100 sequences of microbes -particularly bacteria and archaea- with a coincidence of between 77% and 100% with an identity percentage of 100%.
We then returned to the home page and that second time we chose Human to search the human genome, we repeated the same operation and after a few seconds the result appeared which we screen captured again (image 2). And it turns out that the sequence entered coincides with 74 sequences of the human genome, with a coincidence of between 66% and 100% and a percentage of identity of 100%.
And that indicates that the sequence of that initial PCR primer that is supposed to be specific to SARS-CoV-2 actually corresponds to 74 fragments of the human genome and a hundred microbial fragments as well!
We then decided to repeat the operation but with the final or reverse primer – which is CTCCCTTTGTGTGTGT – and the results were similar.
Since these were very short sequences -about twenty genetic letters or nucleotides- we decided to try again but with the target sequence defined by these two primers, i.e. the sequence of the supposed SARS-CoV-2 genome that is between the initial primer and the final primer . Obviously, for this we needed the sequence that is oﬃcially claimed to be the “SARS-CoV-2 genome” and although thousands of laboratories claim to have isolated and sequenced it -a false claim as we have explained in previous reports- we decided to go to the National Centre for Biotechnology Information website: https://www.ncbi.nlm.nih.gov/nuccore/NC_045512.2?report=genbank&to=29903. Once there, we located the “target sequence”, a fragment of 108 nucleotides located between positions 12,690 and 12,797 of the “genome”, which is this one:
ATGAGCTTAGTCCTGTTGCACTACGACAGATGTTGTGCCGGTACACAAACTGCTTGCACTGAT GACAATGCGTTAGCTTACAACAACAAAGGGAG.
With this we repeated the steps previously described and the results were again surprising since there appeared again a hundred microbe sequences with a percentage of a match of 100% and four sequences of the human genome with an identity percentage between 83% and 95%. The matches were therefore lower but the important thing is that we continue to find fragments of the supposed “target sequence” of SARS-CoV-2 both in microbes and in our own genome.
Truly astonished we took a further step and tested with the gene considered at that time as the most specific of SARS-CoV-2, the E gene that is supposed to generate the envelope proteins and is located between positions 26,245 and 26,472:
ATGTACTCATTCGTTTCGGAAGAGACAGGTACTACGTTAATAGTTAATAGCGTACTTCTCTTGCTTTCGTGGTATTCTTGCTAGTTACACTAGCCATCCTGCTTCGATTGTGCGTACTGCTGCAATATTGTTAACGTGAGTCTTGTAAAACCTTTACGTTTACTCGTGTTAAAATCTGAATTCTTCTAGAGTTCGATTCTGGTCTAA.
We repeated with it the steps already described and the result was even more surprising because despite its length another hundred microbe sequences appeared with a percentage of identity of 100% and 10 sequences of the human genome with a percentage of identity between 80% and 100%. And similar results were obtained with a fragment chosen at random and with the N gene which they say corresponds to the proteins of the SARS-CoV-2 nucleocapsid.
We finally decided to test with the S gene which is said to generate the structural “spike” proteins that are key to entry into the cell and was subsequently considered to be the most specific SARS-CoV-2 gene. Since it is a gene whose sequence is much longer – 3821 nucleotides between positions 21,563 and 25,384 – we tested with two fragments chosen at random within that gene and the first – TTGGCAAAATTCAAGACTCACTTTC – resulted in another hundred microbe sequences and 93 sequences of the human genome and the second – CTTGCTGCTACTAAATGCAGAGTGT – a hundred microbial sequences and 90 of the human genome.
Finally we decided to test with the initiators of the Japan Protocol, the only one that includes target sequences of the S gene and, the reader will have already guessed, the results were once again similar: a hundred microbe sequences and 93 sequences of the human genome with an identity percentage between 94.12% and 100%!
CONCLUSIONS
The consequence of all that we have just explained is clear and immediate: THERE IS NO VALID TEST TO DETECT SARS-COV-2 , neither antibody or antigen tests nor RT-PCR. And we included those based on the supposed gene that codes for the S1 or spike protein. And that means that
ALL THE NUMBERS OF “CASES”, “INFECTED”, “SICK”, “Asymptomatic” OR “DEAD DUE TO COVID-19” LACK A SCIENTIFIC BASE AND ALL “POSITIVES” ARE FALSE POSITIVES, something that should be communicated immediately to those aﬀected and those responsible should be held accountable.
We end by adding that even the WHO itself does not really believe in these tests. Just read the document published last September 11 as a laboratory guide for SARS-CoV-2 entitled Diagnostic tests for SARS-CoV-2 – it is available at https://apps.who.int/iris/rest/bitstreams/1302661/ retrieve – and it literally says on page 5: “Whenever possible, suspected active infection should be tested with a nucleic acid amplification test (NAAT) such as RT-PCR. NAAT tests should target the SARS-CoV-2 genome but since there is no known global circulation of SARS-CoV-1 a Sarbecovirus sequence (presumed to include at least five human and animal coronaviruses including SARS-CoV-1 and SARS-Cov-2) is also a reasonable target”. That is, WHO agrees to use non-specific sequences to detect SARS-CoV-2.
That is not all because the manual later states, “An optimal diagnosis consists of a NAAT test with at least two genome-independent targets of the SARS-CoV-2; however, in areas where transmission is widespread, a simple single-target algorithm can be used.”
The WHO manual states, “One or more negative results do not necessarily rule out SARS-CoV-2 infection. There are a number of factors that can produce a negative result in an infected individual including poor quality of the sample, late collection of the sample, inadequate handling, or technical reasons inherent in the test, such as mutation of the virus or inhibition of PCR.”
What are the judges waiting for to act on their own initiative?
Jesus Garcia Blanca
Note: the author publicly thanks Juan Pedro Aparicio Alcaraz for his patient and meticulous collaborative work in the search for scientific articles and for his tedious work with the BLAST.
THIS REPORT APPEARS IN (https://www.dsalud.com/revistas/numero-242-noviembre-2020/)
Share now!
Author: Thanks for being a reader of this site. Your contributions make this all possible. You can send support to: Kyle Hunt, PO Box 1052, Sorrento FL 32776. Bitcoin address: 1AfppjYZddJzc2C15PXKMsnyBPjPJQezwA . CashApp: Thanks for being a reader of this site. Your contributions make this all possible. You can send support to: Kyle Hunt, PO Box 1052, Sorrento FL 32776. Bitcoin address: 1AfppjYZddJzc2C15PXKMsnyBPjPJQezwA . CashApp: https://cash.app/$thekylehunt