Pandemics

The Lord: True to His word – McKana

The Lord: True to His word

May 19, 2020
McKana
Psalm 12:6 (KJV)

The words of the Lord are pure words: as silver tried in a furnace of earth, purified seven times.

Since we are not out of the woods, a little light about the current pandemic and its deadly potential. The Lord told us through many witnesses, including the writer, that the corona virus is Genetically engineered. We trust the Lord and here, the evidence of their work is presented in short. It is our job to revel the truth.

I have done a lot of Genetic engineering work through basic molecular Biology techniques for therapeutic applications. This is the kind of work I have been doing for over 25 years years. Cloning and expressing gents for therapeutic application. Slicing DNA(restrictive digestion), fusing(ligation), transforming(putting the cloned DNA into cells, bacteria, yeast, cells) and expressing(producing) the protein. Many, many clones:-Hemoglobin for blood substitute, Antibodies, small and big proteins and fusion proteins etc. It is molecular Biology basics. Even though this engineering work sounds a much sophisticated science, it is basic molecular biology techniques, easy to understand and basic science to do.

They used our money, NIH grant, they used our technique-Genetic engeneering, they used our reagents and they used out experimental tools, the enzymes, the human lung cells, the mice and material to engineer the Corona virus.

No one needs advance knowledge of molecular Biology and Genetic Engendering technique to understand what they have done in the lab (You will find out when you read the published scientific paper at the end)

Leaving aside the laboratory jargon/terminologies, what they have done is:-

  1. 1.Change the RNA of two different virus(SARS and Corona) to DNA(Reverse transcription)- RNA to DNA.
  2. 2.Fuse the two DNA through ligation (The back bone of SARS virus and the spike of Corona virus)
  3. 3.Change the fused DNA to RNA(DNA dependent RNA polymerization).DNA back to RNA.
  4. Introduce the cloned viral RNA into cells and propagate the virus.
  5. Harvest the cloned, genetically engineered chimeric/ hybrid virus
  6. Infect human lung epithelial cells as well as infect mice and produce the disease.
  7. Tried to produce Immunotherapy and vaccine which they didn’t fully succeed

In short they cloned a virulent virus strain and made it more infectious (SARS-COV+Spike protein of wild Bat corona virus). The cloning of spike protein from wild Bat corona virus is the most important engineering work they have done which made it more infectious to human lung and mouse lung cells. The spike protien is the surface protein of the corona virus which helps the virus gain entry to cells of the lung and other organs.

The scientific work they have done is published in Nature in April of 2016 for all to see with the intention of creating an epidemic in the lab scale. They got not only epidemic but a pandemic.

After cloning the hybrid virus, the progress they made after 2016 matters much.

The sad part of the story is, the US government stoped the funding for the research when they try to experimental infect primates (monkeys apes etc). They knew it is much close to human, that is why they stopped the fund but number one, they have done the experiment in human lung cell and number two, their experiment suggests the bat corona virus can infect humans, no need to go further. In the meantime they cloned, engeneered a deadly virus. It was very easy for the virus to jump from the mice to human in their own lab, intentionally or not, it did.

Evidently, It is worth mentioning that the location of their virology laboratory they were experimenting with corona virus is few miles, less than 50 miles, from the market they say the pandemic originated.

The Lord told us this pandemic strain is cloned, genetically engineered. True to the words of the Lord, their work tells the same story.

They are not going to come out and tell the world they did this and created pandemic. The laboratory evidence has vanished but the virus is in the population. Future, if there is any future, sequence studies the virus will revel the identity or difference of their lab strain and the virus in the public. Already, mutants of the current pandemic have stated appearing everywhere. One or more can become deadly or the same from the work of the evil one through wicked hands.

As to me, from the words of the Lord and from all the scientific evidence and circumstantial evidence, I am convinced that, this pandemic is the product of cloning through Genetic Engineering in their lab in the place where the pandemic originated. With this potential, they can come up with a variety of deadly infections viruses. The know how is there. They have the potential and the know how to clone and create a deadly epidemic/pandemic..

Here is the article-The first few pages are enough to see what they have been messing up with. https://www.nature.com/articles/nm.3985

Trust The Lord In His word!

The Lord-True to His words May 19, 2020

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9 Comments

  1. MIVAS

    http://www.johnleary.com/index.php/?cat=3&order=DESC
    May 9, 2020, Jesus said: “My people, it is definitely unusual to see snow showers in the middle of May as you are setting all kinds of records for cold at this time of year. As you look at this polar vortex over the Northeast, you can contrast this with unusual heat in California. Such drastic changes in temperature can be created by the HAARP machine in changing the jet stream currents that bring your weather. This machine can be controlled by the deep state people. These people are the same evil people who gave China the money and know how to produce this current corona virus pandemic. Then the Chinese purposely sent infected people to all corners of the earth to spread this virus. It is the plan of the devil and the elite to try and reduce the earth’s population using the spread of this evil virus, even spreading it in your chemtrails. An even deadlier corona virus will be spread in the fall with the intention to bring about a martial law that would give the deep state an opportunity to kill more people and give the evil ones more dictatorial power over your people. There is also a plan to use mandatory vaccines to weaken people’s immune systems and even kill people with the new virus. So do not take any vaccines for any reason. I will bring My faithful to My refuges when your lives are threatened. You could also see My Warning and a call to come to My refuges in the fall so My faithful are not killed. The martial law will give your leaders an opportunity for total control over your people so they can give you over to the Antichrist to start the Great Tribulation. Be prepared to come to My refuges when I call My faithful.”

  2. David Carmack

    Brilliant synopsis. I’m a doctor and surgeon and my research claim to the EXACT same conclusions which can be found here for those interested. https://youtu.be/D2clDNMWjjs
    Thx you

  3. Daniel Noah

    To All: Dr. Luc Montagnier, the French Virologist, who was awarded the Nobel Prize in medicine for discovery of HIV, in 1983, stated that 2019n-CoV was man made in a lab. It has been speculated that 2019 n-CoV is a variant of Coronavirus derived from an animal source which got transmitted to humans. Considering the change of specificity for host, we decided to study the sequences of spike glycoprotein(S protein) of the virus. S proteins are surface proteins that help the virus in host recognition and attachment. Thus, a change in these proteins can be reflected as a change of host specificity of the virus. To know the alterations in S protein gene of 2019-nCoV with respect to all other viruses. A mutiple sequence alignment between the S protein amino acid sequence of 2019-nCoV, Bat-SARS-like, SARS-GZ02 and MERS, revealed that S protein has evolved with closest significant diversity from the SARS-GZ02. Since the S protein of 2019-nCoV shares closest ancestry with SARS GZ02, the sequence coding for spike proteins of these two viruses were compared using multiAlin software, We found four new insertions in the protein of 2019-nCoV-“GTNGTKR” (IS1, “HKNNKS” (IS2), “GDSSSG” (IS3) and “QTNSPRRA” (IS4). To our surprise, these sequence insertions were not only absent in S protein of SARS but were also not observed in any other member of the Coronaviridae family. This is startling as it is quite unlikely for a virus to have acquired such a unique insertions naturally in a short duration of time. The insertions were observed to be present in all genomic sequences of 2019-nCoV virus available from the recent clinical isolates. To know the source of these insertions in 2019-nCoV a local alignment was done with BLASTp using these insertions as query with all virus genome. Unexpectedly, all the insertions got aligned with Human immunodeficiency Virus-1 (HIV-1). Further analysis revealed that aligned sequences of HIV-1 with 2019-nCov were derived from surface glycoprotein gp120 (amino acid sequence positions: 404-409 , 462-467, 136-150) and fromGag protein (336-384 amino acid) Gag protein of HIV is involved ..To get structural insights and to understand the role of these insertions in 2019-nCoV glcoprotein, we modeled it’s structure based on available structure of SARS spike glycoprotein (PDP: 6ACD.1.A) The comparison of the modelled structure reveals that although inserts1,2 and 3 are at non-contiguous locations in the protein primary sequence, they fold to constitute the part of the glycoprotein binding sight that recognizes the host receptor. The insert 1 corresponds to the NTD (N-terminal domain) and the inserts 2 and 3 correspond theCTD(C terminal domain)of the S1 subunit in the 2019-nCoV spike glycoprotein. The insert 4 ia at the junction of theSD1(sub domain) and SD2(sub domain 2) of the S1 subunit. We speculate, that these insertions provide additional flexibility to the glycoprotein binding site by forming a hydrophillic loop in the protein structure that ma facillitate or enhance virus host interactions. Although, the 4 inserts represent discontigous short stretches of amino acids in spike glycoprotein of 2019-nCoV, the fact that all three of them share amino acid identity or similarity with HIV-1 gp120 and HIV-Gag(among all annotated virus proteins) suggests that this is not a random fortuitous finding. In other words, one may sporadically expect a fortuitous match for a stretch of 6-12 contiguous amino acid residues in an unrelated protein. However, it is unlikely that all 4 inserts in the 2019-nCoV spike glycoprotein fortuituously match with 2 key structural proteins of an unrelated virus(HIV-1). The amino acid residues of inserts 1,2 and 3 of 2019-nCoV spike glycoprotein that mapped to HIV-1 were a part of the V4, V5 and VI domains respectively ingp120. Since the 2019-nCoV inserts mapped to variable regions of HIV-1, they were not ubiquitous in HIV-1gp120, but were limited to selected sequences of HIV-1, primarily from Asia and Africa. TheHIV-1 Gag protein enabls interaction of virus with negatively charged host surface and a high positive charge on the Gag protein is a key feature fr the host-virus interaction. On analyzing the pI values for each of the 4 inserts in 2019-nCoV and the corresponding stretches of amino acid residues from HIV-1 proteins we found that: the pI values were very similar for each pair analzed. And most of these pI values were 10=2. Of note, despite gaps in inserts 3 and 4 the pI values werecomparabl;e. This uniformity in the pI values for all 4 inserts, merits further investigation. None of these 4 inserts are present in any other coronavirus This 2019-nCoV has been further engineered…the mistake of 2018-nCoV was that it did not kill the estimated number of people,for the people, to demand/accept a solution/vaccine. This is why they fudged the numbers…the death’s are about 25% top heavy for their needed projections. ‘They’ need some real kill numbers for their agenda to go forward.There is too much resistance at the moment, which is why an enhanced variant will be sprayed on people, to up the kill numbers , sufficient to vaccine inclusion this fall. Daniel

  4. Daniel Noah

    To All: Dr. Luc Montagnier, the French Virologist, who was awarded the Nobel Prize in medicine for discovery of HIV, in 1983, stated that 2019n-CoV was man made in a lab. It has been speculated that 2019 n-CoV is a variant of Coronavirus derived from an animal source which got transmitted to humans. Considering the change of specificity for host, we decided to study the sequences of spike glycoprotein(S protein) of the virus. S proteins are surface proteins that help the virus in host recognition and attachment. Thus, a change in these proteins can be reflected as a change of host specificity of the virus. To know the alterations in S protein gene of 2019-nCoV with respect to all other viruses. A mutiple sequence alignment between the S protein amino acid sequence of 2019-nCoV, Bat-SARS-like, SARS-GZ02 and MERS, revealed that S protein has evolved with closest significant diversity from the SARS-GZ02. Since the S protein of 2019-nCoV shares closest ancestry with SARS GZ02, the sequence coding for spike proteins of these two viruses were compared using multiAlin software, We found four new insertions in the protein of 2019-nCoV-“GTNGTKR” (IS1, “HKNNKS” (IS2), “GDSSSG” (IS3) and “QTNSPRRA” (IS4). To our surprise, these sequence insertions were not only absent in S protein of SARS but were also not observed in any other member of the Coronaviridae family. This is startling as it is quite unlikely for a virus to have acquired such a unique insertions naturally in a short duration of time. The insertions were observed to be present in all genomic sequences of 2019-nCoV virus available from the recent clinical isolates. To know the source of these insertions in 2019-nCoV a local alignment was done with BLASTp using these insertions as query with all virus genome. Unexpectedly, all the insertions got aligned with Human immunodeficiency Virus-1 (HIV-1). Further analysis revealed that aligned sequences of HIV-1 with 2019-nCov were derived from surface glycoprotein gp120 (amino acid sequence positions: 404-409 , 462-467, 136-150) and fromGag protein (336-384 amino acid) Gag protein of HIV is involved ..To get structural insights and to understand the role of these insertions in 2019-nCoV glcoprotein, we modeled it’s structure based on available structure of SARS spike glycoprotein (PDP: 6ACD.1.A) The comparison of the modelled structure reveals that although inserts1,2 and 3 are at non-contiguous locations in the protein primary sequence, they fold to constitute the part of the glycoprotein binding sight that recognizes the host receptor. The insert 1 corresponds to the NTD (N-terminal domain) and the inserts 2 and 3 correspond theCTD(C terminal domain)of the S1 subunit in the 2019-nCoV spike glycoprotein. The insert 4 ia at the junction of theSD1(sub domain) and SD2(sub domain 2) of the S1 subunit. We speculate, that these insertions provide additional flexibility to the glycoprotein binding site by forming a hydrophillic loop in the protein structure that ma facillitate or enhance virus host interactions. Although, the 4 inserts represent discontigous short stretches of amino acids in spike glycoprotein of 2019-nCoV, the fact that all three of them share amino acid identity or similarity with HIV-1 gp120 and HIV-Gag(among all annotated virus proteins) suggests that this is not a random fortuitous finding. In other words, one may sporadically expect a fortuitous match for a stretch of 6-12 contiguous amino acid residues in an unrelated protein. However, it is unlikely that all 4 inserts in the 2019-nCoV spike glycoprotein fortuituously match with 2 key structural proteins of an unrelated virus(HIV-1). The amino acid residues of inserts 1,2 and 3 of 2019-nCoV spike glycoprotein that mapped to HIV-1 were a part of the V4, V5 and VI domains respectively ingp120. Since the 2019-nCoV inserts mapped to variable regions of HIV-1, they were not ubiquitous in HIV-1gp120, but were limited to selected sequences of HIV-1, primarily from Asia and Africa. TheHIV-1 Gag protein enabls interaction of virus with negatively charged host surface and a high positive charge on the Gag protein is a key feature fr the host-virus interaction. On analyzing the pI values for each of the 4 inserts in 2019-nCoV and the corresponding stretches of amino acid residues from HIV-1 proteins we found that: the pI values were very similar for each pair analzed. And most of these pI values were 10=2. Of note, despite gaps in inserts 3 and 4 the pI values werecomparabl;e. This uniformity in the pI values for all 4 inserts, merits further investigation. None of these 4 inserts are present in any other coronavirus This 2019-nCoV has been further engineered…the mistake of 2018-nCoV was that it did not kill the estimated number of people,for the people, to demand/accept a solution/vaccine. This is why they fudged the numbers…the death’s are about 25% top heavy for their needed projections. ‘They’ need some real kill numbers for their agenda to go forward.There is too much resistance at the moment, which is why an enhanced variant will be sprayed on people, to up the kill numbers , sufficient to vaccine inclusion this fall. Daniel

  5. Catherine

    When I read the word of God, it says that plagues/pestilences are coming because of the sin and because we are in the last days. I don’t see anything else. Of course God has his people in this world and the devil has his people but we call the people to repent and we don’t blame other people. Jesus and the apostels never blame people, they blamed the sin.

    https://www.youtube.com/watch?v=UgDQ2lkI07o Conspirancy theories : No, thank you

  6. Mark N

    Catherine…I listened to the YouTube video , Conspiracy theories: No, thank you. I thought it was wonderful, I saved it as a favorite and will come back to it for reassurance. Thank You.

  7. KarenO

    Thank you, Mc Kana, for referring us to an excellent article.
    I was wondering WHY anyone would work SO hard to spread the theory that such mutations of the coronavirus could be achieved in “normal” mutations in animals…especially when we’ve seen mutations don’t create a drastically different organism.
    ***
    The only reason I come up with is: they want to convince you that any vaccines would be “safe.”
    Due to the fact we don’t know a long term effect of the virus – ie. other complications that may arise, we have no guarantee that a current “fix” would have the intended effect, even on a yearly vaccine.
    ***
    From my personal observation, what we are seeing, both in advancement of PPE & protecting essential workers in their workplace are two things.
    1) Concentration of the virus seems to matter (People who’ve been in personal close contact (one carrier close enough to your face to cough into it) in speed of transferrence.
    2) A different length of incubation for DIFFERENT populations.
    ***
    We still have to be careful in the wearing of masks & proximity, simply because we can carry it without being aware of it. It doesn’t mean that the person not wearing a mask won’t get sick, it only means that we did our very best, which is all the Lord asks us to do.
    ***
    We’re called to the truth and to be “shrewd as snakes,” & harmless as doves (Matthew 10:16 paraphrased)

    When we are told that an effective vaccine is 1-2 years away, & within 2 MONTHS, we hear that a vaccine is quickly possible & that they used Rhesus MONKEYS (reading the Nature article Mc Kana referred to will give you an idea as to why they came up with THAT so quickly)
    it is highly suspect.
    ***
    Correct me if I wrong – but, the problem that I see with any vaccine they claim disables the virus is that they don’t have a reassurance that the virus cannot adapt to the vaccines, mutating again in its host.
    Does this vaccine work in disabling the virus mid-disease for everyone? Children showing different symptoms than the adults do? Does it work to keep everyone perpetually safe from that specific virus?
    ***
    It would have to be something that warns the body What type of antibodies to create. (Artificial intelligence)
    ***
    There IS an ulterior motive… reducing the population (which used to be war…abortion… & now this virus that decimates older, poorer, & disabled people).
    Possibly also to convince us, with fear, that you &/or your family are STILL at risk in spite of the vaccine.

    Blessings. Be safe for them as you seek to spread His Good news.

  8. McKana

    Dr David Carmack.
    I listened to your lecture of May 7, 2020(2hrs 38mts). You have covered a lot of very important material and delivered good messages. It is a good timely material to learn from.
    Thank you for the good presentation and the compliment you gave me.

    The Lord through His loyal servants has given us His word, what matters most.
    The Noble prize winner has proven from the sequence.
    The Doctors have confirmed.
    The scientists have ascertained.
    The analysts have given their analysis
    In conclusion, with certainty is Covid 19 is man made.
    Thank you all and God bless you.

  9. Eyes Open

    Thank you for this excellent post and discussion. I have learned much. And I truly believe the point of the vaccine will be primarily for identification. Whether it kills or saves lives I don’t think is the primary goal ….harsh to say but operation warp speed and the Dod and hhs contract with apiject speaks volumes. They are prepping to “mark” humanity. ID2020 will work in conjunction with the rfid gps tracking system and provide quantum dot certification marks to let authorities know you have been properly “vaccinated”. Or not. As for me….NOT.

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