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Conversations with Raven S2EP5
Another "outbreak* table top exercise set in July 2025???
The last one was SARS outbreak and we got CDC-NIH funded HIV SARS Cov-2 from Ralph Baric and Zheelee (the bat lady) made here in North Carolina and somehow transported to CDC BSL4 lab in Wuhan. The glycoproteins are immediate evidence of human tampering... explanation at bottom of this description!
NIPAH exercise link:
https://publichealthpolicyjournal.com/federal-report-simulates-july-4th-2025-bioterror-attack-as-the-fda-goes-rogue/
Mahe Ohna ✌️ Favour ALL
[email protected]
Ravens's Music Videos Playlist:
https://youtube.com/playlist?list=PLoFIKheyukLDwQhUdgNrTCgnwHw7LC8gc&feature=shared
Raven's Music on YT (all five LPs vailable on almost all music streaming platforms):
https://youtube.com/channel/UCC0bhTADohUTFJg9rqkjF3A?feature=shared
Raven's Laugh Podcasts
https://www.spreaker.com/podcast/laugh-podcasts--5686542
Buy me a coffee to keep my technology and service active?
https://ko-fi.com/ravenkeefer
From India NIH:
The NiV genome codes for six structural proteins, namely, fusion protein (F), attachment glycoprotein (G), matrix protein (M), phosphoprotein (P), nucleoprotein (N), and the large RNA-dependent RNA polymerase protein (L). Further, the P gene codes for three non-structural proteins that include proteins C, W, and V (Fig. 5) (Sun et al. 2018). The N, P, and L proteins, in conjunction with the viral RNA, form the virus ribonucleoprotein (vRNP) complex, that regulates transcription of the viral genome and viral replication (Ranadheera et al. 2018) The NiV F protein is heavily glycosylated and mediates viral entry and integration into the host membrane (Aguilar et al. 2006). Studies have confirmed that altering the glycosylation pattern in F protein diminishes its fusion efficacy. At the same time, different investigations have reported that the N-glycans on NiV G glycoprotein act as a decoy and protect the viral envelope from antibody-mediated neutralization. (emphasis hardened G glycoprotein acting as decoy preventing antibiotic and anti-body from mediation, dead giveaway and perhaps, the attempt to blame bats again? as proof of gain of function. Locations also happening to be where CDC or contractor labs are working on the specific pathogens? MERS isn't any different.)
The last one was SARS outbreak and we got CDC-NIH funded HIV SARS Cov-2 from Ralph Baric and Zheelee (the bat lady) made here in North Carolina and somehow transported to CDC BSL4 lab in Wuhan. The glycoproteins are immediate evidence of human tampering... explanation at bottom of this description!
NIPAH exercise link:
https://publichealthpolicyjournal.com/federal-report-simulates-july-4th-2025-bioterror-attack-as-the-fda-goes-rogue/
Mahe Ohna ✌️ Favour ALL
[email protected]
Ravens's Music Videos Playlist:
https://youtube.com/playlist?list=PLoFIKheyukLDwQhUdgNrTCgnwHw7LC8gc&feature=shared
Raven's Music on YT (all five LPs vailable on almost all music streaming platforms):
https://youtube.com/channel/UCC0bhTADohUTFJg9rqkjF3A?feature=shared
Raven's Laugh Podcasts
https://www.spreaker.com/podcast/laugh-podcasts--5686542
Buy me a coffee to keep my technology and service active?
https://ko-fi.com/ravenkeefer
From India NIH:
The NiV genome codes for six structural proteins, namely, fusion protein (F), attachment glycoprotein (G), matrix protein (M), phosphoprotein (P), nucleoprotein (N), and the large RNA-dependent RNA polymerase protein (L). Further, the P gene codes for three non-structural proteins that include proteins C, W, and V (Fig. 5) (Sun et al. 2018). The N, P, and L proteins, in conjunction with the viral RNA, form the virus ribonucleoprotein (vRNP) complex, that regulates transcription of the viral genome and viral replication (Ranadheera et al. 2018) The NiV F protein is heavily glycosylated and mediates viral entry and integration into the host membrane (Aguilar et al. 2006). Studies have confirmed that altering the glycosylation pattern in F protein diminishes its fusion efficacy. At the same time, different investigations have reported that the N-glycans on NiV G glycoprotein act as a decoy and protect the viral envelope from antibody-mediated neutralization. (emphasis hardened G glycoprotein acting as decoy preventing antibiotic and anti-body from mediation, dead giveaway and perhaps, the attempt to blame bats again? as proof of gain of function. Locations also happening to be where CDC or contractor labs are working on the specific pathogens? MERS isn't any different.)
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By Raven KeeferAnother "outbreak* table top exercise set in July 2025???
The last one was SARS outbreak and we got CDC-NIH funded HIV SARS Cov-2 from Ralph Baric and Zheelee (the bat lady) made here in North Carolina and somehow transported to CDC BSL4 lab in Wuhan. The glycoproteins are immediate evidence of human tampering... explanation at bottom of this description!
NIPAH exercise link:
https://publichealthpolicyjournal.com/federal-report-simulates-july-4th-2025-bioterror-attack-as-the-fda-goes-rogue/
Mahe Ohna ✌️ Favour ALL
[email protected]
Ravens's Music Videos Playlist:
https://youtube.com/playlist?list=PLoFIKheyukLDwQhUdgNrTCgnwHw7LC8gc&feature=shared
Raven's Music on YT (all five LPs vailable on almost all music streaming platforms):
https://youtube.com/channel/UCC0bhTADohUTFJg9rqkjF3A?feature=shared
Raven's Laugh Podcasts
https://www.spreaker.com/podcast/laugh-podcasts--5686542
Buy me a coffee to keep my technology and service active?
https://ko-fi.com/ravenkeefer
From India NIH:
The NiV genome codes for six structural proteins, namely, fusion protein (F), attachment glycoprotein (G), matrix protein (M), phosphoprotein (P), nucleoprotein (N), and the large RNA-dependent RNA polymerase protein (L). Further, the P gene codes for three non-structural proteins that include proteins C, W, and V (Fig. 5) (Sun et al. 2018). The N, P, and L proteins, in conjunction with the viral RNA, form the virus ribonucleoprotein (vRNP) complex, that regulates transcription of the viral genome and viral replication (Ranadheera et al. 2018) The NiV F protein is heavily glycosylated and mediates viral entry and integration into the host membrane (Aguilar et al. 2006). Studies have confirmed that altering the glycosylation pattern in F protein diminishes its fusion efficacy. At the same time, different investigations have reported that the N-glycans on NiV G glycoprotein act as a decoy and protect the viral envelope from antibody-mediated neutralization. (emphasis hardened G glycoprotein acting as decoy preventing antibiotic and anti-body from mediation, dead giveaway and perhaps, the attempt to blame bats again? as proof of gain of function. Locations also happening to be where CDC or contractor labs are working on the specific pathogens? MERS isn't any different.)
The last one was SARS outbreak and we got CDC-NIH funded HIV SARS Cov-2 from Ralph Baric and Zheelee (the bat lady) made here in North Carolina and somehow transported to CDC BSL4 lab in Wuhan. The glycoproteins are immediate evidence of human tampering... explanation at bottom of this description!
NIPAH exercise link:
https://publichealthpolicyjournal.com/federal-report-simulates-july-4th-2025-bioterror-attack-as-the-fda-goes-rogue/
Mahe Ohna ✌️ Favour ALL
[email protected]
Ravens's Music Videos Playlist:
https://youtube.com/playlist?list=PLoFIKheyukLDwQhUdgNrTCgnwHw7LC8gc&feature=shared
Raven's Music on YT (all five LPs vailable on almost all music streaming platforms):
https://youtube.com/channel/UCC0bhTADohUTFJg9rqkjF3A?feature=shared
Raven's Laugh Podcasts
https://www.spreaker.com/podcast/laugh-podcasts--5686542
Buy me a coffee to keep my technology and service active?
https://ko-fi.com/ravenkeefer
From India NIH:
The NiV genome codes for six structural proteins, namely, fusion protein (F), attachment glycoprotein (G), matrix protein (M), phosphoprotein (P), nucleoprotein (N), and the large RNA-dependent RNA polymerase protein (L). Further, the P gene codes for three non-structural proteins that include proteins C, W, and V (Fig. 5) (Sun et al. 2018). The N, P, and L proteins, in conjunction with the viral RNA, form the virus ribonucleoprotein (vRNP) complex, that regulates transcription of the viral genome and viral replication (Ranadheera et al. 2018) The NiV F protein is heavily glycosylated and mediates viral entry and integration into the host membrane (Aguilar et al. 2006). Studies have confirmed that altering the glycosylation pattern in F protein diminishes its fusion efficacy. At the same time, different investigations have reported that the N-glycans on NiV G glycoprotein act as a decoy and protect the viral envelope from antibody-mediated neutralization. (emphasis hardened G glycoprotein acting as decoy preventing antibiotic and anti-body from mediation, dead giveaway and perhaps, the attempt to blame bats again? as proof of gain of function. Locations also happening to be where CDC or contractor labs are working on the specific pathogens? MERS isn't any different.)