A Comparative Experimental and Computational Study on the Nature of the Pangolin-CoV and COVID-19 Omicron

The relationship between pangolin-CoV and SARS-CoV-2 has been a subject of debate. Further evidence of a special relationship between the two viruses can be found by the fact that all known COVID-19 viruses have an abnormally hard outer shell (low M disorder, i.e., low content of intrinsically disordered residues in the membrane (M) protein) that so far has been found in CoVs associated with burrowing animals, such as rabbits and pangolins, in which transmission involves virus remaining in buried feces for a long time. While a hard outer shell is necessary for viral survival, a harder inner shell could also help. For this reason, the N disorder range of pangolin-CoVs, not bat-CoVs, more closely matches that of SARS-CoV-2, especially when Omicron is included. The low N disorder (i.e., low content of intrinsically disordered residues in the nucleocapsid (N) protein), first observed in pangolin-CoV-2017 and later in Omicron, is associated with attenuation according to the Shell-Disorder Model. Our experimental study revealed that pangolin-CoV-2017 and SARS-CoV-2 Omicron (XBB.1.16 subvariant) show similar attenuations with respect to viral growth and plaque formation. Subtle differences have been observed that are consistent with disorder-centric computational analysis.

[1]  R. Baric,et al.  Host range, transmissibility and antigenicity of a pangolin coronavirus , 2023, Nature Microbiology.

[2]  W. Chen,et al.  Omicron breakthrough infections in wild‐type SARS‐CoV‐2 vaccinees elicit high levels of neutralizing antibodies against pangolin coronavirus GX_P2V , 2023, Journal of medical virology.

[3]  F. Oriente,et al.  SARS-CoV-2 Affects Both Humans and Animals: What Is the Potential Transmission Risk? A Literature Review , 2023, Microorganisms.

[4]  Y. Tong,et al.  Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3'-UTR , 2022, Emerging microbes & infections.

[5]  James A. Foster,et al.  A Study on the Nature of SARS-CoV-2 Using the Shell Disorder Models: Reproducibility, Evolution, Spread, and Attenuation , 2022, Biomolecules.

[6]  M. Suchard,et al.  The Huanan Seafood Wholesale Market in Wuhan was the early epicenter of the COVID-19 pandemic , 2022, Science.

[7]  Kristian G. Andersen,et al.  The molecular epidemiology of multiple zoonotic origins of SARS-CoV-2 , 2022, Science.

[8]  Y. Tong,et al.  SARS-CoV-2-related pangolin coronavirus exhibits similar infection characteristics to SARS-CoV-2 and direct contact transmissibility in hamsters , 2022, iScience.

[9]  James A. Foster,et al.  Shell Disorder Models Detect That Omicron Has Harder Shells with Attenuation but Is Not a Descendant of the Wuhan-Hu-1 SARS-CoV-2 , 2022, Biomolecules.

[10]  N. Long,et al.  Evidence of SARS-CoV-2 Related Coronaviruses Circulating in Sunda pangolins (Manis javanica) Confiscated From the Illegal Wildlife Trade in Viet Nam , 2022, Frontiers in Public Health.

[11]  M. Nilges,et al.  Bat coronaviruses related to SARS-CoV-2 and infectious for human cells , 2022, Nature.

[12]  L. Poon,et al.  SARS-CoV-2 Omicron variant replication in human bronchus and lung ex vivo , 2022, Nature.

[13]  A. Sigal Milder disease with Omicron: is it the virus or the pre-existing immunity? , 2022, Nature Reviews Immunology.

[14]  J. Bhiman,et al.  Early assessment of the clinical severity of the SARS-CoV-2 omicron variant in South Africa: a data linkage study , 2022, The Lancet.

[15]  K. Kupferschmidt Where did ‘weird’ Omicron come from? , 2021, Science.

[16]  P. Rheeder,et al.  Decreased severity of disease during the first global omicron variant covid-19 outbreak in a large hospital in tshwane, south africa , 2021, International Journal of Infectious Diseases.

[17]  Wenfeng Qian,et al.  Evidence for a mouse origin of the SARS-CoV-2 Omicron variant , 2021, bioRxiv.

[18]  Bum-Tae Kim,et al.  Comparison of Plaque Size, Thermal Stability, and Replication Rate among SARS-CoV-2 Variants of Concern , 2021, bioRxiv.

[19]  S. Lal,et al.  SARS coronavirus outbreaks past and present—a comparative analysis of SARS-CoV-2 and its predecessors , 2021, Virus Genes.

[20]  W. Müller,et al.  Morphogenetic (Mucin Expression) as Well as Potential Anti-Corona Viral Activity of the Marine Secondary Metabolite Polyphosphate on A549 Cells , 2020, Marine drugs.

[21]  Kai Zhao,et al.  Addendum: A pneumonia outbreak associated with a new coronavirus of probable bat origin , 2020, Nature.

[22]  T. Drew,et al.  The effect of temperature on persistence of SARS-CoV-2 on common surfaces , 2020, Virology journal.

[23]  Zhènglì Shí,et al.  Characteristics of SARS-CoV-2 and COVID-19 , 2020, Nature Reviews Microbiology.

[24]  James A. Foster,et al.  Shell Disorder Analysis Suggests That Pangolins Offered a Window for a Silent Spread of an Attenuated SARS-CoV-2 Precursor among Humans , 2020, Journal of proteome research.

[25]  Robin C. Whytock,et al.  Pangolins and bats living together in underground burrows in Lopé National Park, Gabon , 2020, African journal of ecology.

[26]  James A. Foster,et al.  A Novel Strategy for the Development of Vaccines for SARS-CoV-2 (COVID-19) and Other Viruses Using AI and Viral Shell Disorder , 2020, Journal of proteome research.

[27]  Ziding Zhang,et al.  Isolation of SARS-CoV-2-related coronavirus from Malayan pangolins , 2020, Nature.

[28]  Natacha S. Ogando,et al.  SARS-coronavirus-2 replication in Vero E6 cells: replication kinetics, rapid adaptation and cytopathology , 2020, bioRxiv.

[29]  P. Vollmar,et al.  Virological assessment of hospitalized patients with COVID-2019 , 2020, Nature.

[30]  James A. Foster,et al.  Shell disorder analysis predicts greater resilience of the SARS-CoV-2 (COVID-19) outside the body and in body fluids , 2020, Microbial Pathogenesis.

[31]  D. Rajgor,et al.  The many estimates of the COVID-19 case fatality rate , 2020, The Lancet Infectious Diseases.

[32]  Jia-Fu Jiang,et al.  Identifying SARS-CoV-2-related coronaviruses in Malayan pangolins , 2020, Nature.

[33]  Tao Zhang,et al.  Probable Pangolin Origin of SARS-CoV-2 Associated with the COVID-19 Outbreak , 2020, Current Biology.

[34]  Y. Tong,et al.  Repurposing of clinically approved drugs for treatment of coronavirus disease 2019 in a 2019-novel coronavirus-related coronavirus model , 2020, Chinese medical journal.

[35]  B. Foley,et al.  Evolutionary history, potential intermediate animal host, and cross‐species analyses of SARS‐CoV‐2 , 2020, Journal of medical virology.

[36]  Gerard Kian-Meng Goh,et al.  Nipah shell disorder, modes of infection, and virulence , 2020, Microbial Pathogenesis.

[37]  M. Gismondi,et al.  ViralPlaque: a Fiji macro for automated assessment of viral plaque statistics , 2019, PeerJ.

[38]  Lukasz Kurgan,et al.  Sequence Similarity Searching , 2018, Current protocols in protein science.

[39]  S. Gianni,et al.  How order and disorder within paramyxoviral nucleoproteins and phosphoproteins orchestrate the molecular interplay of transcription and replication , 2017, Cellular and Molecular Life Sciences.

[40]  C. Broder,et al.  Pathogenic Differences between Nipah Virus Bangladesh and Malaysia Strains in Primates: Implications for Antibody Therapy , 2016, Scientific Reports.

[41]  A. Dunker,et al.  Correlating Flavivirus virulence and levels of intrinsic disorder in shell proteins: protective roles vs. immune evasion. , 2016, Molecular bioSystems.

[42]  V. Uversky,et al.  Detection of links between Ebola nucleocapsid and virulence using disorder analysis. , 2015, Molecular bioSystems.

[43]  Fabian Sievers,et al.  Clustal Omega , 2014, Current protocols in bioinformatics.

[44]  B. Fielding,et al.  The Coronavirus Nucleocapsid Is a Multifunctional Protein , 2014, Viruses.

[45]  A. Dunker,et al.  Understanding Viral Transmission Behavior via Protein Intrinsic Disorder Prediction: Coronaviruses , 2012, Journal of pathogens.

[46]  Sonia Longhi,et al.  Intrinsic disorder in measles virus nucleocapsids , 2011, Proceedings of the National Academy of Sciences.

[47]  D. Weissman,et al.  Antiviral Activities in Human Saliva , 2011, Advances in dental research.

[48]  J. Fahy,et al.  Airway mucus function and dysfunction. , 2010, The New England journal of medicine.

[49]  A Keith Dunker,et al.  A comparative analysis of viral matrix proteins using disorder predictors , 2008, Virology Journal.

[50]  M. Luo,et al.  Structure of the Vesicular Stomatitis Virus Nucleoprotein-RNA Complex , 2006, Science.

[51]  Sonia Longhi,et al.  Structural disorder and modular organization in Paramyxovirinae N and P. , 2003, The Journal of general virology.

[52]  Julie D Thompson,et al.  Multiple Sequence Alignment Using ClustalW and ClustalX , 2003, Current protocols in bioinformatics.

[53]  P. Tompa Intrinsically unstructured proteins. , 2002, Trends in biochemical sciences.

[54]  T. Ganz Antimicrobial polypeptides in host defense of the respiratory tract. , 2002, The Journal of clinical investigation.

[55]  L. C. Drickamer,et al.  Burrows and Burrow-Cleaning Behavior of House Mice (Mus musculus domesticus) , 2001 .

[56]  Posada How does recombination affect phylogeny estimation? , 2000, Trends in ecology & evolution.

[57]  H. Dyson,et al.  Intrinsically unstructured proteins: re-assessing the protein structure-function paradigm. , 1999, Journal of molecular biology.

[58]  T. Ganz,et al.  Innate Antimicrobial Activity of Nasal Secretions , 1999, Infection and Immunity.

[59]  I. Mandel The Functions of Saliva , 1987 .

[60]  T. Nicholas,et al.  ALVEOLAR TYPE I AND TYPE II CELLS , 1984 .

[61]  S. D. Black,et al.  Corrected: The Rise of SARS-CoV-2 (COVID-19) Omicron Subvariant Pathogenicity , 2023 .

[62]  S. Longhi,et al.  Structural disorder within paramyxovirus nucleoproteins and phosphoproteins. , 2012, Molecular bioSystems.

[63]  Obradovic,et al.  Predicting Binding Regions within Disordered Proteins. , 1999, Genome informatics. Workshop on Genome Informatics.