Medical, Genomic, and Evolutionary Aspects of the Peptide Sharing between Pathogens, Primates, and Humans

Darja Kanduc, Yehuda Shoenfeld

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PDF(216 KB)
Global Medical Genetics ›› 2020, Vol. 7 ›› Issue (02) : 64-67. DOI: 10.1055/s-0040-1716334
Original Article
Original Article

Medical, Genomic, and Evolutionary Aspects of the Peptide Sharing between Pathogens, Primates, and Humans

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Abstract

Comparing mammalian proteomes for molecular mimicry with infectious pathogens highlights the highest levels of heptapeptide sharing between pathogens and human, murine, and rat proteomes, while the peptide sharing level is minimal (or absent) with proteomes from nonhuman primates such as gorilla, chimpanzee, and rhesus macaque. From the medical point of view, the data might be useful to clinicians and vaccinologists to develop and evaluate immunomodulatory and immunotherapeutic approaches. As a matter of fact, primates seem to be unreliable animal models for revealing potential autoimmune events in preclinical testing of immunotherapies. In terms of genomics, the scarce or absent peptide sharing between pathogens and primates versus the massive peptide sharing existing between pathogens and humans lets foresee mechanisms of pathogen sequence insertion/deletion/alteration that have differently operated in mammals over evolutionary timescales. Why and how the human genome has been colonized by pathogen sequences and why and how primates escaped such a colonization appears to be the new scientific challenge in our efforts to understand not only the origin of Homo sapiens but also his autoimmune diseasome.

Keywords

peptide sharing / cross-reactivity / autoimmunity / nonhuman primates / preclinical tests

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Darja Kanduc, Yehuda Shoenfeld. Medical, Genomic, and Evolutionary Aspects of the Peptide Sharing between Pathogens, Primates, and Humans. Global Medical Genetics, 2020, 7(02): 64‒67 https://doi.org/10.1055/s-0040-1716334

References

[1]
Tengvall K, Huang J, Hellström C, et al. Molecular mimicry between Anoctamin 2 and Epstein-Barr virus nuclear antigen 1 associates with multiple sclerosis risk. Proc Natl Acad Sci U S A 2019; 116(34): 16955-16960
[2]
Cunningham MW. Molecular mimicry, autoimmunity, and infection: the cross-reactive antigens of Group A Streptococci and their sequelae. Microbiol Spectr 2019; 7(04): 10
[3]
Gonciarz W, Matusiak A, Rudnicka K, et al. Autoantibodies to a specific peptide epitope of human Hsp60 (ATVLA) with homology to Helicobacter pylori HspB in H. pylori-infected patients. APMIS 2019; 127(03): 139-149
[4]
Baranova SV, Dmitrienok PS, Buneva VN, Nevinsky GA. Autoantibodies in HIV-infected patients: cross site-specific hydrolysis of H1 histone and myelin basic protein. Biofactors 2019; 45(02): 211-222
[5]
Kanduc D, Shoenfeld Y. Human papillomavirus epitope mimicry and autoimmunity: the molecular truth of peptide sharing. Pathobiology 2019; 86(5-6): 285-295
[6]
Kanduc D, Shoenfeld Y. From anti-EBV immune responses to the EBV diseasome via cross-reactivity. Global Med Genet 2020
[7]
Kanduc D. From hepatitis C virus immunoproteomics to rheumatology via cross-reactivity in one table. Curr Opin Rheumatol 2019; 31(05): 488-492
[8]
Bonvalet M, Ollila HM, Ambati A, Mignot E. Autoimmunity in narcolepsy. Curr Opin Pulm Med 2017; 23(06): 522-529
[9]
Kanduc D, Shoenfeld Y. On the molecular determinants of the SARS-CoV-2 attack. Clin Immunol 2020; 215: 108426
[10]
Kanduc D, Polito A. From viral infections to autistic neurodevelopmental disorders via cross-reactivity. J Psychiatry Brain Sci 2018; 3: 14
[11]
Polito A, Polimeno R, Kanduc D. Peptide sharing between Parvovirus B19 and DNA methylating/histone modifying enzymes: a potential link to childhood acute lymphoblastic leukemia. Int J Pediatr Child Health 2017; 5: 29-39
[12]
Kanduc D. Epstein-Barr virus, immunodeficiency, and cancer: a potential crossreactivity connection. Intern Med Rev 2018; 4: 1-17
[13]
Wachtman L, Mansfield K.Viral diseases of nonhuman primates. In Abee C, Mansfield K, Tardif S, Morris T, eds. Nonhuman Primates in Biomedical Research. Vol. II: Diseases. Oxford, UK: Academic Press; Elsevier; 2012
[14]
McCracken MK, Gromowski GD, Garver LS, et al. Route of inoculation and mosquito vector exposure modulate dengue virus replication kinetics and immune responses in rhesus macaques. PLoS Negl Trop Dis 2020; 14(04): e0008191
[15]
Bhaumik SK, Kulkarni RR, Weldon WC, et al. Immune priming and long-term persistence of memory B cells after inactivated poliovirus vaccine in macaque models: support for at least 2 doses. Clin Infect Dis 2018; 67(Suppl. 01): S66-S77
[16]
Woolsey C, Jankeel A, Matassov D, et al. Immune correlates of postexposure vaccine protection against Marburg virus. Sci Rep 2020; 10(01): 3071
[17]
Yu J, Tostanoski LH, Peter L, et al. DNA vaccine protection against SARS-CoV-2 in rhesus macaques. Science 2020; 6284
[18]
Jackson LA, Anderson EJ, Rouphael NG, et al; mRNA-1273 Study Group. An mRNA vaccine against SARS-CoV-2 - preliminary report. N Engl J Med 2020; ; NEJMoa2022483. DOI: 10.1056/NEJMoa2022483.
[19]
Available at: https://www.fda.gov/vaccines-blood-biologics/vaccines
[20]
Pieczenik G. Are the universes of antibodies and antigens symmetrical?. Reprod Biomed Online 2003; 6(02): 154-156
[21]
Kanduc D. Homology, similarity, and identity in peptide epitope immunodefinition. J Pept Sci 2012; 18(08): 487-494
[22]
Kanduc D. Pentapeptides as minimal functional units in cell biology and immunology. Curr Protein Pept Sci 2013; 14(02): 111-120
[23]
Chen C, Li Z, Huang H, Suzek BE, Wu CH. UniProt Consortium. A fast Peptide Match service for UniProt Knowledgebase. Bioinformatics 2013; 29(21): 2808-2809
[24]
Clark KB, Onlamoon N, Hsiao HM, Perng GC, Villinger F. Can non-human primates serve as models for investigating dengue disease pathogenesis?. Front Microbiol 2013; 4: 305
[25]
McAuliffe J, Vogel L, Roberts A, et al. Replication of SARS coronavirus administered into the respiratory tract of African Green, rhesus and cynomolgus monkeys. Virology 2004; 330(01): 8-15
[26]
Hogan RJ. Are nonhuman primates good models for SARS?. PLoS Med2006; 3 (09) e411 , author reply e415
[27]
Roberts A, Paddock C, Vogel L, Butler E, Zaki S, Subbarao K. Aged BALB/c mice as a model for increased severity of severe acute respiratory syndrome in elderly humans. J Virol 2005; 79(09): 5833-5838
[28]
Nagata N, Iwata-Yoshikawa N, Taguchi F. Studies of severe acute respiratory syndrome coronavirus pathology in human cases and animal models. Vet Pathol 2010; 47(05): 881-892
[29]
Glazko G, Veeramachaneni V, Nei M, Makałowski W. Eighty percent of proteins are different between humans and chimpanzees. Gene 2005; 346: 215-219
[30]
Koonin EV, Dolja VV, Krupovic M. Origins and evolution of viruses of eukaryotes: the ultimate modularity. Virology2015; 479-480: 2-25
[31]
Kanduc D. The comparative biochemistry of viruses and humans: an evolutionary path towards autoimmunity. Biol Chem 2019; 400(05): 629-638
[32]
Kanduc D, Stufano A, Lucchese G, Kusalik A. Massive peptide sharing between viral and human proteomes. Peptides 2008; 29(10): 1755-1766
[33]
Kanduc D, Shoenfeld Y. Inter-pathogen peptide sharing and the original antigenic sin: solving a paradox. Open Immunol J 2018; 8: 11-27

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