PMID- 34574906 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240403 IS - 2227-9032 (Print) IS - 2227-9032 (Electronic) IS - 2227-9032 (Linking) VI - 9 IP - 9 DP - 2021 Aug 30 TI - SARS-CoV-2: Origin, Intermediate Host and Allergenicity Features and Hypotheses. LID - 10.3390/healthcare9091132 [doi] LID - 1132 AB - The goal of this study is to investigate the probable intermediate hosts and the allergenicity of the notorious virus SARS-CoV-2 to understand how this virus emerged. The phylogenetic analysis of the virus spike proteins indicates that SARS-CoV-2 falls into various small subclades that include a bat coronavirus RaTG13, suggesting bats as a likely natural origin. Refined alignment of the spike protein in NCBI found several fragments that are specific to SARS-CoV-2 and/or SARS-CoV are specific to Rattus norvegicus and/or Mus musculus, suggesting that rodents are the intermediate reservoir of SARS-CoV-2 and SARS-CoV. To evaluate the allergenicity values, the binding affinities of human leukocyte antigen (HLA) class I or II molecules with the spike proteins were calculated, and the results showed that both SARS-CoV-2 and SARS-CoV are predicted to bind to fourteen HLA class I and II molecules with super-high HLA allele-peptide affinities. The infection rate of individuals who have HLA alleles with very high binding affinities who might become infected and develop into refractory patients if there were no medical or non-medical interventions is about 7.36% and 4.78% of Chinese and Americans, respectively. Extremely high temperature and exceptionally low precipitation, the common climate factors between the outbreak sites of COVID-19 in Wuhan in 2019 and SARS in Guangdong in 2002, might have promoted coronavirus evolution into more virulent forms. Our hypothesis suggests that early immunization with an allergenically-engineered virus, in combination with continued surveillance of meteorological factors and viral mutations, may be one of the most powerful prophylactic modalities to fight this virus. FAU - Huang, Yuyi AU - Huang Y AD - The Second Affiliated Hospital, The State Key Laboratory of Respiratory Disease, Guangdong Provincial Key Laboratory of Allergy & Clinical Immunology, Guangzhou Medical University, Guangzhou 510260, China. FAU - Xie, Junmou AU - Xie J AD - The Second Affiliated Hospital, The State Key Laboratory of Respiratory Disease, Guangdong Provincial Key Laboratory of Allergy & Clinical Immunology, Guangzhou Medical University, Guangzhou 510260, China. FAU - Guo, Yuhe AU - Guo Y AD - The Second Affiliated Hospital, The State Key Laboratory of Respiratory Disease, Guangdong Provincial Key Laboratory of Allergy & Clinical Immunology, Guangzhou Medical University, Guangzhou 510260, China. FAU - Sun, Weimin AU - Sun W AD - The Second Affiliated Hospital, The State Key Laboratory of Respiratory Disease, Guangdong Provincial Key Laboratory of Allergy & Clinical Immunology, Guangzhou Medical University, Guangzhou 510260, China. FAU - He, Ying AU - He Y AD - The Second Affiliated Hospital, The State Key Laboratory of Respiratory Disease, Guangdong Provincial Key Laboratory of Allergy & Clinical Immunology, Guangzhou Medical University, Guangzhou 510260, China. FAU - Liu, Kequn AU - Liu K AD - Wuhan Regional Climate Center, Wuhan 430074, China. FAU - Yan, Jie AU - Yan J AD - The Second Affiliated Hospital, The State Key Laboratory of Respiratory Disease, Guangdong Provincial Key Laboratory of Allergy & Clinical Immunology, Guangzhou Medical University, Guangzhou 510260, China. FAU - Tao, Ailin AU - Tao A AUID- ORCID: 0000-0002-0584-921X AD - The Second Affiliated Hospital, The State Key Laboratory of Respiratory Disease, Guangdong Provincial Key Laboratory of Allergy & Clinical Immunology, Guangzhou Medical University, Guangzhou 510260, China. FAU - Zhong, Nanshan AU - Zhong N AD - The State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China. LA - eng PT - Journal Article DEP - 20210830 PL - Switzerland TA - Healthcare (Basel) JT - Healthcare (Basel, Switzerland) JID - 101666525 PMC - PMC8466535 OTO - NOTNLM OT - MHC binding affinity OT - SARS-CoV-2 OT - allergenicity OT - early immunization OT - intermediary reservoir OT - self-limitation OT - spike protein OT - spontaneous mutation COIS- The authors declare no conflict of interest. EDAT- 2021/09/29 06:00 MHDA- 2021/09/29 06:01 PMCR- 2021/08/30 CRDT- 2021/09/28 01:14 PHST- 2020/11/13 00:00 [received] PHST- 2021/08/26 00:00 [revised] PHST- 2021/08/27 00:00 [accepted] PHST- 2021/09/28 01:14 [entrez] PHST- 2021/09/29 06:00 [pubmed] PHST- 2021/09/29 06:01 [medline] PHST- 2021/08/30 00:00 [pmc-release] AID - healthcare9091132 [pii] AID - healthcare-09-01132 [pii] AID - 10.3390/healthcare9091132 [doi] PST - epublish SO - Healthcare (Basel). 2021 Aug 30;9(9):1132. doi: 10.3390/healthcare9091132.