In silico prediction of interaction between Nipah virus attachment glycoprotein and host cell receptors Ephrin-B2 and Ephrin-B3 in domestic and peridomestic mammals

被引:0
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作者
Hoque, Ananya Ferdous [1 ]
Rahman, Md. Mahfuzur [1 ,5 ]
Lamia, Ayeasha Siddika [1 ]
Islam, Ariful [2 ]
Klena, John D. [3 ]
Satter, Syed Moinuddin [1 ]
Epstein, Jonathan H. [2 ]
Montgomery, Joel M. [3 ]
Hossain, Mohammad Enayet [1 ]
Shirin, Tahmina [4 ]
Jahid, Iqbal Kabir [5 ]
Rahman, Mohammed Ziaur [1 ,6 ]
机构
[1] Icddr b, Infect Dis Div IDD, 68 Shaheed Tajuddin Ahmed Sarani, Dhaka 1212, Bangladesh
[2] Ecohlth Alliance, 520 8th Ave Ste 1200, New York, NY 10018 USA
[3] Ctr Dis Control & Prevent, Viral Special Pathogens Branch, 1600 Clifton Rd NE, Atlanta, GA 30333 USA
[4] Inst Epidemiol Dis Control & Res IEDCR, Dhaka 1212, Bangladesh
[5] Jashore Univ Sci & Technol, Dept Microbiol, Jashore 7408, Bangladesh
[6] Icddr b, Infect Dis Div, One Hlth Lab, 68 Shaheed Tajuddin Ahmed Sarani, Dhaka 1212, Bangladesh
关键词
Molecular docking; Protein-protein interaction; Nipah virus; Glycoprotein; Ephrin; CRYSTAL-STRUCTURE; WEB SERVER; PROTEIN; TRANSMISSION; INFECTION; PATHOGENESIS; RECOGNITION; MALAYSIA; MODEL;
D O I
10.1016/j.meegid.2023.105516
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Nipah virus (NiV) is a lethal bat-borne zoonotic virus that causes mild to acute respiratory distress and neurological manifestations in humans with a high mortality rate. NiV transmission to humans occurs via consumption of bat-contaminated fruit and date palm sap (DPS), or through direct contact with infected individuals and livestock. Since NiV outbreaks were first reported in pigs from Malaysia and Singapore, non-neutralizing antibodies against NiV attachment Glycoprotein (G) have also been detected in a few domestic mammals. NiV infection is initiated after NiV G binds to the host cell receptors Ephrin-B2 and Ephrin-B3. In this study, we assessed the degree of NiV host tropism in domestic and peridomestic mammals commonly found in Bangladesh that may be crucial in the transmission of NiV by serving as intermediate hosts. We carried out a protein-protein docking analysis of NiV G complexes (n = 52) with Ephrin-B2 and B3 of 13 domestic and peridomestic species using bioinformatics tools. Protein models were generated by homology modelling and the structures were validated for model quality. The different protein-protein complexes in this study were stable, and their binding affinity (Delta G) scores ranged between-8.0 to-19.1 kcal/mol. NiV Bangladesh (NiV-B) strain displayed stronger binding to Ephrin receptors, especially with Ephrin-B3 than the NiV Malaysia (NiV-M) strain, correlating with the observed higher pathogenicity of NiV-B strains. From the docking result, we found that Ephrin receptors of domestic rat (R. norvegicus) had a higher binding affinity for NiV G, suggesting greater susceptibility to NiV infections compared to other study species. Investigations for NiV exposure to domestic/peridomestic animals will help us knowing more the possible role of rats and other animals as intermediate hosts of NiV and would improve future NiV outbreak control and prevention in humans and domestic animals.
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