Serveur d'exploration MERS

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Evolutionary relationship analysis of Middle East respiratory syndrome coronavirus 4a and 4b protein coding sequences.

Identifieur interne : 000566 ( PubMed/Checkpoint ); précédent : 000565; suivant : 000567

Evolutionary relationship analysis of Middle East respiratory syndrome coronavirus 4a and 4b protein coding sequences.

Auteurs : Jin Il Kim [Corée du Sud] ; Sehee Park [Corée du Sud] ; Joon-Yong Bae [Corée du Sud] ; Man-Seong Park [Corée du Sud]

Source :

RBID : pubmed:30944524

Descripteurs français

English descriptors

Abstract

The 4a and 4b proteins of the Middle East respiratory syndrome coronavirus (MERS-CoV) have been described for their antagonism on host innate immunity. However, unlike clustering patterns of the complete gene sequences of human and camel MERS-CoVs, the 4a and 4b protein coding regions did not constitute species-specific phylogenetic groups. Moreover, given the estimated evolutionary rates of the complete, 4a, and 4b gene sequences, the 4a and 4b proteins might be less affected by species-specific innate immune pressures. These results suggest that the 4a and 4b proteins of MERS-CoV may function against host innate immunity in a manner independent of host species and/or evolutionary clustering patterns.

DOI: 10.4142/jvs.2019.20.e1
PubMed: 30944524


Affiliations:


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pubmed:30944524

Le document en format XML

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<div type="abstract" xml:lang="en">The 4a and 4b proteins of the Middle East respiratory syndrome coronavirus (MERS-CoV) have been described for their antagonism on host innate immunity. However, unlike clustering patterns of the complete gene sequences of human and camel MERS-CoVs, the 4a and 4b protein coding regions did not constitute species-specific phylogenetic groups. Moreover, given the estimated evolutionary rates of the complete, 4a, and 4b gene sequences, the 4a and 4b proteins might be less affected by species-specific innate immune pressures. These results suggest that the 4a and 4b proteins of MERS-CoV may function against host innate immunity in a manner independent of host species and/or evolutionary clustering patterns.</div>
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