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Molecular and biological characterization of influenza A viruses isolated from human fecal samples.
Al Khatib, Hebah A; Coyle, Peter V; Al Maslamani, Muna A; Al Thani, Asmaa A; Pathan, Sameer A; Yassine, Hadi M.
  • Al Khatib HA; Biomedical Research Center, Qatar University, Doha 2713, Qatar. Electronic address: h.alkhatib@qu.edu.qa.
  • Coyle PV; Virology Laboratory, Hamad Medical Corporation, Doha 3050, Qatar. Electronic address: PCoyle@hamad.qa.
  • Al Maslamani MA; Communicable Diseases Center, Hamad Medical Corporation, Doha 3050, Qatar. Electronic address: malmaslamani@hamad.qa.
  • Al Thani AA; Biomedical Research Center, Qatar University, Doha 2713, Qatar; Department of Biomedical Sciences, College of Health Sciences-QU Health, Qatar University, Doha 2713, Qatar. Electronic address: aaja@qu.edu.qa.
  • Pathan SA; Emergency Medicine, Hamad Medical Corporation, Doha 3050, Qatar.
  • Yassine HM; Biomedical Research Center, Qatar University, Doha 2713, Qatar; Department of Biomedical Sciences, College of Health Sciences-QU Health, Qatar University, Doha 2713, Qatar. Electronic address: hyassine@qu.edu.qa.
Infect Genet Evol ; 93: 104972, 2021 09.
Article in English | MEDLINE | ID: covidwho-1274364
ABSTRACT
Human influenza viruses are occasionally detected in the stools of influenza patients.

OBJECTIVES:

Here, we investigated the molecular and biological characteristics of intestinal influenza viruses and their potential role in virus transmission.

METHODS:

Fecal samples were first screened for the presence of influenza viral RNA using RT-qPCR. Positive fecal samples were subjected to cell culture. Isolated viruses were then sequenced using MiSeq platform. Replication kinetics and receptor binding affinity were also evaluated.

RESULTS:

Influenza RNA was detected in stool samples of 41% (36/87) of influenza A positive patients. Among the 36 stool samples subjected to viral isolation, 5 showed virus growth. Sequence analysis of isolated viruses revealed two distinct mutation patterns in fecal viruses. Set I viruses was able to replicate to higher titers in cell culture despite the limited number of mutations (6 mutations) compared to set II viruses (>10 mutations). Functional analysis of both sets revealed the ability to replicate efficiently in differentiated human bronchial cells. Receptor binding testing has also demonstrated their ability to bind α 2,3 and α 2,6 sialic acid receptors.

CONCLUSION:

The ability of fecal influenza viruses to replicate in intestinal cells and human 3D bronchial cells might suggest their possible contribution in virus transmission.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Influenza A virus / Influenza, Human Type of study: Experimental Studies / Observational study Limits: Adolescent / Adult / Aged / Humans / Middle aged / Young adult Country/Region as subject: Asia Language: English Journal: Infect Genet Evol Journal subject: Biology / Communicable Diseases / Genetics Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Influenza A virus / Influenza, Human Type of study: Experimental Studies / Observational study Limits: Adolescent / Adult / Aged / Humans / Middle aged / Young adult Country/Region as subject: Asia Language: English Journal: Infect Genet Evol Journal subject: Biology / Communicable Diseases / Genetics Year: 2021 Document Type: Article