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Human Species D Adenoviruses Isolated from Diarrheal Feces Show Low Infection Rates in Primary Nasal Epithelial Cells

Bibliographic Data

ID15719685
AuthorsMalik Aydin (0000-0002-1340-9687, Helios Universitätsklinikum Wuppertal, corresponding author), Sebastian Schellhorn (0000-0002-2786-7734, Witten/Herdecke University), Stefan Wirth (0000-0003-4576-3987, Witten/Herdecke University), Wenli Zhang (0000-0001-9077-4189, Witten/Herdecke University), Anja Ehrhardt (0000-0002-6639-4888, Witten/Herdecke University)
Year2021
Volume8
Issue7
Pages563-563
Publication date2021-06-30
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children8070563
PMID34208817
OpenAlexW3174928519
LanguageEN
References cited57

The importance of adenovirus (Ad) research is significantly increasing with respect to virotherapy for vaccine development, tumor, and gene therapy. Due to the different species and subtypes of this virus, the characterization of the biological significance of especially rare Ad is necessary. Previously, rare Ad types 70, 73, and 74 were originally isolated from fecal samples of immunocompromised patients and they represent recombinants of other Ad types. Here we investigated transduction experiments of these reporter gene tagged Ad types in primary cells exemplified by subject-derived primary nasal epithelial cells (NAEPCs). To analyze the transduction rates, we performed flow cytometry, quantitative polymerase chain reaction (PCR), and cytokine analyses 25 h post-infection. We found that, in contrast to Ad type 5 (as a positive control), the transduction rates of NAEPCs with Ad types 70, 73, and 74 were interestingly low. The major Ad receptor (coxsackievirus-adenovirus receptor and CD46) expression levels showed no significant change after infection with Ad types 70, 73 and 74. Moreover, Interleukin 6 (IL-6) was not released after in vitro Ad transduction. Due to the high risk of developing life-threatening complications in immunocompromised patients by these human species D Ads, even more attention needs to be investigated into the development of diagnostic and therapeutic concepts to prevent and treat those opportunistic infections in susceptible patients

Biology · Coxsackievirus · Cytokine · Enterovirus · Flow cytometry · Gene · Gene expression · Oncolytic virus · Receptor · Reporter gene · Signal transduction · Transduction (biophysics · Virotherapy · Virus · CAR-T cell therapy research · Viral gastroenteritis research and epidemiology · Virus-based gene therapy research · Cell Biology · Genetics · Immunology · Virology

Highly citedNo

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