Bacterial Lipopolysaccharide Destabilizes Influenza Viruses

ABSTRACT Depending on the specific viral pathogen, commensal bacteria can promote or reduce the severity of viral infection and disease progression in their hosts. Influenza A virus (IAV) has a broad host range, comprises many subtypes, and utilizes different routes of transmission, including the fe...

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Autores principales: Christopher Bandoro, Jonathan A. Runstadler
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Publicado: American Society for Microbiology 2017
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spelling oai:doaj.org-article:d26f25fab674490e806764d4fb8ccd222021-11-15T15:22:05ZBacterial Lipopolysaccharide Destabilizes Influenza Viruses10.1128/mSphere.00267-172379-5042https://doaj.org/article/d26f25fab674490e806764d4fb8ccd222017-10-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00267-17https://doaj.org/toc/2379-5042ABSTRACT Depending on the specific viral pathogen, commensal bacteria can promote or reduce the severity of viral infection and disease progression in their hosts. Influenza A virus (IAV) has a broad host range, comprises many subtypes, and utilizes different routes of transmission, including the fecal-oral route in wild birds. It has been previously demonstrated that commensal bacteria can interact with the host’s immune system to protect against IAV pathogenesis. However, it is unclear whether bacteria and their products may be interacting directly with IAV to impact virion stability. Herein we show that gastrointestinal (GI) tract bacterial isolates in an in vitro system significantly reduce the stability of IAV. Moreover, bacterial lipopolysaccharide (LPS), found on the exterior surfaces of bacteria, was sufficient to significantly decrease the stability of both human and avian viral strains in a temperature-dependent manner, including at the relevant temperatures of their respective hosts and the external aquatic habitat. The subtype and host origin of the viruses were shown to affect the extent to which IAV was susceptible to LPS. Furthermore, using a receptor binding assay and transmission electron microscopy, we observed that LPS binds to and alters the morphology of influenza virions, suggesting that direct interaction with the viral surface contributes to the observed antiviral effect of LPS on influenza. IMPORTANCE Influenza A virus (IAV), transmitted primarily via the fecal-oral route in wild birds, encounters high concentrations of bacteria and their products. Understanding the extent to which bacteria affect the infectivity of IAV will lead to a broader understanding of viral ecology in reservoir hosts and may lead to insights for the development of therapeutics in respiratory infection. Herein we show that bacteria and lipopolysaccharide (LPS) interact with and destabilize influenza virions. Moreover, we show that LPS reduces the long-term persistence and freeze-thaw stability of IAV, which is important information for modeling the movement and emergence of novel strains from animal hosts. Our results, demonstrating that the subtype and host origin of a virus also influence its susceptibility to LPS, raise key questions about the fitness of viruses in reservoir hosts, their potential to transmit to humans, and the importance of bacterial-viral interactions in viral ecology.Christopher BandoroJonathan A. RunstadlerAmerican Society for Microbiologyarticlebacteriaenvironmental microbiologyinfluenzalipopolysaccharidemicrobiomevirologyMicrobiologyQR1-502ENmSphere, Vol 2, Iss 5 (2017)
institution DOAJ
collection DOAJ
language EN
topic bacteria
environmental microbiology
influenza
lipopolysaccharide
microbiome
virology
Microbiology
QR1-502
spellingShingle bacteria
environmental microbiology
influenza
lipopolysaccharide
microbiome
virology
Microbiology
QR1-502
Christopher Bandoro
Jonathan A. Runstadler
Bacterial Lipopolysaccharide Destabilizes Influenza Viruses
description ABSTRACT Depending on the specific viral pathogen, commensal bacteria can promote or reduce the severity of viral infection and disease progression in their hosts. Influenza A virus (IAV) has a broad host range, comprises many subtypes, and utilizes different routes of transmission, including the fecal-oral route in wild birds. It has been previously demonstrated that commensal bacteria can interact with the host’s immune system to protect against IAV pathogenesis. However, it is unclear whether bacteria and their products may be interacting directly with IAV to impact virion stability. Herein we show that gastrointestinal (GI) tract bacterial isolates in an in vitro system significantly reduce the stability of IAV. Moreover, bacterial lipopolysaccharide (LPS), found on the exterior surfaces of bacteria, was sufficient to significantly decrease the stability of both human and avian viral strains in a temperature-dependent manner, including at the relevant temperatures of their respective hosts and the external aquatic habitat. The subtype and host origin of the viruses were shown to affect the extent to which IAV was susceptible to LPS. Furthermore, using a receptor binding assay and transmission electron microscopy, we observed that LPS binds to and alters the morphology of influenza virions, suggesting that direct interaction with the viral surface contributes to the observed antiviral effect of LPS on influenza. IMPORTANCE Influenza A virus (IAV), transmitted primarily via the fecal-oral route in wild birds, encounters high concentrations of bacteria and their products. Understanding the extent to which bacteria affect the infectivity of IAV will lead to a broader understanding of viral ecology in reservoir hosts and may lead to insights for the development of therapeutics in respiratory infection. Herein we show that bacteria and lipopolysaccharide (LPS) interact with and destabilize influenza virions. Moreover, we show that LPS reduces the long-term persistence and freeze-thaw stability of IAV, which is important information for modeling the movement and emergence of novel strains from animal hosts. Our results, demonstrating that the subtype and host origin of a virus also influence its susceptibility to LPS, raise key questions about the fitness of viruses in reservoir hosts, their potential to transmit to humans, and the importance of bacterial-viral interactions in viral ecology.
format article
author Christopher Bandoro
Jonathan A. Runstadler
author_facet Christopher Bandoro
Jonathan A. Runstadler
author_sort Christopher Bandoro
title Bacterial Lipopolysaccharide Destabilizes Influenza Viruses
title_short Bacterial Lipopolysaccharide Destabilizes Influenza Viruses
title_full Bacterial Lipopolysaccharide Destabilizes Influenza Viruses
title_fullStr Bacterial Lipopolysaccharide Destabilizes Influenza Viruses
title_full_unstemmed Bacterial Lipopolysaccharide Destabilizes Influenza Viruses
title_sort bacterial lipopolysaccharide destabilizes influenza viruses
publisher American Society for Microbiology
publishDate 2017
url https://doaj.org/article/d26f25fab674490e806764d4fb8ccd22
work_keys_str_mv AT christopherbandoro bacteriallipopolysaccharidedestabilizesinfluenzaviruses
AT jonathanarunstadler bacteriallipopolysaccharidedestabilizesinfluenzaviruses
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