Literature DB >> 29212934

Influenza A Virus Reassortment Is Limited by Anatomical Compartmentalization following Coinfection via Distinct Routes.

Mathilde Richard1, Sander Herfst1, Hui Tao2, Nathan T Jacobs2, Anice C Lowen3.   

Abstract

Exchange of gene segments through reassortment is a major feature of influenza A virus evolution and frequently contributes to the emergence of novel epidemic, pandemic, and zoonotic strains. It has long been evident that viral diversification through reassortment is constrained by genetic incompatibility between divergent parental viruses. In contrast, the role of virus-extrinsic factors in determining the likelihood of reassortment has remained unclear. To evaluate the impact of such factors in the absence of confounding effects of segment mismatch, we previously reported an approach in which reassortment between wild-type (wt) and genetically tagged variant (var) viruses of the same strain is measured. Here, using wt/var systems in the A/Netherlands/602/2009 (pH1N1) and A/Panama/2007/99 (H3N2) strain backgrounds, we tested whether inoculation of parental viruses into distinct sites within the respiratory tract limits their reassortment. Using a ferret (Mustella putorius furo) model, either matched parental viruses were coinoculated intranasally or one virus was instilled intranasally whereas the second was instilled intratracheally. Dual intranasal inoculation resulted in robust reassortment for wt/var viruses of both strain backgrounds. In contrast, when infections were initiated simultaneously at distinct sites, strong compartmentalization of viral replication was observed and minimal reassortment was detected. The observed lack of viral spread between upper and lower respiratory tract tissues may be attributable to localized exclusion of superinfection within the host, mediated by innate immune responses. Our findings indicate that dual infections in nature are more likely to result in reassortment if viruses are seeded into similar anatomical locations and have matched tissue tropisms.IMPORTANCE Genetic exchange between influenza A viruses (IAVs) through reassortment can facilitate the emergence of antigenically drifted seasonal strains and plays a prominent role in the development of pandemics. Typical human influenza infections are concentrated in the upper respiratory tract; however, lower respiratory tract (LRT) infection is an important feature of severe cases, which are more common in the very young, the elderly, and individuals with underlying conditions. In addition to host factors, viral characteristics and mode of transmission can also increase the likelihood of LRT infection: certain zoonotic IAVs are thought to favor the LRT, and transmission via small droplets allows direct seeding into lower respiratory tract tissues. To gauge the likelihood of reassortment in coinfected hosts, we assessed the extent to which initiation of infection at distinct respiratory tract sites impacts reassortment frequency. Our results reveal that spatially distinct inoculations result in anatomical compartmentalization of infection, which in turn strongly limits reassortment.
Copyright © 2018 American Society for Microbiology.

Entities:  

Keywords:  compartmentalization; diversity; ferret; influenza A virus; reassortment

Mesh:

Substances:

Year:  2018        PMID: 29212934      PMCID: PMC5809721          DOI: 10.1128/JVI.02063-17

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  54 in total

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Authors:  Rogier Bodewes; Joost H C M Kreijtz; Geert van Amerongen; Marine L B Hillaire; Stella E Vogelzang-van Trierum; Nella J Nieuwkoop; Peter van Run; Thijs Kuiken; Ron A M Fouchier; Albert D M E Osterhaus; Guus F Rimmelzwaan
Journal:  J Virol       Date:  2013-01-30       Impact factor: 5.103

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  15 in total

Review 1.  A Guide for the Use of the Ferret Model for Influenza Virus Infection.

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Journal:  Am J Pathol       Date:  2019-10-23       Impact factor: 4.307

2.  Tissue tropisms opt for transmissible reassortants during avian and swine influenza A virus co-infection in swine.

Authors:  Xiaojian Zhang; Hailiang Sun; Fred L Cunningham; Lei Li; Katie Hanson-Dorr; Matthew W Hopken; Jim Cooley; Li-Ping Long; John A Baroch; Tao Li; Brandon S Schmit; Xiaoxu Lin; Alicia K Olivier; Richard G Jarman; Thomas J DeLiberto; Xiu-Feng Wan
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3.  A Novel Reassortant Avian H7N6 Influenza Virus Is Transmissible in Guinea Pigs via Respiratory Droplets.

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Journal:  Front Microbiol       Date:  2019-01-22       Impact factor: 5.640

Review 4.  The Development and Use of Reporter Influenza B Viruses.

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6.  Construction and identification of influenza plasmid pool imparting high yields to candidate vaccine viruses in Vero cell at low temperature.

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7.  Parallel evolution between genomic segments of seasonal human influenza viruses reveals RNA-RNA relationships.

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Journal:  Elife       Date:  2021-08-27       Impact factor: 8.140

8.  A(H1N1)pdm09 Influenza Viruses Replicating in Ferret Upper or Lower Respiratory Tract Differed in Onward Transmission Potential by Air.

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9.  A large effective population size for established within-host influenza virus infection.

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10.  Neutralising antibodies in Spike mediated SARS-CoV-2 adaptation.

Authors:  S A Kemp; D A Collier; R Datir; Iatm Ferreira; S Gayed; A Jahun; M Hosmillo; C Rees-Spear; P Mlcochova; Ines Ushiro Lumb; David J Roberts; Anita Chandra; N Temperton; K Sharrocks; E Blane; Jag Briggs; Gils Mj van; Kgc Smith; J R Bradley; C Smith; R Doffinger; L Ceron-Gutierrez; G Barcenas-Morales; D D Pollock; R A Goldstein; A Smielewska; J P Skittrall; T Gouliouris; I G Goodfellow; E Gkrania-Klotsas; Cjr Illingworth; L E McCoy; R K Gupta
Journal:  medRxiv       Date:  2020-12-29
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