Evidence map›Paper›PMID 25673727›Full record

ArticleJournal of virology2015

Domestic pigs are susceptible to infection with influenza B viruses.

Zhiguang Ran, Huigang Shen, Yuekun Lang, Elizabeth A Kolb, Nuri Turan, Laihua Zhu, Jingjiao Ma, Bhupinder Bawa, Qinfang Liu, Haixia Liu and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
11.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

  1. Pooled it
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  7. Pseudotyped Viruses for Influenza.Advances in experimental medicine and biology · 2023
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 3 institutions in 1 country.

Zhiguang RanDepartment of Biology and Microbiology, South Dakota State University, Brookings, South Dakota, USA Department of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, South Dakota, USA.
Huigang ShenDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, Kansas, USA.
Yuekun LangDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, Kansas, USA.
Elizabeth A KolbDepartment of Biology and Microbiology, South Dakota State University, Brookings, South Dakota, USA.
Nuri TuranDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, Kansas, USA.
Laihua ZhuDepartment of Biology and Microbiology, South Dakota State University, Brookings, South Dakota, USA Department of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, South Dakota, USA.
Jingjiao MaDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, Kansas, USA.
Bhupinder BawaDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, Kansas, USA.
Qinfang LiuDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, Kansas, USA.
Haixia LiuDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, Kansas, USA.
Megan QuastDepartment of Biology and Microbiology, South Dakota State University, Brookings, South Dakota, USA.
Gabriel SextonDepartment of Biology and Microbiology, South Dakota State University, Brookings, South Dakota, USA.
Florian KrammerDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Ben M HauseDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, Kansas, USA.
Jane Christopher-HenningsDepartment of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, South Dakota, USA.
Eric A NelsonDepartment of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, South Dakota, USA.
Juergen RichtDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, Kansas, USA.
Feng LiDepartment of Biology and Microbiology, South Dakota State University, Brookings, South Dakota, USA Department of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, South Dakota, USA feng.li@sdatate.edu wma@vet.k-state.edu.
Wenjun MaDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, Kansas, USA feng.li@sdatate.edu wma@vet.k-state.edu.
Kansas State University · USSouth Dakota State University · USIcahn School of Medicine at Mount Sinai · US

Funding

NIAID NIH HHS HHSN266200700005CNIAID NIH HHS HHSN272201400006CPHS HHS HHSN266200700005CPHS HHS HHSN272201400006C
6 · The paper itself

Abstract

unlabelledInfluenza B virus (IBV) causes seasonal epidemics in humans. Although IBV has been isolated from seals, humans are considered the primary host and reservoir of this important pathogen. It is unclear whether other animal species can support the replication of IBV and serve as a reservoir. Swine are naturally infected with both influenza A and C viruses. To determine the susceptibility of pigs to IBV infection, we conducted a serological survey for U.S. Midwest domestic swine herds from 2010 to 2012. Results of this study showed that antibodies to IBVs were detected in 38.5% (20/52) of sampled farms, and 7.3% (41/560) of tested swine serum samples were positive for IBV antibodies. Furthermore, swine herds infected with porcine reproductive and respiratory syndrome virus (PRRSV) showed a higher prevalence of IBV antibodies in our 2014 survey. In addition, IBV was detected in 3 nasal swabs collected from PRRSV-seropositive pigs by real-time RT-PCR and sequencing. Finally, an experimental infection in pigs, via intranasal and intratracheal routes, was performed using one representative virus from each of the two genetically and antigenically distinct lineages of IBVs: B/Brisbane/60/2008 (Victoria lineage) and B/Yamagata/16/1988 (Yamagata lineage). Pigs developed influenza-like symptoms and lung lesions, and they seroconverted after virus inoculation. Pigs infected with B/Brisbane/60/2008 virus successfully transmitted the virus to sentinel animals. Taken together, our data demonstrate that pigs are susceptible to IBV infection; therefore, they warrant further surveillance and investigation of swine as a potential host for human IBV. IMPORTANCE: IBV is an important human pathogen, but its ability to infect other species, for example, pigs, is not well understood. We showed serological evidence that antibodies to two genetically and antigenically distinct lineages of IBVs were present among domestic pigs, especially in swine herds previously infected with PRRSV, an immunosuppressive virus. IBV was detected in 3 nasal swabs from PRRSV-seropositive pigs by real-time reverse transcription-PCR and sequencing. Moreover, both lineages of IBV were able to infect pigs under experimental conditions, with transmissibility of influenza B/Victoria lineage virus among pigs being observed. Our results demonstrate that pigs are susceptible to IBV infections, indicating that IBV is a swine pathogen, and swine may serve as a natural reservoir of IBVs. In addition, pigs may serve as a model to study the mechanisms of transmission and pathogenesis of IBVs.

Indexed as

Sus scrofaAnimalsAntibodies, ViralInfluenza B virusLungMidwestern United StatesNasal MucosaOrthomyxoviridae InfectionsReal-Time Polymerase Chain ReactionSequence Analysis, DNASeroepidemiologic StudiesAntibodies, Viral

Identifiers

PMID25673727
PMCPMC4403465
OpenAlexW2002762006

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.