Evidence map›Paper›PMID 27791106›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Synthetically derived bat influenza A-like viruses reveal a cell type- but not species-specific tropism.

Étori Aguiar Moreira, Samira Locher, Larissa Kolesnikova, Hardin Bolte, Teresa Aydillo, Adolfo García-Sastre, Martin Schwemmle, Gert Zimmer

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
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  11. Reverse Genetics of Bat Influenza A Viruses.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Structural and inhibitor sensitivity analysis of influenza B-like viral neuraminidases derived from Asiatic toad and spiny eel.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  16. Article
  17. Influenza Reverse Genetics-Historical Perspective.Cold Spring Harbor perspectives in medicine · 2021
    Review
  18. Review
  19. Article
  20. Bat-Borne Influenza A Viruses: An Awakening.Cold Spring Harbor perspectives in medicine · 2021
    Review
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

8 authors at 4 institutions in 2 countries.

Étori Aguiar MoreiraInstitute of Virology, University Medical Center Freiburg, D-79104 Freiburg, Germany.
Samira LocherDivision of Virology, Institute of Virology and Immunology, CH-3147 Mittelhäusern, Switzerland.
Larissa KolesnikovaInstitute of Virology, Philipps-University, D-35043 Marburg, Germany.
Hardin BolteInstitute of Virology, University Medical Center Freiburg, D-79104 Freiburg, Germany.
Teresa AydilloDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Adolfo García-SastreDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Martin SchwemmleInstitute of Virology, University Medical Center Freiburg, D-79104 Freiburg, Germany; martin.schwemmle@uniklinik-freiburg.de gert.zimmer@ivi.admin.ch.
Gert ZimmerDivision of Virology, Institute of Virology and Immunology, CH-3147 Mittelhäusern, Switzerland; martin.schwemmle@uniklinik-freiburg.de gert.zimmer@ivi.admin.ch.
Icahn School of Medicine at Mount Sinai · USUniversity Medical Center Freiburg · DEPhilipps University of Marburg · DEUniversity of Freiburg · DE

Funding

NIAID NIH HHS HHSN272201400008C
6 · The paper itself

Abstract

Two novel influenza A-like viral genome sequences have recently been identified in Central and South American fruit bats and provisionally designated "HL17NL10" and "HL18NL11." All efforts to isolate infectious virus from bats or to generate these viruses by reverse genetics have failed to date. Recombinant vesicular stomatitis virus (VSV) encoding the hemagglutinin-like envelope glycoproteins HL17 or HL18 in place of the VSV glycoprotein were generated to identify cell lines that are susceptible to bat influenza A-like virus entry. More than 30 cell lines derived from various species were screened but only a few cell lines were found to be susceptible, including Madin-Darby canine kidney type II (MDCK II) cells. The identification of cell lines susceptible to VSV chimeras allowed us to recover recombinant HL17NL10 and HL18NL11 viruses from synthetic DNA. Both influenza A-like viruses established a productive infection in MDCK II cells; however, HL18NL11 replicated more efficiently than HL17NL10 in this cell line. Unlike conventional influenza A viruses, bat influenza A-like viruses started the infection preferentially at the basolateral membrane of polarized MDCK II cells; however, similar to conventional influenza A viruses, bat influenza A-like viruses were released primarily from the apical site. The ability of HL18NL11 or HL17NL10 viruses to infect canine and human cells might reflect a zoonotic potential of these recently identified bat viruses.

Indexed as

batchiropteraemerging virusesinfluenzaorthomyxoviridae

Identifiers

PMID27791106
PMCPMC5111703
OpenAlexW2535572369

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.