Evidence map›Paper›PMID 31013314›Full record

ArticlePloS one2019

Consensus and variations in cell line specificity among human metapneumovirus strains.

Naganori Nao, Ko Sato, Junya Yamagishi, Maino Tahara, Yuichiro Nakatsu, Fumio Seki, Hiroshi Katoh, Aiko Ohnuma, Yuta Shirogane, Masahiro Hayashi and 4 more

Abstract readConsensus Statement
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
–field-weighted citation impact
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

42 citing papers in PubMed.

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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

14 authors.

Naganori NaoDepartment of Virology 3, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Ko SatoVirus Research Center, Clinical Research Division, Sendai Medical Center, Sendai, Japan.
Junya YamagishiReserach Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Maino TaharaDepartment of Virology 3, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Yuichiro NakatsuDepartment of Virology 3, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Fumio SekiDepartment of Virology 3, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Hiroshi KatohDepartment of Virology 3, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Aiko OhnumaReserach Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Yuta ShiroganeDepartment of Virology 3, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
Masahiro HayashiDepartment of Dermatology, Faculty of Medicine, Yamagata University, Yamagata, Japan.
Tamio SuzukiDepartment of Dermatology, Faculty of Medicine, Yamagata University, Yamagata, Japan.
Hideaki KikutaPediatric Clinic, Touei Hospital, Sapporo, Japan.
Hidekazu NishimuraVirus Research Center, Clinical Research Division, Sendai Medical Center, Sendai, Japan.
Makoto TakedaDepartment of Virology 3, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.ORCID 0000-0002-8194-7727

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human metapneumovirus (HMPV) has been a notable etiological agent of acute respiratory infection in humans, but it was not discovered until 2001, because HMPV replicates only in a limited number of cell lines and the cytopathic effect (CPE) is often mild. To promote the study of HMPV, several groups have generated green fluorescent protein (GFP)-expressing recombinant HMPV strains (HMPVGFP). However, the growing evidence has complicated the understanding of cell line specificity of HMPV, because it seems to vary notably among HMPV strains. In addition, unique A2b clade HMPV strains with a 180-nucleotide duplication in the G gene (HMPV A2b180nt-dup strains) have recently been detected. In this study, we re-evaluated and compared the cell line specificity of clinical isolates of HMPV strains, including the novel HMPV A2b180nt-dup strains, and six recombinant HMPVGFP strains, including the newly generated recombinant HMPV A2b180nt-dup strain, MG0256-EGFP. Our data demonstrate that VeroE6 and LLC-MK2 cells generally showed the highest infectivity with any clinical isolates and recombinant HMPVGFP strains. Other human-derived cell lines (BEAS-2B, A549, HEK293, MNT-1, and HeLa cells) showed certain levels of infectivity with HMPV, but these were significantly lower than those of VeroE6 and LLC-MK2 cells. Also, the infectivity in these suboptimal cell lines varied greatly among HMPV strains. The variations were not directly related to HMPV genotypes, cell lines used for isolation and propagation, specific genome mutations, or nucleotide duplications in the G gene. Thus, these variations in suboptimal cell lines are likely intrinsic to particular HMPV strains.

Indexed as

A549 CellsCell LineCytopathogenic Effect, ViralGreen Fluorescent ProteinsHEK293 CellsHeLa CellsHumansMetapneumovirusRespiratory Tract InfectionsGreen Fluorescent Proteins

Identifiers

PMID31013314
PMCPMC6478314

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Registered trials

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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.