Evidence map›Paper›PMID 36564834›Full record

ArticleBMC veterinary research2022

Detection and sequence analysis of Canine morbillivirus in multiple species of the Mustelidae family.

Zsófia Lanszki, József Lanszki, Gábor Endre Tóth, Tamás Cserkész, Gábor Csorba, Tamás Görföl, András István Csathó, Ferenc Jakab, Gábor Kemenesi

Open access · goldAbstract read
In one paragraph

Article in BMC veterinary research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Zsófia LanszkiNational Laboratory of Virology, University of Pécs, 7624, Pécs, Hungary. lanszkizsofi@gmail.com.
József LanszkiBalaton Limnological Research Institute, 8237, Tihany, Hungary.
Gábor Endre TóthNational Laboratory of Virology, University of Pécs, 7624, Pécs, Hungary.
Tamás CserkészDepartment of Zoology, Hungarian Natural History Museum, 1088, Budapest, Hungary.
Gábor CsorbaDepartment of Zoology, Hungarian Natural History Museum, 1088, Budapest, Hungary.
Tamás GörfölNational Laboratory of Virology, University of Pécs, 7624, Pécs, Hungary.
András István CsathóIndependent Researcher, 5830, Battonya, Hungary.
Ferenc JakabNational Laboratory of Virology, University of Pécs, 7624, Pécs, Hungary.
Gábor KemenesiNational Laboratory of Virology, University of Pécs, 7624, Pécs, Hungary.
University of Pecs · HUHungarian Natural History Museum · HUUniversity of Kaposvár · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCanine morbillivirus (canine distemper virus, CDV) is a member of the Paramyxoviridae family. Canine distemper is a serious viral disease that affects many mammalian species, including members of the Mustelidae family. These animals have an elusive nature, which makes related virological studies extremely challenging. There is a significant knowledge gap about the evolution of their viruses and about the possible effects of these viruses to the population dynamics of the host animals. Spleen and lung tissue samples of 170 road-killed mustelids belonging to six species were collected between 1997 and 2022 throughout Hungary and tested for CDV with real-time RT-PCR.

resultsThree species were positive for viral RNA, 2 out of 64 Steppe polecats (Mustela eversmanii), 1 out of 36 European polecats (Mustela putorius) and 2 out of 36 stone martens (Martes foina); all 18 pine martens (Martes martes), 10 least weasels (Mustela nivalis) and 6 stoats (Mustela erminea) tested negative. The complete CDV genome was sequenced in five samples using pan-genotype CDV-specific, amplicon-based Nanopore sequencing. Based on the phylogenetic analysis, all five viral sequences were grouped to the Europe/South America 1 lineage and the distribution of one sequence among trees indicated recombination of the Hemagglutinin gene. We verified the recombination with SimPlot analysis.

conclusionsThis paper provides the first CDV genome sequences from Steppe polecats and additional complete genomes from European polecats and stone martens. The infected specimens of various species originated from distinct parts of the country over a long time, indicating a wide circulation of CDV among mustelids throughout Hungary. Considering the high virulence of CDV and the presence of the virus in these animals, we highlight the importance of conservation efforts for wild mustelids. In addition, we emphasize the importance of full genomic data acquisition and analysis to better understand the evolution of the virus. Since CDV is prone to recombination, specific genomic segment analyses may provide less representative evolutionary traits than using complete genome sequences.

Indexed as

DistemperDistemper Virus, CanineDog DiseasesMustelidaeAnimalsAnimals, WildDogsFerretsPhylogenySequence AnalysisCanine distemper virusCarnivoraDisease ecologyMinIONMustelidsNGSProtected speciesTailingThird generation sequencingWildlife disease

Identifiers

PMID36564834
PMCPMC9789673
OpenAlexW4312133464

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.