Evidence map›Paper›PMID 24885530›Full record

ArticleBMC veterinary research2014

Phylogeny of Mycoplasma bovis isolates from Hungary based on multi locus sequence typing and multiple-locus variable-number tandem repeat analysis.

Kinga M Sulyok, Zsuzsa Kreizinger, Lilla Fekete, Szilárd Jánosi, Nóra Schweitzer, Ibolya Turcsányi, László Makrai, Károly Erdélyi, Miklós Gyuranecz

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Article in BMC veterinary research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.3field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  3. Antimicrobial Susceptibility ofAntibiotics (Basel, Switzerland) · 2020
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  4. Population Genomic Analysis ofMicroorganisms · 2020
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  5. Article
  6. Article
  7. A review of mycoplasma diagnostics in cattle.Journal of veterinary internal medicine · 2018
    Review
  8. Article
  9. Article
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  11. Article
  12. Article
4 · The record

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5 · Who and what money

Authors and funding

9 authors at 5 institutions in 1 country.

Kinga M Sulyok
Zsuzsa Kreizinger
Lilla Fekete
Szilárd Jánosi
Nóra Schweitzer
Ibolya Turcsányi
László Makrai
Károly Erdélyi
Miklós GyuraneczInstitute for Veterinary Medical Research, Centre for Agricultural Research, Hungarian Academy of Sciences, Hungária körút 21, Budapest 1143, Hungary. m.gyuranecz@gmail.com.
National Food Chain Safety Office · HUHUN-REN Veterinary Medical Research Institute · HUCentre for Agricultural Research · HUHungarian Academy of Sciences · HUMagyar Agrár- és Élettudományi Egyetem · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMycoplasma bovis is an important pathogen causing pneumonia, mastitis and arthritis in cattle worldwide. As this agent is primarily transmitted by direct contact and spread through animal movements, efficient genotyping systems are essential for the monitoring of the disease and for epidemiological investigations. The aim of this study was to compare and evaluate the multi locus sequence typing (MLST) and the multiple-locus variable-number tandem repeat (VNTR) analysis (MLVA) through the genetic characterization of M. bovis isolates from Hungary.

resultsThirty one Hungarian M. bovis isolates grouped into two clades by MLST. Two strains had the same sequence type (ST) as reference strain PG45, while the other twenty nine Hungarian isolates formed a novel clade comprising five subclades. Isolates originating from the same herds had the same STs except for one case. The same isolates formed two main clades and several subclades and branches by MLVA. One clade contained the reference strain PG45 and three isolates, while the other main clade comprised the rest of the strains. Within-herd strain divergence was also detected by MLVA. Little congruence was found between the results of the two typing systems.

conclusionsMLST is generally considered an intermediate scale typing method and it was found to be discriminatory among the Hungarian M. bovis isolates. MLVA proved to be an appropriate fine scale typing tool for M. bovis as this method was able to distinguish closely related strains isolated from the same farm. We recommend the combined use of the two methods for the genotyping of M. bovis isolates. Strains have to be characterized first by MLST followed by the fine scale typing of identical STs with MLVA.

Indexed as

AnimalsCattleGenetic VariationHungaryMinisatellite RepeatsMultilocus Sequence TypingMycoplasma bovisPhylogenyTuberculosis, Bovine

Identifiers

PMID24885530
PMCPMC4019563
OpenAlexW2030495776

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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.