Evidence map›Paper›PMID 21536150›Full record

ArticleInfection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases2011

Comparative genomics and the role of lateral gene transfer in the evolution of bovine adapted Streptococcus agalactiae.

Vincent P Richards, Ping Lang, Paulina D Pavinski Bitar, Tristan Lefébure, Ynte H Schukken, Ruth N Zadoks, Michael J Stanhope

Open access · greenAbstract readComparative Study
In one paragraph

Article in Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 2 pooled it
12.9field-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

62 citing papers in PubMed, 2 syntheses or guidelines pooled it, 119 citations in OpenAlex.

  1. Prevalence and antimicrobial resistance ofOpen veterinary journal · 2025
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  11. How GBS Got Its Hump: Genomic Analysis of Group BPathogens (Basel, Switzerland) · 2022
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  14. Detection of virulence associated genes inIranian journal of veterinary research · 2022
    Article
  15. The fall and rise of group BMicrobial genomics · 2021
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  18. Antimicrobial Resistance and Virulence Factor ofInfection and drug resistance · 2021
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  19. Article
  20. Evidence of Common Isolates ofFrontiers in microbiology · 2021
    Article

2 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Vincent P RichardsDepartment of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.
Ping Lang
Paulina D Pavinski Bitar
Tristan Lefébure
Ynte H Schukken
Ruth N Zadoks
Michael J Stanhope
New York State College of Veterinary Medicine · USCornell University · US

Funding

Evolutionary genomics and population genetics of pathogenic streptococciR01AI073368 · NIAID · CORNELL UNIVERSITY · PI STANHOPE, MICHAEL J · 2008 to 2012
$2.3M
NIAID NIH HHS AI073368-01A2NIAID NIH HHS R01 AI073368
6 · The paper itself

Abstract

In addition to causing severe invasive infections in humans, Streptococcus agalactiae, or group B Streptococcus (GBS), is also a major cause of bovine mastitis. Here we provide the first genome sequence for S. agalactiae isolated from a cow diagnosed with clinical mastitis (strain FSL S3-026). Comparison to eight S. agalactiae genomes obtained from human disease isolates revealed 183 genes specific to the bovine strain. Subsequent polymerase chain reaction (PCR) screening for the presence/absence of a subset of these loci in additional bovine and human strains revealed strong differentiation between the two groups (Fisher exact test: p<0.0001). The majority of the bovine strain-specific genes (∼ 85%) clustered tightly into eight genomic islands, suggesting these genes were acquired through lateral gene transfer (LGT). This bovine GBS also contained an unusually high proportion of insertion sequences (4.3% of the total genome), suggesting frequent genomic rearrangement. Comparison to other mastitis-causing species of bacteria provided strong evidence for two cases of interspecies LGT within the shared bovine environment: bovine S. agalactiae with Streptococcus uberis (nisin U operon) and Streptococcus dysgalactiae subsp. dysgalactiae (lactose operon). We also found evidence for LGT, involving the salivaricin operon, between the bovine S. agalactiae strain and either Streptococcus pyogenes or Streptococcus salivarius. Our findings provide insight into mechanisms facilitating environmental adaptation and acquisition of potential virulence factors, while highlighting both the key role LGT has played in the recent evolution of the bovine S. agalactiae strain, and the importance of LGT among pathogens within a shared environment.

Indexed as

Evolution, MolecularGene Transfer, HorizontalGenome, BacterialAnimalsBacterial ProteinsCattleDNA Transposable ElementsDrug Resistance, BacterialFemaleFructoseGene OrderHumansMastitis, BovineMetabolic Networks and PathwaysMultigene FamilyMutagenesis, InsertionalBacterial ProteinsDNA Transposable ElementsFructoseRecombinasesVirulence Factors

Identifiers

PMID21536150
PMCPMC3139733
OpenAlexW2145704137

What OpenQuestion holds

Textmetadata
LicenceTDM
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.