Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2012;7(7):e40458.
doi: 10.1371/journal.pone.0040458. Epub 2012 Jul 11.

Comparative genotypic and phenotypic characterisation of methicillin-resistant Staphylococcus aureus ST398 isolated from animals and humans

Affiliations
Comparative Study

Comparative genotypic and phenotypic characterisation of methicillin-resistant Staphylococcus aureus ST398 isolated from animals and humans

Dorota M Jamrozy et al. PLoS One. 2012.

Abstract

The high prevalence of methicillin-resistant Staphylococcus aureus (MRSA) ST398 among pigs in certain European countries and North America and its occurrence in other animal species raises a question concerning the molecular mechanisms mediating the success of this lineage. In this study a panel of S. aureus strains belonging to sequence type (ST) 5 (n = 4), ST8 (n = 5), ST15 (n = 5), ST22 (n = 8), clonal complex (CC) 30 (n = 8), CC97 (n = 8), CC130 (n = 4), CC151 (n = 4) and ST398 (n = 18) were screened by DNA microarray and PCR for the carriage of virulence and antimicrobial resistance genes. Isolates belonging to the same sequence type/clonal complex (ST/CC) were found to share similar virulence gene profiles. The ST398 lineage displayed the lowest content of virulence genes, which consisted mainly of genes detected among the majority or all of the analysed lineages. All MRSA ST398 isolates lacked accessory virulence genes that were detected in other ST/CC. In contrast to virulence genotype, the antimicrobial resistance genes profiles varied between isolates belonging to the same ST/CC and profile similarities could be observed for isolates from different lineages. MRSA ST398 isolates in particular displayed significant diversity and high content of antimicrobial resistance genes. This was comparable with certain MRSA belonging to other sequence types particularly the equine MRSA ST8. The apparent lack of significant virulence genes among MRSA ST398 strains, demonstrates that the lineage features a unique genetic background but no ST398-specific virulence markers could be identified.

PubMed Disclaimer

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Superantigen gene profiles.
UPGMA dendrogram displaying clustering and genetic similarity (using Jaccard’s coefficient) of superantigen gene profiles of analysed strains. Black box – positive; grey – ambiguous; white/blank – negative.
Figure 2
Figure 2. agr and set gene profiles.
UPGMA dendrogram displaying clustering and genetic similarity (using Jaccard’s coefficient) of agr and set gene profiles of analysed strains. Black box – positive; grey – ambiguous; white/blank – negative.
Figure 3
Figure 3. Leukocidin, haemolysin and other virulence gene profiles.
UPGMA dendrogram displaying clustering and genetic similarity (using Jaccard’s coefficient) of leukocidin, haemolysin and other virulence gene profiles of analysed strains. Black box – positive; grey – ambiguous; white/blank – negative.
Figure 4
Figure 4. Adhesion gene profiles.
UPGMA dendrogram displaying clustering and genetic similarity (using Jaccard’s coefficient) of adhesion gene profiles of analysed strains. Black box – positive; grey – ambiguous; white/blank – negative.
Figure 5
Figure 5. Antimicrobial resistance genotypes and phenotypes.
UPGMA dendrogram displaying clustering and genetic similarity (using Jaccard’s coefficient) of antimicrobial resistance gene profiles of analysed strains. Black box – positive; grey – ambiguous; white/blank – negative. The far right column shows antimicrobial resistance phenotype. PEN, penicillin; FOX, cefoxitin; GEN, gentamicin; KAN, kanamycin; SPE, spectinomycin; CLI, clindamycin; ERY, erythromycin; CIP, ciprofloxacin; CHL, chloramphenicol; FFC, florfenicol; TET, tetracycline; TIA, tiamulin; TMP, trimethoprim; i, inducible.

Similar articles

Cited by

References

    1. Feil EJ, Cooper JE, Grundmann H, Robinson DA, Enright MC, et al. How clonal is Staphylococcus aureus? J Bacteriol. 2003;185(11):3307–3316. - PMC - PubMed
    1. Herron-Olson L, Fitzgerald JR, Musser JM, Kapur V. Molecular correlates of host specialization in Staphylococcus aureus. PLoS One. 2007;2(10):e1120. - PMC - PubMed
    1. Guinane CM, Ben Zakour NL, Tormo-Mas MA, Weinert LA, Lowder BV, et al. Evolutionary genomics of Staphylococcus aureus reveals insights into the origin and molecular basis of ruminant host adaptation. Genome Biol Evol. 2010;2:454–466. - PMC - PubMed
    1. Lowder BV, Guinane CM, Ben Zakour NL, Weinert LA, Conway-Morris A, et al. Recent human-to-poultry host jump, adaptation, and pandemic spread of Staphylococcus aureus. Proc Natl Acad Sci U S A. 2009;106(46):19545–19550. - PMC - PubMed
    1. Walther B, Monecke S, Ruscher C, Friedrich AW, Ehricht R, et al. Comparative molecular analysis substantiates zoonotic potential of equine methicillin-resistant Staphylococcus aureus. J Clin Microbiol. 2009;47(3):704–710. - PMC - PubMed

Publication types

MeSH terms