Staphylococcus brunensis sp. nov. isolated from human clinical specimens with a staphylococcal cassette chromosome-related genomic island outside of the rlmH gene bearing the ccrDE recombinase gene complex

Author:

Kovařovic Vojtěch1,Finstrlová Adéla1ORCID,Sedláček Ivo2ORCID,Petráš Petr3,Švec Pavel2ORCID,Mašlaňová Ivana1ORCID,Neumann-Schaal Meina4ORCID,Šedo Ondrej5,Botka Tibor1ORCID,Staňková Eva2,Doškař Jiří1ORCID,Pantůček Roman1ORCID

Affiliation:

1. Department of Experimental Biology, Division of Genetics and Molecular Biology, Faculty of Science, Masaryk University , Brno, Czech Republic

2. Department of Experimental Biology, Czech Collection of Microorganisms, Faculty of Science, Masaryk University , Brno, Czech Republic

3. Reference Laboratory for Staphylococci, National Institute of Public Health , Praha, Czech Republic

4. Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures , Braunschweig, Germany

5. Central European Institute of Technology, Masaryk University , Brno, Czech Republic

Abstract

ABSTRACT Novel species of coagulase-negative staphylococci, which could serve as reservoirs of virulence and antimicrobial resistance factors for opportunistic pathogens from the genus Staphylococcus , are recognized in human and animal specimens due to advances in diagnostic techniques. Here, we used whole-genome sequencing, extensive biotyping, MALDI-TOF mass spectrometry, and chemotaxonomy to characterize five coagulase-negative strains from the Staphylococcus haemolyticus phylogenetic clade obtained from human ear swabs, wounds, and bile. Based on the results of polyphasic taxonomy, we propose the species Staphylococcus brunensis sp. nov. (type strain NRL/St 16/872 T = CCM 9024 T = LMG 31872 T = DSM 111349 T ). The genomic analysis revealed numerous variable genomic elements, including staphylococcal cassette chromosome (SCC), prophages, plasmids, and a unique 18.8 kb-long genomic island SbCI ccrDE integrated into the ribosomal protein L7 serine acetyltransferase gene rimL . SbCI ccrDE has a cassette chromosome recombinase ( ccr ) gene complex with a typical structure found in SCCs. Based on nucleotide and amino acid identity to other known ccr genes and the distinct integration site that differs from the canonical methyltransferase gene rlmH exploited by SCCs, we classified the ccr genes as novel variants, ccrDE . The comparative genomic analysis of SbCI ccrDE with related islands shows that they can accumulate virulence and antimicrobial resistance factors creating novel resistance elements, which reflects the evolution of SCC. The spread of these resistance islands into established pathogens such as Staphylococcus aureus would pose a great threat to the healthcare system. IMPORTANCE The coagulase-negative staphylococci are important opportunistic human pathogens, which cause bloodstream and foreign body infections, mainly in immunocompromised patients. The mobile elements, primarily the staphylococcal cassette chromosome mec , which confers resistance to methicillin, are the key to the successful dissemination of staphylococci into healthcare and community settings. Here, we present a novel species of the Staphylococcus genus isolated from human clinical material. The detailed analysis of its genome revealed a previously undescribed genomic island, which is closely related to the staphylococcal cassette chromosome and has the potential to accumulate and spread virulence and resistance determinants. The island harbors a set of conserved genes required for its mobilization, which we recognized as novel cassette chromosome recombinase genes ccrDE . Similar islands were revealed not only in the genomes of coagulase-negative staphylococci but also in S. aureus . The comparative genomic study contributes substantially to the understanding of the evolution and pathogenesis of staphylococci.

Funder

Ministerstvo Školství, Mládeže a Tělovýchovy

Ministerstvo Zdravotnictví Ceské Republiky

Masarykova Univerzita

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Cell Biology,Microbiology (medical),Genetics,General Immunology and Microbiology,Ecology,Physiology

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