Background: Coagulase-negative staphylococci belonging to S. haemolyticus, S. hominis subsp. hominis, S. simulans, and S. warneri are often described as etiological factors of infections. Staphylococci are a phylogenetically coherent group; nevertheless, there are differences among the species which may be important to clinicians.
Methods: We investigated selected virulence factors and antibiotic resistance that were phenotypically demonstrated, the presence and expression of genes encoding the virulence factors, and the type of the SCCmec cassette.
Results: The differences between the tested species were revealed. A great number of isolates produced a biofilm and many of them contained single icaADBC operon genes. Clear differences between species in the lipolytic activity spectrum could be related to their ability to cause various types of infections. Our studies also revealed the presence of genes encoding virulence factors homologous to S. aureus in the analysed species such as enterotoxin and pvl genes, which were also expressed in single isolates of S. simulans and S. warneri. S. haemolyticus and S. hominis subsp. hominis isolates were resistant to all clinically important antibiotics including ß-lactams. The identified SCCmec cassettes belonged to IV, V, VII, and IX type but most of the detected cassettes were non-typeable. Among the investigated species, S. hominis subsp. hominis isolates accumulated virulence genes typical for S. aureus in the most efficient way and were widely resistant to antibiotics.
Conclusions: Our results clearly indicated significant differences between the tested species, which might be a result of the horizontal gene transfer (HGT) and can lead to the formation and selection of multi-drug resistant strains as well as strains with new virulence features. Such strains can have a new clinical relevance.
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http://dx.doi.org/10.1186/s12879-020-4841-2 | DOI Listing |
Pathogens
November 2022
Faculty of Health Sciences, Universiti Sultan Zainal Abidin, Kuala Nerus 21300, Malaysia.
is a coagulase-negative (CoNS) commensal capable of causing serious systemic infections in humans. The emergence of multidrug-resistant strains is of concern but little is known about the characteristics of this organism, particularly from Malaysia. Here, we present the comparative genome analysis of ShoR14, a multidrug-resistant, methicillin-resistant blood isolate from Terengganu, Malaysia.
View Article and Find Full Text PDFIndian J Med Microbiol
March 2023
Laboratorio de Microbiología General, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León, Av. Pedro de Alba S/N, Col. Ciudad Universitaria, 66450, San Nicolás de los Garza, Nuevo León, México. Electronic address:
Microbiol Spectr
August 2022
Department of Veterinary Microbiology, Faculty of Veterinary Science, Chulalongkorn Universitygrid.7922.e, Bangkok, Thailand.
Staphylococcus haemolyticus and Staphylococcus hominis subsp. are common coagulase-negative staphylococcus opportunistic pathogens. In Thailand, the clinical strains 1864 and 48 and S.
View Article and Find Full Text PDFBMC Vet Res
June 2022
Istituto Zooprofilattico Sperimentale della Sardegna "G. Pegreffi", Via Vienna 2, 07100, Sassari, Italy.
Background: In a collaboration between animal and human health care professionals, we assessed the genetic characteristics shared by non-aureus staphylococci (NAS) infecting humans and dairy ewes to investigate their relatedness in a region concentrating half of the total National sheep stock. We examined by PCR 125 ovine and 70 human NAS for biofilm production, pyrogenic toxins, adhesins, autolysins genes, and accessory gene regulator (agr) locus. The microtiter plate assay (MPA) was used for the phenotypic screening of biofilm production.
View Article and Find Full Text PDFFood Sci Technol Int
July 2023
Faculty of Agriculture, University of Belgrade, Nemanjina 6 Str., Belgrade 11000, Serbia.
The aim of this study was to select autochthonous lactic acid bacteria (LAB) isolates with antilisterial activity from Zlatar cheese and to evaluate the ability of selected LAB to control growth during soft white cheese production. The genotype characterization of isolated LAB (n = 93) was done using PCR method by 16S rRNA sequencing. In this way, the following isolates were detected: ssp.
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