The prevalence of multidrug resistance in Staphylococcus hominis isolated from clinical materials
The treatment of infections caused by Staphylococcus hominis remains a challenge, mainly due to the increasing resistance of these bacteria to antibiotics. The aim of the study was to determine antibiotic resistance in 62 strains S. hominis isolated from clinical materials, and to identify the molec...
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Veröffentlicht in: | Scientific reports 2025-01, Vol.15 (1), p.414-12, Article 414 |
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Zusammenfassung: | The treatment of infections caused by
Staphylococcus hominis
remains a challenge, mainly due to the increasing resistance of these bacteria to antibiotics. The aim of the study was to determine antibiotic resistance in 62 strains
S. hominis
isolated from clinical materials, and to identify the molecular basis of resistance to antibiotics. Forty-six strains were both methicillin-resistant and harbored the
mecA
gene. Twenty-three of these strains had
mec
complex A and
ccr
complex AB1. Such a combination of the
mec
and
ccr
complexes does not correspond to any cassettes that have been demonstrated so far. However, over 80% of the tested strains were multidrug-resistant, of which as many as 12 were resistant to at least seven antibiotics. More than a half of strains harbored the
tetK
,
acc(6’)-Ie aph(2’’)
, and
ant(4’)-I
genes.
erm(C)
was the most common resistant gene to antibiotics from the MLS group. Two strains had as many as five antibiotic resistance genes from the tested groups (
erm(C), msr(A), msr(B), mph(C), lnu(A)
). The presence of the
vga
gene encoding resistance to streptogramins A was detected in one strain. All of strains were sensitive to vancomycin. However, 11 of them had reduced sensitivity to this antibiotic and eight of them were characterized by a heterogeneous resistance profile to this antibiotic. Our results clearly shows increasing threat of
S.
hominis
caused by their multi-resistance. Moreover, these bacteria can constitute a reservoir of resistance genes for more pathogenic bacteria. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-024-84500-2 |