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. 2025 Jan 2;15(1):597.
doi: 10.1038/s41598-024-84307-1.

Clonal shift and impact of azithromycin use on antimicrobial resistance of Staphylococcus aureus isolated from bloodstream infection during the COVID-19 pandemic

Collaborators, Affiliations

Clonal shift and impact of azithromycin use on antimicrobial resistance of Staphylococcus aureus isolated from bloodstream infection during the COVID-19 pandemic

Carolina de Oliveira Whitaker et al. Sci Rep. .

Abstract

Staphylococcus aureus is a relevant pathogen in bloodstream infections (BSI), and the emergency of the COVID-19 pandemic increased its antimicrobial resistance. S. aureus isolates from BSI (September/2019 - March/2021) were analyzed phenotypically and molecularly, in addition to the clinical features of the patients. Of 88 S. aureus isolates recovered from 85 patients, 25 were isolated before the pandemic and 63 during it, and 16 were from patients with COVID-19. A rate of 45.5% of methicillin-resistant isolates (MRSA) were found, and 5% of them were ceftaroline susceptible dose-dependent. Daptomycin non-susceptibility was observed in 9.1% of isolates. The USA800/ST5/SCCmecIV lineage was prevalent among MRSA isolates (41.8%). Besides, 30.2% of the isolates were associated with community-associated MRSA (CA-MRSA) genotypes. There was a significant impact on the resistance rates for cefoxitin, clindamycin and erythromycin among S. aureus isolates from BSI in COVID-19 patients and association with the previous use of azithromycin by them (p < 0.05). A clonal alternation and an increase in the emergence of CA-MRSA lineages were also found, highlighting the importance of constant microbiological surveillance.

Keywords: S. aureus; Antimicrobial resistance; Bloodstream infection; COVID-19; MRSA lineages.

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Conflict of interest statement

Declarations. Competing interests: The authors declare no competing interests. Ethical approval: The study was approved by the Human Research Ethics Committee of HUCFF (CAAE 40458520.7.0000.5257).

Figures

Fig. 1
Fig. 1
Antimicrobial resistance rates among S. aureus isolated during (A) and before the COVID-19 pandemic (B). * p-value < 0.05. CFX – Cefoxitin; CIP – Ciprofloxacin; CLI – Clindamycin; ERI – Erythromycin; GEN – Gentamycin; PEN – Penicillin G; RIF – Rifampicin; TSX - Trimethoprim-sulfamethoxazole; iMLSB - inducible macrolide-lincosamide-streptogramin B resistance.
Fig. 2
Fig. 2
Dendrogram of the PFGE patterns and characteristics related to the genetic background of 40 MRSA isolates recovered from bloodstream infection. LV: Latin American Variant; SCCmec: Staphylococcal cassette chromosome mec; ST: Sequence Type; MIC: Minimal Inhibitory Concentration in mg/L; Oxa: oxacillin; Van: vancomycin; Dap: daptomycin; Cef: ceftaroline; CA: Community acquisition; HA: hospital acquisition; AAH: Acquisition in another hospital; HCA: Healthcare acquisition; na: not applicable (strain isolated before pandemic); ep: episode; *: pvl gene positive; **: pvl gene and ACME positive; a: susceptible-dose dependent for ceftaroline.

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