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Published on: December 4, 2015
Swine as reservoirs of zoonotic borderline oxacillin-resistant Staphylococcus aureus ST398
S C L Santos1, M M S Saraiva2, A L B Moreira Filho3
1Department of Animal Science, College for Agricultural Sciences, Federal University of Paraiba (UFPB), Rod. PB079 Km12, s/n, 58397-000, Areia, PB, Brazil.
Abstract:
Methicillin resistance mediated by the mecA gene in Staphylococcus aureus, also known as "true MRSA", is typically associated with high oxacillin MIC values (≥8 mg/L). Because non-mecA-mediated oxacillin resistant S. aureus phenotypes can also cause hard-to-treat diseases in humans, their misidentification as methicillin-susceptible S. aureus strains (MSSA) can compromise the efficiency of the antimicrobial therapy. These strains have been refereed as Borderline Oxacillin-Resistant S. aureus (BORSA) but their characterization and role in clinical microbiology have been neglected. Considering the increasing importance of livestock-associated methicillin-resistant S. aureus ST398 (LA-MRSA) as an emerging zoonotic pathogen worldwide, this study aimed to report the genomic context of oxacillin resistance in porcine S. aureus ST398 strains. S. aureus isolates were recovered from asymptomatic pigs from three herds. Oxacillin MIC values ranged from 4 to 32 mg/L. MALDI-TOF-confirmed isolates were screened for mecA and mecC by PCR and genotyped by means of PFGE and Rep-PCR. Seven isolates were whole genome sequenced. None of the isolates harbored the mecA gene or its variants. Although all seven sequenced isolates belonged to one sequence type (ST398), two different spa types (t571 and t1471) were identified. All isolates harbored conserved blaZ gene operon and no mutations on genes encoding for penicillin-binding-proteins were detected. Genes conferring resistance against other drugs such as aminoglycosides, chloramphenicol, macrolide, lincosamide and streptogramin (MLS), tetracycline and trimethoprim were also detected. Isolates also harbored virulence genes encoding for adhesins (icaA; icaB; icaC; icaD; icaR), toxins (hlgA; hlgB; hlgC; luk-PV) and protease (aur). Pigs can serve as reservoirs of non-mecA-mediated oxacillin-resistant ST398 strains potentially pathogenic to humans. Considering that mecA has been the main target to screen methicillin-resistant staphylococci, the occurrence of BORSA phenotypes is probably underestimated in livestock.
Insights
Pigs carry oxacillin-resistant Staphylococcus aureus ST398 strains lacking the mecA gene, posing a potential human health risk. These Borderline Oxacillin-Resistant S. aureus (BORSA) may be underestimated in livestock surveillance.
Area of Science:
- Microbiology
- Genomics
- Antimicrobial Resistance
Background:
- Methicillin resistance in Staphylococcus aureus (MRSA) is typically mecA-mediated.
- Non-mecA-mediated oxacillin-resistant strains (BORSA) can cause difficult-to-treat infections and may be misidentified.
- Livestock-associated MRSA ST398 is an emerging zoonotic pathogen.
Purpose of the Study:
- To investigate the genomic context of oxacillin resistance in porcine Staphylococcus aureus ST398.
- To characterize oxacillin resistance mechanisms in S. aureus isolates from pigs.
Main Methods:
- Oxacillin MIC determination.
- mecA and mecC screening by PCR.
- Genotyping using PFGE and Rep-PCR.
- Whole genome sequencing of selected isolates.
Main Results:
- All seven sequenced porcine S. aureus ST398 isolates lacked the mecA gene.
- Oxacillin MIC values ranged from 4 to 32 mg/L.
- Isolates harbored blaZ, virulence genes, and resistance genes for other antibiotics.
- Two different spa types (t571 and t1471) were identified within ST398.
Conclusions:
- Pigs can act as reservoirs for non-mecA-mediated oxacillin-resistant S. aureus ST398 strains.
- The prevalence of BORSA phenotypes in livestock may be underestimated due to reliance on mecA screening.
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