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Epidemiology of borderline oxacillin-resistant Staphylococcus aureus in pediatric cystic fibrosis
Timothy Ronan Leahy1, Yvonne C W Yau, Eshetu Atenafu
1Institute of Molecular Medicine, St James's Hospital, James's St, Dublin 8, Ireland. leahyt@tcd.ie.
Insights
Borderline oxacillin-resistant Staphylococcus aureus (BORSA) is common in children with cystic fibrosis and lacks mecA. Antibiotic use may drive BORSA development, but it did not worsen disease progression compared to MRSA.
Area of Science:
- Infectious Diseases
- Microbiology
- Pediatrics
Background:
- Cystic fibrosis (CF) patients are susceptible to Staphylococcus aureus infections.
- Methicillin resistance in S. aureus can be mediated by mecA or other mechanisms, leading to MRSA or BORSA phenotypes.
- Understanding resistance patterns in CF is crucial for effective treatment.
Purpose of the Study:
- To evaluate risk factors for acquisition of borderline oxacillin-resistant Staphylococcus aureus (BORSA) versus mecA-positive methicillin-resistant Staphylococcus aureus (MRSA) in children with CF.
- To analyze the molecular epidemiology of these resistant strains.
- To assess the impact of BORSA and MRSA on disease progression in pediatric CF patients.
Main Methods:
- Retrospective single-center study of children with CF and positive respiratory cultures for BORSA or MRSA.
- Collection of clinical and epidemiological data from the 12 months preceding the index culture.
- Microbiological and molecular characterization of isolates and assessment of clinical outcomes.
Main Results:
- Eighteen of 34 eligible children (53%) had BORSA; 16 acquired BORSA only.
- Prior MSSA colonization (P < 0.0001) and use of oral cephalexin (P < 0.01) or inhaled tobramycin (P < 0.03) were associated with BORSA acquisition.
- BORSA isolates were often hyper β-lactamase producers, susceptible to more antibiotics, and showed no strain relatedness. No difference in disease progression was observed between BORSA and MRSA groups.
Conclusions:
- A significant proportion of methicillin-resistant S. aureus in pediatric CF patients are BORSA lacking mecA.
- Antibiotic pressure may contribute to the emergence of BORSA in this population.
- Further prospective studies are needed to clarify the clinical significance of BORSA in CF.
Abstract:
A single-center retrospective study was undertaken in children with cystic fibrosis (CF) to evaluate (1) risk factors for acquisition; (2) molecular epidemiology; and (3) impact on disease progression of borderline oxacillin-resistant Staphylococcus aureus (BORSA) versus mecA-positive methicillin-resistant Staphylococcus aureus (MRSA). The study comprised of (1) identification of all children with at least one respiratory specimen positive for either BORSA or MRSA during the study period; (2) compilation of relevant clinical and epidemiological data from 12-month period leading up to first positive (index) culture; (3) microbiological and molecular characterization of index isolates and (4) measurement of subsequent clinical outcome. Thirty-eight children were identified with at least one positive isolate; 4 were excluded due to insufficient clinical or laboratory data. Eighteen children (53%) grew BORSA in their index culture. Children who acquired BORSA only (n = 16) were more likely to have had prior MSSA colonization (P < 0.0001). Usage of oral cephalexin (P < 0.01) and inhaled tobramycin (P < 0.03) prior to index culture was significantly and independently associated with acquisition of BORSA. The majority of BORSA isolates were hyper β-lactamase producers and susceptible to a greater range of antibiotics. Strain relatedness was not evident within the BORSA group. There was no difference in disease progression between the two groups. This is the first study to demonstrate that a significant proportion of S. aureus isolates with methicillin resistance in the CF population are BORSAs that lack mecA. Antibiotic pressure may lead to the development of BORSA in CF patients. Prospective studies are needed to assess its clinical impact.
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