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Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus (MRSA)
Published on: February 10, 2011
Methicillin-susceptible and -resistant Staphylococcus aureus with high-level antiseptic and low-level mupirocin
Hamed Ghasemzadeh-Moghaddam1, Alex van Belkum, Rukman Awang Hamat
11 Department of Medical Microbiology and Parasitology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia , Serdang, Malaysia .
Abstract:
The prevalence and spread of mupirocin and antiseptic resistance among colonizing and infectious Staphylococcus aureus were determined. S. aureus isolated from anterior nares and infection sites of patients hospitalized in the largest tertiary care referral hospital in Malaysia was investigated for mupirocin and antiseptic susceptibility testing, and for PCR detection of mupA, qacA/B, and smr genes. Twelve isolates showed resistance to mupirocin by disk diffusion, of which 10 (3.8%) harbored the mupA gene. Minimum inhibitory concentrations (MICs) ranged from 64 to 768 μg/ml for mupA positive and below 46 μg/ml for negative isolates. The mupA was more common among ST239 isolates (70%). The qacA/B was carried in 67 out of 95 methicillin-resistant Staphylococcus aureus (MRSA) (70.5%) and 3 out of 164 methicillin-susceptible Staphylococcus aureus (MSSA) (1.8%), while smr was carried in 6 out of 95 MRSA (6.3%) strains. MICs ranged from 3.9 to 15.6 μg/ml for benzethonium chloride (BTC) and benzalkonium chloride (BKC), and from 10.3 to 20.7 μg/ml for chlorhexidine digluconate (CHG). Isolates with qacA/B and smr or qacA/B alone showed higher MIC (20.7 μg/ml for CHG and 15.6 μg/ml for BTC and BKC) than the isolates that lacked antiseptic resistance genes (10.3 μg/ml for CHG and 3.9 μg/ml for BTC and BKC). In 16 cases, ST239 was isolated from the infection site and the nares simultaneously, and shared identical resistance patterns (qacAB or qacAB+smr), suggesting possible endogenous infection. Spread of low-level mupirocin resistance expressing ST239 MRSA and high-level resistance expressing emerging ST1, co-existing with antiseptic-resistant genes showing elevated MICs, should be monitored for effective infection control.
Insights
Mupirocin and antiseptic resistance in Staphylococcus aureus, particularly ST239 MRSA, is prevalent in Malaysian hospitals. Monitoring these resistant strains is crucial for effective infection control.
Area of Science:
- Microbiology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Staphylococcus aureus is a common cause of hospital-acquired infections.
- Mupirocin and antiseptics are vital for controlling S. aureus colonization and infections.
- Emergence of resistance threatens treatment efficacy.
Purpose of the Study:
- To determine the prevalence and spread of mupirocin and antiseptic resistance in S. aureus.
- To investigate the genetic basis of resistance (mupA, qacA/B, smr genes).
- To understand the relationship between resistance, bacterial strains (ST239, MRSA, MSSA), and clinical outcomes.
Main Methods:
- Isolation of S. aureus from nares and infection sites of hospitalized patients.
- Antimicrobial susceptibility testing (disk diffusion, MICs) for mupirocin and antiseptics.
- PCR detection of mupA, qacA/B, and smr resistance genes.
Main Results:
- 10 (3.8%) S. aureus isolates harbored the mupA gene, conferring mupirocin resistance.
- The mupA gene was more common in ST239 isolates (70%).
- qacA/B and smr genes were frequently found in MRSA (70.5% and 6.3%, respectively) but rarely in MSSA (1.8%).
- Isolates with antiseptic resistance genes showed significantly higher MICs for benzethonium chloride, benzalkonium chloride, and chlorhexidine digluconate.
- ST239 strains with identical resistance patterns were isolated from both nares and infection sites, suggesting endogenous spread.
Conclusions:
- Widespread mupirocin and antiseptic resistance exists in S. aureus within a Malaysian tertiary hospital.
- ST239 MRSA strains are significant carriers of both mupirocin (mupA) and antiseptic resistance genes (qacA/B, smr).
- Co-occurrence of resistance genes leads to elevated MICs, necessitating enhanced infection control strategies and monitoring of emerging resistant strains like ST1.
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