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. 2015 Dec 14;60(2):1121-8.
doi: 10.1128/AAC.02011-15. Print 2016 Feb.

Clinical and Molecular Features of Decreased Chlorhexidine Susceptibility among Nosocomial Staphylococcus aureus Isolates at Texas Children's Hospital

Affiliations

Clinical and Molecular Features of Decreased Chlorhexidine Susceptibility among Nosocomial Staphylococcus aureus Isolates at Texas Children's Hospital

J Chase McNeil et al. Antimicrob Agents Chemother. .

Abstract

One of the strategies utilized to decrease infections in the hospital setting relies on topical antimicrobials and antiseptics. While their use is beneficial, concerns arise over the potential to develop resistance or tolerance to these agents. We examined nosocomial Staphylococcus aureus isolates from 2007 to 2013 for the presence of genes associated with tolerance to chlorhexidine. Isolates and patients were identified from an S. aureus surveillance study at Texas Children's Hospital. Nosocomial S. aureus isolates (those causing infection at ≥72 h of hospitalization) were identified and underwent PCR for the qacA or qacB (qacA/B) and smr genes associated with elevated minimum bactericidal concentrations of chlorhexidine. Molecular typing with pulsed-field gel electrophoresis (PFGE), multilocus sequence typing (MLST), and agr typing and a review of the medical record were performed. Two hundred forty-seven nosocomial S. aureus infections were identified. Overall, 111 isolates carried one or both genes (44.9%); 33.1% were positive for smr, 22.7% were positive for qacA/B, and 10.9% of the isolates possessed both genes. The smr-positive isolates were more often resistant to methicillin, ciprofloxacin, and/or clindamycin. The isolates positive for qacA/B were more often associated with indwelling central venous catheters and a vancomycin MIC of ≥2 μg/ml. Isolates carrying either smr or qacA/B were associated with a diagnosis of bacteremia. The smr-positive isolates more often belonged to sequence type 8 (ST8) than the isolates that were positive for qacA/B. Mupirocin resistance was detected in 2.8% of the isolates. Antiseptic-tolerant S. aureus strains are common in our children's hospital and are associated with decreased susceptibility to other systemic antimicrobials and with bloodstream infections. Further work is needed to understand the implications that these organisms have on the hospital environment and antiseptic use in the future.

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Figures

FIG 1
FIG 1
Temporal trends in the presence of smr and qacA/B. (A) Total number of both MRSA and methicillin-susceptible S. aureus (MSSA) isolates per year. (B) Proportion of isolates bearing smr, qacA/B, or both per year of study.

References

    1. Wisplinghoff H, Seifert H, Tallent SM, Bischoff T, Wenzel RP, Edmond MB. 2003. Nosocomial bloodstream infections in pediatric patients in United States hospitals: epidemiology, clinical features and susceptibilities. Pediatr Infect Dis J 22:686–691. doi:10.1097/01.inf.0000078159.53132.40. - DOI - PubMed
    1. Blackburn RM, Henderson KL, Minaji M, Muller-Pebody B, Johnson AP, Sharland M. 2012. Exploring the epidemiology of hospital-acquired bloodstream infections in children in England (January 2009–March 2010) by linkage of national hospital admissions and microbiological databases. J Pediatr Infect Dis Soc 1:284–292. doi:10.1093/jpids/pis084. - DOI - PubMed
    1. Murray MT, Krishnamurthy G, Corda R, Turcotte RF, Jia H, Bacha E, Saiman L. 2014. Surgical site infections and bloodstream infections in infants after cardiac surgery. J Thorac Cardiovasc Surg 148:259–265. doi:10.1016/j.jtcvs.2013.08.048. - DOI - PubMed
    1. Grohskopf LA, Sinkowitz-Cochran RL, Garrett DO, Sohn AH, Levine GL, Siegel JD, Stover BH, Jarvis WR, Pediatric Prevention Network . 2002. A national point-prevalence survey of pediatric intensive care unit-acquired infections in the United States. J Pediatr 140:432–438. doi:10.1067/mpd.2002.122499. - DOI - PubMed
    1. Stoll BJ, Hansen N, Fanaroff AA, Wright LL, Carlo WA, Ehrenkranz RA, Lemons JA, Donovan EF, Stark AR, Tyson JE, Oh W, Bauer CR, Korones SB, Shankaran S, Laptook AR, Stevenson DK, Papile LA, Poole WK. 2002. Late-onset sepsis in very low birth weight neonates: the experience of the NICHD Neonatal Research Network. Pediatrics 110:285–291. doi:10.1542/peds.110.2.285. - DOI - PubMed

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