Abstract

Clindamycin is indicated in the treatment of skin and soft-tissue infections caused by Staphylococcal species. Treatment of an infection caused by a strain carrying inducible erm gene using clindamycin or any non-inducer macrolide can lead to clinical failure. The present study was aimed to detect inducible-clindamycin resistance (MLSBi) among S. aureus isolates in Port Harcourt, Nigeriaand to study the relationship between clindamycin and methicillin-resistant <i S. aureus (MRSA).Two hundred and five (205) non-duplicate Staphylococcus aureus previously isolated from human sources were randomly collected from three health facilities- University of Port Harcourt Teaching Hospital, Braithwaite Memorial Specialist Hospital and De-Integrated Laboratories-all located in Port Harcourt, Nigeria, for this study from August, 2012 to July, 2013. Isolates were grouped as hospital in-patient (termed hospital- acquired – Nosocomial; n = 76) and out- patient cases (community-acquired; n = 129) Staphylococcus aureus . The isolates collected were reconfirmed following standard laboratory protocols. All confirmed isolates were stored in glycerol at +4°C (later sub-cultured for various phenotypic analyses). Using the disk diffusion method, detection of MRSA was carried out with 1μg of oxacillin (OXOID) placed on Mueller-Hinton agar with 4% NaCl supplementation).Antimicrobial susceptibility testing was performed using Erythromycin (15μg) and Clindamycin (2μg) both obtained from OXOID, UK. All clindamycin-sensitive isolates that were also erythromycin-resistant were subjected to D-Test phenotype (Inducible-clindamycin resistance). Among the 205 S. aureus isolates studied, Forty-four (21.5%) showed resistance to erythromycin, while 38 of these erythromycin-resistant isolates were simultaneously sensitive to clindamycin. Overall, out of 205 isolates, inducible-clindamycin resistance was detected in 23 (11.2%) of the isolates. These 23 (inducible MLSB phenotype) are among 38 erythromycin-resistant S. aureus that were simultaneously sensitive (phenotypically) to clindamycin. Ten (4.9%) of the total (205) study isolates expressed constitutive resistance to clindamycin. Oxacillin Resistance (MRSA) was detected in 25 (12.2%) of the 205 isolates. Among the 38 erythromycin-resistant S. aureus, four were MRSA while 3 (75%) of the 4 erythromycin-resistant MRSA expressed inducible resistance to clindamycin. 20 (58.8%) of 34 erythromycin-resistant MSSA expressed inducible resistance to clindamycin. MRSA phenotype was not significantly correlated (p=0.9430) to inducible-clindamycin resistance. Inducible clindamycin-resistance often leads to treatment failure. The clinical microbiology laboratories in Nigeria should consider routine testing and reporting of inducible clindamycin resistance in S. aureus . There is also the need for sustained surveillance of antimicrobial susceptibilities of S. aureus in this region.

Highlights

  • The determination of antimicrobial susceptibility pattern of a clinical isolate is very important for the effective management of infected patients

  • All confirmed isolates were stored at +4°Cand later sub cultured to carry out antibiotic susceptibility testing against Oxacillin (1μg) (MRSA) and D-Test (Inducible clindamycin resistance) using Erythromycin (15μg) and Clindamycin (2μg)

  • Two hundred and five (205) non-duplicate isolates of Staphylococcus aureus cultivated from different clinicalspecimens between August, 2012 and July, 2013, Table 4 shows inducible clindamycin resistance

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Summary

Introduction

The determination of antimicrobial susceptibility pattern of a clinical isolate is very important for the effective management of infected patients. This is moreso in the light of the emergence of multidrug-resistant microorganisms. In view of the Easter Godwin Nwokah and Samuel Douglas Abbey: Inducible-Clindamycin Resistance in Staphylococcus aureus Isolates in Rivers State, Nigeria gradual depletion in the armamentarium of antimicrobial agents effective against S. aureus, there has been renewed interest in the use of the Macrolide(erythromycin, clarithromycin)-Lincosamide (clindamycin, lincomycin)Streptogramin B (quinupristin-dalfopristin) (MLSB) antibiotics to treat S. aureus infections with clindamycin being the preferred agent due to its excellent pharmacokinetic properties [5,6]. MLSB antibiotics structurally related, exhibit similar mode of action. They inhibit bacterial protein synthesis by binding to 23s rRNA, which is a part of large ribosomal subunit

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