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INTERNATIONAL JOURNAL OF CURRENT RESEARCH IN BIOLOGY AND MEDICINE ISSN: 2455-944X www.darshanpublishers.com DOI:10.22192/ijcrbm Volume 2, Issue 7-2017 Original Research Article Prevalence and resistance pattern of methicillin-resistant coagulase negative Staphylococci among orthopaedic patients in a tertiary institution in North western Nigeria Ayokunnumi F. Obajuluwa 1*, Josiah A. Onaolapo 2, Busayo O. Olayinka 2, Gbonjubola O. Adeshina 2 1 Department of Pharmaceutics and Pharmaceutical Microbiology, Faculty of Pharmaceutical sciences, Kaduna State University, Kaduna, Nigeria. 2 Department of Pharmaceutics and Pharmaceutical Microbiology, Faculty of Pharmaceutical sciences, Ahmadu Bello University, Zaria, Nigeria. *Corresponding author: funkeyomi6874@gmail.com Abstract Background: Increasing rate of antibiotic resistance in coagulase negative Staphylococci is of great concern especially methicillin resistant coagulase negative Staphylococci (MRCoNS). It causes increased mortality, morbidity and increased health care costs Objective: The aim of this study was to determine the prevalence of methicillin resistance among the coagulase negative Staphylococci isolates from orthopaedic patients in Ahmadu Bello University Teaching Hospital in North-west Nigeria and their resistance pattern to antibiotics. Method: In this study, 114 clinical samples were collected from orthopaedic patients in Ahmadu Bello University Teaching Hospital, located in North West Nigeria. Biochemical tests were carried out to isolate the coagulase negative Staphylococci while Cefoxitin disc diffusion test was used to determine their methicillin resistance. Antibiotic susceptibility test was carried out using disc agar diffusion method. Results: Using biochemical test 74 Staphylococci isolates were confirmed to be coagulase negative, 48 out of CoNS isolates were found to be methicillin resistant. The antibiotics susceptibility test carried out on the MRCoNS isolates showed the resistance pattern to be in this order: ampicllin (100%), amoxicillin-clavulanic acid (87.5%), ceftriaxone (87.5%), clindamycin (60.5%) and erythromycin (54.2), 39.6% were multi-drug resistant. Conclusion: High prevalence of methicillin-resistant coagulase negative staphylococci was observed in this study. The MRCoNS were generally resistant to beta lactam antibiotics. Keywords: Coagulase, Staphylococci, orthopaedics, methicillin resistance. DOI: http://dx.doi.org/10.22192/ijcrbm.2017.02.07.002 Introduction Coagulase negative Staphylococci (CoNS) belong to the family Micrococcaceae and several species has been identified. Since the 1970s, it has been suggested that CoNS are of great importance as true pathogens, and they have become a common cause of a wide variety of infections (Dubois et al., 2010; Otto, 2009). CoNS colonize different parts of human skin and mucous membrane, this is the major source of endogenous infection by CoNS (Roth and James, 1988, Becker et al., 2014). They are associated with 9

the use of implant, once inserted, foreign bodies can placed on the plates and incubated at 37 0 C for 18 become colonized by CoNS and the success of the hours after which zone of inhibition diameter was respective medical procedure is significantly impaired, measured in reflected light. An inhibition zone resulting in enormous medical and economic burdens. diameter 21 mm was reported as methicillin resistant They have also been recognised as the cause of and 22 mm was considered as methicillin susceptible prosthetic valve endocarditis, neurosurgical shunt (CLSI, 2013). infection and infection of prosthetic orthopaedic devices (Huebner & Goldmann, 1999; Zong et al., Antibiotics susceptibility test 2011) Increasing rates of antibiotic resistance in CoNS is a great problem and this is limiting our therapeutic options. Methicillin resistance in Staphylococci emerged from the acquisition of the meca gene encoded by penicillin-binding protein 2a (PBP2a), a transpeptidase conferring broad-spectrum beta- lactam resistance (IWG -SCC, 2009). Over the last decade, methicillin resistant Staphylococci strains have become endemic in hospitals worldwide. Also, they are now an endemic community pathogen in many geographical regions (Tiwari and Sen, 2006; Lowy, 1998), the strains have also been reported to be implicated in causing progressively increased mortality, morbidity and increased health care costs (Cosgrove et al., 2003; Tiwari et al., 2008). This study was aimed at determining the prevalence of methicillin-resistant coagulase negative Staphylococci among the orthopaedic patients in Ahmadu Bello University and their antibiotics resistance pattern. Materials and Methods Isolation and classification of Staphylococci After obtaining consent clinical samples were collected aseptically from the skin, beddings and wounds of orthopaedic patients in Ahmadu Bello University Teaching Hospital, North-west Nigeria. Biochemical tests were performed on the purified isolates to classify the Staphylococci isolates based on their coagulase properties. API STAPH identification kit (biomerieux, Inc.,Durham,NC) was used to further characterize the coagulase negative Staphylococci into species. Kirby Bauer disk diffusion method was used to determine the antibiotics susceptibility test of the methicillin - resistant CoNS isolates according to the Clinical and Laboratory Standards Institute (CLSI) (Clinical and Laboratory Standards Institute., 2012). The following antibiotics was used: Cefoxitin 30μg, Ceftriaxone 30μg, Vancomycin 30μg, Ampicillin 10μg, Gentamicin 10μg, Pefloxacin 5μg, Ciprofloxacin 5μg, Amoxicillin-clavulanic acid 30μg, Erythromycin 15μg and Clindamycin 2μg (Oxoid Ltd. Basingstoke, London). Determination of resistance pattern of MRCoNS isolates Joint initiative by the European Centre for Disease Prevention and Control (ECDC), and the Centre for Disease Prevention and Control (CDC) gave a standard method for proper description of multidrugresistant (MDR), extensively drug -resistant (XDR) and pandrug resistant (PDR) profiles, in their conclusion, acquired, non-susceptibility to at least one agent in three or more antimicrobial categories were considered MDR, while non-susceptibility to at least one agent in all but two or fewer antimicrobial categories (i.e bacterial isolates remain susceptible to only one or two antimicrobial categories) were considered XDR. PDR was considered as non susceptibility to all agents in all antimicrobial categories (Magiorakos et al, 2012, Silpi et al, 2016). This was used as the standard for the characterization of resistance profile of MRCoNS isolates in this study. Results Detection of methicillin resistance Clinical Laboratory Standards Institute (CLSI) has recommended cefoxitin disc diffusion method for the detection of Methicillin-reistant Staphylococcus aureus due to its ability to enhance induction of PBP2a. A 0.5 Mc Farland standard suspension of the isolate was made and a lawn culture was done on Mueller Hinton Agar plate. Cefoxitin 30 µg discs were 10 Isolation and classification of Staphylococci A total number of 114 samples were collected from the orthopaedic patients, with the use of conventional methods 74 (64.1%) were confirmed to be coagulase negative Staphylococci. The characterization of the CoNS isolates is presented in Table 1, 10(13.5%) were undetermined.

Antibiotics susceptibility Table 1: Identification of Staphylococci species Staphylococci species Number of isolates (%) S. xylosus 23 (31.1) S. lentus 8 (10.8) S. hominis 8 (10.8) S. cohnii cohnii 4 (5.4) S. epidermidis 3 (4.1) S. cohnii ureal. 2 (2.7) S. lugdunensis 2 (2.7) S. hyicus 2 (2.7) S. caprae 1 (1.4) S. warneri 1 (1.4) S. sciuri 1 (1.4) S. chromogens 1 (1.4) S. capitis 1 (1.4) S. haemolyticus 1 (1.4) Gentamicin and ciprofloxacin were the most active (95.8%) (Table 2) Table 2: Antibiotic susceptibility of MRCoNS No of CoNS isolates (%) n= 48 Antibiotics Resistant Intermediate Sensitive Vancomycin 3 (6.3) - 45 (93.8) Ampicillin 48 (100) - - Ceftriaxone 34 (70.8) 8 (16.7) 6 (12.5) Amoxicillin-clavulanic 42 (87.5) - 6 (12.5) Pefloxacin 7 (14.6) 1 (2.1) 40 (83.3) Gentamicin 1 (2.1) 1 (2.1) 46 (95.8) Erythromycin 12(25.0) 14 (29.2) 22 (45.8) Clindamycin 14 (29.2) 15 (31.3) 19 (39.6) Ciprofloxacin 1 (2.1) 1 (2.1) 46 (95.8) Detection of methicillin resistance Methicillin resistance was detected in 48 (64.9%) out of the 74 CoNS isolates Resistance pattern of MRCoNS isolates Out of the 48 MRCoNS, 14 (29.2%) were multi-drug resistant (Fig. 1). The MRCoNS isolates were generally resistant to beta-lactam antibiotics. 11

Fig.1: Incidence of MDR, XDR and PDR among the MRCoNSisolates Discussion Prevalence of methicillin resistance observed in this study was high (64.9%), in Nigeria where this research was carried out there were reports on methicillinresistant Staphylococcus aureus but not much has been reported about methicillin-resistant coagulase negative Staphylococci in clinical setting. However the prevalence observed in this study was consistent with the reports from other parts of the world: 67.5% prevalence of MRCoNS was reported from blood cultures of septicaemia patients in Turkey (Ko Ksai et al, 2009) and 45% prevalence from surgical wounds (Rahman et al, 2013), 52% from a tertiary care hospital in Iran (Sharma et al, 2010). Iyamba et al, 2014 reported 60% prevalence of MRCoNS from surgical site infections from Kinshasa. The high prevalence of MRCoNS should be of great concern to health institutions and the community at large due to its antibiotics multi-resistance challenge and the financial burden on the in-patients especially here in Nigeria, a developing country. Antibiotic resistant coagulase negative Staphylococci has emerged as a major cause of morbidity and mortality in hospital setting. The level of antibiotics resistance in MRCoNS isolates observed in this study is high, this is an indication of possible misuse of antibiotics by the patients before hospital admission or possible acquiring of resistant strains through nosocomial infections since coagulase negative staphylococci has been reported to be an agent of nosocomial infections (Washington et al, 2001). There is a great need for a campaign against misuse and abuse of antibiotics in our society. 12 The isolates were generally resistant to beta lactam antibiotics, lincosamine and macrolides which are cheap readily available antibiotics. In a report by Diekema et al, 2001, resistance to penicillin among the coagulase-negative staphylococci (CoNS) approaches 90 to 95 percent, resistance to methicillin and semisynthetic penicillins has been observed in more than 80 percent of CoNS isolates; these isolates are often resistant to multiple classes of antibiotics in addition to beta-lactams, therefore limiting traditional treatment options, like those with semi-synthetic penicillins. Iyamba et al, 2014 reported high resistant of MRCoNS isolates to ampicillin (beta lactam), erythromycin (macrolide), clindamycin (lincosamine) and ciprofloxacin. The multidrug resistance observed may also be probably due to the ability of MRCoNS strains to produce biofilms. Staphylococci are known as especially good biofilm formers, which is due primarily to the production of a series of surface molecules that promote extracellular matrix formation (Otto, 2008). However, high antibiotics susceptibility was observed with gentamicin (95.8%), ciprofloxacin (95.8%) and vancomycin (93.8%). Even though vancomycin is a drug of choice in the treatment of methicillin-resistant infections (Whitener et al, 2004) 6.2% resistance was observed in this study, this correspond with previous reports from Nigeria (Alo et al, 2013, Obajuluwa et al, 2016) even though vancomycin is not a readily available drug in the country.

Conclusion Huebner, J. & Goldmann, D. A. (1999).Coagulase - negative staphylo-cocci: role as pathogens. Annu In this study high prevalence of methicillin-resistant Rev Med 50, 223 236. coagulase negative staphylococci was observed Lowy F.D (1998). Staphylococcus aureus infections. therefore importance should be accorded to the New England Journal of Medicine. 339:520-532. isolation of coagulase negative and their antibiotics Iyamba J.M., Wambale J.M., Lukukula C.M., za susceptibility studies. Also there is the need for proper Balega Takaisi-Kikuni N., (2014). High prevalence surveillance studies and preventive measures in our of methicillin-resistant Staphylococci strains hospitals to control the emergence and spread of isolated from surgical wound sites in Kinshasa. MRCoNS. It suggested from the findings in this study PanAfr Med J. 18:322 that gentamicin and ciprofloxacin be used in the Koksai F., Yasar H. and Samasti M. (2009). treatment of methicilli-resistant coagulase negative Antibiotics resistance pattern of coagulase negative staphylococcal infections. staphylococcus strains isolated from blood cultures of septicemic patients in Turkey. Microbiological Research; `164(4);404-410. References Magiorakos, A.P.; Srinivasan, A.; Carey, R.B.; Carmeli, Y.; Falagas, M.E.; Giske, C.G.; Harbarth, Alo Moses, Ugah Uchenna, and Okoro Nworie, S.; Hindler, J.F.; Kahlmeter, G.; Olsson-Liljequist, (2013). Epidemiology of Vancomycin Resistant B. (2012). Multidrug -resistant, extensively drugresistant and pandrug-resistant bacteria: An Staphylococcus aureus among Clinical Isolates in a Tertiary Hospital in Abakaliki, Nigeria. American international expert proposal for interim standard Journal of Epidemiology and Infectious Disease 1, definitions for acquired resistance. Clin. Microbiol. no. 3: 24-26. doi: 10.12691/ajeid-1-3-2. Infect, 18, 268 281. Becker K, Heilmann C, Peters G. (2014). Coagulasenegative staphylococci. Clin Microbiol Rev; Adeshina G.O and Igwe J.C.. (2016). Antibiotics Obajuluwa A.F., Onaolapo J.A., Olayinka B.O., 27:870. resistance pattern of Staphylococcus aureus Clinical and Laboratory Standards Institute (2012). isolates from orthopaedic patients in Ahmadu Bello Performance standards for antimicrobial University Teaching Hospital, Zaria, Nigeria. susceptibility testing: 22nd informational European Journal of advanced research in supplement. M100- S22. Wayne, PA. biological and life sciences vol 4No 3; 8-13. Clinical and Laboratory Standards Institute. (2013). Otto M.(2008). Staphylococcal biofilms. Curr Top Performance standards for antimicrobial Microbiol Immunol.; 322: 207-228. susceptibility testing approved standard M100-S23. Otto, M. (2009). Staphylococcus epi dermidis the Clinical and Laboratory Standards Institute, accidental pathogen Int J Antimicrob Agents 29 Wayne, PA. (Suppl. 3), S23 S32. Cosgrove, S.E., Sakoulas, G. and Perencevich, Rahman A., Hossain M.A., Paul S.K., Sultan S., E.N(2003). Comparison of mortality associated Hagne W., Kabir M.R., Hogue S.M. (2013). with methicillin resistant and methicillin sensitive. Methicillin-resistant coagulase negative Stapphylococcus aureus bactermia: a metaanalysis. Clin Infect Dis. 36: 53 59 method. Mymensingh Med. J. 22(2):229-31. Staphylococci (MRCoNS) by disk diffusion Diekema DJ, Pfaller MA, Schmitz FJ, et al. (2001). Roth RR, James WD. (1988). Microbial ecology of the Survey of infections due to Staphylococcus skin. Annu Rev Microbiol; 42:441. species: frequency of occurrence and antimicrobial Silpi B., Priyanka S. and Monali R. (2016). Multidrug susceptibility of isolates collected in the United resistant and extensively drug resistant bacteria: A States, Canada, Latin America, Europe, and the study. Journal of Pathogens: 1-5. Western Pacific region for the SENTRY Sharma V., Jindal N. and Devi P. (2010). Prevalence Antimicrobial Surveillance Program, 1997-1999. of methicillin-resistant coagulae negative Clin Infect Dis; 32 Suppl 2:S114. Staphylococci in a tertiatry care hospital. Iran J Dubois,D.,Leyssene,D.,Chacornac,J.P.,Kostrzewa,M., Microbiol.; 2(4): 185 188. Schmit,P.O.,Talon, R., Bonnet, R. & Delmas, J. Tiwari H.K and Sen M.R. (2006). Em ergence of (2010). Identification of a variety of vancomycin resistant Staphylococcus aureus Staphylococcus species by matrix-assisted laser (VRSA) from a tertiary hospital from northern part desorption ionization- time of flight mass of india. BMC Infectious Diseases. 6:156-161. spectrometry. JClinMicrobiol 48, 941 945. 13

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