Please use this identifier to cite or link to this item: http://repository.kln.ac.lk/handle/123456789/27010
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dc.contributor.authorPathirana, M. P. P. M.-
dc.contributor.authorDanushka, W. A. S.-
dc.contributor.authorAthukorala, N. N.-
dc.contributor.authorNiroshan, D. M. M. P.-
dc.contributor.authorKaluaddaraarachchi, A.-
dc.contributor.authorNayanathara, R. K. A. B.-
dc.contributor.authorPerera, P. D. V. M.-
dc.date.accessioned2023-11-08T07:17:08Z-
dc.date.available2023-11-08T07:17:08Z-
dc.date.issued2023-
dc.identifier.citationPathirana M. P. P. M.; Danushka W. A. S.; Athukorala N. N.; Niroshan D. M. M. P.; Kaluaddaraarachchi A.; Nayanathara R. K. A. B.; Nayanathara R. K. A. B.; Perera P. D. V. M. (2023) Determination of Staphylococcus spp. present as contaminants on public door handles of an institute and analysis of their antibiogram, Proceedings of the International Conference on Applied and Pure Sciences (ICAPS 2023-Kelaniya) Volume 3, Faculty of Science, University of Kelaniya Sri Lanka. Page 170en_US
dc.identifier.urihttp://repository.kln.ac.lk/handle/123456789/27010-
dc.description.abstractpositive, Antibiotic resistanceStaphylococcus are potential pathogens that cause a range of infections, ranging from mild abscesses to severe septicemia. The objective of this study was to identify Staphylococcus present as surface contaminants and to analyze their antibiogram. KAATSU International University’s door knobs were sampled using cotton swabs that had been dipped in peptone water and incubated it for 18-24 hours at 37C0 . Incubated samples were inoculated on mannitol salt agar plates and incubated for 24 hours at 37°C. Gram staining and biochemical tests such as catalase, coagulase were carried out for further identification of the isolates. The disc diffusion method was used for antibiotic sensitivity testing (ABST) following the guidelines of the Clinical and Laboratory Standards Institute (CLSI). For coagulase-positive isolates, cefoxitin (30 g), erythromycin (10 g), gentamicin (10 g), vancomycin (30 g), and oxacillin (1 µg) were used. Novobiocin (5 mg), erythromycin (10 mg), gentamicin (10 mg), and vancomycin (30 mg) were utilized for coagulase-negative isolates. All 37 door handle samples were collected; 91.89% (n =31) were pure growth samples. Out of those samples, 64.86% (n = 24) were identified as Coagulase positive Staphylococcus aureus and 18.91% (n = 7) were identified as coagulase negative Staphylococcus. Out of 24 samples, 24.16% (n = 7) isolates were found to be Methicillin resistant Staphylococcus aureus (MRSA) strains. Rates of MRSA isolates showed resistance to erythromycin 100% (n = 7) and Oxacillin 14.28%. In (CoNS) coagulase negative Staphylococcus 71.42% (n = 5) were identified as Staphylococcus epidermidis, and 28.57% (n = 2) were Staphylococcus saprophyticus. Coagulase negative Staphylococcus showed 100% sensitivity to vancomycin, gentamycin (10 ug), and oxacillin, and 42.86% (n = 4) of the isolates showed resistance to erythromycin. Staphylococcus aureus with a considerable rate of MRSA was discovered in this investigation. [Contaminated door handles can be a source of transmission of MRSA.] This research can be used to find effective disinfectants and proper cleaning techniques to minimize the spread of Staphylococcus through door handlesen_US
dc.publisherFaculty of Science, University of Kelaniya Sri Lankaen_US
dc.subjectDoor handles, Methicillin resistant Staphylococcus aureus, Coagulase negative, Coagulaseen_US
dc.titleDetermination of Staphylococcus spp. present as contaminants on public door handles of an institute and analysis of their antibiogramen_US
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