Minimum inhibitory concentration of vancomycin to methicillin resistant Staphylococcus aureus isolated from different clinical samples at a tertiary care hospital in Nepal

被引:33
作者
Kshetry, Arjun Ojha [1 ]
Pant, Narayan Dutt [2 ]
Bhandari, Raju [1 ]
Khatri, Sabita [1 ]
Shrestha, Krishma Laxmi [1 ]
Upadhaya, Shambhu Kumar [1 ]
Poudel, Asia [1 ]
Lekhak, Binod [1 ]
Raghubanshi, Bijendra R. [3 ]
机构
[1] Goldengate Int Coll, Dept Microbiol, Kathmandu, Nepal
[2] Grande Int Hosp, Dept Microbiol, Kathmandu, Nepal
[3] KIST Med Coll & Teaching Hosp, Dept Microbiol, Lalitpur, Nepal
关键词
S; aureus; MRSA; VRSA; VISA; Nepal; SUSCEPTIBILITY; PREVALENCE; INFECTIONS; MRSA; COMMUNITY; CARRIAGE; VRSA;
D O I
10.1186/s13756-016-0126-3
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Methicillin resistant Staphylococcus aureus (MRSA) has evolved as a serious threat to public health. It has capability to cause infections not only in health care settings but also in community. Due to the multidrug resistance shown by MRSA, there are limited treatment options for the infections caused by this superbug. Vancomycin is used as the drug of choice for the treatment of infections caused by MRSA. Different studies from all around the world have documented the emergence of strains of S. aureus those are intermediate sensitive or resistant to vancomycin. And recently, there have been reports of reduced susceptibility of MRSA to vancomycin, from Nepal also. So the main purpose of this study was to determine the minimum inhibitory concentration (MIC) of vancomycin to methicillin resistant S. aureus isolated from different clinical specimens. Methods: Total 125 strains of S. aureus isolated from different clinical samples at KIST Medical College and Teaching Hospital, Lalitpur, Nepal from Nov 2012 to June 2013, were subjected to MRSA detection by cefoxitin disc diffusion method. The minimum inhibitory concentrations of vancomycin to confirmed MRSA strains were determined by agar dilution method. Yellow colored colonies in mannitol salt agar, which were gram positive cocci, catalase positive and coagulase positive were confirmed to be S. aureus. Results: Among, total 125 S. aureus strains isolated; 47(37.6%) were MRSA. Minimum inhibitory concentrations of vancomycin to the strains of MRSA ranged from 0.125 mu g/ml to 1 mu g/ml. Conclusion: From our findings we concluded that the rate of isolation of MRSA among all the strains of S. aureus isolated from clinical samples was very high. However, none of the MRSA strains were found to be vancomycin intermediate-sensitive or vancomycin-resistant.
引用
收藏
页数:6
相关论文
共 40 条
[1]  
Amatya R, 2014, Nepal Med Coll J, V16, P42
[2]   Determination of minimum inhibitory concentrations [J].
Andrews, JM .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2001, 48 :5-16
[3]  
Arora Shilpa, 2010, J Lab Physicians, V2, P78, DOI 10.4103/0974-2727.72154
[4]  
Awasthi T. R., 2015, Nepal Journal of Biotechnology, V3, P55, DOI 10.3126/njb.v3i1.14232
[5]  
Baral R., 2011, Health Renaissance, V9, P78, DOI 10.3126/hren.v9i2.4977
[6]   Waves of resistance: Staphylococcus aureus in the antibiotic era [J].
Chambers, Henry F. ;
DeLeo, Frank R. .
NATURE REVIEWS MICROBIOLOGY, 2009, 7 (09) :629-641
[7]   Method-specific performance of vancomycin MIC susceptibility tests in predicting mortality of patients with methicillin-resistant Staphylococcus aureus bacteraemia [J].
Chen, Shey-Ying ;
Liao, Chun-Hsing ;
Wang, Jiun-Ling ;
Chiang, Wen-Chu ;
Lai, Mei-Shu ;
Chie, Wei-Chu ;
Chang, Shan-Chwen ;
Hsueh, Po-Ren .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2014, 69 (01) :211-218
[8]  
Clinical and Laboratory Standarad Institute, 2012, M100S22 CLSI
[9]   Community-Associated Methicillin-Resistant Staphylococcus aureus: Epidemiology and Clinical Consequences of an Emerging Epidemic [J].
David, Michael Z. ;
Daum, Robert S. .
CLINICAL MICROBIOLOGY REVIEWS, 2010, 23 (03) :616-+
[10]   The molecular evolution of methicillin-resistant Staphylococcus aureus [J].
Deurenberg, R. H. ;
Vink, C. ;
Kalenic, S. ;
Friedrich, A. W. ;
Bruggeman, C. A. ;
Stobberingh, E. E. .
CLINICAL MICROBIOLOGY AND INFECTION, 2007, 13 (03) :222-235