Nasal colonisation, antimicrobial susceptibility and genotypic pattern of Staphylococcus aureus among agricultural biotechnology students in Besut, Terengganu, east coast of Malaysia

被引:20
|
作者
Zarizal, Suhaili [1 ,2 ]
Yeo, Chew Chieng [3 ]
Faizal, Ghazali Mohd [1 ]
Chew, Ching Hoong [4 ]
Zakaria, Zainul Amiruddin [2 ,5 ]
Al-Obaidi, Mazen M. Jamil [2 ]
Amin, Nordin Syafinaz [6 ]
Nasir, Mohd Desa Mohd [2 ,5 ]
机构
[1] Univ Sultan Zainal Abidin, Sch Anim Sci, Fac Bioresources & Food Ind, Besut Campus, Besut 22200, Terengganu, Malaysia
[2] Univ Putra Malaysia, Dept Biomed Sci, Fac Med & Hlth Sci, Serdang, Selangor, Malaysia
[3] Univ Sultan Zainal Abidin, Fac Med, Kuala Terengganu, Terengganu, Malaysia
[4] Univ Sultan Zainal Abidin, Fac Hlth Sci, Gong Badak, Terengganu, Malaysia
[5] Univ Putra Malaysia, Lab Halal Sci Res, Halal Prod Res Inst, Serdang, Malaysia
[6] Univ Putra Malaysia, Dept Med Microbiol & Parasitol, Fac Med & Hlth Sci, Serdang, Selangor, Malaysia
关键词
antimicrobial susceptibility profiles; methicillin-resistant Staphylococcus aureus; methicillin-susceptible Staphylococcus aureus; nasal carriage; pvl; macrolide-lincosamide-streptogramin B; METHICILLIN-RESISTANT; TOXIN GENES; STRAINS; PREVALENCE; CARRIAGE; MRSA; EMERGENCE; POPULATION; HOSPITALS; BLOOD;
D O I
10.1111/tmi.13090
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
BackgroundThis study aimed to profile the antimicrobial susceptibility and presence of resistance and virulence genes of methicillin-susceptible Staphylococcus aureus (MSSA) and MRSA nasal carriage, by means of genotypic analyses, in students of a tertiary institution in the state of Terengganu, east coast of Malaysia. MethodsA total of 370 agricultural biotechnology students from Universiti Sultan Zainal Abidin in Besut, Terengganu, were enrolled in this study. Antimicrobial susceptibility profiles were evaluated by standard methods. PCR detection of resistance and virulence genes was performed on S. aureus that were methicillin-resistant, macrolide-lincosamide-streptogramin B (MLSB)-positive phenotype and/or positive for the leukocidin (pvl) gene followed by staphylococcal cassette chromosome mec (SCCmec), staphylococcal protein A (spa) and accessory gene regulator (agr) typing. ResultsOne hundred and nineteen of 370 students carried S. aureus (32%); 18 of the isolates were MRSA (15%). Erythromycin resistance was detected in 20% (24/119) of which 15% (18/119) were MRSA and 5% (6/119) MSSA. Among the 24 erythromycin-resistant isolates, D-test was positive in 29% (7/24) displaying inducible MLSB, whereas the remaining 71% (17/24) showed constitutive MLSB phenotypes. Nine (7.6%) of 119 isolates were pvl positive: 44% MRSA (4/9) and 56% MSSA (5/9). Staphylococcal surface protein sasX gene was present in 92% of MRSA and 8% of MSSA isolates. The majority of MRSA isolates were agr type I (15/18; 83%). Five spa types identified with spa t037 were predominant, followed by spa types (t304 and t8696) as newly reported Malaysian MRSA in a community setting. ConclusionThe presence of MRSA with SCCmec of hospital-associated features and globally recognised spa types in community setting is worrisome. Furthermore, the presence of MLSB strains among multidrug-resistant (MDR) S. aureus with sasX as well as pvl-positive isolates highlights the potential risk of a community setting in facilitating the dissemination of both virulence and resistance determinants.
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页码:905 / 913
页数:9
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