尼日利亚奥贡州Sagamu市常见复方中草药革兰氏阴性菌分离株微生物质量评价及延伸谱β-内酰胺酶基因检测

O. Olaniran, S. Ajayi, O. Oluwatobi, O. Adeleke
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引用次数: 0

摘要

背景:中药复方在疾病治疗中的使用呈上升趋势。这些草药中有许多不是在卫生条件下生产的,与草药相关的安全问题可能对免疫功能低下和老年人产生更大的影响。本研究旨在确定当地配制的草药混合物的微生物负荷,并检测任何分离的革兰氏阴性菌病原体的扩展谱β -内酰胺酶(ESBL)基因。方法:从尼日利亚奥贡州Sagamu镇(Sagamu市场、Ita-Oba路和Isale Oko)的三个地点随机购买了50种当地草药混合物。采用平板计数法测定平均活菌总数(MTVB)、平均大肠菌群总数(MTC)和平均真菌总数(MTF)。分离的细菌在不同的细菌培养基上培养,分离的真菌在马铃薯葡萄糖琼脂上培养。分离物在培养基上生长后用常规生化试验进行鉴定。采用Kirby-Bauer纸片扩散法测定菌株的药敏型。采用改良双盘协同试验对ESBL进行表型检测,随后采用聚合酶链反应(PCR)法扩增检测blaTEM、blaCTX-M和blaSHV基因。结果:检出细菌38例(76.0%),真菌25例(50.0%)。10份(20.0%)和14份(28.0%)样品的平均细菌和真菌负荷分别超过105CFU/mL或g。19份(38.0%)草药样品中有总大肠菌群。分离得到8个细菌属51株和4个真菌属28株。革兰氏阴性32株(62.7%),阳性19株(37.3%)。金黄色葡萄球菌是最常见的分离菌(33.3%),曲霉菌是最常见的分离菌(60.7%)。16株(84.2%)金黄色葡萄球菌和26株(81.3%)革兰氏阴性分离株多重耐药,32株革兰氏阴性分离株中6株(18.8%)为ESBL产生菌。26株多重耐药革兰氏阴性菌中有7株(27%)检出esbl编码基因,其中TEM和SHV最常见(14.8%),CTX-M仅检出1株。结论:本研究报告了微生物污染物的存在,超过了世界卫生组织规定的105 CFU/g的安全限值。由于缺乏微生物质量标准,使用当地配制的草药对健康构成重大风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of microbial quality and detection of extended spectrum β-lactamase genes in Gram-negative bacterial isolates of herbal mixtures commonly hawked in Sagamu metropolis, Ogun State, Nigeria
Background: The use of herbal mixtures in the treatment of diseases is on the rise. Many of these herbal drugs are not produced under hygienic conditions and safety issues associated with herbal medicines may have an exacerbated impact in immunocompromised and elderly individuals. This study aimed to determine the microbial loads of locally prepared herbal mixtures and detect extended spectrum beta-lactamase (ESBL) genes  in any isolated Gram-negative bacteria pathogen. Methodology: Fifty local herbal mixtures were purchased randomly from three locations in Sagamu town (Sagamu market, Ita-Oba Road and Isale  Oko) in Ogun State, Nigeria. The mean total viable bacterial (MTVB), mean total coliform (MTC), and mean total fungal (MTF) counts were  determined by the plate count method. The bacterial isolates were streaked on differential bacteriological media while the fungi isolates were  grown on potato dextrose agar. The isolates were identified upon growth on culture media using conventional biochemical tests. Antibiotic  susceptibility pattern of the isolates was determined using Kirby-Bauer disk diffusion technique. Phenotypic detection of ESBL was done by the  modified double disc synergy test followed by amplification detection of blaTEM, blaCTX-M and blaSHV genes with polymerase chain reaction (PCR)  assay. Results: Bacteria and fungi were isolated from 38 (76.0%) and 25 (50.0%) of the herbal samples respectively. Ten (20.0%) and 14 (28.0%) of the  samples had mean bacterial and fungal load that exceeded 105CFU/mL or g, respectively. Nineteen (38.0%) of the herbal samples analyzed had total  coliforms. Fifty-one isolates belonging to eight bacterial genera and 28 fungi isolates belonging to four fungal genera were obtained. Thirty-  two (62.7%) of the bacterial isolates were Gram-negative while 19 (37.3%) isolates were Gram-positive. Staphylococcus aureus was the most  common bacterial isolate (33.3%) while Aspergillus species was the most prevalent fungus (60.7%). Sixteen (84.2%) S. aureus and 26 (81.3%) Gram- negative isolates were multidrug resistant, and 6 (18.8%) of 32 Gram-negative isolates were ESBL producers. ESBL-encoding genes were detected in  7 (27%) of the 26 multidrug resistant Gram-negative bacteria with TEM and SHV being the most prevalent 4 (14.8%) while CTX-M was identified in  only one isolate. Conclusion: This study reported the presence of microbial contaminants which exceeded the safety limits of 105 CFU/g according  to World Health Organization. The use of locally prepared herbal medicines poses a major health risk due to the lack of microbial quality standards. 
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