健康人类肠道菌群在阿比让Côte科特迪瓦社区环境中\(\beta\) -内酰胺酶产肠杆菌科和\(\beta\) -内酰胺耐药性相关基因的出现和传播中的作用

Ouattara Mohamed Baguy, Affou Séraphin Wognin, T. Anatole, Gbonon M’bengue Valérie Carole, Kouassi Koffi Gédeon, Guédé Kipré Bertin, T. Bertin, K. Fernique, Kouadio Kouamé Innocent, D. S. Kpoda, Abraham Ayayi, Konate Ali, Guessennd Nathalie Kouadio, Kamenan Alphonse, Dosso Mireille
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引用次数: 0

摘要

在发展中国家的社区中过度使用β-内酰胺类抗生素已将健康的人类肠道菌群转变为耐抗生素生物的储存库。在社区环境中产生广谱β-内酰胺酶(ESBL)的肠杆菌科的患病率仍未确定。为了获得ESBL肠杆菌的数据,从2019年8月至2020年2月从居住在阿比让市区并在Côte科特迪瓦巴斯德研究所进行医疗咨询的个人中收集了265份粪便样本。在MacConkey上分离肠杆菌科分离株,采用API 20E图库进行鉴定,采用临床实验室标准协会光盘扩散法进行药敏试验。采用单路和多重PCR检测扩展谱β-内酰胺酶(TEM、SHV、GES、PER、VEB、ctxm1、ctxm2、ctxm8和ctxm9)。人类粪便菌株包括513种多重耐药肠杆菌。513株肠杆菌中75株(14.6%)产生ESBLs, 438株(85.4%)产生高水平头孢菌素酶。产广谱β-内酰胺酶的肠杆菌主要有大肠杆菌(46.7%)、肺炎克雷伯菌(17.3%)、阴沟肠杆菌(13.3%)、产气肠杆菌(6.7%)、奇异变形杆菌(6.7%)、氧化克雷伯菌(4%)、普通变形杆菌(2.7%)、克塞利柠檬酸杆菌(1.3%)和弗伦地柠檬酸杆菌(1.3%)。菌株对β -内酰胺类抗生素(含抑制剂的青霉素、单巴坦、头孢菌素)耐药(100%),但对碳青霉烯类抗生素(imipsamen、msamopacen、Ertapenem)耐药(1.3%)。对喹诺酮类药物和氨基糖苷类药物的耐药率分别为22.9% ~ 43.3%和7.9 ~ 35.1%。检测到耐药基因TEM、SHV、ctxm1、ctxm2、ctxm8和ctxm9。未检出GES和PER基因。科特迪瓦社区环境中与基因相关的ESBL-PE的高粪便携带率突出了传播和传播的风险,因为健康人是借来的潜在患者。
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Role of Healthy Human Gut Microbiota in the Emergence and Dissemination of Extended-Spectrum \(\beta\)-lactamase-Producing Enterobacteriaceae and Genes Associated with \(\beta\)-lactam Resistance in Community Settings in Abidjan, Côte d'Ivoire
Overuse of β-lactam antibiotics in communities in developing countries has transformed healthy human intestinal flora into a reservoir of antibiotic-resistant organisms. The prevalence of extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae in community settings remains undetermined. In order to obtain data on ESBL enterobacteria, 265 stool samples were collected from August 2019 to February 2020 from individuals residing in the urban districts of Abidjan and attending medical consultations at the Institut Pasteur de Côte d'Ivoire. Isolates belonging to family Enterobacteriaceae were isolated on MacConkey and identified using the API 20E galerie and antibiotic susceptibility was determined using Clinical Laboratory Standard Institute disc diffusion method. Detection of extended spectrum β-lactamases (TEM, SHV, GES, PER, VEB, CTXM 1, CTXM 2, CTXM 8 and CTXM 9) was done by simplex and multiplex PCR. The human stools strains consisted of 513 species of Enterobacteria multidrug resistants. Among the 513 strains, 75 (14.6%) of the enterobacterial strains produced ESBLs, while 438 (85.4%) produced high-level cephalosporinases. Enterobacteria producing extended-spectrum β-lactamase we dominated by the species Escherichia coli (46.7%), Klebsiella pneumoniae (17.3%), Enterobacter cloacae (13.3%), Enterobacter aerogenes (6.7%), Proteus mirabilis (6.7%), Klebsiella oxytoca (4%), Proteus vulgaris (2.7%), Citrobacter koseri (1.3%), and Citrobacter freundii (1.3%). Strains were resistant (100%) to antibiotics from beta-lactam family (penicillin with inhibitor, monobactam, cephalosporin) but low level resistant (1,3%) was observed to carbapenem (imipénème, méropénème, Ertapenem). The rate of resistance to quinolones and aminoglycosides were respectively between 22.9% - 43.3% and 7.9-35.1%. The resistance genes TEM, SHV, CTXM 1, CTXM 2, CTXM 8 and CTXM 9 were detected. No GES and PER genes were not detected. The high fecal carriage rate of ESBL-PE associated with genes in community settings of Ivory Coast highlights the risk for transmission and dissemination because healthy people are potential patients on borrowed time.
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