Tabassum Tahani, Hossain Md Sakib, Ercumen Ayse, Benjamin-Chung Jade, Abedin Md Foysal, Rahman Mahbubur, Jahan Farjana, Haque Munima, Mahmud Zahid Hayat
Laboratory of Environmental Health, Health Systems and Population Studies Division, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, 1212, Bangladesh.
Biotechnology Program, Department of Mathematics and Natural Sciences, BRAC University, Merul Badda, Dhaka, Bangladesh.
Heliyon. 2024 Jul 9;10(14):e34367. doi: 10.1016/j.heliyon.2024.e34367. eCollection 2024 Jul 30.
Antimicrobial resistance (AMR) is a rising health concern worldwide. As an indicator organism, , specifically extended-spectrum β-lactamase (ESBL) producing , can be used to detect AMR in the environment and estimate the risk of transmitting resistance among humans, animals and the environment. This study focused on detecting cefotaxime resistant in floor swab samples from 49 households in rural villages in Bangladesh. Following isolation of cefotaxime resistant , DNA extracted from isolates was subjected to molecular characterization for virulence and resistance genes, determination of resistance to multiple classes of antibiotics to define multidrug resistant (MDR) and extensively drug resistant (XDR) strains, and the biofilm forming capacity of the isolates. Among 49 households, floor swabs from 35 (71 %) households tested positive for cefotaxime resistant . Notably, all of the 91 representative isolates were ESBL producers, with the majority (84.6 %) containing the gene, followed by the and genes detected in 22.0 % and 6.6 % of the isolates, respectively. All isolates were MDR, and one isolate was XDR. In terms of pathogenic strains, 8.8 % of the isolates were diarrheagenic and 5.5 % were extraintestinal pathogenic (ExPEC). At 25 °C, 45 % of the isolates formed strong biofilm, whereas 43 % and 12 % formed moderate and weak biofilm, respectively. On the other hand, at 37 °C, 1.1 %, 4.4 % and 93.4 % of the isolates were strong, moderate and weak biofilm formers, respectively, and 1.1 % showed no biofilm formation. The study emphasizes the importance of screening and characterizing cefotaxime resistant from household floors in a developing country setting to understand AMR exposure associated with floors.
抗菌药物耐药性(AMR)是全球日益严重的健康问题。作为指示生物,[具体名称未给出],特别是产超广谱β-内酰胺酶(ESBL)的[具体名称未给出],可用于检测环境中的AMR,并估计人类、动物和环境之间传播耐药性的风险。本研究重点检测孟加拉国农村49户家庭地板拭子样本中产头孢噻肟耐药[具体名称未给出]的情况。分离出产头孢噻肟耐药[具体名称未给出]后,从分离株中提取的DNA进行毒力和耐药基因的分子特征分析,测定对多类抗生素的耐药性以定义多重耐药(MDR)和广泛耐药(XDR)菌株,以及分离株的生物膜形成能力。在49户家庭中,35户(71%)家庭的地板拭子检测出产头孢噻肟耐药[具体名称未给出]呈阳性。值得注意的是,所有91株代表性分离株均为ESBL生产者,大多数(84.6%)含有[具体基因名称未给出]基因,其次分别在22.0%和6.6%的分离株中检测到[具体基因名称未给出]和[具体基因名称未给出]基因。所有分离株均为MDR,1株为XDR。在致病菌株方面,8.8%的分离株具有致腹泻性,5.5%为肠外致病性[具体名称未给出](ExPEC)。在25℃时,45%的分离株形成强生物膜,而43%和12%分别形成中度和弱生物膜。另一方面,在37℃时,1.1%、4.4%和93.4%的分离株分别为强、中度和弱生物膜形成者,1.1%未显示生物膜形成。该研究强调了在发展中国家环境中对家庭地板上的产头孢噻肟耐药[具体名称未给出]进行筛查和特征分析以了解与地板相关的AMR暴露的重要性。