SAMRC Microbial Water Quality Monitoring Centre, University of Fort Hare, Alice, South Africa.
Department of Biochemistry and Microbiology, Applied and Environmental Microbiology Research Group, University of Fort Hare, Alice, South Africa.
PLoS One. 2021 Jul 21;16(7):e0254753. doi: 10.1371/journal.pone.0254753. eCollection 2021.
Globally, there is an increasing occurrence of multidrug-resistant (MDR) Enterobacteriaceae with extended-spectrum β-lactamases (ESBLs) and/or plasmid-encoded AmpC (pAmpC) β-lactamases in clinical and environmental settings of significant concern. Therefore, we aimed to evaluate the occurrence of ESBL/pAmpC genetic determinants, and some essential non-β-lactam genetic determinants in the MDR phenotypic antimicrobial resistance in Enterobacteriaceae isolates recovered from hospital wastewater. We collected samples from two hospitals in Amathole and Chris Hani District Municipalities in the Eastern Cape Province, South Africa, within October and November 2017. Using the matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF), we identified a total of 44 presumptive Enterobacteriaceae isolates. From this, 31 were identified as the targeted Enterobacteriaceae members. Thirty-six percent of these belonged to Klebsiella oxytoca, while 29% were Klebsiella pneumoniae. The other identified isolates included Citrobacter freundii and Escherichia coli (10%), Enterobacter asburiae (6%), Enterobacter amnigenus, Enterobacter hormaechei, and Enterobacter kobei (3%). We established the antibiotic susceptibility profiles of these identified bacterial isolates against a panel of 18 selected antibiotics belonging to 11 classes were established following established guidelines by the Clinical and Laboratory Standard Institute. All the bacterial species exhibited resistance phenotypically against at least four antibiotic classes and were classified as MDR. Notably, all the bacterial species displayed resistance against cefotaxime, ampicillin, nalidixic acid, and trimethoprim-sulfamethoxazole. The generated multiple antibiotic resistance indices ranged between 0.5 to 1.0, with the highest value seen in one K. oxytoca isolated. Molecular characterization via the Polymerase Chain Reaction uncovered various ESBLs, pAmpCs, and other non-β-lactam encoding genes. Of the phenotypically resistant isolates screened for each class of antibiotics, the ESBLs detected were blaCTX-M group (including groups 1, 2, and 9) [51.6% (16/31)], blaTEM [32.3% (10/31)], blaOXA-1-like [19.4% (6/31)], blaSHV [12.9% (4/31)], blaPER [6.5% (2/31)], blaVEB [3.2% (1/31)], blaOXA-48-like and blaVIM [15.4% (2/13)], and blaIMP [7.7% (1/13)]. The pAmpC resistance determinants detected were blaCIT [12.9% (4/31)], blaFOX [9.7% (3/31)], blaEBC [6.5% (2/31)], and blaDHA [3.2% (1/31)]. The frequencies of the non-β-lactam genes detected were catII [79.2% (19/24)], tetA [46.7% (14/30)], sulI and sulII [35.5% (11/31)], tetB [23.3% (7/30)], aadA [12.9% (4/31)], tetC [10% (3/30)], and tetD [3.3% (1/30)]. These results indicate that hospital wastewater is laden with potentially pathogenic MDR Enterobacteriaceae with various antibiotic resistance genes that can be spread to humans throughout the food chain, provided the wastewaters are not properly treated before eventual discharge into the environment.
在全球范围内,临床和环境领域中出现了越来越多的具有广泛耐药性(MDR)的肠杆菌科细菌,这些细菌同时具有超广谱β-内酰胺酶(ESBLs)和/或质粒编码的 AmpC(pAmpC)β-内酰胺酶,这令人高度关注。因此,我们旨在评估在从医院废水中分离出的具有多重耐药表型的肠杆菌科细菌中,ESBL/pAmpC 遗传决定因素以及一些重要的非β-内酰胺遗传决定因素的发生情况。我们于 2017 年 10 月至 11 月期间在南非东开普省的阿马托勒和哈尼地区市政收集了来自两家医院的样本。使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF),我们总共鉴定出 44 株疑似肠杆菌科分离株。其中 31 株被鉴定为目标肠杆菌科成员。这些分离株中有 36%属于产酸克雷伯氏菌,而 29%属于肺炎克雷伯氏菌。其他鉴定出的分离株包括弗氏柠檬酸杆菌和大肠杆菌(10%)、阴沟肠杆菌(6%)、阿氏肠杆菌、霍氏肠杆菌和科比肠杆菌(3%)。我们根据临床和实验室标准协会制定的既定指南,建立了这些鉴定出的细菌分离株对 18 种选定抗生素的药敏谱,这些抗生素属于 11 类抗生素。所有细菌种类在表型上都至少对 4 种抗生素类别的药物具有耐药性,被归类为多重耐药菌。值得注意的是,所有细菌种类都对头孢噻肟、氨苄西林、萘啶酸和复方磺胺甲噁唑表现出耐药性。生成的多重抗生素耐药指数在 0.5 到 1.0 之间,在一株产酸克雷伯氏菌中最高。通过聚合酶链反应进行的分子特征分析揭示了各种 ESBLs、pAmpCs 和其他非β-内酰胺编码基因。在对每类抗生素进行筛选的表型耐药分离株中,检测到的 ESBLs 包括 blaCTX-M 组(包括组 1、2 和 9)[51.6%(16/31)]、blaTEM [32.3%(10/31)]、blaOXA-1-like [19.4%(6/31)]、blaSHV [12.9%(4/31)]、blaPER [6.5%(2/31)]、blaVEB [3.2%(1/31)]、blaOXA-48-like 和 blaVIM [15.4%(2/13)]和 blaIMP [7.7%(1/13)]。检测到的 pAmpC 耐药决定因素包括 blaCIT [12.9%(4/31)]、blaFOX [9.7%(3/31)]、blaEBC [6.5%(2/31)]和 blaDHA [3.2%(1/31)]。检测到的非β-内酰胺基因的频率包括 catII [79.2%(19/24)]、tetA [46.7%(14/30)]、sulI 和 sulII [35.5%(11/31)]、tetB [23.3%(7/30)]、aadA [12.9%(4/31)]、tetC [10%(3/30)]和 tetD [3.3%(1/30)]。这些结果表明,医院废水中存在具有各种抗生素耐药基因的潜在致病性多重耐药肠杆菌科细菌,如果废水在最终排放到环境之前没有得到适当处理,这些耐药基因可能会通过食物链传播给人类。