Whole Genome Sequencing of Antibiotic Resistant Genes in Isolates from Surfaces in a Science Laboratory.

IF 1.8 Q3 PHARMACOLOGY & PHARMACY
Christiana Jesumirhewe, Aisha Olamide Abdusalam, Werner Ruppitsch
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Abstract

Objectives Isolates obtained from laboratory surfaces were identified and characterized. Materials and Methods Ten consecutive isolates were obtained from 30 sample surfaces of a University Science Laboratory in Edo State Nigeria in May, 2021. Swabs of surfaces from the laboratory were obtained aseptically. The sample swabs were streaked on MacConkey, eosin methylene blue, mannitol salt, and nutrient agar plates, respectively, and incubated appropriately. Distinct colonies were randomly obtained from culture plates and characterized phenotypically. Matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) was used to analyze four isolates (40%) obtained by selection criteria. Susceptibility testing using antibiotics was performed for the identified isolates by Kirby-Bauer method for 15 antibiotics. Isolate characterization and identification of resistance determinants were determined using whole genome sequencing (WGS). Results Microorganisms identified included Leclercia adecarboxylata, Enterobacter hormaechei, Atlantibacter hermanii, and Stenotrophomonas maltophilia. Three identified isolates were antibiotics-resistant and were investigated by WGS. Resistance genes were found in all (100%) of the resistant laboratory isolates. The resistance determinants included β-lactamase genes, aminoglycoside modifying enzymes, qnr genes, sulfonamide, tetracycline, and trimethoprim resistance genes, respectively. Two isolates carried ESBL genes and blaCTX-M-15 was detected. Conclusion Our study displays the dissemination of antibiotic resistance among isolates obtained from surface of a University Science Laboratory. To the best of our knowledge, we have reported the first genomic characterization of resistance to antibiotics in isolates obtained from surfaces of a University Science Laboratory in Nigeria.
科学实验室表面分离物抗生素耐药基因的全基因组测序。
目的:对从实验室表面获得的分离株进行鉴定和表征。材料和方法:2021年5月,从尼日利亚埃多州一所大学科学实验室的30个样品表面连续获得10株分离株。从实验室无菌获得表面拭子。将样本拭子分别在麦康基、伊红亚甲基蓝、甘露醇盐和营养琼脂板上划线,并适当孵育。从培养板上随机获得不同的菌落,并具有表型特征。采用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)对筛选标准获得的4株分离菌(40%)进行分析。采用Kirby-Bauer法对15种抗生素进行药敏试验。采用全基因组测序(WGS)技术对分离物的特性和耐药决定因素进行鉴定。结果:鉴定出的微生物包括枯叶乳杆菌、嗜麦芽肠杆菌、hermanii大西洋抗菌菌和嗜麦芽窄养单胞菌。鉴定出的3株菌株耐药,经WGS调查。在所有(100%)耐药实验室分离株中均发现耐药基因。耐药决定因素包括β-内酰胺酶基因、氨基糖苷修饰酶基因、qnr基因、磺胺、四环素和甲氧苄氨嘧啶耐药基因。2株分离株携带ESBL基因,检测到blaCTX-M-15。结论:我们的研究显示了从某大学科学实验室表面获得的分离株中抗生素耐药性的传播。据我们所知,我们已经报告了从尼日利亚一所大学科学实验室表面获得的分离株对抗生素耐药性的首次基因组特征。
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来源期刊
CiteScore
3.60
自引率
5.90%
发文量
79
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