Antimicrobial Activity of Ten Local Actinobacterial Strains against ESKAPE, Bacillus subtilis and Pseudomonas baetica Pathogens

Maryam Hazim Abduljaba, T. Salih
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引用次数: 1

Abstract

Aims: The study included the isolation, purification, cultural characteristics, antimicrobial activities and molecular identification of local actinobacterial strains isolated from different locations north of Iraq. Methodology: Oligotrophic medium supplemented with the antifungals cycloheximide (50 mg/l) and nystatin (30 mg/l) was used for preliminary isolation. ISP-3 medium was chosen as a potential medium for subsequent purification of actinobacterial strains. The cultural characteristics of all isolated actinobacterial strains were elucidated on International Streptomyces Project media (ISP2-ISP-7). 16S rRNA marker gene was used for molecular identification using 27F and 1492R universal primers. Results: Ten isolates were biologically active against tested ESKAPE, Bacillus subtilis and pseudomonas paetica pathogens when cultured on different ISPs media under the OSMAC approach. Six representative isolates that exhibited antimicrobial activity against all or almost tested bacteria were sequenced using 16S rRNA gene. The sequences were compared with those of other actinobacterial strains that are found in Genebank database to find the best similarity and the close reference strains to our isolates. Five of the sequenced strains have been identified as Streptomyces species; MT5, MT8, MT12, MT23 and MT26 and one was identified as a rare actinobacterial strain Lentzea sp.; MT4. Nucleotide sequences have been provided and deposited in the National Center for Biotechnology Information NCBI under the accession numbers ON514131, ON514133, ON514134, ON514135, ON514136 and ON514130 respectively.
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10株放线菌对ESKAPE、枯草芽孢杆菌和baetica假单胞菌的抑菌活性研究
目的:研究从伊拉克北部不同地点分离的放线菌菌株的分离、纯化、培养特性、抑菌活性和分子鉴定。方法:采用添加抗真菌药环己亚胺(50 mg/l)和制霉菌素(30 mg/l)的寡营养培养基进行初步分离。选择ISP-3培养基作为后续纯化放线菌菌株的潜在培养基。在国际链霉菌计划培养基(ISP2-ISP-7)上鉴定了所有分离的放线菌菌株的培养特性。16S rRNA标记基因采用27F和1492R通用引物进行分子鉴定。结果:10株分离菌株在不同培养基上均具有抗ESKAPE、枯草芽孢杆菌和乳酸假单胞菌的活性。使用16S rRNA基因对6株具有代表性的对所有或几乎所有被测细菌具有抗菌活性的分离株进行了测序。与Genebank数据库中其他放线菌的序列进行比较,找到与我们分离的放线菌最相似的菌株和最接近的参考菌株。经测序的菌株中有5个被鉴定为链霉菌;MT5、MT8、MT12、MT23和MT26,其中1株为罕见放线菌Lentzea sp.;MT4。核苷酸序列已提供并保存在国家生物技术信息中心NCBI,登录号分别为ON514131、ON514133、ON514134、ON514135、ON514136和ON514130。
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