尼日利亚Yankari禁猎区采采蝇中铜绿假单胞菌的分离、鉴定及药敏分析

Youssouf M. Mouliom, D. Achukwi, Mohammed Mamman, E. O. Balogun, M. N. Shuaibu, Junaidu Kabir
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摘要

微生物群参与其媒介能力,可能有助于开发新的疾病控制工具。据报道,铜绿假单胞菌普遍存在于自然环境、人类和动物中。它已被用于植物的生物防治。方法:采集自尼日利亚Yankari野生动物保护区的采采蝇25只,在无菌条件下解剖。在标准培养基中连续培养中肠。然后对疑似分离物进行生化测试。采用16S rRNA基因序列进行基因型鉴定。阳性分离物还进行了对17种抗菌素的敏感性试验。结果:25只蝇中8只(32%)铜绿假单胞菌阳性。他们的氧化酶、过氧化氢酶、柠檬酸盐和运动试验呈阳性,脲酶、吲哚、甲基红试验呈阴性。16S rRNA基因分析证实了分离株的身份,并与其他菌株建立了系统发育关系。该菌株对氟喹诺酮类药物敏感,对氯霉素敏感。对氨基糖苷类、青霉素、红霉素、克林霉素和亚胺培耐药。结论:P. aeruginosa在采采蝇肠道中存在,是采采蝇可培养肠道菌群的重要组成部分。研究它是否能在调节蝇媒介的能力中发挥作用是至关重要的。
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Isolation, Characterization and Antimicrobial Susceptibility Pattern of Pseudomonas aeruginosa from Tsetse Flies Captured in Yankari Game Reserve, Nigeria
microbiota is involved in their vector competence and may help in developing novel disease control tools. Pseudomonas aeruginosa is reported to be ubiquitous in the natural environment, humans, and animals. It has been used for biocontrol in plants. Methods: Twenty-five live tsetse flies, collected from Yankari Game Reserve, Nigeria, were dissected under sterile conditions. The midgut was incubated successively in standard culture media. Suspected isolates were then subjected to biochemical tests. The 16S rRNA gene sequence was used to confirm the genotype. The positive isolate was also tested for susceptibility to 17 antimicrobials. Results: Eight (32%) of the 25 flies tested were positive for P. aeruginosa. They were positive for oxidase, catalase, citrate, and motility tests and negative for urease, indole, Methyl Red tests. Analysis of 16S rRNA gene confirmed the identity of the isolate, and the phylogenetic relationship with other strains was established. The isolate was sensitive to fluoroquinolones and intermediate to chloramphenicol. Drug resistance was observed against aminoglycosides, penicillin, erythromycin, clindamycin and imipenem Conclusion: The presence of P. aeruginosa in tsetse gut contributes to the repertoire of cultivable tsetse gut bacteria. It is crucial to investigate whether it could play a role in modulating the fly vector’s competence.
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