利用nsomb幼虫研究肠杆菌致病性、毒力及阿莫西林-生物表面活性剂协同作用的新动物模型

IF 3.9 3区 生物学 Q2 MICROBIOLOGY
Sergy Patrick Junior Bissoko, Christian Aimé Kayath, Saturnin Nicaise Mokemiabeka, Frédéric Yannick Okouakoua, David Charles Roland Moukala, Duchel Jeanedvi Kinouani Kinavouidi
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引用次数: 0

摘要

在不断扩大的致病菌研究领域中,昆虫幼虫越来越多地被用作复杂的感染模型。这项创新研究旨在评估一种替代模型,用于分析宿主与病原体的相互作用,并利用腓尼基蛾幼虫的生物系统评估抗菌治疗的效果。采用针对16S rRNA、编码III型分泌系统(T3SS)组分的毒力基因和Hsp60基因的PCR技术,鉴定出鼠伤寒沙门菌、肺炎克雷伯菌、阴沟肠杆菌和肠致病性大肠杆菌(EPEC) 4种主要致病性肠杆菌科细菌,检出率为100%。毒力评价结果表明,将105 CFU/µL浓度的菌株注射到小褐家鼠幼虫体内,对其致病性评价最佳。高毒力菌株e。大肠杆菌EPEC菌株E2、肺炎克雷伯菌K4、鼠伤寒沙门氏菌S4和阴沟肠杆菌en2导致幼虫存活率显著降低,血淋巴细菌负荷高达2.5 × 106 CFU/µL。治疗评价显示,阿莫西林+生物表面活性剂联合用药在延长幼虫存活方面最有效。某些菌株的存活率在24 h时达到80%,在72 h时保持相对较高的存活率,最高可达70%。相比之下,单独使用阿莫西林表现出不稳定和持续时间较短的疗效。这些发现强调了腓尼基幼虫作为探索宿主-病原体相互作用和评估抗生素和生物表面活性剂联合抗菌治疗协同效果的有价值的替代模型的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Novel Animal Model of Enterobacteria Pathogenicity, Virulence, and Amoxicillin—Biosurfactant Synergic Using Nsombé (Rhynchophorus phoenicis Larvae)

Novel Animal Model of Enterobacteria Pathogenicity, Virulence, and Amoxicillin—Biosurfactant Synergic Using Nsombé (Rhynchophorus phoenicis Larvae)

Insect larvae are increasingly being employed as sophisticated infection models in the expanding field of pathogenic bacterial research. This innovative study aims to evaluate an alternative model for analyzing host-pathogen interactions and assessing the efficacy of antimicrobial treatments using the biological system of Rhynchophorus phoenicis larvae. Using PCR techniques targeting 16S rRNA, virulence genes encoding Type III secretion system (T3SS) components, and the Hsp60 gene, four major pathogenic Enterobacteriaceae were identified with 100% detection rates: Salmonella Typhimurium, Klebsiella pneumoniae, Enterobacter cloacae, and enteropathogenic Escherichia coli (EPEC). Virulence assessment revealed that injection of bacterial strains at a concentration of 105 CFU/µL into R. phoenicis larvae was optimal for evaluating pathogenicity. Highly virulent strains—E. coli EPEC strain E2, K. pneumoniae K4, S. Typhimurium S4, and E. cloacae En2—caused significantly reduced larval survival, with bacterial loads in the hemolymph reaching up to 2.5 × 106 CFU/µL. Treatment evaluation showed that the amoxicillin + biosurfactant combination was the most effective in prolonging larval survival across all time points. Survival rates peaked at 80% at 24 h and remained relatively high at up to 70% at 72 h for certain strains. In contrast, amoxicillin alone demonstrated variable and less sustained efficacy. These findings underscore the potential of R. phoenicis larvae as a valuable alternative model for exploring host–pathogen interactions and assessing the synergistic efficacy of combined antimicrobial treatments involving antibiotics and biosurfactants.

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来源期刊
MicrobiologyOpen
MicrobiologyOpen MICROBIOLOGY-
CiteScore
8.00
自引率
0.00%
发文量
78
审稿时长
20 weeks
期刊介绍: MicrobiologyOpen is a peer reviewed, fully open access, broad-scope, and interdisciplinary journal delivering rapid decisions and fast publication of microbial science, a field which is undergoing a profound and exciting evolution in this post-genomic era. The journal aims to serve the research community by providing a vehicle for authors wishing to publish quality research in both fundamental and applied microbiology. Our goal is to publish articles that stimulate discussion and debate, as well as add to our knowledge base and further the understanding of microbial interactions and microbial processes. MicrobiologyOpen gives prompt and equal consideration to articles reporting theoretical, experimental, applied, and descriptive work in all aspects of bacteriology, virology, mycology and protistology, including, but not limited to: - agriculture - antimicrobial resistance - astrobiology - biochemistry - biotechnology - cell and molecular biology - clinical microbiology - computational, systems, and synthetic microbiology - environmental science - evolutionary biology, ecology, and systematics - food science and technology - genetics and genomics - geobiology and earth science - host-microbe interactions - infectious diseases - natural products discovery - pharmaceutical and medicinal chemistry - physiology - plant pathology - veterinary microbiology We will consider submissions across unicellular and cell-cluster organisms: prokaryotes (bacteria, archaea) and eukaryotes (fungi, protists, microalgae, lichens), as well as viruses and prions infecting or interacting with microorganisms, plants and animals, including genetic, biochemical, biophysical, bioinformatic and structural analyses. The journal features Original Articles (including full Research articles, Method articles, and Short Communications), Commentaries, Reviews, and Editorials. Original papers must report well-conducted research with conclusions supported by the data presented in the article. We also support confirmatory research and aim to work with authors to meet reviewer expectations. MicrobiologyOpen publishes articles submitted directly to the journal and those referred from other Wiley journals.
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