首页> 外文期刊>BMC Microbiology >Bacterial diversity analysis of larvae and adult midgut microflora using culture-dependent and culture-independent methods in lab-reared and field-collected Anopheles stephensi-an Asian malarial vector
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Bacterial diversity analysis of larvae and adult midgut microflora using culture-dependent and culture-independent methods in lab-reared and field-collected Anopheles stephensi-an Asian malarial vector

机译:在实验室饲养和田间采集的按蚊亚洲疟疾病媒中,采用依赖于培养和不依赖于培养的方法,对幼虫和成年中肠菌群进行细菌多样性分析

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Background Mosquitoes are intermediate hosts for numerous disease causing organisms. Vector control is one of the most investigated strategy for the suppression of mosquito-borne diseases. Anopheles stephensi is one of the vectors of malaria parasite Plasmodium vivax. The parasite undergoes major developmental and maturation steps within the mosquito midgut and little is known about Anopheles-associated midgut microbiota. Identification and characterization of the mosquito midgut flora is likely to contribute towards better understanding of mosquito biology including longevity, reproduction and mosquito-pathogen interactions that are important to evolve strategies for vector control mechanisms. Results Lab-reared and field-collected A. stephensi male, female and larvae were screened by "culture-dependent and culture-independent" methods. Five 16S rRNA gene library were constructed form lab and field-caught A. stephensi mosquitoes and a total of 115 culturable isolates from both samples were analyzed further. Altogether, 68 genera were identified from midgut of adult and larval A. stephensi, 53 from field-caught and 15 from lab-reared mosquitoes. A total of 171 and 44 distinct phylotypes having 85 to 99% similarity with the closest database matches were detected among field and lab-reared A. stephensi midgut, respectively. These OTUs had a Shannon diversity index value of 1.74–2.14 for lab-reared and in the range of 2.75–3.49 for field-caught A. stephensi mosquitoes. The high species evenness values of 0.93 to 0.99 in field-collected adult and larvae midgut flora indicated the vastness of microbial diversity retrieved by these approaches. The dominant bacteria in field-caught adult male A. stephensi were uncultured Paenibacillaceae while in female and in larvae it was Serratia marcescens, on the other hand in lab-reared mosquitoes, Serratia marcescens and Cryseobacterium meninqosepticum bacteria were found to be abundant. Conclusion More than fifty percent of the phylotypes were related to uncultured class of bacteria. Interestingly, several of the bacteria identified are related to the known symbionts in other insects. Few of the isolates identified in our study are found to be novel species within the gammaproteobacteria which could not be phylogenetically placed within known classes. To the best of our knowledge, this is the first attempt to study the midgut microbiota of A. stephensi from lab-reared and field-collected adult and larvae using "culture-dependent and independent methods".
机译:背景技术蚊子是许多致病生物的中介宿主。病媒控制是抑制蚊子传播疾病的最受研究的策略之一。斯蒂芬按蚊是疟原虫间日疟原虫的媒介之一。寄生虫在蚊子中肠内经历主要的发育和成熟步骤,对与按蚊相关的中肠微生物群知之甚少。蚊中肠菌群的鉴定和表征可能有助于更好地了解蚊子生物学,包括寿命,繁殖和蚊-病原体相互作用,这些对于发展媒介控制机制的策略至关重要。结果通过“依赖于培养和不依赖于培养”的方法筛选了实验室饲养的和田间采集的A. stephensi雄性,雌性和幼虫。通过实验室和现场捕获的斯蒂芬斯蚊(A. stephensi)蚊子构建了五个16S rRNA基因文库,并进一步分析了两个样品中的115种可培养分离株。总共从成年幼虫和斯蒂芬斯幼虫的中肠中鉴定出68属,从田间捕获的蚊子中鉴定出53属,并且在实验室饲养的蚊子中鉴定出了15属。分别在田间和实验室饲养的A. stephensi中肠中共检测到171种和44种与最近的数据库匹配具有85%至99%相似性的不同系统型。这些OTU在实验室饲养的香农多样性指数值为1.74–2.14,在野外捕获的斯蒂芬斯蚊为2.75–3.49。在田间采集的成虫和幼虫中肠菌群中,物种均匀度值较高,为0.93至0.99,这表明通过这些方法可以回收大量的微生物。田间捕获的成年雄性A. stephensi中的主要细菌是未经培养的芽孢杆菌科,而在雌性和幼虫中则是粘质沙雷氏菌,另一方面,在实验室饲养的蚊子中,粘质沙雷氏菌和Meninqosepticum细菌均富含。结论超过百分之五十的系统型与未经培养的细菌有关。有趣的是,鉴定出的几种细菌与其他昆虫中已知的共生菌有关。在我们的研究中,几乎没有发现分离物是γ-变形杆菌内的新物种,无法在系统发育上置于已知类别内。据我们所知,这是首次尝试使用“依赖于文化的方法和独立的方法”从实验室饲养的和田间采集的成年幼虫中研究Stephensi的中肠微生物群。

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