马来西亚细恙螨及其他寄生鸟类恙虫的分子种划分分析。

IF 2
Praveena Rajasegaran, Kim-Kee Tan, Jing Jing Khoo, Mohammad Saiful Mansor, Mohd K S Ahmad Khusaini, Sazaly AbuBakar, Zubaidah Ya'cob, Benjamin L Makepeace
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引用次数: 0

摘要

恙螨(无虫目)在具有医学重要性的节肢动物中是独特的,因为只有幼虫(恙螨)是寄生的,这可能导致人畜共患恙虫病的传播。直到最近,使用分子方法进行恙螨物种区分的研究一直非常有限,特别是对于那些寄生于鸟类宿主的恙螨,这方面的数据仍然很少。本研究基于线粒体细胞色素c氧化酶亚基I (COI)基因,通过DNA提取、PCR和测序,生成马来西亚地区寄生鸟类恙螨的DNA条形码。将来自马来西亚8种鸟类相关恙虫的54条COI序列与来自各国7个属的50条GenBank序列相结合,进行DNA条形码和系统发育分析。95个COI条形码的正确识别率分别为96.84%(最佳匹配)和86.31%(最佳接近匹配)。DNA条形码分析有效地将本研究的8个名义种聚为各自的属。lorius、Neoschoengastia gallinarum、Parascoschoengastia heynemani、Leptotrombidium imphalum和blakkaartia acuscutellaris的遗传差异小于3%,它们都形成了一个单系分支,证实了它们的同种性。与之相反的是,褐斑小圆虫(Toritrombicula densipiliata)、桃齿龙(Odontacarus audyi)和deliense细恙虫(Leptotrombidium deliense)的种内差异分别为17.64%、15.49%和11.63%。这些差异,通过划界分析得到不同实体的证据支持,表明这些种群中潜在的隐性多样性。总之,这项研究首次对马来西亚的鸟类恙虫进行了分子遗传分析,揭示了不同程度的遗传分化。我们的发现强调了DNA条形码在理解恙螨多样性和帮助准确鉴定方面的实用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular species delimitation analysis of Leptotrombidium spp. and other chigger species parasitizing birds in Malaysia.

Molecular species delimitation analysis of Leptotrombidium spp. and other chigger species parasitizing birds in Malaysia.

Molecular species delimitation analysis of Leptotrombidium spp. and other chigger species parasitizing birds in Malaysia.

Molecular species delimitation analysis of Leptotrombidium spp. and other chigger species parasitizing birds in Malaysia.

Trombiculid mites (Acariformes) are unique among arthropods of medical importance in that only the larval instar (chigger) is parasitic, which can result in the transmission of zoonotic scrub typhus. The use of molecular approaches for chigger species discrimination has been very limited until recently, especially for those parasitizing bird hosts, where data remain scarce. Here, we aimed to generate DNA barcodes of chiggers parasitizing birds in Malaysia based on the mitochondrial cytochrome c oxidase subunit I (COI) gene following DNA extraction, PCR and sequencing. Fifty-four COI sequences from 8 bird-associated chigger species in Malaysia were combined with 50 GenBank sequences comprising 7 genera from various countries for DNA barcode and phylogenetic analysis. The correct identification rates for the 95 COI barcodes were 96.84% (Best Match) and 86.31% (Best-Close Match). DNA barcode analyses effectively clustered the 8 nominal species from this study into their respective genera. Genetic divergence of less than 3% was observed within Ascoschoengastia lorius, Neoschoengastia gallinarum, Parascoschoengastia heynemani, Leptotrombidium imphalum, and Blankaartia acuscutellaris, all of which formed a monophyletic clade, confirming their conspecific nature. Conversely, intraspecific divergences of 17.64%, 15.49%, and 11.63% were obtained for Toritrombicula densipiliata, Odontacarus audyi, and Leptotrombidium deliense. These divergences, supported by evidence of distinct entities through delimitation analyses, indicate potential cryptic diversity within these populations. In conclusion, this study represents the first molecular genetic analysis of bird chiggers in Malaysia, revealing varying levels of genetic divergence. Our findings highlight the utility of DNA barcoding for understanding chigger diversity and aiding in accurate identification.

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