泰国西部主要疟疾病媒微小按蚊自然种群中与寻找宿主行为相关的嗅觉途径的遗传变异

IF 3.5 2区 医学 Q1 PARASITOLOGY
Kanchon Pusawang, Daibin Zhong, Patchara Sriwichai, Yudthana Samung, Atiporn Saeung, Kittipat Aupalee, Pradya Somboon, Anuluck Junkum, Somsakul Pop Wongpalee, Jassada Saingamsook, Jetsumon Sattabongkot, Liwang Cui, Guiyun Yan
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引用次数: 0

摘要

背景:疟疾的传播取决于受感染的按蚊叮咬人类,二氧化碳、宿主气味和体温是主要的引诱剂。在泰缅边境,一种主要的疟疾媒介小按蚊(Funestus组)比Maculatus组的物种对人类宿主表现出更强的偏好。阐明这种摄食行为的遗传基础对于改进疟疾控制策略至关重要。方法:2019年7月至2020年11月,在泰国德省塔松阳区采用牛诱法、人诱法和疾控灯诱法采集野生按蚊。对标本进行形态学鉴定,并通过细胞色素c氧化酶亚基1 (cox1)基因的Sanger测序进行确认。然后我们对An进行了全基因组测序。根据寻找寄主行为分类的最小雌性:牛饵收集(COW)、人在室内着陆(HLI)和人在室外着陆(HLO),以研究寄主偏好的遗传决定因素。结果:雌性小按蚊占总样本的25%(504/ 1997)。Cox1测序结果显示,287个标本中有143个独特的单倍型,形成了A(181个序列)和B(106个序列)两大系统发育谱系,提示潜在的隐型多样性。An的全基因组测序。来自COW、HLI和HLO组的最小谱系A产生12,659,785个变异。过滤后,非同义单核苷酸多态性(nssnp)残留68,975个。比较三个合并组的等位基因频率(经fdr校正的p值)。根据收集方法(反映寄主寻找行为)对Minimus雌性进行分类,提出了这些行为变化的遗传基础。嗅觉途径基因中的差异nssnp可能在功能上与这一重要疟疾媒介的寄主寻找有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic variation in olfactory pathways associated with host-seeking behavior in natural populations of Anopheles minimus, a primary malaria vector in western Thailand.

Background: Malaria transmission hinges on infected Anopheles mosquitoes biting humans, with carbon dioxide (CO2), host odor, and body heat acting as key attractants. Along the Thai-Myanmar border, Anopheles minimus (the Funestus Group), a primary malaria vector, exhibits a stronger preference for human hosts than species of the Maculatus Group. Elucidating the genetic basis of this feeding behavior is essential for improving malaria control strategies.

Methods: Wild Anopheles mosquitoes were collected in Tha Song Yang district, Tak province, Thailand, from July 2019 to November 2020, using cow-baited traps, human landing catches, and Center for Disease Control (CDC) light traps. Specimens were identified morphologically and confirmed by Sanger sequencing of the cytochrome c oxidase subunit 1 (cox1) gene. We then performed whole-genome sequencing on An. minimus females categorized by host-seeking behavior: cow-baited collection (COW), human landing indoor (HLI), and human landing outdoor (HLO) to investigate the genetic determinants of host preference.

Results: Anopheles minimus females accounted for 25% of total samples (504/1,997). Cox1 sequencing revealed 143 unique haplotypes among 287 specimens, forming two major phylogenetic lineages, A (181 sequences) and B (106 sequences), suggestive of potential cryptic diversity. Whole-genome sequencing of An. minimus Lineage A from COW, HLI, and HLO groups yielded 12,659,785 variants. After filtering, 68,975 non-synonymous single-nucleotide polymorphisms (nsSNPs) remained. Comparing allele frequencies across the three pooled groups (FDR-adjusted p-value < 0.001) yielded 2,629, 2,948, and 4,369 significant nsSNPs, respectively. Gene Ontology (GO) analysis of genes harboring these nsSNPs showed strong enrichment for olfaction-related terms. The top six nsSNPs with olfactory annotations from each group comparison were selected for validation; Sanger sequencing confirmed their association with host-seeking preference. The VectorBase gene IDs for these candidate nsSNPs are AMIN001807, AMIN001339, AMIN003886, AMIN000912, AMIN003926, AMIN011060, AMIN002342, and AMIN015480.

Conclusions: The observed significant genomic variance in field-collected An. minimus females, categorized by collection methods (reflecting host-seeking behavior), proposes a genetic underpinning for these behavioral variations. Differential nsSNPs within olfactory pathway genes might be functionally linked to host-seeking in this important malaria vector.

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来源期刊
Parasites & Vectors
Parasites & Vectors 医学-寄生虫学
CiteScore
6.30
自引率
9.40%
发文量
433
审稿时长
1.4 months
期刊介绍: Parasites & Vectors is an open access, peer-reviewed online journal dealing with the biology of parasites, parasitic diseases, intermediate hosts, vectors and vector-borne pathogens. Manuscripts published in this journal will be available to all worldwide, with no barriers to access, immediately following acceptance. However, authors retain the copyright of their material and may use it, or distribute it, as they wish. Manuscripts on all aspects of the basic and applied biology of parasites, intermediate hosts, vectors and vector-borne pathogens will be considered. In addition to the traditional and well-established areas of science in these fields, we also aim to provide a vehicle for publication of the rapidly developing resources and technology in parasite, intermediate host and vector genomics and their impacts on biological research. We are able to publish large datasets and extensive results, frequently associated with genomic and post-genomic technologies, which are not readily accommodated in traditional journals. Manuscripts addressing broader issues, for example economics, social sciences and global climate change in relation to parasites, vectors and disease control, are also welcomed.
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