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中国南京市(双翅目:蚊科)的精细尺度遗传结构与感染情况

Fine-scale genetic structure and infection of (Diptera: Culicidae) in Nanjing city, China.

作者信息

Zhang Heng-Duan, Gao Jian, Xing Dan, Guo Xiao-Xia, Li Chun-Xiao, Dong Yan-De, Zheng Zhong, Ma Zu, Wu Zhi-Ming, Zhu Xiao-Juan, Zhao Ming-Hui, Liu Qin-Mei, Yan Ting, Chu Hong-Liang, Zhao Tong-Yan

机构信息

State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, China.

Department of Disinfection and Vector Control, Jiangsu Provincial Center for Disease Control and Prevention, Nanjing, China.

出版信息

Front Genet. 2022 Aug 30;13:827655. doi: 10.3389/fgene.2022.827655. eCollection 2022.

DOI:10.3389/fgene.2022.827655
PMID:36110209
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9468874/
Abstract

is an indigenous primary vector of dengue and Zika viruses in China. is a gram-negative and common intracellular bacteria, which is maternally inherited endosymbionts and could expand their propagation in host populations by means of various manipulations. Compared with research on the dispersion of at the macrospatial level (mainly at the country or continent level), little is known about its variation and infection at the microspatial level, which is essential for its management. Meanwhile, no local cases of dengue fever have been recorded in the history of Nanjing, which implies that few adulticides have been applied in the city. Thus, the present study examines how the population varies and the infection status of each population among microspatial regions of Nanjing City. The genetic structure of 17 populations collected from urban, urban fringe, and rural regions of Nanjing City was investigated based on 9 microsatellite loci and the mitochondrial gene. The infection status of each population was also assessed with A- and B-specific primers. Nine out of 58 tested pairs of microsatellite markers were highly polymorphic, with a mean PIC value of 0.560, and these markers were therefore chosen for microsatellite genotyping analysis. The Na value of each population was very high, and the urban area populations (7.353 ± 4.975) showed a lower mean value than the urban fringe region populations (7.866 ± 5.010). A total of 19 haplotypes were observed among 329 individuals via haplotype genotyping, with the highest diversity observed among the urban fringe populations (Hd = 0.456) and the lowest among the urban populations (Hd = 0.277). Each population showed significant departure from HWE, and significant population expansion was observed in only three populations from the urban (ZSL), urban fringe (HAJY), and rural areas (HSZY) ( < 0.05). Combined with DAPC analysis, all the populations were adequately allocated to two clades with significant genetic differences according to population structure analysis, and the best K value was equal to two. AMOVA results showed that most (96.18%) of the genetic variation detected in occurred within individuals (F = 0.22238, < 0.0001), while no significant positive correlation was observed via isolation by distance (IBD) analysis ( = 0.03262, = 0.584). The TCS network of all haplotypes showed that haplotype 1 (H1) and haplotype 4 (H4) were the most frequent haplotypes among all populations, and the haplotype frequency significantly increased from urban regions (36.84%) to rural regions (68.42%). Frequent migration was observed among populations from rural to urban regions via the urban fringe region, with four direct migration routes between rural and urban regions. Furthermore, genotyping results showed that most of the individuals of each population were coinfected with A and B. The independent infection rate of A was slightly higher than that of B, and no significant differences were observed among different regions. In the microspatial environment of Nanjing City, the urban fringe region is an important region for the dispersion of populations between rural and urban areas, and A and B coinfection is the most common infection status in all populations among different regions.

摘要

是中国登革热和寨卡病毒的本土主要传播媒介。是一种革兰氏阴性且常见的细胞内细菌,是母系遗传的内共生体,可通过各种方式在宿主种群中扩大其传播。与在宏观空间层面(主要是国家或大陆层面)对其扩散的研究相比,人们对其在微观空间层面的变异和感染情况知之甚少,而这对其管理至关重要。同时,南京历史上未记录到本地登革热病例,这意味着该市很少使用杀虫剂。因此,本研究考察了南京市微观空间区域内种群如何变化以及每个种群的感染状况。基于9个微卫星位点和线粒体基因,对从南京市城市、城市边缘和农村地区采集的17个种群的遗传结构进行了调查。还用A和B特异性引物评估了每个种群的感染状况。58对测试的微卫星标记中有9对具有高度多态性,平均PIC值为0.560,因此选择这些标记进行微卫星基因分型分析。每个种群的Na值都非常高,城市地区种群(7.353±4.975)的平均值低于城市边缘地区种群(7.866±5.010)。通过单倍型基因分型在329个个体中总共观察到19种单倍型,城市边缘种群的多样性最高(Hd = 0.456),城市种群的多样性最低(Hd = 0.277)。每个种群均显著偏离哈迪 - 温伯格平衡(HWE),仅在城市(ZSL)、城市边缘(HAJY)和农村地区(HSZY)的三个种群中观察到显著的种群扩张(P < 0.05)。结合判别分析主成分分析(DAPC),根据种群结构分析,所有种群被充分分配到两个具有显著遗传差异的进化枝中,最佳K值等于2。分子方差分析(AMOVA)结果表明,中检测到的大部分遗传变异(96.18%)发生在个体内部(F = 0.22238,P < 0.0001),而通过距离隔离分析(IBD)未观察到显著的正相关(r = 0.03262,P = 0.584)。所有单倍型的TCS网络表明,单倍型1(H1)和单倍型4(H4)是所有种群中最常见的单倍型,单倍型频率从城市地区(36.84%)到农村地区(68.42%)显著增加。观察到种群从农村地区经城市边缘地区向城市地区频繁迁移,农村和城市地区之间有四条直接迁移路线。此外,基因分型结果表明,每个种群的大多数个体同时感染了A和B。A的独立感染率略高于B,不同区域之间未观察到显著差异。在南京市的微观空间环境中,城市边缘地区是种群在农村和城市地区之间扩散的重要区域,A和B共感染是不同区域所有种群中最常见的感染状况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/1e9d895b7ac3/fgene-13-827655-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/9a2d402007b5/fgene-13-827655-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/4a47426da138/fgene-13-827655-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/b1d475c1352c/fgene-13-827655-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/3e312ecfa187/fgene-13-827655-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/44851a431a14/fgene-13-827655-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/1e9d895b7ac3/fgene-13-827655-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/9a2d402007b5/fgene-13-827655-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/4a47426da138/fgene-13-827655-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/b1d475c1352c/fgene-13-827655-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/3e312ecfa187/fgene-13-827655-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/44851a431a14/fgene-13-827655-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d0/9468874/1e9d895b7ac3/fgene-13-827655-g006.jpg

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