滇缅边境及其他地区5种疟原虫18S核糖体DNA测序及系统发育树构建[j]。

Mu-xin Chen, Jia-xu Chen, Wei Liu, Xin-yu Feng, Shen-bo Chen, Shao-hong Chen, Yu-chun Cai, Bin Xu, Wei Hu
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引用次数: 0

摘要

目的:利用18S核糖体DNA分析中缅边境及其他地区5种疟原虫的序列变异并构建系统发育树。方法:采集2000 - 2015年滇缅边境等地区疟疾患者血样(或DNA)。从血样中提取DNA,扩增18S rDNA片段,测序并与GenBank中的相关序列比对。系统发育树分别采用邻居连接法(NJ)、最大似然法(ML)和最大简约法(MP)构建。结果:共采集疟疾患者血样或DNA 94份。所有样品均成功扩增出18S rDNA。序列比对结果显示,恶性疟原虫、间日疟原虫、疟疾疟原虫、卵形疟原虫和诺氏疟原虫的18S rDNA序列差异分别为0-0.2%、0-0.1%、0-0.1%、0-0.1%和0。三种方法构建的系统发育树具有一致性。系统发育分析表明,所研究的疟原虫有五大分支。恶性疟原虫分支与来自喀麦隆(KC428741、KC428742)、巴西(KC906718)和马来西亚(HQ283221)的分离株聚集在GenBank中。间日疟分支与来自喀麦隆(HF945443)、印度(HM014361, JQ627158)和哥伦比亚(U83877)的分离株聚集在一起。Pv11、Pv18和Pv21与Macaca fascicularis分离株P. cynomolgi(L07559)有较密切的系统发育关系。云南省疟疟样本Pm1、Pm3、Pm4聚在一起形成一个小分支,再与海南省样本聚在一起,呈现出地理多样性。所有卵形疟原虫分离株均与越南分离株EU935736和AF387038聚集在一起。所有分离株均聚集在一个分支,与缅甸分离株(GU816250和GU816246)亲缘关系密切。结论:滇缅边境及其他地区5种疟原虫18S rDNA基因差异无统计学意义。用NJ、MP和ML方法构建的系统发育树具有一致性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Sequencing and Phylogenetic Tree Construction of 18S Ribosomal DNA from Five Species of Plasmodium from Yunnan Border between China and Myanmar and Other Areas].

Objective: To analyze sequence variation and construct phylogenetic tree based on 18S ribosomal DNA among five species of Plasmodium in Yunnan border between China and Myanmar and other areas.

Methods: Blood samples (or DNA samples)from malaria patients were collected from 2000 to 2015 in Yunnan border and Myanmar and other areas. DNA was extracted from blood samples, and the 18S rDNA fragment was amplified, sequenced and aligned with relevant sequences available in the GenBank. The phylogenetic tree was constructed by methods of neighbor joining (NJ), maximum likelihood (ML), and maximum parsimony (MP), respectively.

Results: A total of 94 blood samples or DNA from malaria patients were collected. The 18S rDNA was successfully amplified from all the samples. Sequence alignment revealed variations of 0-0.2%, 0-0.1%, 0-0.1%, 0-0.1% and 0 for 18S rDNA sequence among Plasmodium falciparum, P. vivax, P. malariae, P. ovale and P. knowlesi, respectively. The phylogenetic tree constructed with the three method showed consistency. Phylogenic analysis revealed that there were five big branches of Plasmodium spp. studied. The P. falciparum branch clustered with the isolates from Cameroon(KC428741, KC428742), Brazil(KC906718), and Malaysia(HQ283221) in GenBank. The P. vivax branch clustered with isolates from Cameroon(HF945443), India (HM014361, JQ627158), and Colombia (U83877). However, the samples Pv11, Pv18 and Pv21 formed a small branch that showed closer phylogenetic relationship with P. cynomolgi(L07559), an isolate from Macaca fascicularis. Moreover, P. malariae samples from Yunnan Province including Pm1, Pm3 and Pm4 clustered to form a small branch, and then clustered with samples from Hainan Province, showing geographical diversity. All the isolates of P. ovale clustered with isolates from Vietnam(EU935736 and AF387038). All the isolates of P. knowlesi clustered into a branch, and showed close relationship with those from Myanmar (GU816250 and GU816246).

Conclusion: There is no significant difference in 18S rDNA gene of the five species of Plasmodium from Yunnan border between China and Myanmar and other areas. The phylogenetic tree constructed with the NJ, MP and ML methods shows consistency.

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