基于18S rrna巢式PCR的云南边境地区疟原虫种类鉴定及序列分析

Cang-lin Zhang, Hong-ning Zhou, Ren-hua Nie, Hui Liu, Jian Wang, Chun-fu Li, Ya-ming Yang
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引用次数: 0

摘要

目的:采用基于18S rRNA的巢式PCR方法对云南省边境地区恶性疟疾和间日疟疾患者血样进行分析,并比较18S rRNA序列。方法:收集2004 - 2011年缅甸拉扎、南卡江、芒东、乃威地区和云南勐腊、腾冲、盈江地区恶性疟原虫或间日疟原虫感染镜检阳性的血液或滤血标本。对样品进行18S rrna巢式PCR,对PCR产物进行测序和爆破。采用MEGA软件(6.06版)邻接法构建系统发育树。结果:镜检发现恶性疟原虫感染256例,间日疟原虫感染219例。基于18S rrna的PCR进一步证实242份样本存在恶性疟原虫感染,176份样本存在间日疟原虫感染,57份样本存在混合感染。镜检结果与PCR结果符合率为81.7%(388/475)。不一致率与寄生虫密度显著相关(Spearman’s r=-0.408, p)。结论:巢式PCR在镜检单一感染的样本中发现57个样本存在混合感染。云南省7个县市的18S rRNA序列差异不显著。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Species Identification and Sequence Analysis of Plasmodium spp. in Border Areas of Yunnan Province by 18S rRNA-based Nested PCR]

Objective: To analyze blood samples from patients with falciparum malaria and vivax malaria in border areas of Yunnan Province, using 18S rRNA-based nested PCR, and compare 18S rRNA sequences.

Methods: Blood or filter blood samples with positive microscopic results for Plasmodium falciparum or P. vivax infection were collected from Laza, Nankajiang, Mangdong and Nawei of Myanmar, and from Mengla, Tengchong and Yingjiang of Yunnan Province between 2004 and 2011. 18S rRNA-based nested PCR was conducted on the samples, and PCR products were sequenced and blasted. Phylogenetic tree was constructed using the neighbor-joining method with MEGA software (version 6.06).

Results: Microscopic examination revealed P. falciparum infection in 256 samples and P. vivax infection in 219 samples. The 18S rRNA-based PCR further confirmed P. falciparum infection in 242 samples, P. vivax infection in 176 samples, and mixed infection in 57 samples. The consistency rate was 81.7% (388/475) between microscopic and PCR results. The inconsistency rate significantly correlated with parasite density (Spearman’s r=-0.408, P<0.05). Sequence alignment revealed 11 and 10 homologous sequences for P. falciparum and P. vivax 18S rRNA gene, comprising 2.9%(6/205) and 22.5%(27/120) variable sites, respectively. The 18S rRNA of P. falciparum clustered with that from Cameroon(GenBank accession number KC428742), but was distantly related with the S-type 18S rRNA from the Netherlands (U36465) and Brazil (U36466 and U36467). The 18S rRNA of P. vivax clustered with A-type 18S rRNA from Thailand (U07367), but was distantly related with the C-type 18S rRNA from Thailand(U07368).

Conclusion: Nested PCR revealed mixed infection in 57 samples among those identified with single infection by microscopy. There is no significant difference in 18S rRNA sequence in seven counties/cities in Yunnan Province.

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