[Mutations of Plasmodium falciparum Multidrug Resistance 1 Gene in Imported Plasmodium falciparum in Wuhan].

Xi-shuai Jia, Shui-mao Zhou, Ming-xing Xu, Yan Yang, Kai Wu
{"title":"[Mutations of Plasmodium falciparum Multidrug Resistance 1 Gene in Imported Plasmodium falciparum in Wuhan].","authors":"Xi-shuai Jia,&nbsp;Shui-mao Zhou,&nbsp;Ming-xing Xu,&nbsp;Yan Yang,&nbsp;Kai Wu","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To identify Plasmodium falciparum multidrug resistance 1(Pfmdr1) point mutations in imported Plasmodium falciparum in Wuhan.</p><p><strong>Methods: </strong>Blood samples were collected from returnees infected with P. falciparum in endemic areas of Africa and Myanmar during 2010-2015 in Wuhan City. Nested PCR primers were specifically designed for Pfmdr1 gene loci 86, 1042 and 1246 of P. falciparum. The Pfmdr1 gene was then amplified by nested PCR, and the products were digested by restriction enzyme ApoⅠ, AseⅠ and EcoRⅤ, respectively. The mutation rate for loci 86, 1042 and 1246 was analyzed. Results A total of 187 patients with falciparum malaria were involved in the study. Pfmdr1 was amplified from all the blood samples. Restriction enzyme digestion revealed mutation rate of 19.3%(36/187), 4.3% (8/187) and 9.6%(18/187) for loci 86, 1042 and 1246, respectively. In detail, the mutation rate for loci 86, 1042 and 1246 was 20.6%(36/175), 2.9%(5/175) and 10.3%(18/175) respectively in the 175 samples from Africa, and only 3 cases with locus 1042 mutation were found in the 12 samples from Myanmar.</p><p><strong>Results: </strong>A total of 187 patients with falciparum malaria were involved in the study. Pfmdr1 was amplified from all the blood samples. Restriction enzyme digestion revealed mutation rate of 19.3%(36/187), 4.3% (8/187) and 9.6%(18/187) for loci 86, 1042 and 1246, respectively. In detail, the mutation rate for loci 86, 1042 and 1246 was 20.6%(36/175), 2.9%(5/175) and 10.3%(18/175) respectively in the 175 samples from Africa, and only 3 cases with locus 1042 mutation were found in the 12 samples from Myanmar.</p><p><strong>Conclusion: </strong>The loci 86, 1042 and 1246 mutations of Pfmdr1 have all been found in the samples from Africa, with only one point mutation (locus 1042) found in samples from Myanmar.</p>","PeriodicalId":23981,"journal":{"name":"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases","volume":"34 6","pages":"489-92"},"PeriodicalIF":0.0000,"publicationDate":"2016-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: To identify Plasmodium falciparum multidrug resistance 1(Pfmdr1) point mutations in imported Plasmodium falciparum in Wuhan.

Methods: Blood samples were collected from returnees infected with P. falciparum in endemic areas of Africa and Myanmar during 2010-2015 in Wuhan City. Nested PCR primers were specifically designed for Pfmdr1 gene loci 86, 1042 and 1246 of P. falciparum. The Pfmdr1 gene was then amplified by nested PCR, and the products were digested by restriction enzyme ApoⅠ, AseⅠ and EcoRⅤ, respectively. The mutation rate for loci 86, 1042 and 1246 was analyzed. Results A total of 187 patients with falciparum malaria were involved in the study. Pfmdr1 was amplified from all the blood samples. Restriction enzyme digestion revealed mutation rate of 19.3%(36/187), 4.3% (8/187) and 9.6%(18/187) for loci 86, 1042 and 1246, respectively. In detail, the mutation rate for loci 86, 1042 and 1246 was 20.6%(36/175), 2.9%(5/175) and 10.3%(18/175) respectively in the 175 samples from Africa, and only 3 cases with locus 1042 mutation were found in the 12 samples from Myanmar.

Results: A total of 187 patients with falciparum malaria were involved in the study. Pfmdr1 was amplified from all the blood samples. Restriction enzyme digestion revealed mutation rate of 19.3%(36/187), 4.3% (8/187) and 9.6%(18/187) for loci 86, 1042 and 1246, respectively. In detail, the mutation rate for loci 86, 1042 and 1246 was 20.6%(36/175), 2.9%(5/175) and 10.3%(18/175) respectively in the 175 samples from Africa, and only 3 cases with locus 1042 mutation were found in the 12 samples from Myanmar.

Conclusion: The loci 86, 1042 and 1246 mutations of Pfmdr1 have all been found in the samples from Africa, with only one point mutation (locus 1042) found in samples from Myanmar.

武汉输入性恶性疟原虫多药耐药基因突变分析[j]。
目的:鉴定武汉市输入性恶性疟原虫多药耐药1(Pfmdr1)点突变。方法:采集2010-2015年武汉市非洲和缅甸流行区归国人员恶性疟原虫感染血样。针对恶性疟原虫Pfmdr1基因86、1042和1246位点设计巢式PCR引物。然后用巢式PCR扩增Pfmdr1基因,产物分别用ApoⅠ、AseⅠ和EcoRⅤ酶切。分析了86、1042和1246位点的突变率。结果本研究共纳入187例恶性疟疾患者。从所有血液样本中扩增出Pfmdr1。限制性内切酶酶切结果显示,86、1042和1246位点的突变率分别为19.3%(36/187)、4.3%(8/187)和9.6%(18/187)。其中,来自非洲的175份样本中86、1042和1246位点的突变率分别为20.6%(36/175)、2.9%(5/175)和10.3%(18/175),来自缅甸的12份样本中仅发现3例1042位点突变。结果:本研究共纳入187例恶性疟疾患者。从所有血液样本中扩增出Pfmdr1。限制性内切酶酶切结果显示,86、1042和1246位点的突变率分别为19.3%(36/187)、4.3%(8/187)和9.6%(18/187)。其中,来自非洲的175份样本中86、1042和1246位点的突变率分别为20.6%(36/175)、2.9%(5/175)和10.3%(18/175),来自缅甸的12份样本中仅发现3例1042位点突变。结论:Pfmdr1的86、1042和1246位点突变均在非洲发现,仅在缅甸发现1个位点突变(1042位点)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信