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恶性疟原虫药物治疗后配子体密度增加但流行率未增加。

Increased density but not prevalence of gametocytes following drug treatment of Plasmodium falciparum.

作者信息

Ali Eltayeb, Mackinnon Margaret J, Abdel-Muhsin Abdel-Muhsin A, Ahmed Salah, Walliker David, Babiker Hamza A

机构信息

Sudan Atomic Energy Commission, Khartoum, Sudan.

出版信息

Trans R Soc Trop Med Hyg. 2006 Feb;100(2):176-83. doi: 10.1016/j.trstmh.2005.04.021. Epub 2005 Oct 27.

Abstract

We monitored post-treatment Plasmodium falciparum among patients treated with chloroquine (CQ) and sulfadoxine-pyrimethamine (SP; Fansidar in a village in eastern Sudan. Parasites were examined on day 0 (pre-treatment), day 7, day 14 and day 21 (post-treatment) during the transmission season. A further sample was taken 2 months later (day 80) at the start of the dry season. Asexual forms and gametocytes were detected by microscopy, and reverse transcriptase polymerase chain reaction (RT-PCR) was used to detect expression of gametocyte-specific proteins pfs 25 and pfg 377. Gametocyte carriage, as revealed by microscopy, increased significantly following CQ and SP treatment, reaching a maximum between days 7 and 14. When measured by RT-PCR, however, there was no significant difference in gametocyte rate between day 0 and days 7 or 14. RT-PCR gametocyte rates dropped dramatically by day 80 post treatment but were still 33% and 8% in the CQ- and SP-treated group at this time. Alleles associated with drug resistance of P. falciparum to chloroquine (the chloroquine resistance transporter, pfcrt, and multidrug resistance, pfmdr1) and to pyrimethamine (dihydrofolate reductase, dhfr) were seen at a high frequency at the beginning of treatment and increased further through time following both drug treatments. Infections with drug-resistant parasites tended to have higher gametocyte prevalence than drug-sensitive infections.

摘要

我们在苏丹东部一个村庄对接受氯喹(CQ)和磺胺多辛-乙胺嘧啶(SP;Fansidar)治疗的患者进行了治疗后恶性疟原虫监测。在传播季节,于第0天(治疗前)、第7天、第14天和第21天(治疗后)对寄生虫进行检查。在旱季开始时(第80天)又采集了一份样本。通过显微镜检测无性体和配子体,并使用逆转录酶聚合酶链反应(RT-PCR)检测配子体特异性蛋白pfs 25和pfg 377的表达。显微镜检查显示,CQ和SP治疗后配子体携带率显著增加,在第7天至第14天达到最高。然而,通过RT-PCR测量时,第0天与第7天或第14天之间的配子体率没有显著差异。治疗后第80天,RT-PCR检测的配子体率急剧下降,但此时CQ治疗组和SP治疗组仍分别为33%和8%。在治疗开始时,与恶性疟原虫对氯喹(氯喹抗性转运蛋白,pfcrt,和多药抗性,pfmdr1)以及对乙胺嘧啶(二氢叶酸还原酶,dhfr)耐药相关的等位基因出现频率较高,并且在两种药物治疗后随时间进一步增加。耐药寄生虫感染的配子体流行率往往高于药物敏感感染。

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