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恶性疟原虫中对乙胺嘧啶耐药的突变

Pyrimethamine resistant mutations in Plasmodium falciparum.

作者信息

Thaithong S, Chan S W, Songsomboon S, Wilairat P, Seesod N, Sueblinwong T, Goman M, Ridley R, Beale G

机构信息

Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.

出版信息

Mol Biochem Parasitol. 1992 Jun;52(2):149-57. doi: 10.1016/0166-6851(92)90047-n.

Abstract

Three mutations in Plasmodium falciparum yielding increased resistance to pyrimethamine were obtained following treatment with chemical mutagens and selection in presence of pyrimethamine. From parasite clone TM4/8.2 a mutant, TM4/8.2/4.1, was produced which raised pyrimethamine resistance about 500 times and was found to involve an amino acid change in the DHFR-TS enzyme molecule from Ser108 to Asn108. A clone of another isolate, T9/94, yielded a mutant, T9/94/300.300, raising pyrimethamine resistance about 10 times and involving an amino acid change from Ile164 to Met164. However, another mutant from T9/94, T9/94/M1-1(b3), although it raised the pyrimethamine resistance 100 times, did not involve any changes in the coding sequence of the DHFR-TS gene, but resulted in the production of about twice as much DHFR-TS enzyme as the original clone T9/94. No amplification of the DHFR-TS gene was detected. It is concluded that changes in pyrimethamine resistance of malaria parasites may arise in at least 2 ways: (1) by structural changes in the DHFR domain of the DHFR-TS gene (as previously found by other workers); (2) by other changes, possibly affecting the expression of the DHFR-TS gene. The relative importance of these 2 mechanisms in causing resistance in wild populations of P. falciparum is discussed.

摘要

在用化学诱变剂处理并在乙胺嘧啶存在的情况下进行选择后,获得了恶性疟原虫中三个对乙胺嘧啶产生更高抗性的突变体。从寄生虫克隆TM4/8.2中产生了一个突变体TM4/8.2/4.1,其乙胺嘧啶抗性提高了约500倍,并且发现这涉及二氢叶酸还原酶-胸苷酸合成酶(DHFR-TS)酶分子中的一个氨基酸变化,即从Ser108变为Asn108。另一个分离株T9/94的一个克隆产生了一个突变体T9/94/300.300,其乙胺嘧啶抗性提高了约10倍,涉及一个氨基酸变化,即从Ile164变为Metl64。然而,来自T9/94的另一个突变体T9/94/M1-1(b3),尽管其乙胺嘧啶抗性提高了100倍,但在DHFR-TS基因的编码序列中没有任何变化,而是导致产生的DHFR-TS酶量约为原始克隆T9/94的两倍。未检测到DHFR-TS基因的扩增。得出的结论是,疟原虫对乙胺嘧啶抗性的变化可能至少通过两种方式产生:(1) 通过DHFR-TS基因的DHFR结构域中的结构变化(如其他研究人员先前发现的);(2) 通过其他变化,可能影响DHFR-TS基因的表达。讨论了这两种机制在导致恶性疟原虫野生种群抗性方面的相对重要性。

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