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[从海南省分离的恶性疟原虫中Pfcrt和Pfmdr1基因的点突变]

[The point mutations in Pfcrt and Pfmdr1 genes in Plasmodium falciparum isolated from Hainan Province].

作者信息

Guan Ya-Yi, Tang Lin-Hua, Hu Ling, Feng Xiao-Ping, Liu De-Quan

机构信息

National Institute of Parasitic Diseases, Chinese Center for Diseases Control and Prevention, Shanghai 200025, China.

出版信息

Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2005 Jun 30;23(3):135-9.

Abstract

OBJECTIVE

To evaluate the point mutations in Pfcrt and Pfmdr1 genes in Plasmodium falciparum isolated from Hainan Province.

METHODS

Nested polymerase chain reaction and restriction fragment length polymorphism were used to detect the point mutations at codon 76 of Pfcrt and at codon 86, 1246 of Pfmdr1 in P. falciparum isolates. Chloroquine resistance was measured by the in vitro microtest recommended by WHO.

RESULTS

In 36 samples tested, 28 were successfully amplified for Pfcrt, 64.3% of them carried mutant allele at codon 76, 21.4% with wild allele K76 and 14.3% with mixed allele mutation. While for Pfmdr1, 3.4% isolates displayed the 86Y mutation, 89.7% with wild allele N86 and 6.9% with the mixed alleles in 29 isolates which were amplified successfully for N86Y. No point mutation in Pfmdr1 at codon 1246 was found in 13 isolates from the total 36 samples. By the in vitro test, 72.2% (26/36) showed resistance to chloroquine. The 76T and 86Y mutant alleles were present in both in vitro susceptible and resistant isolates. There was a significant difference between susceptible and resistant isolates carrying 76T mutant codon (P < 0.05), but no significant difference was found in Pfmdr1 (P < 0.05).

CONCLUSION

There is a significant difference of the 76T prevalence in Pfcrt gene between the susceptible isolate and resistant one of P. falciparum to chloroquine in vitro. The Pfcrt 76T may be used as a predictive marker for chloroquine resistance surveillance.

摘要

目的

评估从海南省分离出的恶性疟原虫中Pfcrt和Pfmdr1基因的点突变情况。

方法

采用巢式聚合酶链反应和限制性片段长度多态性方法检测恶性疟原虫分离株中Pfcrt基因第76位密码子以及Pfmdr1基因第86、1246位密码子的点突变。按照世界卫生组织推荐的体外微量试验方法测定氯喹抗性。

结果

在检测的36份样本中,28份成功扩增出Pfcrt基因,其中64.3%在第76位密码子携带突变等位基因,21.4%为野生型K76等位基因,14.3%为混合等位基因突变。对于Pfmdr1基因,在成功扩增出N86Y的29份分离株中,3.4%的分离株显示第86位密码子发生Y突变,89.7%为野生型N86等位基因,6.9%为混合等位基因。在全部36份样本中的13份分离株中未发现Pfmdr1基因第1246位密码子的点突变。通过体外试验,72.2%(26/36)显示对氯喹耐药。第76位密码子的T突变等位基因和第86位密码子的Y突变等位基因在体外敏感和耐药分离株中均有存在。携带第76位密码子T突变的敏感株和耐药株之间存在显著差异(P<0.05),但Pfmdr1基因无显著差异(P>0.05)。

结论

体外氯喹敏感和耐药的恶性疟原虫分离株中,Pfcrt基因第76位密码子T突变的发生率存在显著差异。Pfcrt基因第76位密码子T突变可作为氯喹耐药监测的预测标志物。

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