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无症状疟疾感染中多种恶性疟原虫裂殖子表面抗原-2等位基因的年龄依赖性携带情况。

Age-dependent carriage of multiple Plasmodium falciparum merozoite surface antigen-2 alleles in asymptomatic malaria infections.

作者信息

Ntoumi F, Contamin H, Rogier C, Bonnefoy S, Trape J F, Mercereau-Puijalon O

机构信息

Institut Pasteur, Unite de Parasitologie Experimentale, Paris, France.

出版信息

Am J Trop Med Hyg. 1995 Jan;52(1):81-8. doi: 10.4269/ajtmh.1995.52.81.

Abstract

Genetic diversity of the merozoite surface antigen-2 gene of the human malaria parasite Plasmodium falciparum has been analyzed in a Senegalese village where malaria is holoendemic. A cross-sectional survey of 65 residents was performed in 1992 during the high transmission season. Plasmodium falciparum was detected both by microscopy (77% positive samples) and DNA amplification using a single (29% or 38% positive samples, depending on the primers used) or nested polymerase chain reaction (PCR) (78% positive samples). The overlap between the positive nested PCR and microscopic examination was not complete. The PCR fragments were analyzed for size polymorphism on agarose gels, and were subsequently assigned to the major allelic families 3D7 or FC27 by hybridization with family-specific probes. Both allelic families were found, with a slightly higher prevalence for FC27. Chimeric alleles that failed to hybridize under stringent conditions to the reference probes were also observed. Some were typed using a novel PCR approach, using hybrid pairs of primers, consisting of a family-specific sense oligonucleotide combined with an antisense oligonucleotide specific for the other family. Combining typing techniques, 82% of the positive PCR results yielded more than one band. Both the overall number of fragments and the number of allelic types per carrier were markedly reduced around the age of 15 years. The number of DNA fragments decreased abruptly from an average of four per carrier before the age of 15 years to an average of two in individuals more than 15 years of age.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在疟疾高度流行的塞内加尔一个村庄,对人类疟原虫恶性疟原虫裂殖子表面抗原-2基因的遗传多样性进行了分析。1992年在高传播季节对65名居民进行了横断面调查。通过显微镜检查(77%阳性样本)以及使用单重(根据所用引物,29%或38%阳性样本)或巢式聚合酶链反应(PCR)(78%阳性样本)进行DNA扩增来检测恶性疟原虫。巢式PCR阳性结果与显微镜检查之间的重叠并不完全。对PCR片段在琼脂糖凝胶上进行大小多态性分析,随后通过与家族特异性探针杂交将其归为主要等位基因家族3D7或FC27。两个等位基因家族均被发现,FC27的流行率略高。还观察到在严格条件下未能与参考探针杂交的嵌合等位基因。一些通过一种新的PCR方法进行分型,该方法使用引物杂交对,由家族特异性正义寡核苷酸与另一家族特异性反义寡核苷酸组成。综合分型技术,82%的PCR阳性结果产生不止一条带。在15岁左右,每个携带者的片段总数和等位基因类型数量均显著减少。DNA片段数量从15岁前每个携带者平均四条突然降至15岁以上个体平均两条。(摘要截短至250字)

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