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[应用分子技术对输入性丝虫病的鉴别诊断(2006 - 2009年)]

[Differential diagnosis of imported filariasis by molecular techniques (2006-2009)].

作者信息

Jiménez Maribel, González Luis Miguel, Bailo Begoña, Blanco Alejandra, García Luz, Pérez-González Francisco, Fuentes Isabel, Gárate Teresa

机构信息

Servicio de Parasitología, Centro Nacional de Parasitología, Instituto de Salud Carlos III, Majadahonda, Madrid, España.

出版信息

Enferm Infecc Microbiol Clin. 2011 Nov;29(9):666-71. doi: 10.1016/j.eimc.2011.06.012. Epub 2011 Sep 8.

DOI:10.1016/j.eimc.2011.06.012
PMID:21906850
Abstract

INTRODUCTION

The last few years has seen an increase in the number of immigrants and travellers from endemic areas where filariasis are mainly caused by Loa loa (L. loa), Mansonella perstans (M. perstans) and Wuchereria bancrofti (W. bancrofti) species. These demographic changes has led to the need for better filariae species-specific molecular diagnostic tests to solve problems, as alternatives to the more time consuming classic parasitology methods. Thus, the objective of the present work was the implementation of optimised molecular protocols (nested-PCR and ITS1-RFLP) developed in our laboratory, for the differential diagnosis of filarial parasites. The results obtained were compared with those obtained using the conventional parasitological methods.

MATERIAL AND METHODS

A total of 523 samples (517 peripheral blood, 5 adult worms and one vitreous body) were sent to Parasitology Department of the National Microbiology Centre, Carlos II Research Institute (ISCIII), from 47 Health Centres in the Autonomous Regions of Spain, from 2006 to 2009. The samples were studied by the Knott technique, nested-PCR and ITS1-RFLP.

RESULTS

The molecular techniques applied on blood samples showed to be more sensitive that Knott's concentration technique in the diagnosis of both L. loa (n=12 versus n=4) and M. perstans (n=57 versus n=25) infections.

CONCLUSIONS

The nested-PCR and ITS1-RFLP are potential diagnostic tools for daily routine laboratory species-specific and sensitive detection of L. loa and M. perstans filarial species in immigrant population and travellers from endemic areas where these filarial species are co-endemic. Knott's concentration technique was less sensitive than molecular methods and should be carried out as a complementary diagnostic assay.

摘要

引言

在过去几年中,来自丝虫病主要由罗阿丝虫(L. loa)、常现曼森线虫(M. perstans)和班氏吴策线虫(W. bancrofti)引起的流行地区的移民和旅行者数量有所增加。这些人口结构的变化导致需要更好的针对丝虫物种的分子诊断测试来解决问题,作为耗时较长的传统寄生虫学方法的替代方法。因此,本研究的目的是实施我们实验室开发的优化分子方案(巢式PCR和ITS1-RFLP),用于丝虫寄生虫的鉴别诊断。将获得的结果与使用传统寄生虫学方法获得的结果进行比较。

材料与方法

2006年至2009年期间,来自西班牙自治区47个健康中心的523份样本(517份外周血、5条成虫和1份玻璃体)被送至卡洛斯二世研究所(ISCIII)国家微生物中心寄生虫学系。通过Knott技术、巢式PCR和ITS1-RFLP对样本进行研究。

结果

应用于血液样本的分子技术在诊断罗阿丝虫(n = 12对n = 4)和常现曼森线虫(n = 57对n = 25)感染方面比Knott浓缩技术更敏感。

结论

巢式PCR和ITS1-RFLP是日常实验室针对来自这些丝虫物种共流行的流行地区的移民和旅行者进行罗阿丝虫和常现曼森线虫物种特异性和灵敏检测的潜在诊断工具。Knott浓缩技术不如分子方法敏感,应作为补充诊断方法进行。

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