Detection of Entamoeba histolytica by Recombinase Polymerase Amplification

被引:33
|
作者
Nair, Gayatri
Rebolledo, Mauricio
White, A. Clinton, Jr.
Crannell, Zachary
Richards-Kortum, R. Rebecca
Pinilla, A. Elizabeth
Ramirez, Juan David
Lopez, M. Consuelo
Castellanos-Gonzalez, Alejandro
机构
[1] Univ Texas Med Branch, Dept Internal Med, Galveston, TX 77555 USA
[2] Rice Univ, Dept Bioengn, Houston, TX USA
[3] Univ Rosario, Fac Ciencias Natr & Matemat, Bogota, Colombia
[4] Univ Nacl Colombia, Dept Med Interna, Bogota, Colombia
[5] Univ Nacl Colombia, Dept Salud Publ, Bogota, Colombia
基金
美国国家卫生研究院;
关键词
REAL-TIME-PCR; DISPAR; ASSAY; DIFFERENTIATION; MOSHKOVSKII; DNA;
D O I
10.4269/ajtmh.15-0276
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Amebiasis is an important cause of diarrheal disease worldwide and has been associated with childhood malnutrition. Traditional microscopy approaches are neither sensitive nor specific for Entamoeba histolytica. Antigen assays are more specific, but many cases are missed unless tested by molecular methods. Although polymerase chain reaction (PCR) is effective, the need for sophisticated, expensive equipment, infrastructure, and trained personnel limits its usefulness, especially in the resource-limited, endemic areas. Here, we report development of a recombinase polymerase amplification (RPA) method to detect E. histolytica specifically. Using visual detection by lateral flow (LF), the test was highly sensitive and specific and could be performed without additional equipment. The availability of this inexpensive, sensitive, and field-applicable diagnostic test could facilitate rapid diagnosis and treatment of amebiasis in endemic regions.
引用
收藏
页码:591 / 595
页数:5
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