Differentiation of Oesophagostomum bifurcum from Necator americanus by PCR using genetic markers in spacer ribosomal DNA

被引:61
作者
Romstad, A
Gasser, RB
Monti, JR
Polderman, AM
Nansen, P
Pit, DSS
Chilton, NB
机构
[1] UNIV MELBOURNE,DEPT VET SCI,WERRIBEE,VIC 3030,AUSTRALIA
[2] LEIDEN UNIV,FAC MED,DEPT PARASITOL,NL-2300 RC LEIDEN,NETHERLANDS
[3] ROYAL VET & AGR UNIV,DANISH CTR EXPT PARASITOL,DK-1870 FREDERIKSBERG C,DENMARK
[4] MINIST HLTH,DAPAONG,TOGO
基金
澳大利亚研究理事会;
关键词
Oesophagostomum bifurcum; Necator americanus; parasitic nematodes; species identification; internal transcribed spacer; ribosomal DNA; specific PCR;
D O I
10.1006/mcpr.1996.0094
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Oesophagostomiasis in humans due to infection with Oesophagostomum bifurcum (nodular worm) is of major human health significance in northern Togo and Ghana where Necator americanus (human hookworm) also exists at high prevalence. However, very little is known about the transmission patterns of O. bifurcum, partly due to the difficulty in differentiating O. bifurcum from N. americanus at some life-cycle stages using morphological features. To overcome this limitation, a molecular approach utilizing genetic markers in the second internal transcribed spacer (ITS-2) of ribosomal (r) DNA was developed. The ITS-2 sequence of each species was determined, and specific oligonucleotide primers were designed to the regions of greatest sequence difference between the species. Utilizing these primers, rapid PCR assays were developed for the specific amplification of DNA of O. bifurcum or N. americanus, which have the potential to confirm the identity of eggs from faeces and larvae from the intestine or environment. The application of species-specific PCR has important implications for studying the epidemiology and population biology of O. bifurcum. (C) 1997 Academic Press Limited.
引用
收藏
页码:169 / 176
页数:8
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