Low-stringency single specific primer PCR for identification of Leptospira

被引:30
作者
do Oliveira, MAA
Caballero, OL
Vago, AR
Harskeerl, RA
Romanha, AJ
Pena, SDJ
Smpson, AJG
Koury, MC
机构
[1] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Microbiol, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Morfol, BR-31270901 Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Bioquim & Immunol, BR-31270901 Belo Horizonte, MG, Brazil
[4] Ludwig Inst Canc Res, Canc Genet Lab, Sao Paulo, Brazil
[5] Royal Trop Inst, Dept Biomed Res, NL-1105 AZ Amsterdam, Netherlands
[6] Fiocruz MS, Ctr Pesquisas Rene Rachou, Belo Horizonte, MG, Brazil
关键词
D O I
10.1099/jmm.0.04923-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Thirty-five Leptospira serovars from the species Leptospira interrogans, Leptospira borgpetersenii, Leptospira santarosai, Leptospira kirschneri, Leptospira weilii, Leptospira biflexa and Leptospira meyeri were characterized by the low-stringency single specific primer PCR (LSSP-PCR) technique. LSSP-PCR analysis was performed to detect DNA polymorphisms in a 285 bp DNA fragment amplified from genomic DNA with G1 and G2 selected primers. Similar LSSP-PCR profiles were obtained for serovars from the same genomic species, while serovars from non-related species produced distinct multiband patterns. Based on the data from sequence analysis, all genomic fragments amplified with G1 and G2 primers from distinct serovars of Leptospira were 285 bp in length, with nucleotide variation observed most frequently among different genomic species. The simplicity and accuracy of the LSSP-PCR technique were found to be suitable for identification of Leptospira species.
引用
收藏
页码:127 / 135
页数:9
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