TY - JOUR
T1 - Molecular typing of Leptospira spp. based on putative O-antigen polymerase gene (wzy), the benefit over 16S rRNA gene sequence
AU - Wangroongsarb, Piyada
AU - Chanket, Teerarut
AU - Gunlabun, Kata
AU - Long, Do Hoang
AU - Satheanmethakul, Pedcharat
AU - Jetanadee, Siriporn
AU - Thaipadungpanit, Janjira
AU - Wuthiekanun, Vannaporn
AU - Peacock, Sharon J.
AU - Blacksell, Stuart D.
AU - Smythe, Lee D.
AU - Bulach, Dieter M.
AU - Kalambaheti, Thareerat
PY - 2007/6
Y1 - 2007/6
N2 - Molecular typing of leptospiral strains based on variation within putative O-antigen polymerase gene (wzy) was determined among reference strains and those isolated from patients. Using the PCR primers designed from the flanking gene of wzy derived from Leptospira interrogans serovar Copenhageni, all L. interrogans serovars as well as human and rodent leptospiral isolates from Thailand could be amplified. The size of PCR product ranged from 1 to 1.5 kb. The limitation of these primer pairs was the inability to amplify those strains whose sequences differ in the region of the primers, these included Leptospira biflexa (serovar Patoc), Leptospira borgpetersenii (serovar Tarassovi) and Leptospira kirschneri (serovar Bim, Bulgarica, Butembo). Notably, amplification was not limited to L. interrogans as demonstrated by the amplification of some strains from L. kirschneri, Leptospira meyeri, Leptospira noguchii, Leptospira santarosai, L. borgpetersenii and Leptospira weilii. The phylogenetic tree of wzy sequence, inferred by posterior probability of the Bayesian, enabled the categorization of leptospiral serovars into seven genetically related group, of which its differentiation power was better than that of the more highly conserved 16S rRNA gene, which is used extensively for genotyping.
AB - Molecular typing of leptospiral strains based on variation within putative O-antigen polymerase gene (wzy) was determined among reference strains and those isolated from patients. Using the PCR primers designed from the flanking gene of wzy derived from Leptospira interrogans serovar Copenhageni, all L. interrogans serovars as well as human and rodent leptospiral isolates from Thailand could be amplified. The size of PCR product ranged from 1 to 1.5 kb. The limitation of these primer pairs was the inability to amplify those strains whose sequences differ in the region of the primers, these included Leptospira biflexa (serovar Patoc), Leptospira borgpetersenii (serovar Tarassovi) and Leptospira kirschneri (serovar Bim, Bulgarica, Butembo). Notably, amplification was not limited to L. interrogans as demonstrated by the amplification of some strains from L. kirschneri, Leptospira meyeri, Leptospira noguchii, Leptospira santarosai, L. borgpetersenii and Leptospira weilii. The phylogenetic tree of wzy sequence, inferred by posterior probability of the Bayesian, enabled the categorization of leptospiral serovars into seven genetically related group, of which its differentiation power was better than that of the more highly conserved 16S rRNA gene, which is used extensively for genotyping.
KW - 16S rRNA gene
KW - Leptospira
KW - Phylogenetic
KW - wzy
UR - http://www.scopus.com/inward/record.url?scp=34249036078&partnerID=8YFLogxK
U2 - 10.1111/j.1574-6968.2007.00711.x
DO - 10.1111/j.1574-6968.2007.00711.x
M3 - Article
C2 - 17403048
AN - SCOPUS:34249036078
SN - 0378-1097
VL - 271
SP - 170
EP - 179
JO - FEMS Microbiology Letters
JF - FEMS Microbiology Letters
IS - 2
ER -