A unique DNA repair and recombination gene (recN) sequence for identification and intraspecific molecular typing of bacterial wilt pathogen Ralstonia solanacearum and its comparative analysis with ribosomal DNA sequences

被引:9
作者
Kumar, Aundy [1 ]
Prameela, Thekkan Puthiyaveedu [2 ]
Suseelabhai, Rajamma [2 ]
机构
[1] Indian Agr Res Inst, Div Plant Pathol, New Delhi 110012, India
[2] Indian Inst Spices Res, Div Crop Protect, Kozhikode 673012, India
关键词
Bacterial wilt; biovar; DNA repair protein; phylotyping; race; Ralstonia solanacearum; recN gene; BURKHOLDERIA-SOLANACEARUM; PSEUDOMONAS-SOLANACEARUM; PHYLOGENY; DIVERSITY; STRAINS; RACE-3; PROTEINS; DISEASE; PCR;
D O I
10.1007/s12038-013-9312-0
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ribosomal gene sequences are a popular choice for identification of bacterial species and, often, for making phylogenetic interpretations. Although very popular, the sequences of 16S rDNA and 16-23S intergenic sequences often fail to differentiate closely related species of bacteria. The availability of complete genome sequences of bacteria, in the recent years, has accelerated the search for new genome targets for phylogenetic interpretations. The recently published full genome data of nine strains of R. solanacearum, which causes bacterial wilt of crop plants, has provided enormous genomic choices for phylogenetic analysis in this globally important plant pathogen. We have compared a gene candidate recN, which codes for DNA repair and recombination function, with 16S rDNA/16-23S intergenic ribosomal gene sequences for identification and intraspecific phylogenetic interpretations in R. solanacearum. recN gene sequence analysis of R. solanacearum revealed subgroups within phylotypes (or newly proposed species within plant pathogenic genus, Ralstonia), indicating its usefulness for intraspecific genotyping. The taxonomic discriminatory power of recN gene sequence was found to be superior to ribosomal DNA sequences. In all, the recN-sequence-based phylogenetic tree generated with the Bayesian model depicted 21 haplotypes against 15 and 13 haplotypes obtained with 16S rDNA and 16-23S rDNA intergenic sequences, respectively. Besides this, we have observed high percentage of polymorphic sites (S 23.04%), high rate of mutations (Eta 276) and high codon bias index (CBI 0.60), which makes the recN an ideal gene candidate for intraspecific molecular typing of this important plant pathogen.
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收藏
页码:267 / 278
页数:12
相关论文
共 44 条
[21]  
Janse J. D., 1996, Bulletin OEPP, V26, P679, DOI 10.1111/j.1365-2338.1996.tb01512.x
[22]  
KELMAN A, 1954, PHYTOPATHOLOGY, V44, P693
[23]   Visualization of DNA double-strand break repair in live bacteria reveals dynamic recruitment of Bacillus subtilis RecF, RecO and RecN proteins to distinct sites on the nucleoids [J].
Kidane, D ;
Sanchez, H ;
Alonso, JC ;
Graumann, PL .
MOLECULAR MICROBIOLOGY, 2004, 52 (06) :1627-1639
[24]  
Kumar A., 2006, Indian Phytopathology, V59, P281
[25]  
Kumar A, 2004, CURR SCI INDIA, V87, P1555
[26]   Friend or foe: genetic and functional characterization of plant endophytic Pseudomonas aeruginosa [J].
Kumar, A. ;
Munder, A. ;
Aravind, R. ;
Eapen, S. J. ;
Tuemmler, B. ;
Raaijmakers, J. M. .
ENVIRONMENTAL MICROBIOLOGY, 2013, 15 (03) :764-779
[27]   Molecular typing of Japanese strains of Ralstonia solanacearum in relation to the ability to induce a hypersensitive reaction in tobacco [J].
Liu, Yingqin ;
Kanda, Ayami ;
Yano, Kazutaka ;
Kiba, Akinori ;
Hikichi, Yasufumi ;
Aino, Masataka ;
Kawaguchi, Akira ;
Mizoguchi, Sentaro ;
Nakaho, Kazuhiro ;
Shiomi, Hiroshi ;
Takikawa, Yuichi ;
Ohnishi, Kouhei .
JOURNAL OF GENERAL PLANT PATHOLOGY, 2009, 75 (05) :369-380
[28]   BACTERIAL WILT, A NEW DISEASE OF CUSTARD APPLE - SYMPTOMS AND ETIOLOGY [J].
MAYERS, PE ;
HUTTON, DG .
ANNALS OF APPLIED BIOLOGY, 1987, 111 (01) :135-141
[29]   RecN protein and transcription factor DksA combine to promote faithful recombinational repair of DNA double-strand breaks [J].
Meddows, TR ;
Savory, AP ;
Grove, JI ;
Moore, T ;
Lloyd, RG .
MOLECULAR MICROBIOLOGY, 2005, 57 (01) :97-110
[30]   16S rRNA gene sequencing for bacterial pathogen identification in the clinical laboratory [J].
Patel, JB .
MOLECULAR DIAGNOSIS, 2001, 6 (04) :313-321