Differentiation of Acidithiobacillus ferrooxidans and A-thiooxidans strains based on 16S-23S rDNA spacer polymorphism analysis

被引:21
作者
Bergamo, RF
Novo, MTM
Veríssimo, RV
Paulino, LC
Stoppe, NC
Sato, MIZ
Manfio, GP
Prado, PI
Garcia, O
Ottoboni, LMM
机构
[1] Univ Estadual Campinas, Ctr Biol Mol & Engn Genet, BR-13083875 Campinas, SP, Brazil
[2] Univ Estadual Campinas, Ctr Pluridisciplinar Pesquisa Quim Biol & Agr, BR-13083875 Campinas, SP, Brazil
[3] Univ Estadual Paulista, Inst Quim, Dept Bioquim & Tecnol Quim, BR-14800900 Araraquara, SP, Brazil
[4] Co Tecnol Saneamento Ambiental, BR-05489900 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Acidithiobacillus ferrooxidans; Acidithiobacillus thiooxidans; 16S-23S rDNA spacer;
D O I
10.1016/j.resmic.2004.03.009
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Restriction fragment length polymorphism (RFLP) and sequence analyses of the PCR-amplified 16S-23S rDNA intergenic spacer (ITS) were used for differentiating Acidithiobacillus thiooxidans strains from other related acidithiobacilli, including A. ferrooxidans and A. caldus. RFLP fingerprints obtained with AluI, DdeI, HaeIII, HinfI and MspI enabled the differentiation of all Acidithiobacillus reference strains into species groups. The A. thiooxidans strains investigated (metal mine isolates) yielded identical RFLP patterns to the A. thiooxidans type strain (ATCC 19377(T)), except for strain DAMS, which had a distinct pattern for all enzymes tested. Fourteen A. ferrooxidans mine strains were assigned to 3 RFLP groups, the majority of which were grouped with A. ferrooxidans ATCC 23270(T). The spacer region of one representative strain from each of the RFLP groups obtained was subjected to sequence analysis, in addition to eleven additional A. thiooxidans strains isolated from sediment and water samples, and A. caldus DSM 8584(T). The tRNA(IIe) and tRNA(Ala) genes, present in all strains analyzed, showed high sequence similarity. Phylogenetic analysis of the ITS sequences differentiated all three Acidithiobacillus species. Inter- and infraspecific genetic variations detected were mainly due to the size and sequence polymorphism of the ITS3 region. Mantel tests showed no significant correlation between ITS sequence similarity and the geographical origin of strains. The results showed that the 16S-23S rDNA spacer region is a useful target for the development of molecular-based methods aimed at the detection, rapid differentiation and identification of acidithiobacilli. (C) 2004 Elsevier SAS. All rights reserved.
引用
收藏
页码:559 / 567
页数:9
相关论文
共 33 条
  • [1] RFLP of rRNA genes and sequencing of the 16S-23S rDNA intergenic spacer region of ammonia-oxidizing bacteria:: a phylogenetic approach
    Aakra, Å
    Utåker, JB
    Nes, IF
    [J]. INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1999, 49 : 123 - 130
  • [2] [Anonymous], THESIS U NEWCASTLE U
  • [3] *APHA AWWA WPCE, 1998, STAND METH EX WAT WA
  • [4] Bioleaching: Metal solubilization by microorganisms
    Bosecker, K
    [J]. FEMS MICROBIOLOGY REVIEWS, 1997, 20 (3-4) : 591 - 604
  • [5] Evidence for conserved tRNA genes in the 16S-23S rDNA spacer sequence and two rrn operons of Xylella fastidiosa
    Chen, JC
    Banks, D
    Jarret, RL
    Jones, JB
    [J]. CANADIAN JOURNAL OF MICROBIOLOGY, 2000, 46 (12) : 1171 - 1175
  • [6] DUTKA BJ, 1976, METHODS MICROBIOLOGI
  • [7] GARCIA O, 1991, REV MICROBIOL, V22, P1
  • [8] Phylogenetic analysis of Xanthomonas species based upon 16S-23S rDNA intergenic spacer sequences
    Gonçalves, ER
    Rosato, YB
    [J]. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY, 2002, 52 : 355 - 361
  • [9] CLONING, CHARACTERIZATION, AND COMPLEMENTATION OF LESIONS CAUSING ACID SENSITIVITY IN TN5-INDUCED MUTANTS OF RHIZOBIUM-MELILOTI WSM419
    GOSS, TJ
    OHARA, GW
    DILWORTH, MJ
    GLENN, AR
    [J]. JOURNAL OF BACTERIOLOGY, 1990, 172 (09) : 5173 - 5179
  • [10] New approaches to typing and identification of bacteria using the 16S-23S rDNA spacer region
    Gurtler, V
    Stanisich, VA
    [J]. MICROBIOLOGY-SGM, 1996, 142 : 3 - 16