Identification of Lactobacillus strains of goose origin using MALDI-TOF mass spectrometry and 16S-23S rDNA intergenic spacer PCR analysis

被引:50
|
作者
Dec, Marta [1 ]
Urban-Chmiel, Renata [1 ]
Gnat, Sebastian [2 ]
Puchalski, Andrzej [1 ]
Wernicki, Andrzej [1 ]
机构
[1] Univ Life Sci, Fac Vet Med, Inst Biol Bases Anim Dis, Sub Dept Vet Prevent & Avian Dis, PL-20033 Lublin, Poland
[2] Univ Life Sci, Fac Vet Med, Inst Biol Bases Anim Dis, Sub Dept Vet Microbiol, PL-20033 Lublin, Poland
关键词
Lactobacillus; Lactic acid bacteria; Geese; MALDI-TOF mass spectrometry; ITS-PCR; 16S-23S rDNA; DESORPTION IONIZATION-TIME; LACTIC-ACID BACTERIA; GASTROINTESTINAL-TRACT; LACTOCOCCUS-LACTIS; BROILERS;
D O I
10.1016/j.resmic.2014.02.003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The objective of our study was to identify Lactobacillus sp. strains of goose origin using MALDI-TOF mass spectrometry, ITS-PCR and ITS-PCR/RFLP. All three techniques proved to be valuable tools for identification of avian lactobacilli and produced comparable classification results. Lactobacillus strains were isolated from 100% of geese aged 3 weeks to 4 years, but from only 25% of chicks aged 1-10 days. Among the 104 strains isolated, we distinguished 14 Lactobacillus species. The dominant species was Lactobacillus salivarius (35.6%), followed by Lactobacillus johnsonii (18.3%), Lactobacillus ingluviei (11.5%) and Lactobacillus agilis (7.7%). The intact-cell MALDI-TOF mass spectrometry enabled rapid species identification of the lactobacilli with minimal pretreatment. However, it produced more than one identification result for 11.5% examined strains (mainly of the species L. johnsonii). ITS-PCR distinguished 12 genotypes among the isolates, but was not able to differentiate closely related strains, i.e. between Lactobacillus amylovorus and Lactobacillus kitasatonis and between Lactobacillus paracasei, Lactobacillus rhamnosus and Lactobacillus zeae. These species were differentiated by ITS-PCR/RFLP using the restriction enzymes TaqI and MseI. The results obtained indicate that ITS-PCR and ITS-PCR/RFLP assays could be used not only for interspecific, but also for intraspecific, typing. (C) 2014 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:190 / 201
页数:12
相关论文
共 50 条
  • [41] Characterization of the 16S-23S rRNA intergenic spacer regions among strains of the Fusobacterium necrophorum cluster
    Jin, J
    Xu, D
    Narongwanichgarn, W
    Goto, Y
    Haga, T
    Shinjo, T
    JOURNAL OF VETERINARY MEDICAL SCIENCE, 2002, 64 (03): : 273 - 276
  • [42] Presence of a novel 16S-23S rRNA gene intergenic spacer insert in Bradyrhizobium canariense strains
    Safronova, Vera
    Chizhevskaya, Elena
    Bullitta, Simonetta
    Andronov, Evgeny
    Belimov, Andrei
    Charles, Trevor C.
    Lindstrom, Kristina
    FEMS MICROBIOLOGY LETTERS, 2007, 269 (02) : 207 - 212
  • [43] Rapid and direct detection of Clostridium chauvoei by PCR of the 16S-23S rDNA spacer region and partial 23S rDNA sequences
    Sasaki, Y
    Yamamoto, K
    Kojima, A
    Tetsuka, Y
    Norimatsu, M
    Tamura, Y
    JOURNAL OF VETERINARY MEDICAL SCIENCE, 2000, 62 (12): : 1275 - 1281
  • [44] 16S-23S RDNA: Polymorphisms and their use for detection and identification of Xylella fastidiosa strains
    Martinati, Juliana Camargo
    Hansen Pacheco, Flavia Tereza
    Oliveira de Miranda, Vitor Fernandes
    Tsai, Siu Mui
    BRAZILIAN JOURNAL OF MICROBIOLOGY, 2007, 38 (01) : 159 - 165
  • [45] Vibrio alginolyticus 16S-23S intergenic spacer region analysis, and PCR assay for identification of coral pathogenic strain XSBZ03
    Li, Hongyue
    Zhang, Xiang
    Long, Hao
    Hu, Chaoqun
    Zhou, Yongcan
    Wang, Shifeng
    Ke, Shaowen
    Xie, Zhenyu
    DISEASES OF AQUATIC ORGANISMS, 2018, 129 (01) : 71 - 83
  • [46] Specific PCR amplification for the genus Pseudomonas targeting the 3′ half of 16S rDNA and the whole 16S-23S rDNA spacer
    Locatelli, L
    Tarnawski, S
    Hamelin, J
    Rossi, P
    Aragno, M
    Fromin, N
    SYSTEMATIC AND APPLIED MICROBIOLOGY, 2002, 25 (02) : 220 - 227
  • [47] EFFECTIVE IDENTIFICATION OF LACTOBACILLUS PARACASEI SSP. PARACASEI-1 BY 16S-23S rRNA INTERGENIC SPACER REGION SEQUENCING
    Islam, Tariful
    Khan, Md. Iqbal Hassan
    Afroz, Kazi Farhana
    Rahman, Mohammed Zakiur
    Hossain, Md. Shawkat
    Islam, Md. Emdadul
    Billah, Md. Morsaline
    Islam, Kazi Didarul
    JOURNAL OF MICROBIOLOGY BIOTECHNOLOGY AND FOOD SCIENCES, 2016, 6 (01): : 695 - 701
  • [48] Structural analysis and genetic variation of the 16S-23S rDNA internal spacer region from Micrococcus luteus strains
    Haga, S
    Hirano, Y
    Murayama, O
    Millar, BC
    Moore, JE
    Matsuda, M
    LETTERS IN APPLIED MICROBIOLOGY, 2003, 37 (04) : 314 - 317
  • [49] Development of a PCR assay based on the 16S-23S rDNA internal transcribed spacer for identification of strictly anaerobic bacterium Zymophilus
    Felsberg, Jurgen
    Jelinkova, Marketa
    Kubizniakova, Petra
    Matoulkova, Dagmar
    ANAEROBE, 2015, 33 : 85 - 89
  • [50] Analysis of 16S-23S rRNA intergenic spacer regions of Vibrio cholerae and Vibrio mimicus
    Chun, J
    Huq, A
    Colwell, RR
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1999, 65 (05) : 2202 - 2208