High inter-species and low intra-species variation in 16S-23S rDNA spacer sequences of pathogenic avian mycoplasmas offers potential use as a diagnostic tool

被引:36
作者
Ramirez, A. S. [1 ,2 ]
Naylor, C. J. [1 ]
Pitcher, D. G. [3 ]
Bradbury, J. M. [1 ]
机构
[1] Univ Liverpool, Leahurst Vet Teaching Hosp, Dept Vet Pathol, Neston CH64 7TE, England
[2] Univ Las Palmas GC, Fac Vet, Unit Epidemiol & Prevent Med, Las Palmas Gran Canaria 35416, Spain
[3] Hlth Protect Agcy, Resp & Syst Infect Lab, London NW9 5HT, England
关键词
mollicutes; mycoplasma; intergenic spacer region; phylogeny;
D O I
10.1016/j.vetmic.2007.10.023
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In order to investigate its value for phylogenetic analysis, species characterisation and diagnosis, the 16S-23S rDNA intergenic spacer regions (ISRs) of the type strain of 23 avian Mycoplasma species were amplified and the sequences determined. Also sequenced were the reference strains of Mycoplasma iowae serotypes J, K, N, Q and R and a number of field strains of Mycoplasma synoviae, Mycoplasma gallisepticum, Mycoplasma meleagridis and M. iowae. The ISRs demonstrated a high level of size variation (178-2488 bp) between species and did not include RNA genes. Phylogenetic analysis performed using the information conflicted with that based on the 16S rDNA and was therefore not helpful for phylogenetic studies. However, the ISR did appear to be of value for determining species since there was high inter-species variation between all 23 avian Mycoplasma species, and in addition there was low intra-species variation, at least in the four pathogenic species. It could also be very useful as additional information in the description of a new species and as a target for species-specific PCRs. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:279 / 287
页数:9
相关论文
共 32 条
[1]   The vlhA loci of Mycoplasma synoviae are confined to a restricted region of the genome [J].
Allen, JL ;
Noormohammadi, AH ;
Browning, GF .
MICROBIOLOGY-SGM, 2005, 151 :935-940
[2]  
[Anonymous], 1989, Molecular Cloning
[3]  
[Anonymous], 1989, Cladistics, DOI DOI 10.1111/J.1096-0031.1989.TB00562.X
[4]  
Bradbury J M., 2001, Poultry Diseases, V5th, P178
[5]  
BRADBURY JM, 1977, J CLIN MICROBIOL, V5, P531
[6]   Taxonomy of the canine Mollicutes by 16S rRNA gene and 1 6S/23S rRNA intergenic spacer region sequence comparison [J].
Chalker, VJ ;
Brownlie, J .
INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY, 2004, 54 :537-542
[7]   Development of a polymerase chain reaction for the detection of Mycoplasma felis in domestic cats [J].
Chalker, VJ ;
Owen, WMA ;
Paterson, CJI ;
Brownlie, J .
VETERINARY MICROBIOLOGY, 2004, 100 (1-2) :77-82
[8]   CONTROL OF RIBOSOMAL-RNA TRANSCRIPTION IN ESCHERICHIA-COLI [J].
CONDON, C ;
SQUIRES, C ;
SQUIRES, CL .
MICROBIOLOGICAL REVIEWS, 1995, 59 (04) :623-&
[9]   Genotyping of Mycoplasma pneumoniae clinical isolates reveals eight P1 subtypes within two genomic groups [J].
Dorigo-Zetsma, JW ;
Dankert, J ;
Zaat, SAJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (03) :965-970
[10]  
GUTLER V, 1999, GENE, V238, P241