Variable number of tandem aminoacid repeats in adhesion-related CDS products in Mycoplasma hyopneumoniae strains

被引:41
作者
de Castro, Luiza Amaral
Pedroso, Thiago Rodrigues
Kuchiishi, Suzana Satomi
Ramenzoni, Marni
Kich, Jalusa Deon
Zaha, Arnaldo
Vainstein, Marilene Henning
Ferreira, Henrique Bunselmeyer
机构
[1] UFRGS, Ctr Biotechnol, Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande Sul, Dept Biol Mol & Biotecnol, Porto Alegre, RS, Brazil
关键词
aminoacid repeats; VNTR; adhesins; interstrain variability; strain typing; enzootic pneumonia;
D O I
10.1016/j.vetmic.2006.04.022
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Mycoplasma hyopneumoniae genome contains at least 22 regions with a variable number of tandem nucleotide repeats (VNTRs) within coding DNA sequences (CDSs). In this work, the VNTR-containing CDSs were analysed in order to evaluate their degree of variation, possible correlations with antigenic properties, and their potential to be used as a basis for a strain typing PCR assay. We have analysed the VNTRs in five M. hyopneumoniae strains (J, 7448, 7422, PMS, and 232), based on published genomic sequences and on amplified and sequenced DNA segments. These VNTRs are distributed among 12 genes, most of which encode putative surface proteins, including known adhesins. The number of repeat units in any of the VNTRs is highly variable among the analysed strains, but they are, without exception, translationally in frame, and, therefore, code for a variable number of aminoacid repeats (VNTARs). These VNTARs determine putative structural, physicochemical and antigenic variations in the corresponding proteins, with potential implications for aspects associated to M. hyopneumoniae pathogenicity, such as cell adhesion and interactions with the host immune system. Considering that the characterized VNTARs are relatively stable, at least in vitro, and their sizes are strain-specific, we have developed a VNTR-based PCR assay for M. hyopneumoniae strain identification, useful for enzootic pneumonia (EP) diagnosis, strain typing, and distinction of circulating field isolates from vaccine strains in animals vaccinated against EP. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:258 / 269
页数:12
相关论文
共 35 条
[1]  
[Anonymous], 1997, EMBnet News
[2]   Protein and antigenic variability among Mycoplasma hyopneumoniae strains by SDS-PAGE and immunoblot [J].
Assunçao, P ;
De la Fe, C ;
Ramírez, AS ;
Llamazares, OG ;
Poveda, JB .
VETERINARY RESEARCH COMMUNICATIONS, 2005, 29 (07) :563-574
[3]   Evaluation of Mycoplasma hyopneumoniae growth by flow cytometry [J].
Assunçao, P ;
Diaz, R ;
Comas, J ;
Galarreta, CMR ;
González-Llamazares, OR ;
Poveda, JB .
JOURNAL OF APPLIED MICROBIOLOGY, 2005, 98 (05) :1047-1054
[4]   ANTHEPROT:: An integrated protein sequence analysis software with client/server capabilities [J].
Deléage, G ;
Combet, C ;
Blanchet, C ;
Geourjon, C .
COMPUTERS IN BIOLOGY AND MEDICINE, 2001, 31 (04) :259-267
[5]  
Desrosiers R, 2001, J SWINE HEALTH PROD, V9, P233
[6]   Proteolytic processing of the Mycoplasma hyopneumoniae cilium adhesin [J].
Djordjevic, SP ;
Cordwell, SJ ;
Djordjevic, MA ;
Wilton, J ;
Minion, FC .
INFECTION AND IMMUNITY, 2004, 72 (05) :2791-2802
[7]  
EWING JM, 1998, J ED MULTIMEDIA HYPE, V8, P3
[8]   Molecular structures and interactions of repetitive peptides based on wheat glutenin subunits depend on chain length [J].
Feeney, KA ;
Wellner, N ;
Gilbert, SM ;
Halford, NG ;
Tatham, AS ;
Shewry, PR ;
Belton, PS .
BIOPOLYMERS, 2003, 72 (02) :123-131
[9]  
FRIIS NF, 1974, ACTA VET SCAND, V15, P283
[10]  
GARLINGHOUSE LE, 1981, LAB ANIM SCI, V31, P39