Representational difference analysis identifies a strain-specific LPS biosynthesis locus in Bordetella spp.

被引:18
作者
Middendorf, B [1 ]
Gross, R [1 ]
机构
[1] Univ Wurzburg, Biozentrum, Theodor Boveri Inst, Lehrstuhl Mikrobiol, D-97074 Wurzburg, Germany
来源
MOLECULAR AND GENERAL GENETICS | 1999年 / 262卷 / 01期
关键词
Bordetella spp; evolution; lipopolysaccharide biosynthesis; pulsed-field gel electrophoresis; representational difference analysis;
D O I
10.1007/s004380051074
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bordetella pertussis and B. bronchiseptica are genetically very closely related but differ significantly in their virulence properties. Using Representational Difference Analysis (RDA), 11 DNA fragments specific for B. pertussis Tohama I or B. bronchiseptica BB7865 were identified. All B, bronchiseptica BB7865-derived fragments also hybridized with chromosomal DNA from B. bronchiseptica but not from the B. pertussis strains Tohama I and W28, underlining the close phylogenetic relationship between B. bronchiseptica and B. parapertussis. The B. per tussis type strain BP18323 is a special case, as it contains DNA sequences characteristic for both B. pertussis and B, bronchiseptica. As demonstrated by pulsed-field gel electrophoresis, several of the BB7865-derived fragments are present on a single 30-kb XbaI fragment. Based on the sequences of putative coding regions, four of these fragments may code for proteins involved in carbohydrate metabolism or transport. In agreement with this notion, a mutant for one of these loci synthesizes a significantly altered lipopolysaccharide that lacks the O-specific side chains. The analysis of the corresponding genomic region in various Bordetella species showed that this locus is present in B, bronchiseptica and B. parapertussis but not in B. pertussis. This confirms that the RDA approach has identified a novel strain-specific LPS biosynthesis locus which accounts for the differences between the LPS structures elaborated by different Bordetella species.
引用
收藏
页码:189 / 198
页数:10
相关论文
共 52 条
[1]   The identification, cloning and mutagenesis of a genetic locus required for lipopolysaccharide biosynthesis in Bordetella pertussis [J].
Allen, A ;
Maskell, D .
MOLECULAR MICROBIOLOGY, 1996, 19 (01) :37-52
[2]   Molecular and functional analysis of the lipopolysaccharide biosynthesis locus wlb from Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica [J].
Allen, AG ;
Thomas, RM ;
Cadisch, JT ;
Maskell, DJ .
MOLECULAR MICROBIOLOGY, 1998, 29 (01) :27-38
[3]   PBLUESCRIPT-II - GENE-MAPPING VECTORS [J].
ALTINGMEES, MA ;
SHORT, JM .
NUCLEIC ACIDS RESEARCH, 1989, 17 (22) :9494-9494
[4]   BIOCHEMICAL AND IMMUNOLOGICAL COMPARISON OF LIPOPOLYSACCHARIDES FROM BORDETELLA SPECIES [J].
AMANO, K ;
FUKUSHI, K ;
WATANABE, M .
JOURNAL OF GENERAL MICROBIOLOGY, 1990, 136 :481-487
[5]  
[Anonymous], METHOD ENZYMOL
[6]   EVOLUTIONARY RELATIONSHIPS IN THE GENUS BORDETELLA [J].
ARICO, B ;
GROSS, R ;
SMIDA, J ;
RAPPUOLI, R .
MOLECULAR MICROBIOLOGY, 1987, 1 (03) :301-308
[7]   The lipopolysaccharide of Bordetella bronchiseptica acts as a protective shield against antimicrobial peptides [J].
Banemann, A ;
Deppisch, H ;
Gross, R .
INFECTION AND IMMUNITY, 1998, 66 (12) :5607-5612
[8]   IN-VIVO CHARACTERIZATION OF THE UNORTHODOX BVGS 2-COMPONENT SENSOR PROTEIN OF BORDETELLA-PERTUSSIS [J].
BEIER, D ;
SCHWARZ, B ;
FUCHS, TM ;
GROSS, R .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 248 (03) :596-610
[9]  
Bordet J., 1909, ANN I PASTEUR PARIS, V23, P415
[10]  
Chaby R, 1988, PATHOGENESIS IMMUNIT, P247