LIPOPOLYSACCHARIDE HETEROGENEITY IN PASTEURELLA-HAEMOLYTICA ISOLATES FROM CATTLE AND SHEEP

被引:18
作者
ALI, Q
DAVIES, RL
PARTON, R
COOTE, JG
GIBBS, HA
机构
[1] UNIV GLASGOW,DEPT MICROBIOL,GLASGOW G12 8QQ,SCOTLAND
[2] UNIV GLASGOW,DEPT VET MED,GLASGOW G12 8QQ,SCOTLAND
来源
JOURNAL OF GENERAL MICROBIOLOGY | 1992年 / 138卷
关键词
D O I
10.1099/00221287-138-10-2185
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Lipopolysaccharide (LPS) from 40 isolates of Pasteurella haemolytica, comprising 23 serotype A1, seven serotype A2, one serotype T4, one serotype T10 and eight untypable isolates, obtained from diseased and healthy cattle or sheep, was characterized by SDS-PAGE and Western blotting. Ten different SDS-PAGE LPS profiles, five smooth and five rough, were identified among the biotype A and untypable isolates and designated LPS types 1-10. LPS types 1 and 2 were smooth, had similar O-antigen banding-patterns but differed in the low-molecular-mass or core-oligosaccharide regions; type 3 LPS was rough but had a core-oligosaccharide region similar to that of LPS type 1. No similarities were observed between these LPS types and types 6, 7 and 9, which were smooth, and types 4,5,8 and 10, which were rough. Most serotype Al isolates (19/23) were of LPS type 1, whereas two isolates each had LPS of types 2 and 3. The majority (5/7) of serotype A2 isolates possessed type 3 LPS, whereas the remaining two isolates each had LPS of types 4 and 5. There was much greater heterogeneity within the untypable group of isolates, which comprised LPS of types 1 and 9 (two isolates each), and 6, 7, 8 or 10 (one isolate each). Western blotting analysis demonstrated that LPS types 1 and 2 had immunologically identical O-antigen side-chains but differed in their core-oligosaccharide regions, whereas the core-oligosaccharide region of rough LPS type 3 was immunologically very similar to that of LPS type 1. The other LPS types were immunologically unrelated to these three LPS types. The majority (20/23) of serotype A1 isolates originated from cattle and possessed LPS types 1 or 2, different from most (5/7) of the serotype A2 isolates which originated from sheep and possessed LPS of types 3 or 4. However, two of the three ovine serotype Al isolates had the same type 3 LPS as occurred in most of the ovine serotype A2 isolates, suggesting a possible correlation between LPS type and host specificity. This study has demonstrated that LPS diversity within different serotypes of P. haemolytica is greater than was previously thought and that certain LPS types might be host-specific.
引用
收藏
页码:2185 / 2195
页数:11
相关论文
共 42 条
[31]   STRUCTURAL AND ANTIGENIC PROPERTIES OF LIPOPOLYSACCHARIDES FROM SEROTYPE REFERENCE STRAINS OF CAMPYLOBACTER-JEJUNI [J].
PRESTON, MA ;
PENNER, JL .
INFECTION AND IMMUNITY, 1987, 55 (08) :1806-1812
[32]   ELUCIDATION OF THE STRUCTURE OF THE PASTEURELLA-HAEMOLYTICA SEROTYPE-T10 LIPOPOLYSACCHARIDE O-ANTIGEN BY NMR-SPECTROSCOPY [J].
RICHARDS, JC ;
LEITCH, RA .
CARBOHYDRATE RESEARCH, 1989, 186 (02) :275-286
[34]  
RIMSAY RL, 1981, AM J VET RES, V42, P2134
[35]   HETEROGENEITY OF LIPOPOLYSACCHARIDES FROM PSEUDOMONAS-AERUGINOSA - ANALYSIS OF LIPOPOLYSACCHARIDE CHAIN-LENGTH [J].
RIVERA, M ;
BRYAN, LE ;
HANCOCK, REW ;
MCGROARTY, EJ .
JOURNAL OF BACTERIOLOGY, 1988, 170 (02) :512-521
[36]   VARIATION IN CARRIER RATES OF PASTEURELLA-HAEMOLYTICA IN SHEEP .2. DISEASED FLOCKS [J].
SHREEVE, BJ ;
THOMPSON, DA ;
BIBERSTEIN, EL .
JOURNAL OF COMPARATIVE PATHOLOGY, 1972, 82 (01) :111-+
[37]  
STURM S, 1984, ARCH MICROBIOL, V140, P198, DOI 10.1007/BF00454926
[38]   ELECTROPHORETIC TRANSFER OF PROTEINS FROM POLYACRYLAMIDE GELS TO NITROCELLULOSE SHEETS - PROCEDURE AND SOME APPLICATIONS [J].
TOWBIN, H ;
STAEHELIN, T ;
GORDON, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (09) :4350-4354
[39]   IMMUNOTYPE EPITOPES OF NEISSERIA-MENINGITIDIS LIPOOLIGOSACCHARIDE TYPE-1 THROUGH TYPE-8 [J].
TSAI, CM ;
MOCCA, LF ;
FRASCH, CE .
INFECTION AND IMMUNITY, 1987, 55 (07) :1652-1656
[40]  
TSAI CM, 1983, J BACTERIOL, V155, P498, DOI 10.1128/JB.155.2.498-504.1983