Serological crossreactivity between Brucella abortus and Yersinia enterocolitica 0:9 II the use of Yersinia outer proteins for the specific detection of Yersinia enterocolitica infections in ruminants

• Published in: Veterinary microbiology Vol. 47; no. 3; pp. 271 - 280
• Main Authors: Kittelberger, Reinhold, Hilbink, Frans, Hasen, Mike F., Ross, Gail P., Joyce, Maree A., Fenwick, Stan, Heesemann, Jürgen, Wolf-Watz, Hans, Nielsen, Klaus
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 01.12.1995; Elsevier Science
• Subjects: Animals; Antibodies, Bacterial - blood; Antibody Formation; Antigens, Bacterial - immunology; Bacterial diseases; Bacterial Outer Membrane Proteins - immunology; Biological and medical sciences; Brucella abortus; Brucella abortus - immunology; Brucellosis, Bovine - blood; Brucellosis, Bovine - immunology; Cattle; Cattle Diseases; Cross Reactions; Crossreactivity; Electrophoresis, Polyacrylamide Gel; Experimental bacterial diseases and models; False Positive Reactions; Female; Immunoblotting; Infectious diseases; Medical sciences; Ruminants; Time Factors; Yersinia enterocolitica; Yersinia enterocolitica - immunology; Yersinia Infections - blood; Yersinia Infections - immunology; Yersinia Infections - veterinary; YOP; Yersinia enterocolitica; Crossreactivity; Brucella abortus; YOP; Membrane protein; Ruminant animal; Biosynthesis; Veterinary medicine; Brucellaceae; Cross reaction; Bacteria; Diagnosis; Ungulata; Enterobacteriaceae; Bovine; Antibody; External membrane; Infection; Antigen; Vertebrata; Experimental disease; Mammalia; Serological method; Bacteriosis; Brucellosis; Artiodactyla; Detection
• ISSN: 0378-1135; 1873-2542
• DOI: 10.1016/0378-1135(95)00121-2

Yersinia outer protein (YOP) preparations from Y. enterocolitica and Y. pseudotuberculosis were used as antigens in immunoblots for the detection of Yersinia infections in experimentally and naturally infected ruminants. Sera from 9 groups of animals were used: (1) 51 sera from cattle which were false-positive in the standard brucellosis serological tests, (2) 52 sera from brucellosis-negative cattle, (3) 51 sera from a deer herd in which 16 animals were positive in the brucellosis tests and Yersina species were isolated from 5 animals, (4) 50 sera from a deer herd in which sera from all animals were negative in the brucellosis tests, (5) 107 sera from brucellosis-negative cattle which were received from throughout New Zealand, (6) 30 sera from cattle naturally infected with B. abortus and from which B. abortus was isolated, (7) 55 sera from cattle naturally infected with B. abortus, (8) 26 sera from cattle experimentally infected with B. abortus, with mostly high titres in the conventional brucellosis tests, and (9) sera taken weekly from 3 cattle experimentally infected with Y. enterocolitica 0:9. In all 3 Y. enterocolitica 0:9 experimentally infected animals the antibody reactivity against major YOPs in the Y. enterocolitica and in the Y. pseudotuberculosis YOP preparation correlated well with the strength in the classical brucellosis tests and with the staining of smooth lipopolysaccharides (SLPS) in blots, thus confirming the usefulness of YOPs for the detection of Yersinia infections. Sera from naturally infected cattle and deer herds, regardless of whether they were false positive or negative in the brucellosis tests, showed high frequencies of staining in YOP blots (53–58% in cattle and 80–100% in deer), indicating a high prevalence of field infections with Yersinia species in New Zealand. In two of the three sera groups from B. abortus infected animals, antibodies against YOPs were detected with high frequency, showing that dual infections may be common and may interfere with differential serological testing.