Differentiating turkey postvaccination isolants of Pasteurella multocida using arbitrarily primed polymerase chain reaction

被引:28
作者
Hopkins, BA
Huang, THM
Olson, LD
机构
[1] Univ Missouri, Sch Med, Dept Pathol & Anat Sci, Columbia, MO 65211 USA
[2] Univ Missouri, Coll Vet Med, Dept Vet Pathobiol, Columbia, MO 65211 USA
关键词
arbitrarily primed polymerase chain reaction (AP-PCR); Pasteurella multocida; turkeys; vaccine;
D O I
10.2307/1592476
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 [兽医学];
摘要
The chromosomal DNA of 29 field isolants of Pasteurella multocida from commercial turkey farms in Missouri and the avirulent Clemson University (CU) and M-9 vaccine strains of P. multocida were tested using the arbitrarily primed polymerase chain reaction (AP-PCR) in combination with P-32-labeled deoxycytidine triphosphate (dCTP) and high-resolution gel electrophoresis. The 23 field isolants of P. multocida were isolated from outbreaks of fowl cholera in turkey flocks in which vaccination with the CU vaccine had been performed within 2 weeks of the isolation, and it was suspected that the outbreak could have been due to the use of the live CU vaccine. The results of this study showed that: 1) the use of the live CU vaccine can lead to the isolation of the vaccine strain if the outbreak occurs within 2 weeks of vaccination; 2) a higher proportion of field isolants collected during 1983 and 1984, when the usage of the CU vaccine strain was highest on Missouri turkey farms, had PCR-amplified product profiles similar or identical to those of the CU vaccine strain compared with the period between 1987 and 1992, when its use was less; and 3) there was no relationship between the PCR-amplified product profiles and the serotype.
引用
收藏
页码:265 / 274
页数:10
相关论文
共 17 条
[1]
CHARACTERIZATION OF PASTEURELLA-MULTOCIDA ISOLATED FROM FOWL CHOLERA OUTBREAKS ON TURKEY FARMS [J].
BLACKALL, PJ ;
PAHOFF, JL ;
MARKS, D ;
FEGAN, N ;
MORROW, CJ .
AUSTRALIAN VETERINARY JOURNAL, 1995, 72 (04) :135-138
[2]
CARTER GR, 1984, BERGEYS MANUAL SYSTE, V1, P552
[3]
CLONAL ANALYSIS OF PORPHYROMONAS-GINGIVALIS BY THE ARBITRARILY PRIMED POLYMERASE CHAIN-REACTION [J].
CHEN, C ;
SLOTS, J .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 1994, 9 (02) :99-103
[4]
TRANSMISSION OF PASTEURELLA-MULTOCIDA ON CALIFORNIA TURKEY PREMISES IN 1988-89 [J].
CHRISTIANSEN, KH ;
CARPENTER, TE ;
SNIPES, KP ;
HIRD, DW .
AVIAN DISEASES, 1992, 36 (02) :262-271
[5]
FOWL CHOLERA - GEL-DIFFUSION PRECIPITIN TEST FOR SEROTYPING PASTEURELLA-MULTOCIDA FROM AVIAN SPECIES [J].
HEDDLESTON, KL ;
REBERS, PA ;
GALLAGHER, JE .
AVIAN DISEASES, 1972, 16 (04) :925-+
[6]
SEROTYPE IDENTIFICATION OF ACTINOBACILLUS-PLEUROPNEUMONIAE BY ARBITRARILY PRIMED POLYMERASE CHAIN-REACTION [J].
HENNESSY, KJ ;
IANDOLO, JJ ;
FENWICK, BW .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (05) :1155-1159
[7]
DIVERSITY AMONG CLINICAL ISOLATES OF HISTOPLASMA-CAPSULATUM DETECTED BY POLYMERASE CHAIN-REACTION WITH ARBITRARY PRIMERS [J].
KERSULYTE, D ;
WOODS, JP ;
KEATH, EJ ;
GOLDMAN, WE ;
BERG, DE .
JOURNAL OF BACTERIOLOGY, 1992, 174 (22) :7075-7079
[8]
KIM CJ, 1990, AM J VET RES, V51, P207
[10]
APPLICATION OF POLYMERASE CHAIN-REACTION WITH ARBITRARY PRIMER (AP-PCR) TO STRAIN IDENTIFICATION OF PORPHYROMONAS-(BACTEROIDES)-GINGIVALIS [J].
MENARD, C ;
BROUSSEAU, R ;
MOUTON, C .
FEMS MICROBIOLOGY LETTERS, 1992, 95 (2-3) :163-168