EFFICACY OF 3 LIVE VACCINES AGAINST HIGHLY VIRULENT INFECTIOUS BURSAL DISEASE VIRUS IN CHICKENS WITH OR WITHOUT MATERNAL ANTIBODIES

被引:79
作者
TSUKAMOTO, K [1 ]
TANIMURA, N [1 ]
KAKITA, S [1 ]
OTA, K [1 ]
MASE, M [1 ]
IMAI, K [1 ]
HIHARA, H [1 ]
机构
[1] GOTO HATCHERY INC, RES CTR, KAKAMIGAHARA, GIFU 504, JAPAN
关键词
HIGHLY VIRULENT IBDV; INFECTIOUS BURSAL DISEASE; MATERNAL ANTIBODY; VACCINE;
D O I
10.2307/1591863
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Since 1990, highly virulent infectious bursal disease virus (IBDV), which induces high mortality, has been, infecting even vaccinated necks in Japan. We report the efficacy of three live vaccines that are available in Japan. Two mildly attenuated strains (A and B) and one intermediate strain (C) were each tested both in specific-pathogen-free (SPF) chickens and in commercial chickens that have maternal antibodies against IBDV. Chickens were vaccinated at 20 days old and challenged with highly virulent IBDV 10 days pest vaccination. Protection was determined 7 days after challenge by measuring bursa/body weight ratios, histopathological lesions, and antibody responses to IBDV. All three live vaccines conferred protection to SPF chickens. However, only vaccine C protected 100% of vaccinated commercial chickens against highly virulent IBDV; Vaccines A and B respectively protected three-fourths and none of vaccinated commercial chickens from severe bursal lesions. Vaccines A, B, and C and highly virulent IBDV induced bursal lesions in 3%, 0%, 23%, and 61% of inoculated commercial chickens, respectively. These results suggest that serological determination of the optimum vaccination time for each flock is required to effectively control highly virulent IBDV in the field. The optimum vaccination timing could be approximated by titrating the maternal IBDV antibodies of 1-day-old chicks by an enzyme-linked immunosorbent assay or by an agar gel precipitin test.
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页码:218 / 229
页数:12
相关论文
共 16 条
[1]   VP2 SEQUENCES OF RECENT EUROPEAN VERY VIRULENT ISOLATES OF INFECTIOUS BURSAL DISEASE VIRUS ARE CLOSELY-RELATED TO EACH OTHER BUT ARE DISTINCT FROM THOSE OF CLASSICAL STRAINS [J].
BROWN, MD ;
GREEN, P ;
SKINNER, MA .
JOURNAL OF GENERAL VIROLOGY, 1994, 75 :675-680
[2]   PERFORMANCE OF 3 SUCCESSIVE GENERATIONS OF SPECIFIED-PATHOGEN-FREE CHICKENS MAINTAINED AS A CLOSED FLOCK [J].
FURUTA, K ;
OHASHI, H ;
OBANA, J ;
SATO, S .
LABORATORY ANIMALS, 1980, 14 (02) :107-112
[3]   SEQUENCE COMPARISONS OF A HIGHLY VIRULENT INFECTIOUS BURSAL DISEASE VIRUS PREVALENT IN JAPAN [J].
LIN, Z ;
KATO, A ;
OTAKI, Y ;
NAKAMURA, T ;
SASMAZ, E ;
UEDA, S .
AVIAN DISEASES, 1993, 37 (02) :315-323
[4]  
Lukert P. D., 1991, Diseases of poultry., P648
[5]   PATHOGENICITY AND IMMUNOSUPPRESSIVE PROPERTIES OF INFECTIOUS BURSAL DISEASE INTERMEDIATE STRAINS [J].
MAZARIEGOS, LA ;
LUKERT, PD ;
BROWN, J .
AVIAN DISEASES, 1990, 34 (01) :203-208
[6]   IMMUNOSUPPRESSIVE EFFECT OF A HIGHLY VIRULENT INFECTIOUS BURSAL DISEASE VIRUS ISOLATED IN JAPAN [J].
NAKAMURA, T ;
OTAKI, Y ;
NUNOYA, T .
AVIAN DISEASES, 1992, 36 (04) :891-896
[7]   OCCURRENCE OF ACUTE INFECTIOUS BURSAL DISEASE WITH HIGH MORTALITY IN JAPAN AND PATHOGENICITY OF FIELD ISOLATES IN SPECIFIC-PATHOGEN-FREE CHICKENS [J].
NUNOYA, T ;
OTAKI, Y ;
TAJIMA, M ;
HIRAGA, M ;
SAITO, T .
AVIAN DISEASES, 1992, 36 (03) :597-609
[8]   COMPARATIVE PATHOGENESIS OF SEROTYPE-1 AND VARIANT SEROTYPE-1 ISOLATES OF INFECTIOUS BURSAL DISEASE VIRUS AND THEIR EFFECT ON HUMORAL AND CELLULAR IMMUNE COMPETENCE OF SPECIFIC-PATHOGEN-FREE CHICKENS [J].
SHARMA, JM ;
DOHMS, JE ;
METZ, AL .
AVIAN DISEASES, 1989, 33 (01) :112-124
[9]   EFFECT OF MATERNAL ANTIBODY ON TIMING OF INITIAL VACCINATION OF YOUNG WHITE LEGHORN CHICKENS AGAINST INFECTIOUS BURSAL DISEASE VIRUS [J].
SOLANO, W ;
GIAMBRONE, JJ ;
WILLIAMS, JC ;
LAUERMAN, LH ;
PANANGALA, VS ;
GARCES, C .
AVIAN DISEASES, 1986, 30 (04) :648-652
[10]   ASSOCIATION BETWEEN PATHOGENICITY OF INFECTIOUS BURSAL DISEASE VIRUS AND VIRAL-ANTIGEN DISTRIBUTION DETECTED BY IMMUNOHISTOCHEMISTRY [J].
TANIMURA, N ;
TSUKAMOTO, K ;
NAKAMURA, K ;
NARITA, M ;
MAEDA, M .
AVIAN DISEASES, 1995, 39 (01) :9-20