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951.
952.
Kusuhara H Hohdatsu T Seta T Nemoto K Motokawa K Gemma T Watanabe R Huang C Arai S Koyama H 《Veterinary microbiology》2007,120(3-4):217-225
Feline immunodeficiency virus (FIV) vaccine, Fel-O-Vax FIV, was released for sale in the US in 2002. The antibodies of vaccinated cats interfere with serological assays by currently available FIV diagnostic kits. In this study, we investigated whether it is possible to distinguish serologically cats vaccinated with Fel-O-Vax FIV from cats experimentally or naturally infected with FIV. A total of 153 sera taken from 97 cats were used as serum samples. Enzyme linked immunosorbent assay (ELISA) was performed using whole FIV antigen and formalin treated whole FIV antigen, recombinant-gag (r-gag) antigen, and transmembrane (TM) peptide. Statistical analysis was performed using ELISA optical density (O.D.) values obtained with each antigen as variables. Except for the ELISA O.D. values obtained with r-gag antigen, a significant difference in ELISA O.D. values was observed between the vaccinated and the infected groups. However, it was not possible to distinguish both groups unequivocally. Using discriminant analysis, it was possible to distinguish the two groups with an accuracy of 97.1% with two discriminating variables (ELISA O.D. values obtained with formalin treated whole FIV antigen, and TM peptide), 97.8% with three discriminating variables (ELISA O.D. values obtained with whole FIV antigen, formalin treated whole FIV antigen, and TM peptide). Therefore, it was considered possible to distinguish cats vaccinated with Fel-O-Vax FIV from FIV-infected cats by ELISA using two types of antigens including formalin treated whole FIV antigen and TM peptide, or three types of antigens including formalin treated whole FIV antigen, TM peptide and whole FIV antigen. 相似文献
953.
Allan GM Caprioli A McNair I Lagan-Tregaskis P Ellis J Krakowka S McKillen J Ostanello F McNeilly F 《Zoonoses and public health》2007,54(5):214-222
Porcine circovirus type 2 (PCV2) infection is now recognized as the major factor in the development of post-weaning multisystemic wasting syndrome (PMWS). Although Koch's postulates have been fulfilled for PCV2 and PMWS, the severe clinical expression of the disease observed in field cases has been difficult to reproduce experimentally. Some studies have demonstrated that immune stimulation associated with the use of some commercially available swine vaccines may trigger progression of PCV2 infection to disease and lesions characteristic of PMWS. Here we describe the effects on PCV2 infection in an experimental model following the use of a commercially available modified live vaccine to porcine respiratory and reproductive syndrome virus (PRRSV). Although none of the piglets infected with PCV2 developed clinical PMWS, the severity of microscopical lesions and the PCV2 antigen load associated with these lesions were higher in the PRRSV-vaccinated piglets compared with those detected in the PCV2 only infected animals. 相似文献
954.
《Veterinary microbiology》2015,175(2-4):294-303
The human oral microbiome is known to play a significant role in human health and disease. While less well studied, the feline oral microbiome is thought to play a similarly important role. To determine roles oral bacteria play in health and disease, one first has to be able to accurately identify bacterial species present. 16S rRNA gene sequence information is widely used for molecular identification of bacteria and is also useful for establishing the taxonomy of novel species.The objective of this research was to obtain full 16S rRNA gene reference sequences for feline oral bacteria, place the sequences in species-level phylotypes, and create a curated 16S rRNA based taxonomy for common feline oral bacteria.Clone libraries were produced using “universal” and phylum-selective PCR primers and DNA from pooled subgingival plaque from healthy and periodontally diseased cats. Bacteria in subgingival samples were also cultivated to obtain isolates. Full-length 16S rDNA sequences were determined for clones and isolates that represent 171 feline oral taxa. A provisional curated taxonomy was developed based on the position of each taxon in 16S rRNA phylogenetic trees.The feline oral microbiome curated taxonomy and 16S rRNA gene reference set will allow investigators to refer to precisely defined bacterial taxa. A provisional name such as “Propionibacterium sp. feline oral taxon FOT-327” is an anchor to which clone, strain or GenBank names or accession numbers can point. Future next-generation-sequencing studies of feline oral bacteria will be able to map reads to taxonomically curated full-length 16S rRNA gene sequences. 相似文献
955.
956.
Naoyuki AIHARA Noriyuki HORIUCHI Nanase HIKICHI Mariko OCHIAI Yuko HOSODA Yoko ISHIKAWA Yoko SHIMAZAKI Koji OISHI 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2015,77(8):913-918
Infectious bursal disease (IBD) is characterized by immunosuppression due to the depletion of lymphocytes in the atrophied bursa of Fabricius (BF). We have sometimes encountered contradictory findings: chickens infected with the vaccine IBD virus (IBDV) strain have sometimes exhibited a highly atrophied BF, but not immunosuppression. In this study, chickens administered vaccine or wild-type strains of IBDV were later vaccinated with the B1 strain of the Newcastle disease virus (NDV). Bursal changes were examined histologically with a focus on the bursal follicle. The immunoreactivity to NDV was also evaluated with the hemagglutination inhibition test. In gross examination, we observed a few chickens with a severely atrophied BF in vaccine strain-administered groups (vaccine groups), and the level of severity was the same as that in the wild-type strain-administered group (wild-type group). However, these chickens retained humoral antibody responses to NDV and were revealed to possess a higher number of bursal follicles than those of the wild-type group. These results indicated that macroscopic evaluation dose not accurately reflect the immunoreactivity and degree of bursal damage in IBDV-administered chickens. We also found non-immunosuppressed chickens in the wild-type group. These non-immunosuppressed chickens retained a significantly higher number of normal follicles and total follicles according to our statistical analysis. Furthermore, a high correlation coefficient between the NDV-HI titer and the number of normal follicles was found in the wild-type group. These results implied that the retained number of normal follicles is important for the immunoreactivity of chickens infected with IBDV. 相似文献
957.
Mai YAMAMOTO Takashige KASHIMOTO Ping TONG Jianbo XIAO Michiko SUGIYAMA Miyuki INOUE Rie MATSUNAGA Kohei HOSOHARA Kazue NAKATA Kenji YOKOTA Keiji OGUMA Koichiro YAMAMOTO 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2015,77(7):823-828
Vibrio vulnificus is the causative agent of primary septicemia, wound
infection and gastroenteritis in immunocompromised people. In this study, signature-tagged
mutagenesis (STM) was applied to identify the virulence genes of V.
vulnificus. Using STM, 6,480 mutants in total were constructed and divided into
81 sets (INPUT pools); each mutant in a set was assigned a different tag. Each INPUT pool
was intraperitoneally injected into iron-overloaded mice, and in vivo
surviving mutants were collected from blood samples from the heart (OUTPUT pools). From
the genomic DNA of mixed INPUT or OUTPUT pools, digoxigenin-labeled DNA probes against the
tagged region were prepared and used for dot hybridization. Thirty tentatively attenuated
mutants, which were hybridized clearly with INPUT probes but barely with OUTPUT probes,
were negatively selected. Lethal doses of 11 of the 30 mutants were reduced to more than
1/100; of these, the lethal doses of 2 were reduced to as low as 1/100,000.
Transposon-inserted genes in the 11 attenuated mutants were those for IMP dehydrogenase,
UDP-N-acetylglucosamine-2-epimerase, aspartokinase, phosphoribosylformylglycinamidine
cyclo-ligase, malate Na (+) symporter and hypothetical protein. When mice were immunized
with an attenuated mutant strain into which IMP dehydrogenase had been inserted with a
transposon, they were protected against V. vulnificus infection. In this
study, we demonstrated that the STM method can be used to search for the virulence genes
of V. vulnificus. 相似文献
958.
为了评定无针注射器接种猪瘟活疫苗的免疫效果,将300头非免仔猪随机分为6个组,其中3组用无针注射器分别免疫1头份、1/2头份剂量的瘟倍安以及1头份剂量的STTM猪瘟活疫苗,剩下的3组将无针注射器替换成传统的有针注射器进行免疫。30日龄进行首次免疫,55日龄进行二次免疫,免疫后一周内观察猪有无不良反应。首免后第14天、二免后第25天分别采血、分离血清,ELISA试剂盒检测CSFV抗体,计算每组猪抗体阻断率及免疫合格率,统计分析各组之间的差异。实验结果显示,无针注射器与有针注射器接种疫苗均未对猪精神状态、采食、运动造成影响,无针注射器接种部位炎症发生率也低于有针注射器;无针注射器免疫组抗体滴度明显高于有针注射器接种组,即使疫苗使用剂量减半也能达到很好的免疫效果。 相似文献
959.
为解决兽药二维码追溯工作中大批量产品数据信息采集难的问题,利用现有口蹄疫疫苗分装线进行自动化采集系统改造的摸索,通过热转印技术,结合包装线的技改与调试,在不改变生产现状的情况下,建立了适合大批量口蹄疫疫苗产品二维码数据信息的在线自动化采集。每分钟可达120瓶,解决了批量大、手工逐瓶采集不好操作的难题,为其他疫苗产品生产线的自动化改造提供了参考。 相似文献
960.