J. Nišavić, N. Milic, A. Radalj, A. Stanojković, L. Veljović
{"title":"与牛呼吸道疾病相关的牛副流感-3病毒、牛疱疹病毒1和牛呼吸道合胞病毒的实验室诊断","authors":"J. Nišavić, N. Milic, A. Radalj, A. Stanojković, L. Veljović","doi":"10.2298/BAH2101001N","DOIUrl":null,"url":null,"abstract":"The bovine respiratory disease complex (BRDC) is multifactorial and results\n from interactions between host factors, environmental factors, and\n pathogens. A virus, as an initial pathogen alters the animal?s immunity\n supporting the bacterial colonization of the lower respiratory tract. Bovine\n herpesvirus 1 (BHV-1), bovine parainfluenza virus 3 (BPIV-3), and bovine\n respiratory syncytial virus (BRSV) are among the most significant viruses\n associated with BRDC. The disease most often affects young and older\n immunosuppressed animals. Laboratory results depend on the selected sampling\n site of the respiratory tract and proper timing during the period of virus\n shedding. The samples for testing mostly include nasal or nasopharyngeal\n swabs, tracheal wash, bronchoalveolar lavage fluid, or necropsy specimens.\n Virus isolation, although considered as the gold standard, is time-consuming\n and depends on the virus species and sampling conditions. Most of the virus\n identification methods used today are molecular assays (conventional and\n real-time PCR or RT-PCR) that are rapid, sensitive, and specific, which is\n of the essence in veterinary diagnostic laboratories. DNA sequencing is\n mostly used to detect specific genetic mutations and for molecular\n epidemiology of disease outbreaks. Serological diagnosis is performed based\n on the detection of specific antibody presence after infection of\n seronegative animals or a 4-fold specific antibody titer rise in paired\n serum samples. Different assays are available, including virus\n neutralization, complement fixation, haemagglutination inhibition, and\n ELISA. The early and reliable diagnosis is beneficial in the management and\n control of BRDC and is the basis of a timely treatment and prevention\n program.","PeriodicalId":249404,"journal":{"name":"Biotehnologija u stocarstvu","volume":"24 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Laboratory diagnostics of bovine parainfluenza-3 virus, bovine herpesvirus 1, and bovine respiratory syncytial virus associated with bovine respiratory disease\",\"authors\":\"J. Nišavić, N. Milic, A. Radalj, A. Stanojković, L. Veljović\",\"doi\":\"10.2298/BAH2101001N\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The bovine respiratory disease complex (BRDC) is multifactorial and results\\n from interactions between host factors, environmental factors, and\\n pathogens. A virus, as an initial pathogen alters the animal?s immunity\\n supporting the bacterial colonization of the lower respiratory tract. Bovine\\n herpesvirus 1 (BHV-1), bovine parainfluenza virus 3 (BPIV-3), and bovine\\n respiratory syncytial virus (BRSV) are among the most significant viruses\\n associated with BRDC. The disease most often affects young and older\\n immunosuppressed animals. Laboratory results depend on the selected sampling\\n site of the respiratory tract and proper timing during the period of virus\\n shedding. The samples for testing mostly include nasal or nasopharyngeal\\n swabs, tracheal wash, bronchoalveolar lavage fluid, or necropsy specimens.\\n Virus isolation, although considered as the gold standard, is time-consuming\\n and depends on the virus species and sampling conditions. Most of the virus\\n identification methods used today are molecular assays (conventional and\\n real-time PCR or RT-PCR) that are rapid, sensitive, and specific, which is\\n of the essence in veterinary diagnostic laboratories. DNA sequencing is\\n mostly used to detect specific genetic mutations and for molecular\\n epidemiology of disease outbreaks. Serological diagnosis is performed based\\n on the detection of specific antibody presence after infection of\\n seronegative animals or a 4-fold specific antibody titer rise in paired\\n serum samples. Different assays are available, including virus\\n neutralization, complement fixation, haemagglutination inhibition, and\\n ELISA. The early and reliable diagnosis is beneficial in the management and\\n control of BRDC and is the basis of a timely treatment and prevention\\n program.\",\"PeriodicalId\":249404,\"journal\":{\"name\":\"Biotehnologija u stocarstvu\",\"volume\":\"24 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biotehnologija u stocarstvu\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2298/BAH2101001N\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotehnologija u stocarstvu","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2298/BAH2101001N","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Laboratory diagnostics of bovine parainfluenza-3 virus, bovine herpesvirus 1, and bovine respiratory syncytial virus associated with bovine respiratory disease
The bovine respiratory disease complex (BRDC) is multifactorial and results
from interactions between host factors, environmental factors, and
pathogens. A virus, as an initial pathogen alters the animal?s immunity
supporting the bacterial colonization of the lower respiratory tract. Bovine
herpesvirus 1 (BHV-1), bovine parainfluenza virus 3 (BPIV-3), and bovine
respiratory syncytial virus (BRSV) are among the most significant viruses
associated with BRDC. The disease most often affects young and older
immunosuppressed animals. Laboratory results depend on the selected sampling
site of the respiratory tract and proper timing during the period of virus
shedding. The samples for testing mostly include nasal or nasopharyngeal
swabs, tracheal wash, bronchoalveolar lavage fluid, or necropsy specimens.
Virus isolation, although considered as the gold standard, is time-consuming
and depends on the virus species and sampling conditions. Most of the virus
identification methods used today are molecular assays (conventional and
real-time PCR or RT-PCR) that are rapid, sensitive, and specific, which is
of the essence in veterinary diagnostic laboratories. DNA sequencing is
mostly used to detect specific genetic mutations and for molecular
epidemiology of disease outbreaks. Serological diagnosis is performed based
on the detection of specific antibody presence after infection of
seronegative animals or a 4-fold specific antibody titer rise in paired
serum samples. Different assays are available, including virus
neutralization, complement fixation, haemagglutination inhibition, and
ELISA. The early and reliable diagnosis is beneficial in the management and
control of BRDC and is the basis of a timely treatment and prevention
program.