A. G. Dibbern, J. L. Gonçalves, B. G. Alves, J. R. Barreiro, Kevin Anderson, Marcos Veiga dos Santos
{"title":"实时聚合酶链反应检测和枚举不同牛奶样品的金黄色葡萄球菌和无乳链球菌","authors":"A. G. Dibbern, J. L. Gonçalves, B. G. Alves, J. R. Barreiro, Kevin Anderson, Marcos Veiga dos Santos","doi":"10.37496/rbz5220210086","DOIUrl":null,"url":null,"abstract":"- The objective of the present study was to evaluate the qPCR for detection and enumeration of Staphylococcus aureus and Streptococcus agalactiae using different milk samplings in comparison to the conventional microbiology. Four dairy herds with a history of subclinical mastitis caused by S . aureus and S . agalactiae were selected. Sampling approach included milk samples from bulk tank (BT), cow level (composite samples, CO), and mammary quarter level (MQ) from 785 lactating cows. Three consecutive monthly milk samplings were carried out, totaling 3347 MQ milk samples, 912 CO, and 12 from BT. All collected milk samples were subjected to conventional microbiology and qPCR for detection and enumeration of S . aureus and S . agalactiae. The qPCR showed 71.5% of diagnostic sensitivity for S . aureus isolated from MQ milk samples, 71.8% for CO, and 50% for BT milk samples compared with conventional microbiology methodology. Taken together, the diagnostic sensitivity for S . agalactiae isolated from MQ milk samples was 90.2, 87.7 for CO, and 90.9% for BT milk samples. In general, the qPCR methodology enabled the detection of S . aureus and S . agalactiae , regardless of the type of milk sampling. The direct use of milk samples to estimate the counting of S . aureus by qPCR demonstrated lower sensitivity than the counting of S . agalactiae , which can be explained by the","PeriodicalId":49614,"journal":{"name":"Revista Brasileira De Zootecnia-Brazilian Journal of Animal Science","volume":null,"pages":null},"PeriodicalIF":1.0000,"publicationDate":"2023-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Real-time polymerase chain reaction for detection and enumeration of Staphylococcus aureus and Streptococccus agalactiae using different milk samplings\",\"authors\":\"A. G. Dibbern, J. L. Gonçalves, B. G. Alves, J. R. Barreiro, Kevin Anderson, Marcos Veiga dos Santos\",\"doi\":\"10.37496/rbz5220210086\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"- The objective of the present study was to evaluate the qPCR for detection and enumeration of Staphylococcus aureus and Streptococcus agalactiae using different milk samplings in comparison to the conventional microbiology. Four dairy herds with a history of subclinical mastitis caused by S . aureus and S . agalactiae were selected. Sampling approach included milk samples from bulk tank (BT), cow level (composite samples, CO), and mammary quarter level (MQ) from 785 lactating cows. Three consecutive monthly milk samplings were carried out, totaling 3347 MQ milk samples, 912 CO, and 12 from BT. All collected milk samples were subjected to conventional microbiology and qPCR for detection and enumeration of S . aureus and S . agalactiae. The qPCR showed 71.5% of diagnostic sensitivity for S . aureus isolated from MQ milk samples, 71.8% for CO, and 50% for BT milk samples compared with conventional microbiology methodology. Taken together, the diagnostic sensitivity for S . agalactiae isolated from MQ milk samples was 90.2, 87.7 for CO, and 90.9% for BT milk samples. In general, the qPCR methodology enabled the detection of S . aureus and S . agalactiae , regardless of the type of milk sampling. The direct use of milk samples to estimate the counting of S . aureus by qPCR demonstrated lower sensitivity than the counting of S . agalactiae , which can be explained by the\",\"PeriodicalId\":49614,\"journal\":{\"name\":\"Revista Brasileira De Zootecnia-Brazilian Journal of Animal Science\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2023-04-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Revista Brasileira De Zootecnia-Brazilian Journal of Animal Science\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.37496/rbz5220210086\",\"RegionNum\":4,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Agricultural and Biological Sciences\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista Brasileira De Zootecnia-Brazilian Journal of Animal Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.37496/rbz5220210086","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
Real-time polymerase chain reaction for detection and enumeration of Staphylococcus aureus and Streptococccus agalactiae using different milk samplings
- The objective of the present study was to evaluate the qPCR for detection and enumeration of Staphylococcus aureus and Streptococcus agalactiae using different milk samplings in comparison to the conventional microbiology. Four dairy herds with a history of subclinical mastitis caused by S . aureus and S . agalactiae were selected. Sampling approach included milk samples from bulk tank (BT), cow level (composite samples, CO), and mammary quarter level (MQ) from 785 lactating cows. Three consecutive monthly milk samplings were carried out, totaling 3347 MQ milk samples, 912 CO, and 12 from BT. All collected milk samples were subjected to conventional microbiology and qPCR for detection and enumeration of S . aureus and S . agalactiae. The qPCR showed 71.5% of diagnostic sensitivity for S . aureus isolated from MQ milk samples, 71.8% for CO, and 50% for BT milk samples compared with conventional microbiology methodology. Taken together, the diagnostic sensitivity for S . agalactiae isolated from MQ milk samples was 90.2, 87.7 for CO, and 90.9% for BT milk samples. In general, the qPCR methodology enabled the detection of S . aureus and S . agalactiae , regardless of the type of milk sampling. The direct use of milk samples to estimate the counting of S . aureus by qPCR demonstrated lower sensitivity than the counting of S . agalactiae , which can be explained by the
期刊介绍:
The Revista Brasileira de Zootecnia (RBZ; Brazilian Journal of Animal Science) encompasses all fields of Animal Science Research. The RBZ publishes original scientific articles in the areas of Aquaculture, Biometeorology and Animal Welfare, Forage Crops and Grasslands, Animal and Forage Plants Breeding and Genetics, Animal Reproduction, Ruminant and Non-Ruminant Nutrition, and Animal Production Systems and Agribusiness.