Detection and Identification of Salmonella Typhimurium in Bovine Diarrhoeic Fecal Samples by Immunomagnetic Separation and Multiplex PCR Assay
| Autor: | T. Zahraei Salehi, Mohammadreza Mahzounieh, N. Atashparvar, M. G. Nadalian, Hasan Tadjbakhsh |
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| Rok vydání: | 2007 |
| Předmět: |
DNA
Bacterial Diarrhea Salmonella typhimurium Serotype Salmonella Microbiological culture Epidemiology Cattle Diseases Biology Immunomagnetic separation medicine.disease_cause Polymerase Chain Reaction Sensitivity and Specificity Microbiology law.invention Feces law Zoonoses Multiplex polymerase chain reaction medicine Animals Humans Phylogeny Polymerase chain reaction Salmonella Infections Animal General Veterinary General Immunology and Microbiology Immunomagnetic Separation Gene Amplification Public Health Environmental and Occupational Health biology.organism_classification Molecular biology Infectious Diseases Salmonella enterica Cattle |
| Zdroj: | Zoonoses and Public Health. 54:231-236 |
| ISSN: | 1863-2378 1863-1959 |
| DOI: | 10.1111/j.1863-2378.2007.01061.x |
| Popis: | The aim of this study was to use the immunomagnetic separation (IMS) test plus a multiplex polymerase chain reaction (m-PCR) assay to detect Salmonella at genus level and also for the identification of Salmonella enterica serovar Typhimurium in bovine diarrhoeic fecal samples. In all, 400 bovine diarrhoeic fecal specimens were examined by conventional bacterial culture, IMS, and m-PCR. For m-PCR assay, four set primers were selected: 139-141, specific for inv-A gene of Salmonella spp and the RfbJ, FliC and FljB, specific for the rfbJ, FliC and fljB genes of Salmonella Typhimurium or other Salmonella serovars with similar antigenic properties. Thirty-three (8.25%) out of the 400 fecal samples were culture positive for Salmonella serovars. Of these, 66.7% (22 of 33) were Salmonella enterica serovar Typhimurium, and 9.1% (three of 33) were serovar Dublin. In the IMS + m-PCR, four amplified product (663, 526, 284 and 183 bp) were found in all specimens that had serovar Typhimurium (4,5,12:i:1,2), they corresponded, respectively, to the rfbJ, fljB, inv-A and Flic genes of this serovar. In serovar Dublin (1,9,12:g,p:-), Georgia (6,7:b:e,n,z(15)) and, Enteritidis (1,9,12;g,m:-) only one PCR product (284 bp) was amplified from the inv-A gene. In serovars Augustenborg (6,7:i:1,2) and Lindenburg (6,8:i:1,2) three positive bands (526, 284 and 183 bp) were amplified corresponding to the fljB, inv-A and Flic genes, respectively. In serovar Virchow (6,7:r:1,2) two amplified products (284 and 526 bp) from the inv-A and FliC genes were observed. In serovar Gloucster (1,4,12(27):i:1,w) three fragments (183, 284 and 663) from the FliC, inv-A and, rfbJ genes respectively, were observed. In the positive control as expected, four PCR products were amplified corresponding to the FliC, inv-A, fljB and rfbJ genes, respectively. In conclusion, the results of this study showed that detection of Salmonella at genus level with universal ST139-141 primers and identification of Salmonella Typhimurium by using specific primers of O4, H(2):1, 2 and H(1) antigens can potentially permit to more readily evaluate fecal and other types of samples for the presence of these organisms. Compared to bacteriological culture the combination of IMS and m-PCR resulted a faster method for the detection and identification of Salmonella at genus and serovar level by using of universal and specific primers. |
| Databáze: | OpenAIRE |
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