Polyrnerase chain reaction detection of caecal bacteria in case of preventive application of Enterococcus jaecium EK13 against Salmonella enterica subsp Enteritidis in chickens
被引:2
|
作者:
Herich, R
论文数: 0引用数: 0
h-index: 0
机构:Univ Vet Med, Inst Pathol, Kosice 04001, Slovakia
Herich, R
Lauková, A
论文数: 0引用数: 0
h-index: 0
机构:Univ Vet Med, Inst Pathol, Kosice 04001, Slovakia
Lauková, A
Strompfová, V
论文数: 0引用数: 0
h-index: 0
机构:Univ Vet Med, Inst Pathol, Kosice 04001, Slovakia
Strompfová, V
Revajová, V
论文数: 0引用数: 0
h-index: 0
机构:Univ Vet Med, Inst Pathol, Kosice 04001, Slovakia
Revajová, V
Levkut, M
论文数: 0引用数: 0
h-index: 0
机构:Univ Vet Med, Inst Pathol, Kosice 04001, Slovakia
Levkut, M
Pistl, J
论文数: 0引用数: 0
h-index: 0
机构:Univ Vet Med, Inst Pathol, Kosice 04001, Slovakia
Pistl, J
机构:
[1] Univ Vet Med, Inst Pathol, Kosice 04001, Slovakia
The polymerase chain reaction (PCR) was used in combination with microbiology methods for identifying faecal bacteria. The changes were monitor in the bacterial flora of chicken's caecum after preventive peroral application of Enterococcus faecium EK13 and consecutive infection with Salmonella enterica subsp. Enteritidis. The preventive treatment with Enteroccocus faecium EK 13, reduced the numbers of S. enterica subsp. Enteritidis in chicken excreta after 5 days post infection (pi) and in the caecum after 7 days pi. The PCR products 243 bp for Sallmonella spp. and 550 bp for Ent. faecium were amplified. The detection of Salmonella spp. required only simple boiling of the samples. On the contrary, for reliable detection of Ent. jaecium, DNA isolation with commercial avalaible kit was required. The high sensitivity of PCR was confirmed and the exptected specific DNA fragments could be amplified from dilutions containing ten to one CFU (Colony Forming Units).