Primers for Salmonella serovar detection by polymerase chain reaction

Salmonella serovar detection was studied by polymerase chain reaction (PCR). The primers were designed from Salmonella specific clone, A18:2 which was previously constructed and studied for genus specificity through colony hybridization. The primers were subsequently tested for specificity and sensi...

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Published inSoutheast Asian journal of tropical medicine and public health Vol. 29; no. 1; pp. 85 - 90
Main Authors KANTAMA, L, JAYANETRA, P, PILANTANAPAK, A, CHARAENSUB, A
Format Journal Article
LanguageEnglish
Published Bangkok Southeast Asian Ministers of Education Organization, Regional Tropical Medicine and Public Health Network 01.03.1998
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Abstract Salmonella serovar detection was studied by polymerase chain reaction (PCR). The primers were designed from Salmonella specific clone, A18:2 which was previously constructed and studied for genus specificity through colony hybridization. The primers were subsequently tested for specificity and sensitivity and showed that they amplified DNA fragment of all Salmonellae tested but did not amplify all isolates of non-Salmonellae tested. The amplified fragment was confirmed and increased sensitivity by nested PCR. Salmonella isolates amplified by the primers in the first round PCR were all positive in the second round. The sensitivity in the first and second round were 7 pg and 80 fg, respectively. The result indicated that the primers can be used as molecular tool for future field survey of Salmonella both in food and in clinical specimens.
AbstractList Salmonella serovar detection was studied by polymerase chain reaction (PCR). The primers were designed from Salmonella specific clone, A18:2 which was previously constructed and studied for genus specificity through colony hybridization. The primers were subsequently tested for specificity and sensitivity and showed that they amplified DNA fragment of all Salmonellae tested but did not amplify all isolates of non-Salmonellae tested. The amplified fragment was confirmed and increased sensitivity by nested PCR. Salmonella isolates amplified by the primers in the first round PCR were all positive in the second round. The sensitivity in the first and second round were 7 pg and 80 fg, respectively. The result indicated that the primers can be used as molecular tool for future field survey of Salmonella both in food and in clinical specimens.
Author PILANTANAPAK, A
JAYANETRA, P
KANTAMA, L
CHARAENSUB, A
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Keywords Infection
Human
Interest
Salmonella
Food industry
Bacteriosis
Bacteria
Salmonellosis
Diagnosis
Medical screening
Enterobacteriaceae
Language English
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PublicationTitle Southeast Asian journal of tropical medicine and public health
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StartPage 85
SubjectTerms Bacterial diseases
Bacterial diseases of the digestive system and abdomen
Base Sequence
Biological and medical sciences
DNA Primers - genetics
Human bacterial diseases
Humans
Infectious diseases
Medical sciences
Molecular Sequence Data
Polymerase Chain Reaction - methods
Salmonella - genetics
Salmonella Infections - diagnosis
Sensitivity and Specificity
Tropical medicine
Title Primers for Salmonella serovar detection by polymerase chain reaction
URI https://www.ncbi.nlm.nih.gov/pubmed/9740275
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