Simple and rapid detection of Salmonella serovar Enteritidis under field conditions by loop-mediated isothermal amplification

Journal of Applied Microbiology

Volumn 109, Issue 5, 2010, Pages 1715-1723

  Yang, J L ^a,b   Ma, G P ^c   Yang, R ^a   Yang, S Q ^a   Fu, L Z ^a   Cheng, A C ^b   Wang, M S ^b   Zhang, S H ^a   Shen, K F ^a   Jia, R Y ^b   Deng, S X ^b   Xu, Z Y ^d  

^a Poultry Science Institute   (China)

^b SICHUAN AGRICULTURAL UNIVERSITY   (China)

^c China Rural Technology Development Center   (China)

^d HENAN INSTITUTE OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

LAMP; Real time PCR; Salmonella enteritidis; Serovar specific

Indexed keywords

DNA SEQUENCES; ISOTHERMS; POLYMERASE CHAIN REACTION; SALMONELLA;

FIELD CONDITIONS; LOOP MEDIATED ISOTHERMAL AMPLIFICATIONS; LOOP-MEDIATED ISOTHERMAL AMPLIFICATIONS; REAL-TIME PCR; SALMONELLA ENTERITIDIS; SALMONELLA SEROVARS; SEROVAR-SPECIFIC; SEROVARS; SIMPLE++; WATER BATHS;

DNA;

DNA POLYMERASE; PRIMER DNA;

AMPLIFICATION; BACTERIUM; LABORATORY METHOD; POLYMERASE CHAIN REACTION; REAL TIME;

ANIMAL EXPERIMENT; ARTICLE; BACTERIUM DETECTION; CONTROLLED STUDY; GENE AMPLIFICATION; LOOP MEDIATED ISOTHERMAL AMPLIFICATION; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; REAL TIME POLYMERASE CHAIN REACTION; SALMONELLA ENTERITIDIS; SENSITIVITY AND SPECIFICITY; SEROTYPE;

SALMONELLA; SALMONELLA ENTERITIDIS;

EID: 78650469770     PISSN: 13645072     EISSN: 13652672     Source Type: Journal    
DOI: 10.1111/j.1365-2672.2010.04800.x     Document Type: Article

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