Development and Research of PCR Diagnostic Technique to Detect Salmonella

碩士 === 國立中山大學 === 生物科學系研究所 === 91 === ABSTRACT There are more than 2000 serotypes in the typhoid, septic and enteritidis Salmonella strains. This has long been a perplexity for the differentiation of Salmonella and discrimination from other food poisoning bacteria. In this research, we used polymer...

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Main Authors: YEOU-HUN CHIANG, 江有恆
Other Authors: JONG-KANG LIU
Format: Others
Language:zh-TW
Online Access:http://ndltd.ncl.edu.tw/handle/y3385k
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spelling ndltd-TW-091NSYS51120422019-05-15T20:31:59Z http://ndltd.ncl.edu.tw/handle/y3385k Development and Research of PCR Diagnostic Technique to Detect Salmonella 沙門氏菌PCR檢驗技術之開發與研究 YEOU-HUN CHIANG 江有恆 碩士 國立中山大學 生物科學系研究所 91 ABSTRACT There are more than 2000 serotypes in the typhoid, septic and enteritidis Salmonella strains. This has long been a perplexity for the differentiation of Salmonella and discrimination from other food poisoning bacteria. In this research, we used polymerase chain reaction method (PCR) to develop a molecular technique for the detection of Salmonella. An invasion factor invA gene had been used to design the PCR primers. The results showed that under specific PCR conditions, many related bacterias such as Shigella, Yersinia, Serratia, Enterobacter, Vibrio and E. coli could be detected only with the primer annealing temperature ranging from 56℃~66℃. However, all tested Salmonella strains could be detected above 69℃. This is potential of being developed into a rapid method for detecting Salmonella strains in food or clinical specimens. In the future, it can be further increased the accuracy of detection in coordination with multi-primer PCR technique or developed into a biochip for the detection of Salmonella. JONG-KANG LIU 劉仲康 學位論文 ; thesis 60 zh-TW
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language zh-TW
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sources NDLTD
description 碩士 === 國立中山大學 === 生物科學系研究所 === 91 === ABSTRACT There are more than 2000 serotypes in the typhoid, septic and enteritidis Salmonella strains. This has long been a perplexity for the differentiation of Salmonella and discrimination from other food poisoning bacteria. In this research, we used polymerase chain reaction method (PCR) to develop a molecular technique for the detection of Salmonella. An invasion factor invA gene had been used to design the PCR primers. The results showed that under specific PCR conditions, many related bacterias such as Shigella, Yersinia, Serratia, Enterobacter, Vibrio and E. coli could be detected only with the primer annealing temperature ranging from 56℃~66℃. However, all tested Salmonella strains could be detected above 69℃. This is potential of being developed into a rapid method for detecting Salmonella strains in food or clinical specimens. In the future, it can be further increased the accuracy of detection in coordination with multi-primer PCR technique or developed into a biochip for the detection of Salmonella.
author2 JONG-KANG LIU
author_facet JONG-KANG LIU
YEOU-HUN CHIANG
江有恆
author YEOU-HUN CHIANG
江有恆
spellingShingle YEOU-HUN CHIANG
江有恆
Development and Research of PCR Diagnostic Technique to Detect Salmonella
author_sort YEOU-HUN CHIANG
title Development and Research of PCR Diagnostic Technique to Detect Salmonella
title_short Development and Research of PCR Diagnostic Technique to Detect Salmonella
title_full Development and Research of PCR Diagnostic Technique to Detect Salmonella
title_fullStr Development and Research of PCR Diagnostic Technique to Detect Salmonella
title_full_unstemmed Development and Research of PCR Diagnostic Technique to Detect Salmonella
title_sort development and research of pcr diagnostic technique to detect salmonella
url http://ndltd.ncl.edu.tw/handle/y3385k
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