Demonstration of Expression of Six Proteins of the Mammalian Cell Entry (mce1) Operon of Mycobacterium tuberculosis by Anti-Peptide Antibodies, Enzyme-Linked Immunosorbent Assay and Reverse Transcription-Polymerase Chain Reaction

1999 ◽  
Vol 50 (5) ◽  
pp. 519-527 ◽  
Author(s):  
Harboe ◽  
Christensen ◽  
Haile ◽  
Ulvund ◽  
Ahmad ◽  
...  
Keyword(s):  
Polymerase Chain Reaction ◽  
Mycobacterium Tuberculosis ◽  
Mammalian Cell ◽  
Immunosorbent Assay ◽  
Reverse Transcription ◽  
Cell Entry ◽  
Enzyme Linked Immunosorbent Assay ◽  
Chain Reaction ◽  
Polymerase Chain ◽  
Peptide Antibodies

scholarly journals Genotyping ofSalmonellaspp. on the basis of CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)

2018 ◽  
Author(s):  
Calvin Jiksing ◽  
Normah Yusop ◽  
Farhan Nazaie Nasib ◽  
Kenneth Francis Rodrigues
Keyword(s):  
Polymerase Chain Reaction ◽  
Mycobacterium Tuberculosis ◽  
Immunosorbent Assay ◽  
Deoxyribonucleic Acid ◽  
Enzyme Linked Immunosorbent Assay ◽  
Chain Reaction ◽  
Pcr Polymerase Chain Reaction ◽  
Crispr Array ◽  
Polymerase Chain ◽  
Veterinary Laboratory

ABSTRACTAimsBacterial genotyping on the basis of the CRISPR array has been established inMycobacterium tuberculosiswith a method called spacer oligonucleotide typing (spoligotyping). The spoligotyping method had been widely used for both detection and typing ofM. tuberculosiscomplex bacteria. This present study aimed at determining if the CRISPR array inSalmonellaspp. could be applied to establish a correlationship between serogroup and the fingerprint generated by CRISPR typing.Methodology and resultsA total of 30 samples were obtained from Diagnostic Veterinary Laboratory, Kota Kinabalu, Sabah. Serogroup was determined on the basis of ELISA (enzyme-linked immunosorbent assay). Four different serogroups were identified which were serogroup B, C, D, and E. DNA (deoxyribonucleic acid) was extracted and PCR (polymerase chain reaction) was performed using primers which were designed to amplify the CRISPR array inSalmonellagenome. Our results indicate that there is a correlationship between serogroup obtained using ELISA and the profile generated by CRISPR typing.Conclusion, significance and impact of studyCRISPR typing has the potential to be applied for the genotyping ofSalmonella.

Detection and differentiation of Norwalk virus by reverse transcription-polymerase chain reaction and enzyme-linked immunosorbent assay

2002 ◽  
Vol 68 (2) ◽  
pp. 285-290 ◽  
Author(s):  
Masatoshi Tatsumi ◽  
Shuji Nakata ◽  
Yoshiyuki Sakai ◽  
Shinjiro Honma ◽  
Kazuko Numata-Kinoshita ◽  
...  
Keyword(s):  
Polymerase Chain Reaction ◽  
Immunosorbent Assay ◽  
Reverse Transcription ◽  
Enzyme Linked Immunosorbent Assay ◽  
Norwalk Virus ◽  
Chain Reaction ◽  
Polymerase Chain

scholarly journals Enzyme-Linked Immunosorbent Assay Testing of Shoots Grown In Vitro and the Use of Immunocapture-Reverse Transcription-Polymerase Chain Reaction Improve the Detection of Prunus necrotic ringspot virus in Rose

2000 ◽  
Vol 90 (5) ◽  
pp. 522-528 ◽  
Author(s):  
Benoît Moury ◽  
Loïc Cardin ◽  
Jean-Paul Onesto ◽  
Thierry Candresse ◽  
Alain Poupet
Keyword(s):  
Polymerase Chain Reaction ◽  
Immunosorbent Assay ◽  
Reverse Transcription ◽  
Shoot Tips ◽  
Enzyme Linked Immunosorbent Assay ◽  
Chain Reaction ◽  
Simple Method ◽  
Mother Plants ◽  
Polymerase Chain

We developed and evaluated two different methods to improve the detection of the most prevalent virus of rose in Europe, Prunus necrotic ring-spot virus (PNRSV). Immunocapture-reverse transcription-polymerase chain reaction was estimated to be about 100 times more sensitive than double-antibody sandwich-enzyme-linked immunosorbent assay (DAS-ELISA) and showed an equivalent specificity. Based on the observation that PNRSV multiplies actively in young growing tissues (axillary shoots and cuttings), an in vitro culture method allowing rapid (about 15 days) and homogeneous development of dormant axillary buds with high virus titers was standardized. ELISA tests of these young shoots showed, in some cases, a 104 to 105 increase in sensitivity in comparison to adjacent leaf tissues from the rose mother plants. Between 21 and 98% (depending on the season) more samples were identified as positive by using ELISA on samples from shoot tips grown in vitro rather than on leaves collected directly from the PNRSV-infected mother plants. This simple method of growing shoot tips in vitro improved the confidence in the detection of PNRSV and eliminated problems in sampling appropriate tissues.

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