DEVELOPMENT OF THE ALGORITHM FOR IDENTIFICATION OF THE LEVEL OF VIBRIO CHOLERAE CTXA AND TOXR GENE EXPRESSION USING RT-PCR WITH REAL-TIME HYBRIDIZATION-FLUORESCENT REGISTRATION OF RESULTS
https://doi.org/10.21055/0370-1069-2017-3-53-57
Abstract
Objective of the study is to design the algorithm for assessment of expression of the structural and regulatory virulence Vibrio cholerae genes by the model of ctxA and toxR genes encoding and controlling biosynthesis of cholera toxin.
Materials and methods. Utilized were 10 strains of Vibrio cholerae, classical and El Tor biovars. Cloning of gene fragments was carried out through transformation and ligation. RT-PCR was done in “BIS M112” and “Rotor-GeneQ” amplifiers. Processing of the results was performed by means of the software package in set with Rotor-GeneQ (Software 1.8.17.5).
Results and conclusions. Developed has been the algorithm for evaluation of the level of expression of V. cholerae ctxA and toxR genes applying RT-PCR with real-time hybridization-fluorescent registration of results. The stated algorithm allows for rapid and effective statistically significant specification of the expression of structural and regulatory virulence V. cholerae genes and can be used for evaluation of newly discovered cholera vibrio strains.
About the Authors
A. A. KritskyRussian Federation
46, Universitetskaya St., Saratov, 410005
N. B. Cheldyshova
Russian Federation
46, Universitetskaya St., Saratov, 410005
I. V. Tuchkov
Russian Federation
46, Universitetskaya St., Saratov, 410005
N. I. Smirnova
Russian Federation
46, Universitetskaya St., Saratov, 410005
References
1. Smirnova N.I., Cheldyshova N.B., Zadnova S.P., Kutyrev V.V. [Molecular-genetic peculiarities of Vibrio cholerae classica strains that caused epidemic of Asian cholera in Russia in 1942]. Mol. Genet. Mikrobiol., Virusol. 2001; 4: 12–6.
2. Creating Standard Curves with genomic DNA or plasmid DNA templates for use in quantitative PCR. Applied Biosystems; 2003.
3. Livak K.J., Schmittgen T.D. Analysis of relative gene expression data using Real-Time quantitative PCR and the 2–ΔΔCt Method. Methods. 2001; 25(4):402–8. DOI: 10.1006/meth.2001.1262.
4. Malinen E., Kassinen A., Rinttila Т., Palva A. Comparison of real-time PCR with SYBR Green I or 5’-nuclease assays and dot-blot hybridization with rDNA-targeted oligonucleotide probes in quantification of selected faecal bacteria. Microbiology. 2003; 149(Pt 1):269–77. DOI: 10.1099/mic.0.25975-0.
5. Marashi S.M., Bakhshi B., Fooladi A.A., Tavakoli A., Sharifnia A., Pourshafie M.R. Quantitative expression of cholera toxin mRNA in Vibrio cholerae isolates with different CTX cassette arrangements. J. Med. Microbiol. 2012; 61(Pt 8):1071–3. DOI: 10.1099/jmm.0.038752-0.
6. Matson J.S., Withey J.H., DiRita V.J. Regulatory networks controlling Vibrio cholerae virulence gene expression. Infect. Immun. 2007; 75(12):554–29. DOI: 10.1128/IAI.01094-07.
7. Muller P.Y., Janovjak H., Miserez A.R., Dobbie Z. Processing of gene expression data generated by quantitative Real-Time RT-PCR. Biotechniques. 2002; 32(6):1372–9.
8. Palmer S., Wiegand A.P., Maldarelli F., Bazmi H., Mican J.M., Polis М., Dewar R.L., Planta A., Liu S., Metcalf J.A., Mellors J.W., Coffin J.M. New real-time reverse transcriptase-initiated PCR assay with single-copy sensitivity for human immunodeficiency virus type 1 RNA in plasma. J. Clin. Microbiol. 2003; 41(10):4531–6.
9. Sharkey F.H., Banat I.M., Marchant R. Detection and quantification of gene expression in environmental bacteriology. Appl. Environ. Microbiol. 2004; 70(7):3795–806. DOI: 10.1128/AEM.70.7.3795–3806.2004.
10. Smith C.J., Osborn A.M. Advantages and limitations of quantitative PCR(Q-PCR)-based approaches in microbial ecology. FEMS Microbiol. Ecol. 2009; 67(1):6–20. DOI: 10.1111/j.1574-6941.2008.00629.x.
11. Wang Т., Brown M.J. mRNA quantification by real time TaqMan polymerase chain reaction: validation and comparison with RNase protection. Anal. Biochem. 1999; 269(1):198–201. DOI: 10.1006/abio.1999.4022.
12. Fykse E.M., Skogan G., Davies W., Olsen J.S., Blatny J.M. Detection of Vibrio cholerae by real-time nucleic acid sequence-based amplification. Appl. Environ. Microbiol. 2007; 73(5):1457–66. DOI: 10.1128/AEM.01635-06.
Review
For citations:
Kritsky A.A., Cheldyshova N.B., Tuchkov I.V., Smirnova N.I. DEVELOPMENT OF THE ALGORITHM FOR IDENTIFICATION OF THE LEVEL OF VIBRIO CHOLERAE CTXA AND TOXR GENE EXPRESSION USING RT-PCR WITH REAL-TIME HYBRIDIZATION-FLUORESCENT REGISTRATION OF RESULTS. Problems of Particularly Dangerous Infections. 2017;(3):53-57. (In Russ.) https://doi.org/10.21055/0370-1069-2017-3-53-57