期刊论文详细信息
BMC Research Notes
Identification of appropriate reference genes for qPCR studies in Staphylococcus pseudintermedius and preliminary assessment of icaA gene expression in biofilm-embedded bacteria
Scott J Weese1  Thomas WG Gibson2  Devon Metcalf1  Ameet Singh2  Evan C Crawford2 
[1] Department of Pathobiology and Centre for Public Health and Zoonoses, Ontario Veterinary College, University of Guelph, 50 Stone Road, Ontario N1G 2 W1, Canada;Department of Clinical Studies, Ontario Veterinary College, University of Guelph, 50 Stone Road, Ontario N1G 2 W1, Canada
关键词: Reference gene;    Biofilm;    MRSP;    Canine;    qPCR;   
Others  :  1131922
DOI  :  10.1186/1756-0500-7-451
 received in 2014-01-18, accepted in 2014-06-30,  发布年份 2014
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【 摘 要 】

Background

Quantitative PCR is rapidly becoming the standard method for analyzing gene expression in a wide variety of biological samples however it can suffer from significant error if stably expressed reference genes are not identified on which to base the analysis. Suitable reference genes for qPCR experiments on Staphylococcus pseudintermedius have yet to be identified.

Results

Three reference genes in S. pseudintermedius were identified and validated from a set of eight potential genes (proC, gyrB, rplD, rho, rpoA, ftsZ, recA, sodA). Two strains of S. pseudintermedius were used, and primer specificity and efficiency were confirmed and measured. Ranking of the genes with respect to expression stability revealed gyrB, rho and recA as the best reference genes. This combination was used to quantify expression of a single biofilm associated gene, icaA, in logarithmic, stationary and biofilm growth phases, revealing that expression was significantly upregulated in the biofilm growth phase in both strains.

Conclusion

Three reference genes, gyrB, rho and recA, were identified and validated for use as reference genes for quantitative PCR experiments in S. pseudintermedius. Also, the biofilm associated gene icaA was shown to be significantly upregulated in biofilm samples, consistent with its role in biofilm production.

【 授权许可】

   
2014 Crawford et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Weese JS: A review of multidrug resistant surgical site infections. Vet Comp Orthop Traumatol 2008, 21:1.
  • [2]Griffeth GC, Morris DO, Abraham JL, Shofer FS, Rankin SC: Screening for skin carriage of methicillin-resistant coagulase-positive staphylococci and Staphylococcus schleiferi in dogs with healthy and inflamed skin. Vet Dermatol 2008, 19:142-149.
  • [3]Perreten V, Kadlec K, Schwarz S, Andersson UG, Finn M, Greko C, Moodley A, Kania SA, Frank LA, Bemis DA, Franco A, Iurescia M, Battisti A, Duim B, Wagenaar JA, van Duijkeren E, Weese JS, Fitzgerald JR, Rossano A, Guardabassi L: Clonal spread of methicillin-resistant Staphylococcus pseudintermedius in Europe and North America: an international multicentre study. J Antimicrob Chemother 2010, 65:1145-1154.
  • [4]van Duijkeren E, Catry B, Greko C, Moreno MA, Pomba MC, Pyorala S, Ruzauskas M, Sanders P, Threlfall EJ, Torren-Edo J, Torneke K: Review on methicillin-resistant Staphylococcus pseudintermedius. J Antimicrob Chemother 2011, 66:2705-2714.
  • [5]Weese JS, van Duijkeren E: Methicillin-resistant Staphylococcus aureus and Staphylococcus pseudintermedius in veterinary medicine. Vet Microbiol 2010, 140:418-429.
  • [6]Otto M: Staphylococcal Infections: Mechanisms of Biofilm Maturation and Detachment as Critical Determinants of Pathogenicity. Annu Rev Med 2012, 64(1):175-188.
  • [7]Dicicco M, Neethirajan S, Singh A, Weese JS: Efficacy of clarithromycin on biofilm formation of methicillin-resistant Staphylococcus pseudintermedius. BMC Vet Res 2012, 8:225.
  • [8]Fey PD, Olson ME: Current concepts in biofilm formation of Staphylococcus epidermidis. Future Microbiol 2010, 5:917-933.
  • [9]Rohde H, Frankenberger S, Zähringer U, Mack D: Structure, function and contribution of polysaccharide intercellular adhesin (PIA) to Staphylococcus epidermidis biofilm formation and pathogenesis of biomaterial-associated infections. Eur J Cell Biol 2010, 89:103-111.
  • [10]Römling U, Balsalobre C: Biofilm infections, their resilience to therapy and innovative treatment strategies. J Intern Med 2012, 272:541-561.
  • [11]Bustin SA, Benes V, Garson JA, Hellemans J, Huggett J, Kubista M, Mueller R, Nolan T, Pfaffl MW, Shipley GL, Vandesompele J, Wittwer CT: The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments. Clin Chem 2009, 55:611-622.
  • [12]Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, De Paepe A, Speleman F: Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol 2002, 3(7):1-8.
  • [13]Chung PY, Chung LY, Navaratnam P: Identification of novel gene targets in Staphylococcus aureus treated with betulinaldehyde by gene expression profiling analysis. Res Microbiolin press
  • [14]Theis T, Skurray RA, Brown MH: Identification of suitable internal controls to study expression of a Staphylococcus aureus multidrug resistance system by quantitative real-time PCR. J Microbiol Meth 2007, 70:355-362.
  • [15]Singh A, Walker M, Rousseau J, Weese JS: Characterization of the biofilm forming ability of Staphylococcus pseudintermedius from dogs. BMC Vet Res 2013, 9:93.
  • [16]Hellemans J, Mortier G, De Paepe A, Speleman F, Vandesompele J: qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data. Genome Biol 2007, 8(2):R19.
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