EVALUATION AND COMPARISON OF DNA EXTRACTION KITS FOR THE DETECTION OF Clostridium difficile IN SPIKED AND FIELD FAECES FROM PIGLETS BY USING REAL-TIME PCR
DOI:
https://doi.org/10.26873/SVR-323-2017Abstract
In complex samples (faeces, soil, food, etc.), Clostridium difficile is often present in the form of dormant spores that cause reduced effectiveness of DNA extraction. With the aim of determining an optimal DNA extraction procedure from spores, DNA extraction from faecal samples spiked with a known number of C. difficile spores and faecal samples from piglets was performed with three manual protocols, using two commercial kits and subsequent real-time PCR (rtPCR) DNA amplification. DNA extraction protocols, including mechanical disruption by bead beating, gave better results with rtPCR. The SmartHelix DNAid Complex Kit proved to be more efficient than the QIAamp DNA Stool Mini Kit, suggesting that an optimal combination of mechanical, enzymatic, and chemical lysis seems to be required for the best results.
Key words: Clostridium difficile; DNA extraction; real-time PCR; piglets; faeces; spores
OVREDNOTENJE IN PRIMERJAVA KOMERCIALNIH KOMPLETOV ZA IZOLACIJO DNK ZA DOKAZOVANJE BAKTERIJE Clostridium difficile V BLATU PRAŠIČKOV Z METODO PCR V REALNEM ČASU
V kompleksnih vzorcih (blato živali, zemlja, hrana, itd.) je bakterija Clostridium difficile pogosto prisotna v obliki spor, ki so vzrok za slabšo učinkovitost izolacije DNK. Da bi določili optimalni postopek izolacije DNK iz spor, smo s tremi različnimi protokoli in uporabo dveh komercialnih kompletov za izolacijo DNK izolirali DNK iz vzorcev blata z znanim številom C. difficile spor in vzorcev blata prašičkov. DNK smo pomnoževali z metodo PCR v realnem času (rtPCR). Boljše rtPCR rezultate smo dobili pri vzorcih, kjer smo pri izolaciji DNK uporabili tudi mehansko razbitje celic s kroglicami. SmartHelix DNAid Complex Kit je bil učinkovitejši komercialni komplet kot QIAamp DNA Stool Mini Kit, kar nakazuje na optimalno kombinacijo mehanske, encimske in kemične lize za najboljši izplen DNK.
Ključne besede: Clostridium difficile; izolacija DNK; spore; PCR v realnem času; prašički; blato
References
(1) Hensgens MPM, Keesen EC, Squire MM, et al. Clostridium difficile infection in community: a zoonotic disease? Clin Microbiol Infect 2012; 18: 635–45.
(2) Banks A, Brown DJ, Mather H, Coia JE, Wiuff C. Sentinel community Clostridium difficile infection (CDI) surveillance in Scotland, April 2013 to March 2014. Anaerobe 2016; 37: 49–53.
(3) Crobach MJT, Dekkers OM, Wilcox MH, Kuijper EJ. European society of clinical microbiology and infectious diseases (ESCMID): data review and recommendations for diagnosing Clostridium difficile-infection (CDI). Clin Microbiol Infect 2009; 15: 1053–66.
(4) Houser BA, Hattel AL, Jayarao BM. Real-time multiplex polymerase chain reaction assay for rapid detection of Clostridium difficile toxin-encoding strains. Foodborne Pathog Dis 2010; 7: 719–26.
(5) Avbersek J, Cotman M, Ocepek M. Detection of Clostridium difficile in animals: comparison of real-time PCR assays with the culture method. J Med Microbiol 2011; 60: 1119–25.
(6) Miller DN, Bryant JE, Madsen EL, Ghiorse WC. Evaluation and optimization of DNA extraction and purification procedures for soil and sediment samples. Appl Environ Microbiol 1999; 65: 4715–24.
(7) Dauphin LA, Moser BD, Bowen MD. Evaluation of five commercial nucleic acid extraction kits for their ability to inactivate Bacillus anthracis spores and comparison of DNA yields from spores and spiked environmental samples. J Microbiol Methods 2009; 76: 30–7.
(8) Freifeld AG, Simonsen KA, Booth CS, et al. A new rapid method for Clostridium difficile DNA extraction and detection in stool. J Mol Diagn 2012; 14: 274–9.
(9) Sorg JA, Dineen SS. Laboratory maintenance of Clostridium difficile. Curr Protoc Microbiol 2009; 12: 9A.1.1–10.
(10) Avbersek J, Zajc U, Micunovic J, Ocepek M. Improved detection of Clostridium difficile in animals by using enrichment culture followed by LightCycler real-time PCR. Vet Microbiol 2013; 64: 93–100.
(11) Burns DA, Minton NP. Sporulation studies in Clostridium difficile. J Microbiol Methods 2011; 87: 133–8.
(12) Logar K, Kopinc R, Bandelj P, Lapanje A, Ocepek M. Evaluation of combined high-efficiency DNA extraction and real-time PCR for detection of Mycobacterium avium subsp. paratuberculosis in subclinically infected dairy cattle: comparison with faecal culture, milk real-time PCR and milk ELISA. BMC Vet Res 2012; 8: e49 (10 pp.)
https://bmcvetres.biomedcentral.com/articles/10.1186/1746-6148-8-49 (Dec. 2016)
(13) Kim BH, Ramanan R, Cho DH, et al. Simple, rapid and cost-effective method for high quality nucleic acids extraction from different strains of Botryococcus braunii. PLoS ONE 2012; 7: e37770 (90 pp.) http://journals.plos.org/plosone/article? id=10.1371/journal.pone.0037770 (Dec. 2016)