PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2012 | 19 | 2 |

Tytuł artykułu

Efficacy of the detection of Legionella in hot and cold water samples by culture and PCR. I. Standardization of methods

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The aim of the present study was: – to compare methods for concentration and isolation of Legionella DNA from water; – to examine the efficacy of various modifications of PCR test (PCR, semi-nested PCR, and real-time PCR) for the detection of known numbers of Legionella pneumophila in water samples artificially contaminated with the strain of this bacterium and in randomly selected samples of environmental water, in parallel with examination by culture. It was found that filtration is much more effective than centrifugation for the concentration of DNA in water samples, and that the Qiamp DNA Mini-Kit is the most efficient for isolation of Legionella DNA from water. The semi-nested PCR and real-time PCR proved to be the most sensitive methods for detection of Legionella DNA in water samples. Both PCR modifications showed a high correlation with recovery of Legionella by culture (p<0.01), while no correlation occurred between the results of one-stage PCR and culture (p>0.1).

Słowa kluczowe

Wydawca

-

Rocznik

Tom

19

Numer

2

Opis fizyczny

p.289-293,fig.,ref.

Twórcy

  • Department of Zoonoses, Institute of Rural Health, Lublin, Poland
autor
  • Department of Water and Soil Safety, Institute of Rural Health, Lublin, Poland
  • Department of Zoonoses, Institute of Rural Health, Lublin, Poland

Bibliografia

  • 1. Stojek NM, Dutkiewicz J. Legionella and other Gram-negative bacteria in potable water from various rural and urban sources. Ann AgricEnviron Med. 2006; 13: 323-335.
  • 2. Dussere E, Ginevra C, Hallier-Soulier S, Vandenesch F, Festoc G, Etienne J, Jarraud S, Molmeret M. A PCR-based method for monitoringLegionella pneumophila in water samples detects viable but noncultivablelegionellae that can recover their cultivability. Appl Environ Microbiol.2008; 74: 4817-4824.
  • 3. Wellinghausen N, Frost C, Marre R. Detection of legionellae in hospital water samples by quantitative real-time LightCycler PCR. Appl EnvironMicrobiol. 2001; 67: 3985-3993.
  • 4. Szénási Z, Endo T, Yagita K, Veréb I, Nagy E. Epidemiology and laboratory diagnostics of legionellae. Orv Hetil. 2001; 142: 1035-1043.
  • 5. Joly P, Falconnet P-A, André J, Weill N, Reyrolle M, Vandenesch F, Maurin M, Etienne J, Jarraud S. Quantitative real-time Legionella PCRfor environmental water samples: data interpretation. Appl EnvironMicrobiol. 2006; 72: 2801-2808.
  • 6. Yaradou DF, Hallier-Soulier S, Moreau S, Poty F, Hillion Y, Reyrolle M, André J, Festoc G, Delabre K, Vandenesch F, Etienne J, Jarraud S.Integrated real-time PCR for detection and monitoring of Legionellapneumophila in water systems. Appl Environ Microbiol. 2007; 73: 1452-1456.
  • 7. Morio F, Corvec S, Caroff N, Le Gallou F, Drugeon H, Reynaud A. Real-time PCR assay for the detection and quantification of Legionellapneumophila in environmental water samples: utility for daily practice.Int J Hyg Environ Health. 2008; 211: 403-411.
  • 8. Guillemet TA, Lévesque B, Gauvin D, Brousseau N, Giroux JP, Cantin P. Assessment of real-time PCR for quantification of Legionella spp. inspa water. Lett Appl Microbiol. 2010; 51: 639-644.
  • 9. Lee JV, Lai S, Exner M, Lenz J, Gaia V, Casati S, Hartemann P, Lück C, Pangon B, Ricci ML, Scaturro M, Fontana S, Sabria M, Sánchez I,Assaf S, Surman-Lee S. An international trial of quantitative PCR formonitoring Legionella in artificial water systems. Appl Microbiol. 2011.doi: 10.1111/j.1365-2672.2011.04957.x.
  • 10. Ahmadinejad M, Shakibaie MR, Shams K, Khalili M. Detection of Legionella pneumophila in cooling water systems of hospitals andnursing homes of Kerman City, Iran by semi-nested PCR. Int J BiolLife Sci. 2011; 7: 2.
  • 11. Delgado-Viscogliosi P, Solignac L, Delattre JM. Viability PCR, a cultureindependent method for rapid and selective quantification of viableLegionella pneumophila cells in environmental water samples. ApplEnviron Microbiol. 2009; 75: 3502-3512.
  • 12. Fittipaldi M, Codony F, Adrados B, Camper AK, Morató J. Viable realtime PCR in environmental samples: can all data be interpreted directly?Microb Ecol. 2011; 61: 7-12.
  • 13. Atlas RM, Parks LC. Handbook of Microbiological Media. CRC Press, Boca Raton 1993.
  • 14. Maleszewska J, Krogulska B, Bielecka Z, Stypułkowska-Misiurewicz H. Presence of Yersinia organism in the water from private wells. RocznPZH 1988; 39: 396-403.
  • 15. Matuszewska R, Krogulska B. Detection and isolation of bacteria of genus Legionella from water environment. Roczn PZH 2000; 51: 183-190.
  • 16. Stypułkowska-Misiurewicz H, Krogulska B, Pancer K, Matuszewska R. Legionella sp. – investigation of human infection and detection inenvironmental water. Roczn PZH 2001; 52: 1-18 (in Polish).
  • 17. Yanez MA, Barberá VM, Catalán V. Validation of a new seminested PCR-based detection method for Legionella pneumophila. J Microbiol Methods. 2007; 70: 214-217.

Uwagi

rekord w opracowaniu

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-9b541526-796a-4a7b-8660-3e9040206f05
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.