Evaluation of the NASBA nucleic acid amplification system for assessment of the viability of Campylobacter jejuni.

Although NASBA uses RNA as a target molecule for amplification, the nucleic acid amplification system cannot be used for differentiating viable and non-viable C. jejuni. It was shown that 16S rRNA, or the defined sequence within the 16S rRNA enclosed by the primer set applied, is fairly stable and resistant to heating at 100 degrees C. False-positive results can occur in case of direct NASBA detection of C. jejuni in foods. These false positive results due to amplification of RNA from dead cells were eliminated by prior selective enrichment in Preston medium for 24 h at 42 degrees C.

[1]  P. L. Griffiths Morphological changes of Campylobacter jejuni growing in liquid culture , 1993, Letters in applied microbiology.

[2]  S. Notermans,et al.  Existing and emerging foodborne diseases. , 1992, International journal of food microbiology.

[3]  M. Uyttendaele,et al.  Comparison of the Nucleic Acid Amplification System NASBA® and Agar Isolation for Detection of Pathogenic Campylobacters in Naturally Contaminated Poultry. , 1996, Journal of food protection.

[4]  M. Salimans,et al.  Rapid and simple method for purification of nucleic acids , 1990, Journal of clinical microbiology.

[5]  K L Josephson,et al.  Polymerase chain reaction detection of nonviable bacterial pathogens , 1993, Applied and environmental microbiology.

[6]  N. Pace,et al.  Microbial ecology and evolution: a ribosomal RNA approach. , 1986, Annual review of microbiology.

[7]  James M. Jay,et al.  Modern food microbiology , 1970 .

[8]  M. Uyttendaele,et al.  Detection of Campylobacter jejuni added to foods by using a combined selective enrichment and nucleic acid sequence-based amplification (NASBA) , 1995, Applied and environmental microbiology.

[9]  M. Uyttendaele,et al.  Identification of Campylobacter jejuni, Campylobacter coli and campylobacter lari by the nucleic acid amplification system NASBAR. , 1994, The Journal of applied bacteriology.

[10]  P. Klatser,et al.  Assessment of mycobacterial viability by RNA amplification , 1994, Antimicrobial Agents and Chemotherapy.

[11]  D. van Strijp,et al.  NASBATM isothermal enzymatic in vitro nucleic acid amplification optimized for the diagnosis of HIV-1 infection , 1991 .

[12]  B. Kaijser Campylobacter jejuni/coli , 1988, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.

[13]  D. Post,et al.  Culture media for the isolation of campylobacters. , 1995, International journal of food microbiology.

[14]  R. Franco,et al.  Campylobacter jejuni/coli : Methodology of Isolation and Possible Interfering Factors in Primary Culture. , 1996, Journal of food protection.

[15]  R. Beumer,et al.  Detection of the coccoid form of Campylobacter jejuni in chicken products with the use of the polymerase chain reaction. , 1994, International journal of food microbiology.

[16]  A. M. Mckay,et al.  Viable but non‐culturable forms of potentially pathogenic bacteria in water , 1992 .

[17]  R. Colwell,et al.  Viable but nonculturable stage of Campylobacter jejuni and its role in survival in the natural aquatic environment , 1986, Applied and environmental microbiology.