Oxidative metabolism in nonculturable Helicobacter pylori and Vibrio vulnificus cells studied by substrate-enhanced tetrazolium reduction and digital image processing

Growing and nonculturable cells of Helicobacter pylori and Vibrio vulnificus were studied for the capacity to reduce tetrazolium salts in order to elucidate the possible physiological basis for the proposed "viable but nonculturable" (VNC) state. Initial difficulties in obtaining consistent reduction of rho-iodonitrotetrazolium violet (INT) by H. pylori led us to develop a method for studying the effect of adding exogenous substrates on these reactions. The established procedure provided a profile of substrate enhancement of oxidative activity revealed by INT reduction which was related to both the identity and physiological state of the organism studied. Representation and interpretation of these enhancement profiles were facilitated by digital image processing. Nonculturable cells of H. pylori produced by carbon and nitrogen starvation in air lost all INT-reducing capacity in 24 h when stored at 37 degrees C, while 99% of those produced at 4 degrees C retained oxidative activity for at least 250 days when tested in the presence but not in the absence of succinate, alpha-ketoglutarate, or aspartate. Activity was detected at similar levels in cells with coccoid and spiral shapes. In contrast, only 1% of nonculturable cells of V. vulnificus, produced under conditions previously reported to induce the VNC state in this organism, retained intrinsic INT-reducing capacity; no substrate-enhanced activity occurred in the remainder of the population. Thus, there was no common pattern of oxidative activity indicative of a VNC state in both test organisms. Nonculturable cells of H. pylori can retain several different oxidative enzyme activities; whether these indicate viability or the persistence of cells as "bags of enzymes" remains to be established.

[1]  J. Dankert,et al.  Transmission of Helicobacter pylori via faeces , 1993, The Lancet.

[2]  J. Oliver Formation of Viable but Nonculturable Cells , 1993 .

[3]  S. Kjelleberg,et al.  Formation of nonculturable Vibrio vulnificus cells and its relationship to the starvation state , 1991, Applied and environmental microbiology.

[4]  R. Colwell,et al.  Use of autoradiography to assess viability of Helicobacter pylori in water , 1993, Applied and environmental microbiology.

[5]  J Becker-Birck,et al.  Simultaneous determination of the total number of aquatic bacteria and the number thereof involved in respiration , 1978, Applied and environmental microbiology.

[6]  S. Kjelleberg,et al.  Resuscitation of Vibrio vulnificus from the viable but nonculturable state , 1991, Applied and environmental microbiology.

[7]  J. Oliver,et al.  Correlation between virulence and colony morphology in Vibrio vulnificus , 1987, Infection and immunity.

[8]  P. Malfertheiner,et al.  The coccoid forms of Helicobacter pylori. Criteria for their viability , 1993, Epidemiology and Infection.

[9]  A. Moran Coccoid forms of Helicobacter pylori. , 1997, Helicobacter.

[10]  P. Somasegaran,et al.  Comparison of the Pour, Spread, and Drop Plate Methods for Enumeration of Rhizobium spp. in Inoculants Made from Presterilized Peat , 1982, Applied and environmental microbiology.

[11]  B. Marshall,et al.  UNIDENTIFIED CURVED BACILLI IN THE STOMACH OF PATIENTS WITH GASTRITIS AND PEPTIC ULCERATION , 1984, The Lancet.

[12]  B. Tripathi Helicobacter pylori--current status. , 1997, The Journal of the Association of Physicians of India.

[13]  H. Ridgway,et al.  Use of a fluorescent redox probe for direct visualization of actively respiring bacteria , 1992, Applied and environmental microbiology.

[14]  C. Harwood,et al.  Detection of induced β‐galactosidase activity in individual non‐culturable cells of pathogenic bacteria by quantitative cytological assay , 1995, Molecular microbiology.

[15]  C. O'Morain,et al.  CAMPYLOBACTER PYLORI AND RECURRENCE OF DUODENAL ULCERS— A 12-MONTH FOLLOW-UP STUDY , 1987, The Lancet.

[16]  D. Weichart,et al.  Low temperature induced non-culturability and killing of Vibrio vulnificus. , 1992, FEMS microbiology letters.

[17]  C. Harwood,et al.  THE VIABLE BUT NON-CULTURABLE HYPOTHESIS AND MEDICAL BACTERIOLOGY , 1993 .

[18]  G. Tytgat,et al.  Helicobacter pylori and peptic ulcer. , 1995, Scandinavian journal of gastroenterology. Supplement.

[19]  D. Graham,et al.  Water source as risk factor for Helicobacter pylori infection in Peruvian children , 1991, The Lancet.

[20]  C. Catrenich,et al.  Characterization of the morphologic conversion of Helicobacter pylori from bacillary to coccoid forms. , 1991, Scandinavian journal of gastroenterology. Supplement.

[21]  J. Oliver,et al.  Temperature effects on the viable but non‐culturable state of Vibrio vulnificus , 1992 .

[22]  A. Curry,et al.  The Genesis of Coccal Forms of Helicobacter pylori , 1990 .

[23]  H. Flemming,et al.  Use of 5-cyano-2,3-ditolyl tetrazolium chloride for quantifying planktonic and sessile respiring bacteria in drinking water , 1993, Applied and environmental microbiology.

[24]  T. Nyström,et al.  Relative changes in incorporation rates of leucine and methionine during starvation survival of two bacteria isolated from marine waters , 1986 .

[25]  J. Errington,et al.  Use of digitized video microscopy with a fluorogenic enzyme substrate to demonstrate cell‐ and compartment‐specific gene expression in Salmonella enteritidis and Bacillus subtilis , 1994, Molecular Microbiology.

[26]  M. Barer,et al.  Factors affecting the selection and use of tetrazolium salts as cytochemical indicators of microbial viability and activity. , 1993, The Journal of applied bacteriology.

[27]  M. Barer,et al.  Serodiagnosis of Helicobacter pylori infection in childhood , 1990, Journal of clinical microbiology.

[28]  G. King,et al.  Application of a Tetrazolium Salt with a Water-Soluble Formazan as an Indicator of Viability in Respiring Bacteria , 1993, Applied and environmental microbiology.