Culturability and Viability of Salmonella Typhimurium during Photo-Fenton Process at pH 5.5 under Solar Simulated Irradiation

Abstract

Culturability and viability techniques such as plate count on solid agar (PC), Most Probable Number (MPN) and Direct Viable Count-Fluorescence in Situ Hybridation (DVC FISH) were used to study the inactivation of Salmonella typhimurium by photo-Fenton process at pH 5.5. In the presence of only simulated solar irradiation (500 W·m-2), S. typhimurim showed that both culturability measured by MPN and viability (measured by DVC FISH) underwent just a slight decreasing of 2 and 1 log respectively after 240 min of light exposition while culturability measured by PC did not show any change. Results after 48 h of dark conditions did not reveal re-growth. However, when experiment was carried out in the presence of 2 mg L-1 of Fe3+ and 20 mg L-1 of H2O2 and pH 5.5, culturability was strongly affected after 240 min of simulated solar irradiation; nevertheless, viability was only slightly altered (~1 log). During dark period of 48 h changes on culturability and viability were not observed. On the other hand, it was also found that sugar metabolism was affected rather the amino-acids in S. typhimurium cells irradiated at different times upon photo-Fenton conditions. These findings might suggest for the first time that photo-Fenton process at pH 5.5 could induce viable but nonculturable state (VBNC) on waterborne S. typhimurium and that probably sugar metabolism damage could activate the VBNC state.

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J. Rengifo-Herrera, O. Castaño and I. Sanabria, "Culturability and Viability of Salmonella Typhimurium during Photo-Fenton Process at pH 5.5 under Solar Simulated Irradiation," Journal of Water Resource and Protection, Vol. 5 No. 8A, 2013, pp. 21-27. doi: 10.4236/jwarp.2013.58A003.

Conflicts of Interest

The authors declare no conflicts of interest.

References

[1] J. J. Pignatello, E. Oliveros and A. MacKay, “Advanced Oxidation Processes for Organic Contaminant Destruction Based on the Fenton Reaction and Related Chemistry,” Critical Reviews in Environmental Science and Technology, Vol. 36, No. 1, 2006, pp. 1-84. doi:10.1080/10643380500326564
[2] A. G. Rincon and C. Pulgarin, “Comparative Evaluation of Fe3+ and TiO2 Photoassisted Processes in Solar Photocatalytic Disinfection of Water,” Applied Catalysis B: Environmental, Vol. 63, No. 3-4, 2006, pp. 222-231. doi:10.1016/j.apcatb.2005.10.009
[3] S. Malato, P. Fernández-Ibanez, M. I. Maldonado, J. Blanco and W. Gernjak, “Decontamination and Disinfection of Water by Solar Photocatalysis: Recent Overview and Trends,” Catalysis Today, Vol. 147, No. 1, 2009, pp. 1-59. doi:10.1016/j.cattod.2009.06.018
[4] D. Spuhler, J. A. Rengifo-Herrera and C. Pulgarin, “The Effect of Fe2+, Fe3+, H2O2 and the Photo-Fenton Reagent at near Neutral pH on the Solar Disinfection (SODIS) at Low Temperatures of Water Containing Escherichia coli K-12,” Applied Catalysis B: Environmental, Vol. 96, No. 1-2, 2010, pp. 126-141. doi:10.1016/j.apcatb.2010.02.010
[5] I. García-Fernández, M. I. Polo-López, I. Oller and P. Fernández-Ibánez, “Bacteria and Fungi Inactivation Using Fe3+/Sunlight, H2O2/Sunlight and near Neutral Photo-Fenton: A Comparative Study,” Applied Catalysis B: Environmental, Vol. 121-122, 2012, pp. 20-29. doi:10.1016/j.apcatb.2012.03.012
[6] M. Berney, H.-U. Weilenmann, A. Simonetti and T. Egli, “Efficacy of Solar Disinfection of Escherichia coli, Shigella flexneri, Salmonella typhimurium and Vibrio cholera,” Journal of Applied Microbiology, Vol. 101, No. 4, 2006, pp. 828-836. doi:10.1111/j.1365-2672.2006.02983.x
[7] F. Sciacca, J. A. Rengifo-Herrera, J. Wéthé and C. Pulgarin, “Dramatic Enhancement of Solar Disinfection (SO-DIS) of Wild Salmonella sp. in PET Bottles by H2O2 Addition on Natural Water of Burkina Faso Containing Dissolved Iron,” Chemosphere, Vol. 78, No. 9, 2010, pp. 1186-1191. doi:10.1016/j.chemosphere.2009.12.001
[8] A. Moncayo-Lasso, L. E. Mora-Arizmendi, J. A. Rengifo-Herrera, J. Sanabria, N. Benitez and C. Pulgarin, “The Detrimental Influence of Bacteria (E. coli, Shigella and Salmonella) on the Degradation of Organic Compounds (and Vice-Versa) in TiO2 Photocatalysis and near Neutral Photo-Fenton Processes under Simulated Solar Light,” Photochemical & Photobiological Sciences, Vol. 11, No. 5, 2012, pp. 821-827. doi:10.1039/c2pp05290c
[9] D. B. Roszak and R. R. Colwell, “Survival Strategies of Bacteria in the Natural Environment,” Microbiological Reviews, Vol. 51, No. 3, 1987, pp. 365-379.
[10] G. V. Mukamolova, A. S. Kaprylants, D. B. Kell and M. Young, “Adoption of the Transiently Non-Culturable State: A Bacterial Survival Strategy?” Advances in Microbial Physiology, Vol. 47, 2003, pp. 65-129. doi:10.1016/S0065-2911(03)47002-1
[11] A. P. Caro, J. Got, S. Lesne, A. Binard and B. Baleux, “Viability and Virulence of Experimentally Stressed Nonculturable Salmonella typhimurium,” Applied and Environmental Microbiology, Vol. 65, No. 7, 1999, pp. 3229-3232.
[12] J. S. Lesne, S. Berthet, A. Binard, J. Rouxel and F. Humbert, “Changes of Culturability and Virulence of Salmonella typhimurium during Long-Term Starvation under Dessicating Conditions,” International Journal of Food Microbiology, Vol. 60, No. 2-3, 2000, pp. 195-203. doi:10.1016/S0168-1605(00)00311-1
[13] L. A. Bjergbaek and P. Roslev, “Formation of Nonculturable Escherichia coli in Drinking Waters,” Journal of Applied Microbiology, Vol. 99, No. 5, 2005, pp. 1090-1098. doi:10.1111/j.1365-2672.2005.02706.x
[14] C. Almeida, N. F. Azevedo, R. M. Fernandez, C. W. Keewil and M. J. Vieira, “Fluorescent in Situ Hybridization Method Using a Peptide Nucleic Acid Probe for Identification of Salmonella spp. in a Broad Spectrum Samples,” Applied and Environmental Microbiology, Vol. 76, No. 13, 2010, pp. 4476-4485. doi:10.1128/AEM.01678-09
[15] T. García-Armisen and P. Servais, “Enumeration of Viable E. coli in Rivers and Wastewaters by Fluorescent in situ Hybridization,” Journal of Microbiological Methods, Vol. 58, No. 2, 2004, pp. 269-279. doi:10.1016/j.mimet.2004.04.014
[16] S. P. Rivera, L. Flores and J. Sanabria, “Standardization of a Quantification Method for Salmonella spp. and Shigella spp. in Specific Liquid Media,” Colombia Médica, Vol. 41, No. 1, 2010, pp. 60-70.
[17] R. I. Amann, L. Krumholz and D. A. Stahl, “Fluorescent-Oligonucleotide Probing of Whole Cells for Determinative, Phylogenetic, and Environmental Studies in Microbiology,” Journal of Bacteriology, Vol. 172, No. 2, 1990, pp. 762-770.
[18] K. Kogure, U. Simidu and N. A. Taga, “A Tentative Direct Microscopic Method for Counting Living Marine Bacteria,” Canadian Journal of Microbiology, Vol. 25, No. 3, 1979, pp. 415-420.
[19] Regnault, S. Martin-Delautre and P. Grimont, “Problems Associated with the Direct Viable Count Procedure Applied to Gram-Positive Bacteria,” International Journal of Food Microbiology, Vol. 55, No. 1, 2000, pp. 281-284. doi:10.1016/S0168-1605(00)00204-X
[20] S. Norsdentoft, H. Christensen and H. C. Wegener, “Evaluation of a Fluorescence Labelled Oligonucleotide Probe Targeting 23S rRNA for in Situ Detection of Salmonella serovars in Paraffin-Embedded Tissue Sections and Their Rapid Identification in Bacterial Smears,” Journal of Clinical Microbiology, Vol. 35, No. 10, 1997, pp. 2642-2648.
[21] A. G. Rincon and C. Pulgarin, “Bactericidal Action of Illuminated TiO2 on Pure Escherichia coli and Natural Bacteria Consortia: Post Irradiation Events in the Dark and Assessment of the Effective Disinfection Time,” Applied Catalysis B: Environmental, Vol. 49, No. 2, 2004, pp. 99-112. doi:10.1016/j.apcatb.2003.11.013
[22] W. A. M. Hijnen, E. F. Beerendonk and G. J. Medema, “Inactivation Credit of UV Radiation for Viruses, Bacteria and Protozoan (oo)Cysts in Water: A Review,” Water Research, Vol. 40, No. 1, 2006, pp. 3-22. doi:10.1016/j.watres.2005.10.030
[23] R. B. Kapuscinski and R. Mitchell, “Solar Irradiation Induces Sublethal Injury in Escherichia coli in Seawater,” Applied and Environmental Microbiology, Vol. 41, No. 3, 1981, pp. 670-674.
[24] J. A. Imlay, “Cellular Defenses against Superoxide and Hydrogen Peroxide,” Annual Review of Biochemistry, Vol. 77, No. 1, 2008, pp. 755-776. doi:10.1146/annurev.biochem.77.061606.161055
[25] H. Gallard, J. De Laat and B. Legube, “Spectrophotometric Study of the Formation of Iron(III)—Hydroperoxy Complexes in Homogeneous Aqueous Solutions,” Water Research, Vol. 33, No. 13, 1999, pp. 2929-2936. doi:10.1016/S0043-1354(99)00007-X
[26] J. D. Oliver, “Recent Findings of on the Viable but Non Culturable State in Pathogenic Bacteria,” FEMS Microbiology Reviews, Vol. 34, No. 4, 2010, pp. 415-425.
[27] L. Fang, P. Cai, W. Chen, W. Liang, Z. Hong and Q. Huang, “Impact of Cell Wall Structure on the Behaviour of Bacterial Cells in the Binding of Cooper and Cadmium,” Colloid Surface A, Vol. 347, No. 1, 2009, pp. 50-55. doi:10.1016/j.colsurfa.2008.11.041
[28] Z. Cheng and Y. Li, “What Is Responsible for the Initiating Chemistry of Iron-Mediated Lipid Peroxidation: An update,” Chemical Reviews, Vol. 107, No. 3, 2007, pp. 748-766. doi:10.1021/cr040077w
[29] A. Chatti, N. Messaoudi, M. Mihoub and A. Landoulsi, “Effects of Hydrogen Peroxide on the Motility, Catalase and Superoxide Dismutase of Dam and/or seqA Mutant of Salmonella typhimurium,” World Journal of Microbiology and Biotechnology, Vol. 28, No. 1, 2012, pp. 129-133. doi:10.1007/s11274-011-0801-8
[30] M. R. Barer, R. J. Smith, R. P. Cooney and P. T. Kimmitt, “Relationships between Culturability, Activity and Virulence in Pathogenic Bacteria,” Journal of Infection and Chemotherapy, Vol. 6, No. 2, 2000, pp. 108-111. doi:10.1007/PL00012148
[31] I.-S. Kong, T. C. Bates, A. Hülsmann, H. Hassan, B. E. Smith and J. D. Oliver, “Role of Catalase and oxyR in the Viable but Nonculturable State of Vibrio vulnificus,” FEMS Microbiology Ecology, Vol. 50, No. 3, 2004, pp. 133-142. doi:10.1016/j.femsec.2004.06.004
[32] I. J. Sanabria, J. Wist and C. Pulgarin, “Photocatalytic Disinfection Treatments: Viability, Culturability and Metabolic Changes of E. coli Using Different Measurement Methods,” DYNA-Colombia, Vol. 78, No. 166, 2011, pp. 150-157.
[33] J. D. Oliver, M. Dagher and K. Linden, “Induction of Escherichia coli and Salmonella typhimurium into the Viable but Nonculturable State Following Chlorination of Wastewater,” Journal of Water and Health, Vol. 3, No. 3, 2005, pp. 249-257.

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