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Seasonal Levels of the Vibrio Predator Bacteriovorax in Atlantic, Pacific, and Gulf Coast Seawater

DOI: 10.1155/2013/375371

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Abstract:

Bacteriovorax were quantified in US Atlantic, Gulf, and Pacific seawater to determine baseline levels of these predatory bacteria and possible seasonal fluctuations in levels. Surface seawater was analyzed monthly for 1 year from Kailua-Kona, Hawaii; the Gulf Coast of Alabama; and four sites along the Delaware Bay. Screening for Bacteriovorax was performed on lawns of V. parahaemolyticus host cells. Direct testing of 7.5?mL portions of seawater from the Atlantic, Pacific, and Gulf coasts gave mean annual counts ≤12.2 PFU. Spikes in counts were observed at 3 out of 4 sites along the Delaware Bay 1 week after Hurricane Sandy. A comparison of summer versus winter counts showed significantly more Bacteriovorax ( ) in the Delaware Bay during the summer and significantly more ( ) in the Gulf during the winter, but no significant seasonal differences ( ) for Hawaiian seawater. Bacteriovorax counts only correlated with seawater salinity and temperature at one Delaware site ( and , resp.). There was a relatively strong negative correlation between temperature and Bacteriovorax levels ( ) for Gulf seawater. Selected isolates were sequenced and identified by phylogenetic analysis as Bacteriovorax clusters IX, X, XI, and XII. 1. Introduction Vibrio parahaemolyticus and Vibrio vulnificus are important foodborne pathogens associated with the consumption of fish and shellfish, especially oysters, which have long been known to bioconcentrate vibrios within their edible tissues [1, 2]. Vibrio vulnificus also causes life-threatening illness from wound infections acquired in the marine environment [3]. Pathogenic vibrios show seasonal predilection in seawater and shellfish, with high counts during warmer months and low to negligible counts during the colder months [2, 4, 5]. Recently, we showed that naturally occurring Bdellovibrio and like organisms (BALOs) from coastal seawater significantly reduced the levels of V. parahaemolyticus and V. vulnificus in seawater and V. parahaemolyticus in seawater and oysters [6]. Among the BALOs are marine and terrestrial forms, with the marine forms associated with Bacteriovorax, which are exclusively saltwater predators [7, 8]. Bacteriovorax have shown preferential predation toward V. parahaemolyticus when compared to a broad range of potential host bacteria [9–12]. This suggests that Bacteriovorax may invade and kill V. parahaemolyticus in seawater more efficiently than other bacterial pathogens. The life cycle of Bacteriovorax and other BALOs usually involve intracellular invasion of and replication within a host cell, although

References

[1]  S. Earampamoorthy and R. S. Koff, “Health hazards of bivalve mollusk ingestion,” Annals of Internal Medicine, vol. 83, no. 1, pp. 107–110, 1975.
[2]  A. DePaola, L. H. Hopkins, J. T. Peeler, B. Wentz, and R. M. McPhearson, “Incidence of Vibrio parahaemolyticus in U.S. Coastal waters and oysters,” Applied and Environmental Microbiology, vol. 56, no. 8, pp. 2299–2302, 1990.
[3]  J. D. Oliver, “Wound infections caused by Vibrio vulnificus and other marine bacteria,” Epidemiology and Infection, vol. 133, no. 3, pp. 383–391, 2005.
[4]  M. T. Kelly, “Effect of temperature and salinity on Vibrio (Beneckea) vulnificus occurrence in a Gulf Coast environment,” Applied and Environmental Microbiology, vol. 44, no. 4, pp. 820–824, 1982.
[5]  M. L. Motes, A. DePaola, D. W. Cook et al., “Influence of water temperature and salinity on Vibrio vulnificus in Northern Gulf and Atlantic Coast oysters (Crassostrea virginica),” Applied and Environmental Microbiology, vol. 64, no. 4, pp. 1459–1465, 1998.
[6]  G. P. Richards, J. P. Fay, K. A. Dickens, M. A. Parent, D. S. Soroka, and E. F. Boyd, “Predatory bacteria as natural modulators of Vibrio parahaemolyticus and Vibrio vulnificus in seawater and oysters,” Applied and Environmental Microbiology, vol. 78, pp. 7455–7466, 2012.
[7]  S. A. Pi?eiro, H. N. Williams, and O. C. Stine, “Phylogenetic relationships amongst the saltwater members of the genus Bacteriovorax using rpoB sequences and reclassification of Bacteriovorax stolpii as Bacteriolyticum stolpii gen. nov., comb. nov,” International Journal of Systematic and Evolutionary Microbiology, vol. 58, no. 5, pp. 1203–1209, 2008.
[8]  H. N. Williams, B.-F. Turng, and J. I. Kelley, “Survival response of Bacteriovorax in surface biofilm versus suspension when stressed by extremes in environmental conditions,” Microbial Ecology, vol. 58, no. 3, pp. 474–484, 2009.
[9]  S. A. Pineiro, O. C. Stine, A. Chauhan, S. R. Steyert, R. Smith, and H. N. Williams, “Global survey of diversity among environmental saltwater Bacteriovoracaceae,” Environmental Microbiology, vol. 9, no. 10, pp. 2441–2450, 2007.
[10]  V. I. Taylor, P. Baumann, J. L. Reichelt, and R. D. Allen, “Isolation, enumeration, and host range of marine Bdellovibrios,” Archives of Microbiology, vol. 98, no. 2, pp. 101–114, 1974.
[11]  A. Sanchez-Amat and F. Torrella, “Formation of stable bdelloplasts as a starvation-survival strategy of marine bdellovibrios,” Applied and Environmental Microbiology, vol. 56, no. 9, pp. 2717–2725, 1990.
[12]  T. D. Rice, H. N. Williams, and B. F. Turng, “Susceptibility of bacteria in estuarine environments to autochthonous Bdellovibrios,” Microbial Ecology, vol. 35, no. 3, pp. 256–264, 1998.
[13]  J. C. Burnham, T. Hashimoto, and S. F. Conti, “Electron microscopic observations on the penetration of Bdellovibrio bacteriovorus into gram-negative bacterial hosts,” Journal of Bacteriology, vol. 96, no. 4, pp. 1366–1381, 1968.
[14]  M. Eksztejn and M. Varon, “Elongation and cell division in Bdellovibrio bacteriovorus,” Archives of Microbiology, vol. 114, no. 2, pp. 175–181, 1977.
[15]  T. M. Rosche, D. J. Smith, E. E. Parker, and J. D. Oliver, “RpoS involvement and requirement for exogenous nutrient for osmotically induced cross protection in Vibrio vulnificus,” FEMS Microbiology Ecology, vol. 53, no. 3, pp. 455–462, 2005.
[16]  H. N. Williams, M. L. Baer, and J. J. Tudor, “Bdellovibrio stolp and starr,” in Bergey’s Manual of Systematic Bacteriology: The Proteobacteria, G. M. Garrity, D. J. Brenner, N. R. Krieg, and J. T. Staley, Eds., vol. 2, pp. 1040–1053, Springer, New York, NY, USA, 2005.
[17]  H. N. Williams, W. A. Falkler Jr., and D. E. Shay, “Seasonal distribution of bdellovibrios at the mouth of the Patuxent River in the Chesapeake Bay,” Canadian Journal of Microbiology, vol. 28, no. 1, pp. 111–116, 1982.
[18]  H. N. Williams, “A study of the occurrence and distribution of bdellovibrios in estuarine sediment over an annual cycle,” Microbial Ecology, vol. 15, no. 1, pp. 9–20, 1988.
[19]  H. Chen, S. Young, T.-K. Berhane, and H. N. Williams, “Predatory bacteriovorax communities ordered by various prey species,” PLoS ONE, vol. 7, no. 3, Article ID e34174, 2012.
[20]  K. Makino, K. Oshima, K. Kurokawa et al., “Genome sequence of Vibrio parahaemolyticus: a pathogenic mechanism distinct from that of V cholerae,” The Lancet, vol. 361, no. 9359, pp. 743–749, 2003.
[21]  H. Nasu, T. Iida, T. Sugahara et al., “A filamentous phage associated with recent pandemic Vibrio parahaemolyticus O3:K6 strains,” Journal of Clinical Microbiology, vol. 38, no. 6, pp. 2156–2161, 2000.
[22]  Y. Davidov, A. Friedjung, and E. Jurkevitch, “Structure analysis of a soil community of predatory bacteria using culture-dependent and culture-independent methods reveals a hitherto undetected diversity of Bdellovibrio-and-like organisms,” Environmental Microbiology, vol. 8, no. 9, pp. 1667–1673, 2006.
[23]  S. Pineiro, A. Chauhan, T. -K. Brehane, R. Athar, G. Zheng, et al., “Niche partition of Bacteriovorax operational taxonomic units along salinity and temporal gradients in the Chesapeake Bay reveals distinct estuarine strains,” Microbial Ecology, vol. 65, pp. 652–660, 2013.
[24]  M. L. Motes and A. DePaola, “Offshore suspension relaying to reduce levels of Vibrio vulnificus in oysters (Crassostrea virginica),” Applied and Environmental Microbiology, vol. 62, no. 10, pp. 3875–3877, 1996.
[25]  M. L. Motes, A. DePaola, D. W. Cook et al., “Influence of water temperature and salinity on Vibrio vulnificus in Northern Gulf and Atlantic Coast oysters (Crassostrea virginica),” Applied and Environmental Microbiology, vol. 64, no. 4, pp. 1459–1465, 1998.
[26]  C. Audemard, H. I. Kator, M. Rhodes et al., “High salinity relay as a postharvest processing strategy to reduce Vibrio vulnificus levels in Chesapeake Bay oysters (Crassostrea virginica),” Journal of Food Protection, vol. 74, no. 11, pp. 1902–1907, 2011.
[27]  B. A. Froelich, T. C. Williams, R. T. Noble, and J. D. Oliver, “Apparent loss of Vibrio vulnificus in North Carolina oysters coincides with drought-induced increase in salinity,” Applied and Environmental Microbiology, vol. 78, pp. 3885–3889, 2012.

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