2014, Number 2
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Biotecnol Apl 2014; 31 (2)
In vitro modeling of the environmental performance of attenuated strains of Vibrio cholerae O139
Ledón T, Hernández DD, Marrero K, Fando R
Language: Spanish
References: 27
Page: 121-128
PDF size: 388.85 Kb.
ABSTRACT
Vibrio cholerae, serogroups
O1 and
O139, is the causative agent of cholera diarrheal disease. Much of the research aimed to develop oral cholera vaccines is directed to the production of live attenuated strains, such as the
V. cholerae O139 TLP01 and
TLP05 strains. These two strains lack
CTXφ prophage genes and do not produce the hemagglutinin protease, a relevant pathogenesis factor, and the mannose-sensitive hemagglutinin fimbria, which could play an important role in the environmental behavior. In this work, different
in vitro models were used to study the potential environmental performance of these two strains. Their ability to produce different types of biofilms, to acquire rugose phenotype and to resist different environmental stress conditions such as the presence of chlorine, detergents or high salt concentrations, were assessed. Significantly, the
TLP01 and
TLP05 strains displayed characteristics that limit their
in vitro survival under different stress conditions, with respect to controls and wild-type strains. Such behavior under harsh environmental settings may limit their survival and act for their containment while using them as active ingredients for the development of a cholera vaccine candidate.
REFERENCES
Faruque SM, Chowdhury N, Kamruzza- man M, Ahmad QS, Faruque AS, Salam MA, et al. Reemergence of epidemic Vibrio cholerae O139, Bangladesh. Emerg Infect Dis. 2003;9(9):1116-22.
Bishop AL, Camilli A. Vibrio cholerae: lessons for mucosal vaccine design. Expert Rev Vaccines. 2011;10(1):79-94.
Lopez AL, Clemens JD, Deen J, Jodar L. Cholera vaccines for the developing world. Hum Vaccin. 2008;4(2):165-9.
Waldor MK, Mekalanos JJ. Lysogenic conversion by a filamentous phage encoding cholera toxin. Science. 1996;272(5270): 1910-4.
Campos J, Martinez E, Marrero K, Silva Y, Rodriguez BL, Suzarte E, et al. Novel type of specialized transduction for CTX phi or its satellite phage RS1 mediated by filamentous phage VGJ phi in Vibrio chole-rae. J Bacteriol. 2003;185(24):7231-40.
Campos J, Martinez E, Izquierdo Y, Fando R. VEJphi, a novel filamentous phage of Vibrio cholerae able to transduce the cholera toxin genes. Microbiology. 2010; 156(Pt 1):108-15.
Das B, Bischerour J, Barre FX. Molecular mechanism of acquisition of the cholera toxin genes. Indian J Med Res. 2011;133: 195-200.
Ledon T, Ferran B, Perez C, Suzarte E, Vichi J, Marrero K, et al. TLP01, an mshA mutant of Vibrio cholerae O139 as vaccine candidate against cholera. Microbes Infect. 2012;14(11):968-78.
Lipp EK, Huq A, Colwell RR. Effects of global climate on infectious disease: the cholera model. Clin Microbiol Rev. 2002; 15(4):757-70.
Huq A, Sack RB, Nizam A, Longini IM, Nair GB, Ali A, et al. Critical factors influencing the occurrence of Vibrio cholerae in the environment of Bangladesh. Appl Environ Microbiol. 2005;71(8):4645-54.
Kamruzzaman M, Udden SM, Cameron DE, Calderwood SB, Nair GB, Mekalanos JJ, et al. Quorum-regulated biofilms enhance the development of conditionally viable, environmental Vibrio cholerae. Proc Natl Acad Sci USA. 2010;107(4):1588-93.
Chiavelli DA, Marsh JW, Taylor RK. The mannose-sensitive hemagglutinin of Vibrio cholerae promotes adherence to zooplankton. Appl Environ Microbiol. 2001;67(7):3220-5.
Reidl J, Klose KE. Vibrio cholerae and cholera: out of the water and into the host. FEMS Microbiol Rev. 2002;26(2):125-39.
Watnick PI, Kolter R. Steps in the development of a Vibrio cholerae El Tor biofilm. Mol Microbiol. 1999;34(3):586-95.
Watnick PI, Lauriano CM, Klose KE, Croal L, Kolter R. The absence of a flagellum leads to altered colony morphology, biofilm development and virulence in Vibrio cholerae O139. Mol Microbiol. 2001;39(2):223-35.
Yildiz FH, Schoolnik GK. Vibrio cholerae O1 El Tor: identification of a gene cluster required for the rugose colony type, exopolysaccharide production, chlorine resistance, and biofilm formation. Proc Natl Acad Sci USA. 1999;96(7):4028-33.
Kierek K, Watnick PI. The Vibrio cholerae O139 O-antigen polysaccharide is essential for Ca2+-dependent biofilm development in sea water. Proc Natl Acad Sci USA. 2003;100(24):14357-62.
Yildiz FH, Dolganov NA, Schoolnik GK. VpsR, a member of the response regulators of the two-component regulatory systems, is required for expression of vps biosynthesis genes and EPS(ETr)-associated phenotypes in Vibrio cholerae O1 El Tor. J Bacteriol. 2001;183(5):1716-26.
Wai SN, Mizunoe Y, Takade A, Kawabata SI, Yoshida SI. Vibrio cholerae O1 strain TSI-4 produces the exopolysaccharide materials that determine colony morphology, stress resistance, and biofilm formation. Appl Environ Microbiol. 1998; 64(10):3648-55.
Provenzano D, Klose KE. Altered expression of the ToxR-regulated porins OmpU and OmpT diminishes Vibrio cholerae bile resistance, virulence factor expression, and intestinal colonization. Proc Natl Acad Sci USA. 2000;97(18):10220-4.
Van Boekel MAJS. On the use of the Weibull model to describe thermal inactivation of microbial vegetative cells. J Food Microbiol. 2002;74(1-2):139-59.
Lizarraga-Partida ML, Méndez-Gómez E, Rivas-Montano AM, Vargas-Hernández E, Portillo-López A, González-Ramírez AR, et al. Association of Vibrio cholerae with plankton in coastal areas of Mexico. Environ Microbiol. 2009;11(1):201-8.
Sperandio V, Bailey C, Giron JA, DiRita VJ, Silveira WD, Vettore AL, et al. Cloning and characterization of the gene encoding the OmpU outer membrane protein of Vibrio cholerae. Infect Immun. 1996;64(12): 5406-9.
Provenzano D, Lauriano CM, Klose KE. Characterization of the role of the ToxR-modulated outer membrane porins OmpU and OmpT in Vibrio cholerae virulence. J Bacteriol. 2001;183(12):3652-62.
Bina XR, Provenzano D, Nguyen N, Bina JE. Vibrio cholerae RND family efflux systems are required for antimicrobial resistance, optimal virulence factor production, and colonization of the infant mouse small intestine. Infect Immun. 2008;76(8): 3595-605.
Ledón T, Ferran B, Fando R. Estudio de la funcionalidad de ToxR en cepas atenuadas de Vibrio cholerae O139. Rev CENIC Cienc Biol. 2011;42(1):25-28.
Castaneda Chavez Mdel R, Pardio Sedas V, Orrantia Borunda E, Lango Reynoso F. Influence of water temperature and salinity on seasonal occurrences of Vibrio cholerae and enteric bacteria in oyster-producing areas of Veracruz, Mexico. Mar Pollut Bull. 2005;50(12):1641-8.