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22<br />

(2008) analyzed the genetic relatedness <strong>and</strong> geographical distribution <strong>of</strong> V.<br />

parahaemolyticus from the environment <strong>and</strong> cl<strong>in</strong>ical stra<strong>in</strong>s us<strong>in</strong>g seven house<br />

keep<strong>in</strong>g genes (dnE, gyrB, recA, dtdA, pntA, pyrC, tnaA).<br />

2.7.5 Molecular <strong>and</strong> genetic <strong>characteristics</strong> <strong>of</strong> environmental Vibrio<br />

Vibrio <strong>species</strong> are widely distributed <strong>in</strong> the aquatic environment <strong>and</strong> are<br />

considered as autochthonous bacteria <strong>in</strong> the estuar<strong>in</strong>e <strong>and</strong> mar<strong>in</strong>e waters (Nishibuchi<br />

<strong>and</strong> Kaper, 1995). Scientists isolated <strong>and</strong> identified this organism <strong>in</strong> the mar<strong>in</strong>e water<br />

(Faruque et al., 2004, Nair et al., 1988), shrimp <strong>and</strong> oysters (Dalsgaard et al., 1995 a,<br />

Gopal et al., 2005, Sobr<strong>in</strong>ho et al., 2010), sediments (Bhaskar <strong>and</strong> Setty, 1994),<br />

plankton (Lipp <strong>and</strong> Rose, 1997), <strong>and</strong> also from the seafood (Chitov et al., 2009 b,<br />

Sujeewa et al., 2009). Many <strong>in</strong>vestigations were carried out to identify genetic <strong>and</strong><br />

phenotypic differences between cl<strong>in</strong>ical <strong>and</strong> environmental <strong>vibrio</strong>s.<br />

V. cholerae serogroups O1 <strong>and</strong> O139 caused the epidemics <strong>of</strong> cholera. But<br />

other non O1 <strong>and</strong> non O139 serogroups can cause sporadic diarrhoea. Environmental<br />

stra<strong>in</strong>s ma<strong>in</strong>ly belong to V. cholerae serogroup non O1 <strong>and</strong> non O 139 (Faruque et al.,<br />

2004). Cl<strong>in</strong>ical stra<strong>in</strong>s carry the virulence factors for cholera tox<strong>in</strong> (CT) <strong>and</strong> tox<strong>in</strong>-<br />

coregulated pilus (TCP) which is central to the disease process <strong>and</strong> provide adhesion<br />

for the tox<strong>in</strong>s respectively (Chakraborty et al., 2000). Studies found that<br />

environmental stra<strong>in</strong>s <strong>of</strong> V. cholerae rarely carried CT <strong>and</strong> TCP. Water samples from<br />

two major rivers <strong>of</strong> Bangladesh were <strong>in</strong>vestigated for the <strong>pre</strong>sence <strong>of</strong> V. cholerae <strong>and</strong><br />

their virulence associated genes. V. cholerae non O1 <strong>and</strong> non O139 was found <strong>in</strong><br />

89.9% (116/125) <strong>and</strong> 3.2% (4/125) were V. cholerae O1 (Faruque et al., 2004). These<br />

authors found one V. cholerae O1 carry<strong>in</strong>g the TCP <strong>and</strong> CT gene (0.8%) <strong>in</strong> those<br />

environmental samples. Nair et al. (1988) carried out an <strong>in</strong>vestigation on V. cholerae<br />

non O1 from environmental sources <strong>in</strong> India, to describe tox<strong>in</strong> pr<strong>of</strong>ile. They exam<strong>in</strong>ed<br />

for the production <strong>of</strong> CT, shiga-like tox<strong>in</strong> (vero tox<strong>in</strong>), heat stable enterotox<strong>in</strong> <strong>and</strong><br />

haemolys<strong>in</strong>s. Two <strong>of</strong> the stra<strong>in</strong>s (0.5%) produced CT; none <strong>of</strong> them produced shiga-<br />

like tox<strong>in</strong> or heat stable enterotox<strong>in</strong>s. Haemolytic activity was observed <strong>in</strong> 89.7% <strong>of</strong><br />

the stra<strong>in</strong>s. The authors concluded that only a small percentage <strong>of</strong> environmental V.<br />

cholerae non O1 has the ability <strong>of</strong> caus<strong>in</strong>g cholera like symptoms (Nair et al., 1988).

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