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Detection of Enteric Bacteria in Raw Food Samples from Vietnam ...

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24<br />

CHAPTER 1: INTRODUCTION<br />

Virulence plasmids <strong>of</strong> nontyphoidal serotypes are associated with systemic <strong>in</strong>fection <strong>in</strong> both<br />

humans and animals (Jones et al., 1982; Terakado et al., 1983; Gulig and Curtiss III, 1987;<br />

Barrow and Lovell, 1988; Danbara et al., 1992; Fierer et al., 1992; Wallis et al., 1995; Libby<br />

et al., 1997; Rotger and Casadesus, 1999; Bakshi et al., 2003). Among more than 2500<br />

Salmonella serotypes, the virulence plasmid was detected <strong>in</strong> only a small number <strong>of</strong><br />

serotypes, <strong>in</strong>clud<strong>in</strong>g S. Abortusovis, S. Abortusequi, S. Choleraesuis, S. Dubl<strong>in</strong>, S. Enteritidis,<br />

S. Gall<strong>in</strong>arum-Pullorum, S. Typimurium, S. Sendai and S. Paratyphi C (Chiu and Ou, 1996;<br />

Rotger and Casadesus, 1999; Chu and Chiu, 2006). The virulence plasmid appears to be<br />

specific to its host, such as the pSEV plasmid with 60 kb <strong>in</strong> size <strong>in</strong> S. Enteritisis, pSDV <strong>of</strong> 80<br />

kb <strong>in</strong> S. Dubl<strong>in</strong>, 86-kb pSPV <strong>of</strong> S. Gall<strong>in</strong>arum-Pullorum, and 95-kb pSTV plasmid <strong>in</strong><br />

S. Typhimurium and S. Abortusequi (Chu et al., 1999; Chu and Chiu, 2006).<br />

1.2.2. The virulence genes <strong>in</strong> E. coli<br />

Most E. coli are normal components <strong>of</strong> the <strong>in</strong>test<strong>in</strong>al flora, but certa<strong>in</strong> pathogenic stra<strong>in</strong>s carry<br />

virulence genes enabl<strong>in</strong>g <strong>in</strong>test<strong>in</strong>al colonis<strong>in</strong>g and <strong>in</strong>duc<strong>in</strong>g either <strong>in</strong>test<strong>in</strong>al or extra-<strong>in</strong>test<strong>in</strong>al<br />

disease (Orskov and Orskov, 1992; Schroeder et al., 2004). The most frequent cl<strong>in</strong>ical<br />

syndromes caused by a number <strong>of</strong> pathogenic clones <strong>of</strong> E. coli are ur<strong>in</strong>ary tract <strong>in</strong>fections,<br />

bacteremia, men<strong>in</strong>gitis and diarrhoeal disease (Bopp et al., 2003; Dobr<strong>in</strong>dt, 2005; Germon et<br />

al., 2005). In contrast to diarrhoeagenic E.coli, extra<strong>in</strong>test<strong>in</strong>al pathogenic E. coli (ExPEC)<br />

stra<strong>in</strong>s are <strong>in</strong>capable <strong>of</strong> caus<strong>in</strong>g enteric disease but responsible for most extra<strong>in</strong>test<strong>in</strong>al<br />

<strong>in</strong>fections. The <strong>in</strong>fections are caused by three pathotypes: (i) urpathogenic (UPEC) stra<strong>in</strong>s that<br />

cause ur<strong>in</strong>ary tract <strong>in</strong>fections <strong>in</strong> humans, dogs and cats (ii) stra<strong>in</strong>s <strong>in</strong>volved <strong>in</strong> neonatal<br />

men<strong>in</strong>gitis (NMEC) and (iii) stra<strong>in</strong>s that cause septicemia <strong>in</strong> humans and animals (Kuhnert et<br />

al., 2000; Russo and Johnson, 2000; Johnson and Russo, 2002; Bekal et al., 2003).

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