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. 2012 Apr 3:12:51.
doi: 10.1186/1471-2180-12-51.

tkt1, located on a novel pathogenicity island, is prevalent in avian and human extraintestinal pathogenic Escherichia coli

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tkt1, located on a novel pathogenicity island, is prevalent in avian and human extraintestinal pathogenic Escherichia coli

Ganwu Li et al. BMC Microbiol. .

Abstract

Background: Extraintestinal pathogenic Escherichia coli are important pathogens of human and animal hosts. Some human and avian extraintestinal pathogenic E. coli are indistinguishable on the basis of diseases caused, multilocus sequence and phylogenetic typing, carriage of large virulence plasmids and traits known to be associated with extraintestinal pathogenic E. coli virulence.

Results: The gene tkt1 identified by a previous signature-tagged transposon mutagenesis study, was found on a 16-kb genomic island of avian pathogenic Escherichia coli (APEC) O1, the first pathogenic Escherichia coli strain whose genome has been completely sequenced. tkt1 was present in 39.6% (38/96) of pathogenic Escherichia coli strains, while only 6.25% (3/48) of E. coli from the feces of apparently healthy chickens was positive. Further, tkt1 was predominantly present in extraintestinal pathogenic E. coli belonging to the B2 phylogenetic group, as compared to extraintestinal pathogenic E. coli of other phylogenetic groups. The tkt1-containing genomic island is inserted between the metE and ysgA genes of the E. coli K12 genome. Among different extraintestinal pathogenic E. coli of the B2 phylogenetic group, 61.7% of pathogenic Escherichia coli, 80.6% of human uropathogenic E.coli and 94.1% of human neonatal meningitis-causing E. coli, respectively, harbor a complete copy of this island; whereas, only a few avian fecal E. coli strains contained the complete island. Functional analysis showed that Tkt1 confers very little transketolase activity but is involved in peptide nitrogen metabolism.

Conclusion: These results suggest tkt1 and its corresponding genomic island are frequently associated with avian and human ExPEC and are involved in bipeptide metabolism.

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Figures

Figure 1
Figure 1
Prevalence of tkt1 in ExPEC strains.
Figure 2
Figure 2
Genetic organization of the 16 Kb tkt1 genomic island and its flanking regions within the APEC O1 genome, drawn to scale. The ORFs present in this genomic island are listed in the Table 2. There is an islet containing 6 ORFs between the udp and rmuC genes.
Figure 3
Figure 3
The prevalence of tkt1 genomic island in phylogenetic group B2 of ExPEC strains.
Figure 4
Figure 4
Tkt1 could not complement TktA in E. coli K12. 1, APEC O1; 2, APEC O1 Mtkt1; 3, APEC O1 MtktA; 4, BJ502; 5, BJ502-P1; 6, BJ502-P2 and 7 BJ502-P3.

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