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Infection and Immunity, September 2002, p. 5335-5337, Vol. 70, No. 9
0019-9567/02/$04.00+0     DOI: 10.1128/IAI.70.9.5335-5337.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Yersinia High-Pathogenicity Island Contributes to Virulence in Escherichia coli Causing Extraintestinal Infections

Sören Schubert,1* Bertrand Picard,2 Stéphanie Gouriou,2 Jürgen Heesemann,1 and Erick Denamur3

Max von Pettenkofer-Institut für Hygiene und Medizinische Mikrobiologie, 80336 Munich, Germany,1 Laboratoire de Bactériologie-Virologie, 29285 Brest Cedex,2 INSERM U 458, Hôpital Robert Debré, 75395 Paris Cedex 19, France3

Received 27 February 2002/ Returned for modification 24 April 2002/ Accepted 11 June 2002


   ABSTRACT
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The Yersinia high-pathogenicity island (HPI) encodes an iron uptake system mediated by the siderophore yersiniabactin (Ybt) and confers the virulence of highly pathogenic Yersinia species. This HPI is also widely distributed in human pathogenic members of the family of Enterobacteriaceae, above all in extraintestinal pathogenic Escherichia coli (ExPEC). In the present study we demonstrate a highly significant correlation of a functional HPI and extraintestinal virulence in E. coli. Moreover, using a mouse infection model, we show for the first time that the HPI contributes to the virulence of ExPEC.


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Highly pathogenic strains of Yersinia pestis, Y. pseudotuberculosis, and Y. enterocolitica biotype IB possess a genomic island designated the high-pathogenicity island (HPI). This 35- to 45-kb island carries a siderophore-mediated iron uptake system named the yersiniabactin (Ybt) locus, which is required for full virulence expression in Yersinia (4). A unique characteristic of the HPI is its wide distribution in different members of the family of Enterobacteriaceae, especially in extraintestinal pathogenic Escherichia coli (ExPEC) causing urinary tract infection, septicemia, and meningitis in newborns (5, 8, 16). The Ybt siderophore system has been shown to be functional in the vast majority of HPI-positive ExPEC strains, indicating a selective pressure for maintenance of this genetic module (16). However, experimental evidence for a direct impact of the HPI on virulence of ExPEC has not yet been obtained. In this study we determined the distribution and the functionality of the HPI and its relation to virulence in a previously described collection of commensal and extraintestinal E. coli strains that had been tested for extraintestinal virulence in a mouse model (14). Our data indicate a high rate of association of a functional HPI with mouse virulence. The same mouse model was used to evaluate the impact of a functional HPI on virulence by examining two wild-type strains from the collection together with their isogenic Ybt synthesis mutants. In this study, we provide first-time evidence of an impact of the HPI on the virulence of ExPEC.

All 82 E. coli strains of the previously described collection (14), representing isolates with different phylogenetic and virulence traits, were examined (i) for the presence of the Yersinia HPI using PCR and Southern hybridization (16, 17) and (ii) for the functionality of the HPI by analysis of Ybt synthesis using a reporter gene-mediated bioassay (16). The strain collection had previously been surveyed for virulence factors, such as attachment factors (pap, sfa/foc, and afa), an E. coli transmembrane protein involved in neonatal meningitis (ibe10), the alpha-hemolysin (hly), and the aerobactin siderophore (aer) (14). Associations between the presence of HPI, the expression of Ybt, the occurrence of other virulence factors, and mouse lethality were determined by {chi}2 tests and calculations of odds ratios using SigmaStat software (version 2.03; SPSS Inc., Richmond, Calif.). The threshold for statistical significance was a P of <0.05. Comparison of the prevalence of HPI within the different phylogenetic groups A, B1, B2, and D (7) was performed by determining Spearman's rank order correlation using SigmaStat software (9).

First we determined the distribution of HPI within the E. coli strain collection with regard to phylogenetic groups. The HPI was found significantly more frequently in E. coli strains of the phylogenetic group B2 (92%) than in strains of groups A (35%) and B1 (48%) (Table 1). This finding corresponds with that of previous studies on the phylogenetic distribution of the HPI (5) and supports the idea that virulence determinants are accumulated in the phylogenetic group B2, to which most of the EXPEC isolates belong (2, 3, 10). More strikingly, the presence of HPI was significantly associated with lethality in mice (Table 2). As the HPI codes for the Ybt siderophore system, we looked at a functional HPI with regard to Ybt production. The HPI was found to be functional in HPI-positive B2 strains (94%) more often than in corresponding strains of group A (71%) and B1 (45%). Ybt production was significantly associated with E. coli strains that were lethal to mice, which killed 2 to 10 out of 10 mice ({chi}2 = 37.28; P < 0.001). Interestingly, of all the virulence factors examined (pap, sfa/foc, aer, hly, K1 antigen, afa, and ibe10), the functional HPI showed the highest association with lethality in mice (Table 2) (14).


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  		TABLE 1. Correlation between presence of HPI, production of Ybt, and affiliation to each of the phylogenetic groups of E. coli

 

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  		TABLE 2. Relationship between different virulence traits and mouse lethality in E. coli strains of the IA collection (n = 82)

 
Two HPI-positive E. coli strains of the collection (IAI51 and IAI52) (14) with a high-virulence phenotype were selected to determine the impact of HPI on mouse virulence. These strains lack some of the potential virulence factors, such as aerobactin and hemolysin (14). The HPI-encoded Ybt system of the strains was inactivated by insertion of a kanamycin resistance gene cassette into the irp1 gene coding for Ybt synthesis protein HMWP1 as described previously (12). The presence of the kanamycin cassette within irp1 was confirmed by PCR and Southern hybridization. In order to recomplement the mutation of the irp1 gene, plasmid pCP1 was introduced into the mutant strains as described recently for Y. enterocolitica (11). The pCP1 plasmid carries the entire 35-kb core region of the HPI coding for the Ybt siderophore system. Original strains, mutants, and recomplemented strains were examined for the structure of HPI by PCR and Southern hybridization (12) and for Ybt synthesis using a reporter gene-mediated bioassay (16). Pathogen-free female mice of the outbred white Swiss mouse lineage (Swiss OF1-Caw) (age, 4 weeks; body weight, 14 g) were purchased from IFA Credo (Orléans, France). E. coli strains were prepared and isolated as described previously (14), except for the mutant strains, which were grown with kanamycin (40 µg/ml). Groups of 30 mice were subcutaneously inoculated with either wild-type, or mutant, or recomplemented mutant strains (108 CFU). After inoculation, the mice were observed daily for up to 1 week to score for killed mice.

The results of the mouse virulence tests of wild-type strains and mutants correspond entirely with the statistical correlation of HPI with a virulent phenotype. Sixteen out of 30 mice infected by E. coli wild-type strain IAI52 were killed, whereas none of the mice infected with the irp1 mutant died ({chi}2 = 21.82; P < 0.001). Even more pronounced results were obtained using the E. coli IAI51 strain, which killed 28 of 30 mice in comparison to the irp1 mutant (1 of 30; {chi}2 = 48.65; P < 0.001). Introduction of the pCP1 plasmid partially restored the mouse-lethal phenotype of the irp1 mutants with 2 of 10 mice killed by the recomplemented strains. This partial restoration is likely due to the fact that the pCP1 plasmid is rather instable in vivo, as has been reported for Y. enterocolitica previously (11). Thus, the results demonstrate the rather clear-cut impact of the HPI on virulence.

The HPI codes for a siderophore Ybt-mediated iron uptake system. The iron limitation during the colonization and infection of a host organism provides a good reason why an endogenous iron uptake system would be advantageous. This is true for yersiniae, for which the HPI-encoded Ybt is the only endogenous siderophore system. However, E. coli possesses at least one other endogenous siderophore system (enterobactin), and in many pathogenic isolates the aerobactin system is detectable, too. One reason for the predominance of Ybt in ExPEC could be the high iron-binding affinity with an Fe3+-Ybt formation constant (pK) of 36.6 compared to those of Fe3+-enterobactin (35.5) and Fe3+-aerobactin (23.3), which are the other endogenous siderophores in E. coli (13, 15). Interestingly, the irp1 mutant strains that were defective for Ybt siderophore synthesis revealed no growth impairment under iron depletion compared to the parental strains (data not shown). Previously demonstrated has been a dual role of siderophores with (i) delivery of iron to the microbial pathogen and (ii) immunosuppression of the host (1). The iron-binding constants of siderophores alone might therefore not be sufficient to explain their contribution to virulence. An intriguing hypothesis for the association of functional HPI with mouse virulence as well as with the presence of other virulence factors is the gene-regulatory effect of Ybt. It has been shown for yersiniae that, in complex with the HPI-encoded protein YbtA, Ybt acts as a positive regulator of gene expression (6). It is conceivable that genes outside the HPI, e.g., other virulence factors, could be influenced by the Ybt-mediated regulation. Thus, cross talk between different virulence determinants could lead to a regulatory network of virulence expression in E. coli sensed by an iron-limited environment. The present study may encourage further investigations of ascending urinary tract infection or meningitis in animal models to determine the impact of a functional HPI on virulence in these routes of ExPEC infections.


   ACKNOWLEDGMENTS
 
This study was supported by a grant from the Deutsche Forschungsgemeinschaft to S.S. (SCHU 1494/1-1) and partially by a grant from the Programme de Recherche Fondamentale en Microbiologie et Maladies Infectieuses et Parasitaires (MENRT).


   FOOTNOTES
 
* Corresponding author. Mailing address: Max von Pettenkofer-Institut, Pettenkoferstr. 9a, 80336 Munich, Germany. Phone: 49 89 5160 5261. Fax: 49 89 5160 5223. E-mail: schubert{at}pk-i.med.uni-muenchen.de. Back

Editor: V. J. DiRita


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Infection and Immunity, September 2002, p. 5335-5337, Vol. 70, No. 9
0019-9567/02/$04.00+0     DOI: 10.1128/IAI.70.9.5335-5337.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.



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