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Infection and Immunity, September 2007, p. 4664-4669, Vol. 75, No. 9
0019-9567/07/$08.00+0     doi:10.1128/IAI.00972-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Contribution of a Novel Gene, rpeA, Encoding a Putative Autotransporter Adhesin to Intestinal Colonization by Rabbit-Specific Enteropathogenic Escherichia coli{triangledown}

Denisse L. Leyton,1 Louise M. Adams,2 Michelle Kelly,1 Joan Sloan,1 Marija Tauschek,2 Roy M. Robins-Browne,2,3 and Elizabeth L. Hartland1,3*

Australian Bacterial Pathogenesis Program, Department of Microbiology, Monash University, Victoria 3800,1 Australian Bacterial Pathogenesis Program, Department of Microbiology and Immunology, University of Melbourne, Victoria 3010,2 Microbiological Research Unit, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville 3052, Australia3

Received 16 June 2006/ Returned for modification 24 July 2006/ Accepted 26 June 2007


   ABSTRACT
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Rabbit-specific enteropathogenic Escherichia coli (REPEC) is an attaching and effacing pathogen of young rabbits. Using signature-tagged mutagenesis, we identified several known colonization factors of REPEC as well as a gene predicted to encode a novel autotransporter protein. This novel gene was termed rpeA for REPEC plasmid-encoded autotransporter.


   TEXT
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Attaching and effacing (A/E) pathogens induce distinctive lesions on the host intestine that are characterized by localized destruction of intestinal microvilli, intimate attachment of the bacteria to the host cell surface, and rearrangement of cytoskeletal proteins beneath tightly adherent bacteria (5). Rabbit-specific enteropathogenic Escherichia coli (REPEC) is an A/E pathogen of weanling rabbits that induces A/E lesions indistinguishable from those induced by the human pathogens enteropathogenic E. coli (EPEC) and enterohemorrhagic E. coli (EHEC) (1, 14, 17). REPEC-induced disease shows the same clinicopathological features and age and tissue specificity as human infection with EPEC, and as such, REPEC is a useful small animal model for studying the contribution of specific virulence factors to colonization of the host and development of diarrhea (17). In addition to the locus for enterocyte effacement (LEE), strains of REPEC also produce fimbriae that are necessary for colonization, although these vary among different strains and serotypes (4, 20). REPEC O15:H– strain 83/39 produces Ral (rabbit adherence locus) fimbriae, which are encoded by the 95-kb plasmid pRAP (1).

The aim of this study was to identify novel colonization factors in A/E pathogens, using REPEC as a model organism. We used signature-tagged mutagenesis (STM) to screen a library of REPEC O15:H– strain 83/39 transposon mutants simultaneously for loss of virulence in weanling rabbits (Microscience, Wokingham, Berkshire, United Kingdom) (10). Ten pools of 21 mutants were used to infect two 5- to 6-week-old New Zealand White rabbits per pool by oral gavage. Each rabbit received 2 ml of inoculum containing approximately 6 x 106 CFU each of the 21 different mutants pooled from individual cultures grown statically in Penassay broth at 37°C overnight. The optical density at 600 nm of each mutant was checked, and mutants displaying in vitro growth defects were excluded from the screen. The viable count of the inoculum strain was determined by retrospective plating of serial dilutions onto LB agar supplemented with kanamycin. DNA was isolated from the remaining inoculum for amplification of input pool DNA. Infected rabbits were examined daily for 7 days and monitored for body weight and evidence of diarrhea, such as loose stools and soiling of the hind limbs. Stool samples were taken from the rabbits daily using sterile rectal swabs inserted approximately 2 cm into the anus, and the rabbits were killed on day 7 after infection. Collected stools and duodenum, jejunum, ileum, cecum, and colon scrapings were emulsified in 0.5 ml phosphate-buffered saline and plated on MacConkey agar supplemented with rifampin and kanamycin. More than 10,000 colonies were used to extract output pool DNA at day 5 and day 7. Tags from input and output pools were amplified by PCR using primers P2 and STM-R2 (Table 1). Amplified input and output tags were each spotted in duplicate onto Hybond N+ membranes (Amersham Biosciences, Buckinghamshire, United Kingdom), and a digoxigenin-labeled 40-bp oligonucleotide homologous to one of the 21 signature tag sequences was then used to simultaneously probe input and output pools. Twenty-one different hybridizations were performed to detect the 21 tags. Tags that were present in the input pool but absent in the output pool denoted putative attenuated mutants. A derivative of REPEC 83/39, the REPEC {Delta}eae intimin mutant (12), carrying tag H7 was included in each input pool as a negative control and was not recovered from any of the 10 output pools. Twenty-seven mutants that showed weak or absent hybridization signals in the output pool compared to those in the corresponding input pool were identified (Table 2). Marker rescue of the transposon insertion sites of these mutants identified six known LEE-encoded virulence determinants, including escV, escD, rorf8, map, espB, and tir. In addition, we identified three insertions into the ral operon and one insertion into another fimbrial gene, designated z2203, in the genome of EHEC O157:H7 EDL933. Other insertions were found in genes encoding putative cell wall components, regulators, and several hypothetical proteins (Table 2). One novel gene identified by this screen was predicted to encode a member of the serine protease autotransporters of Enterobacteriaceae (SPATE) family of autotransporters, and we termed this gene rpeA for REPEC plasmid-encoded autotransporter.


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  		TABLE 1. Oligonucleotide primers used in this study

 

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  		TABLE 2. Transposon insertion sites of REPEC 83/39 mutants attenuated for colonization

 
A fosmid gene library was constructed from REPEC 83/39 to obtain nucleotide sequence information about rpeA and flanking DNA (Copy Control, Epicenter, Madison, WI). rpeA comprised a 3,684-bp open reading frame flanked by genes that code for hypothetical proteins (Fig. 1). Sequencing of fosmid DNA also revealed that rpeA is located downstream of the ral operon and is therefore carried by the virulence plasmid pRAP (1). rpeA was predicted to encode a 1,228-amino-acid precursor protein with a molecular mass of 135 kDa. Although slightly smaller than other reported SPATE proteins, RpeA exhibited a significant degree of amino acid sequence identity with several SPATE proteins, including Hbp, Tsh, Pic, SepA, EpeA, and the serine protease adhesins App from Neisseria meningitidis and Hap from Haemophilus influenzae (Table 3) (2, 7, 9, 13, 16, 18). Amino acid sequence analysis showed that, similar to other SPATE proteins, RpeA comprised an extended N-terminal leader peptide signal sequence that possessed a conserved extension beginning with an MNKI(F/Y)SLK(F/W/Y)S motif followed closely by a second motif, GLIAVSELAR, comprising conserved aromatic and hydrophobic residues. The C-terminal ß domain of the predicted rpeA product also exhibited a conserved 3-amino-acid motif, (Y/V/I/F/W)-X(E)-(F/W), which is essential for outer membrane localization of Hap (8). RpeA differed from other SPATE proteins, however, in that it did not have a characteristic C-terminal domain cleavage site located between two asparagine residues. This may indicate that the RpeA passenger domain is not cleaved from the outer membrane and instead remains attached to the bacterial surface, similar to the autotransporter Hia from Haemophilus influenzae (19). Alternatively, RpeA may employ a mode of cleavage different from those of other SPATE proteins. Although we made several attempts to express epitope-tagged RpeA consistently in REPEC 83/39, this was unsuccessful (data not shown). In addition, we produced several forms of recombinant RpeA, but all were insoluble, and antibodies generated to the insoluble protein did not recognize native RpeA from REPEC strains. Therefore, we were unable to confirm localization of the protein in REPEC or perform functional assays. Nevertheless, the putative passenger domain of RpeA possessed a potential serine protease motif, GDSGSP, which was conserved in sequence and location in comparison to other SPATE proteins, suggesting that the protein may have protease activity (Fig. 1) (6).


Figure 1
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  		FIG. 1. Schematic representation of a segment of pRAP containing rpeA. The white arrow represents rpeA (3,684 bp), and the dark arrows represent other open reading frames carried by this fragment. HP is hypothetical protein. The domain organization of RpeA is indicated below the fragment and shows the N-terminal cleavage site predicted by the SignalP method and two N-terminal conserved motifs as well as the serine protease motif, the proline-rich tandem repeat in the passenger domain, and the conserved YEF motif at the C terminus. The predicted molecular mass of each domain is indicated in kDa.

 

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  		TABLE 3. Shared amino acid sequence similarity between RpeA and its closest relatives

 
We used primers specific for rpeA (rpeA-F and rpeA-R) to determine the distribution of this gene among REPEC strains and other E. coli pathogens by PCR. We found that rpeA was present in 7 out of 10 REPEC strains tested, and 5 of these 10 strains also carried ral (Table 4). The ral operon was detected using the primer pair ral-F/ral-R (Table 1). All REPEC strains that carried ral also carried rpeA. As rpeA is a novel gene, we also tested its prevalence among other E. coli pathogens, including 25 strains of EPEC, 25 strains of EHEC, and 5 strains each of enteroaggregative E. coli, enteroinvasive E. coli, enterotoxigenic E. coli, and Shigella flexneri, by PCR; however, results for all were negative (data not shown). Therefore, rpeA appears to be present predominantly in strains of REPEC and could not be detected in the other pathotypes of E. coli tested here.


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  		TABLE 4. Prevalence of ral and rpeA among different strains of REPEC

 
Nucleotide sequence analysis suggested that rpeA may be transcriptionally linked to the ral operon (Fig. 1). To determine if rpeA was expressed in the same operon as ral, we extracted whole-cell RNA from two different serotypes of REPEC, namely, wild-type REPEC O15:H– strain 83/39 and wild-type REPEC O103:H2 strain E22. Bacteria were grown to mid-log phase, preparations were treated with DNase, and RNA was purified using an RNeasy mini kit (QIAGEN) according to the manufacturer's instructions. This was followed by a second treatment with DNase. rpeA and ral expression was then analyzed by reverse transcription (RT)-PCR. Random hexamers and Superscript II RNase H– reverse transcriptase (Invitrogen) were used to generate cDNA from purified RNA. PCR of cDNA and a negative control lacking reverse transcriptase was performed with primer pairs rpeA-F/rpeA-R, ralG-F/ralH-R, ralI-F/rpeA-R, and ralI-F/rpeA-RT (Table 1). Primers internal to rpeA were used to detect expression of the gene in both REPEC E22 and REPEC 83/39 (Fig. 2). Primers overlapping ralG and ralH as well as ralI and the start of rpeA were used to determine whether ral and rpeA expression was transcriptionally coupled. In both REPEC E22 and REPEC 83/39, ralG and ralH were expressed from the same mRNA whereas rpeA expression was independent of the most distal ral gene, ralI (Fig. 2).


Figure 2
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  		FIG. 2. Analysis of ral and rpeA expression by RT-PCR in wild-type REPEC strains E22 (left panels) and 83/39 (right panels). (A) Expression analysis of rpeA using primers rpeA-F and rpeA-R, internal to rpeA. (B) Expression of ralG-ralH using primers ralG-F and ralH-R. (C) Expression analysis of ralI-rpeA using primers ralI-F and rpeA-R, yielding a 1,353-bp product. (D) Expression analysis of ralI-rpeA using primers ralI-F and rpeA-RT, yielding a 920-bp product. Std indicates DNA size markers shown in base pairs; DNA indicates the PCR control; RT– indicates RT-PCR in the absence of reverse transcriptase; RT+ indicates PCR from cDNA.

 
Loss of the rpeA transposon mutant 81H5 (REPEC rpeA::mini-Tn5 Km2) from output pools during our STM screen implied that this derivative of REPEC 83/39 was defective for intestinal colonization. To determine whether rpeA contributed to adherence in vitro, we constructed a defined nonpolar deletion mutant of rpeA, using the {lambda} Red recombinase system and primers pKD4rpeA-F and pKD4rpeA-R (Table 1) (3). Fluorescence actin staining of HeLa cells infected with the REPEC {Delta}rpeA mutant showed that the mutant still carried a functional LEE pathogenicity island capable of inducing actin polymerization (data not shown) (11). Quantitative adherence assays comparing wild-type REPEC 83/39 and REPEC {Delta}rpeA were performed as described previously (15) but revealed no significant difference in the abilities of the two strains to adhere to HeLa cells (data not shown). Since REPEC 83/39 produces several adhesins, the expression of one or all of these may mask the activity of RpeA in vitro (11, 14). Therefore, to determine if RpeA possessed host cell binding activity in the absence of other adhesins, we tested the ability of poorly adherent E. coli strain XL1-Blue to adhere to HeLa cells and HCT-8 cells when expressing RpeA from a plasmid. To construct pRpeA, rpeA from REPEC 83/39 was amplified using the primers prpeA-F and prpeA-R (Table 1). The final product was cloned into the BamHI site of pUC18 to generate pRpeA, which was subsequently introduced into E. coli XL1-Blue. The results showed that E. coli XL1-Blue carrying pRpeA was significantly more adherent for both cell types than E. coli XL1-Blue carrying pUC18 alone (Fig. 3), indirectly suggesting by genetic studies that RpeA possessed some host cell binding activity.


Figure 3
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  		FIG. 3. Quantitative adherence of E. coli XL1-Blue carrying pRpeA (white bars) and E. coli XL1-Blue carrying pUC18 (black bars) to HeLa and HCT-8 cells. Results are expressed as percentages of the original inoculum recovered from quadruplicate wells and are the means for at least four independent experiments. *, adherence significantly greater than that of E. coli XL1-Blue carrying pUC18 (P < 0.05; unpaired, two-tailed t test).

 
To assess further the role of rpeA in adherence and colonization of rabbits, we next tested the ability of the defined nonpolar {Delta}rpeA mutant of REPEC 83/39 to colonize weanling rabbits in a single infection. Two groups of six rabbits received 6 x 106 CFU each of wild-type REPEC 83/39 and REPEC {Delta}rpeA. Rectal swabs from animals inoculated with wild-type REPEC 83/39 and the REPEC rpeA mutant were taken each day over a 27-day period to assess levels of colonization, and animals were weighed daily to monitor changes in body weight, which indicates the severity of REPEC-induced disease. The {Delta}rpeA mutant was recovered in lower numbers on 21 of 27 days, took longer to colonize the rabbits, and was cleared more quickly than wild-type REPEC 83/39 (Fig. 4). This lower bacterial burden translated into slightly higher weight gain for rabbits infected with the {Delta}rpeA mutant than for those infected with wild-type REPEC 83/39 (Fig. 4). Overall, rabbits were colonized to significantly higher levels with wild type REPEC 83/39 (≥106 CFU on 28 of 162 group days) than with the {Delta}rpeA mutant (≥106 CFU on 7 of 162 group days; P = 0.0002; Fisher's exact test, two-tailed). These results indicated that when tested with a single infection, rpeA was found to be essential for full colonization of weanling rabbits by REPEC 83/39. In addition, these findings corroborated results from the STM screen where the rpeA transposon mutant 81H5 was not detected in output pools by day 7 when samples were taken for the STM screen.


Figure 4
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  		FIG. 4. Mean weights (circles) and mean log10 numbers of CFU per swab (triangles) of rabbits infected with wild-type REPEC 83/39 (solid shapes) and the REPEC {Delta}rpeA mutant (open shapes). Animals were weighed daily, and fecal swabs were taken daily for 27 days after inoculation. The dotted line indicates the CFU detection limit.

 
Concluding remarks. We have shown previously that REPEC 83/39 requires both ral and eae to colonize the rabbit intestine (12). In this study, the construction of a defined nonpolar mutant of rpeA showed that this novel gene also plays a role in intestinal colonization, albeit a more minor one than either eae or ral. The rpeA mutant took longer to colonize rabbits, was cleared more quickly than wild-type REPEC 83/39, and did not achieve the high bacterial numbers associated with REPEC 83/39 infection. These results explain the identification of rpeA though our STM screen, in which colonization-defective mutants present in lower numbers 7 days after infection were identified by weak or absent hybridization signals in output pool DNA.

The predicted product of rpeA is the latest member of the autotransporter family of proteins and appears most closely related to serine protease adhesins from gram-negative pathogens. The presence of rpeA in a pathogen of rabbits provides an opportunity to study the role of autotransporter adhesins in a small animal model of intestinal colonization. In particular, it will now be possible to assess the contributions of specific domains of autotransporter adhesins, such as the proline-rich region and the serine protease motif, to virulence in a natural infection model.

Nucleotide sequence accession number. The rpeA nucleotide sequence presented in this study was assigned GenBank accession number AY552473.


   ACKNOWLEDGMENTS
 
We gratefully acknowledge Danni Krmek, Shelley Luck, and Louise Taylor for their expert assistance with this work. We thank Microscience Ltd. for making their signature-tagged transposons available for this screen.

This study was supported in part by funding from the Australian National Health and Medical Research Council, the Australian Research Council, and the Murdoch Childrens Research Institute. D.L.L. is the recipient of an Australian Postgraduate Award.


   FOOTNOTES
 
* Corresponding author. Mailing address: Department of Microbiology, Monash University, Victoria 3800, Australia. Phone: (61) 3 9905 4323. Fax: (61) 3 9905 4811. E-mail: Liz.Hartland{at}med.monash.edu.au Back

{triangledown} Published ahead of print on 9 July 2007. Back

Editor: J. B. Bliska


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Infection and Immunity, September 2007, p. 4664-4669, Vol. 75, No. 9
0019-9567/07/$08.00+0     doi:10.1128/IAI.00972-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.




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