Unique Cell Adhesion and Invasion Properties of O:3, the Most Frequent Cause of Human Yersiniosis

Summary

Many enteric pathogens are equipped with multiple cell adhesion factors which are important for host tissue colonization and virulence. Y. enterocolitica, a common food-borne pathogen with invasive properties, uses the surface proteins invasin and YadA for host cell binding and entry. In this study, we demonstrate unique cell adhesion and invasion properties of Y. enterocolitica serotype O:3 strains, the most frequent cause of human yersiniosis, and show that these differences are mainly attributable to variations affecting the function and expression of invasin in response to temperature. In contrast to other enteric Yersinia strains, invasin production in O:3 strains is constitutive and largely enhanced compared to other Y. enterocolitica serotypes, in which invA expression is temperature-regulated and significantly reduced at 37°C. Increase of invasin levels is caused by (i) an IS1667 insertion into the invA promoter region, which includes an additional promoter and RovA and H-NS binding sites, and (ii) a P98S substitution in the invA activator protein RovA rendering the regulator less susceptible to proteolysis. Both variations were shown to influence bacterial colonization in a murine infection model. Furthermore, we found that co-expression of YadA and down-regulation of the O-antigen at 37°C is required to allow efficient internalization by the InvA protein. We conclude that even small variations in the expression of virulence factors can provoke a major difference in the virulence properties of closely related pathogens which may confer better survival or a higher pathogenic potential in a certain host or host environment.

Introduction

Yersinia enterocolitica is a common gram-negative zoonotic pathogen that is able to grow in the environment and cause enteric diseases (Yersiniosis), ranging from enteritis, severe diarrhea, mesenteric lymphadenitis, hepatic or splenic abscesses to postinfectious extraintestinal sequelae such as reactive arthritis and erythema nodosum [1]. Infection by Y. enterocolitica is usually initiated through uptake of contaminated food or water. Following ingestion, the bacteria first colonize the lumen and transmigrate through antigen-sampling M cells across the epithelial lining of the small intestine, resulting in the colonization of the underlying lymphoid tissues (Peyer's patches) [2], [3]. Subsequently, Y. enterocolitica can spread via the lymph and/or blood into the mesenteric lymph nodes or to extraintestinal sites such as liver and spleen [4], [5], [6]. Alternatively, the bacteria may bypass colonization of the Peyer's patches and spread directly from the intestine to the systemic tissues, similar to what has been observed for enteropathogenic Yersinia pseudotuberculosis [7], [8].

Adhesion, invasion and survival in deeper tissues depend on several Yersinia virulence factors encoded on the Yersinia chromosome or the 65–70 kb virulence plasmid (pYV) [9]. Y. enterocolitica produces at least three invasion factors, invasin, Ail (attachment-invasion locus), and YadA (Yersinia adhesin A) which were shown to promote adherence to and invasion into mammalian cells [10], [11], [12]. Invasin, the primary invasion factor, binds with high affinity to beta 1 chain integrin receptors found on the surface of M cells but not on the apical side of brush border cells, and mediates efficient and rapid internalization into host cells [13], [14]. As invasin is strongly expressed at environmental temperature but only weakly at 37°C, it is assumed to support initial colonization and survival of host tissues during the very early stages of an infection [15], [16], [17]. Recent studies showed that the dimeric winged-helix transcriptional regulator RovA controls transcription of the invasin gene (invA) in response to temperature. For this purpose, RovA uses an in-built thermosensor to control its DNA-binding activity and its susceptibility to the proteolytic degradation by ATP-dependent proteases [18].

After the initiation of the infection, the YadA and Ail proteins seem to be the predominant adhesins in infected tissues. Both virulence factors mediate serum resistance and promote tight adherence to extracellular matrix proteins, such as fibronectin and/or collagen, but their contribution to bacterial uptake is relatively small [19], [20], [21], [22], [23], [24], [25]. The yadA gene is located on pYV and its expression, together with the plasmid-encoded type III secretion system (Ysc proteins) and the antiphagocytic effector proteins (Yops) is controlled by the VirF(LcrF) activator. VirF-dependent induction of yadA, yop and ysc expression occurs exclusively at 37°C [26], [27]. Ail is also predominantly expressed at 37°C, and regulated by pH and oxygen content, but the control mechanisms are still unclear [24].

Besides the classical pathogenicity factors, other surface factors also contribute or are required for full virulence. Lipopolysaccharides (LPS) of Y. enterocolitica serotypes O:3 and O:8 are required for successful colonization of the gut and play an important role in the outer membrane integrity of the bacteria [28], [29], [30]. LPS O polysaccharide (O-antigen) mutants were attenuated in virulence and impaired in their ability to colonize the Peyer's patches, liver and spleen [30], [31]. Production of the O-antigen is also temperature-regulated with maximal expression at moderate temperatures [32], [33]. A complex network regulates O-antigen expression at the transcriptional level and the RosA/RosB efflux pump/potassium antiporter system and Wzz, the O-antigen chain length determinant, are indirectly involved in the temperature-dependent control process [33]. In addition, flagella-dependent motility is required to initiate host cell invasion by ensuring migration and cell contact of the bacteria [34].

Most studies on Y. enterocolitica virulence factors and their contribution to virulence were performed using highly mouse-virulent bioserogroup 1B/O:8 strains, in particular Y. enterocolitica 8081v. However, several other human pathogenic Y. enterocolitica strains which are less virulent in mice (e.g. serotypes O:3, O:9 and O:5,27) were also frequently isolated from patients [1]. Among these strains, Y. enterocolitica bioserotype 4/O:3 is by far the most frequent cause of human yersiniosis in Europe and Japan (80–90%). Y. enterocolitica infections are less common in North America. However, since the 1980s, serogroup O:3 strains have emerged as an occasional cause of foodborne outbreaks and replaced O:8 as the predominant serotype of Y. enterocolitica reported to CDC [35], [36], [37], [38]. They mainly originate from domestic pigs (prevalence of 0–65% in fattening pig herds), which are often asymptotic carriers, and in which they commonly colonize the lymphoid tissue of the gut and oropharynx [39], [40]. As only very little is known about the pathogenicity of Y. enterocolitica bioserotype 4/O:3, we compared host cell interactions of different human-, pig- and food-derived Y. enterocolitica isolates and found that expression and function of surface-exposed virulence factors of serotype O:3 strains differ significantly from other Y. enterocolitica serotypes. This may reflect an adaptation of Y. enterocolitica O:3 to the intestine of pigs which make them also highly pathogenic for humans.

Results

Y. enterocolitica O:3 interaction with epithelial cells differs significantly from other Y. enterocolitica serotypes

In order to obtain information about interactions of Y. enterocolitica serotype O:3 (YeO:3) strains with host cells, we first investigated the adhesion and invasion efficiency of two reference strains Y11 and YeO3 and 25 different YeO:3 strains isolated from human patients, animals or food between 2005 and 2008 in Germany (Table S1). None of the serotype O:3 isolates was able to efficiently bind and invade into cultured human epithelial cells when the bacteria were grown at standard culture conditions and similar patterns of host-cell associated bacteria (adhesion and invasion) were obtained when infection was performed at 22–25°C or 37°C (Fig. 1, S1, data not shown). A prolongation of the infection time from 30 min to 3 hours and/or use of other human, porcine and murine epithelial cell lines did not significantly enhance the efficiency of cell adherence (data not shown), indicating that low-efficiency of adhesion and invasion is independent of the cell line and host species. In contrast, all other tested Y. enterocolitica isolates (serotypes O:5,27, O:8 and O:9) adhered very efficiently and were able to enter all tested epithelial cell lines after 30 min with a frequency ranging from 20–30% depending on the serotype and the isolate (Fig. 1, data not shown).

Amotility of Y. enterocolitica O:3 affects cell invasion efficiency

It is known that motility is an important factor enhancing the invasion efficiency of yersiniae [34]. We tested motility of the YeO:3 strains and found that none of the isolates was motile on swimming and swarming agar plates in contrast to other Y. enterocolitica serotypes, e.g. Y. enterocolitica YeO:8 8081v (Fig. 2A, data not shown). Transmission electron microscopy further revealed that YeO:3 strains are not flagellated (Fig. 2B, data not shown), indicating that flagella synthesis is abolished or does not occur under used growth conditions (LB, 25°C). This phenotype was also observed with YeO:3 strains isolated from liver and spleen of BALB/c mice three days post infection (data not shown). Notably, 30–40% of the bacteria isolated from the intestine were flagellated (Fig. S2) and motile after in vitro cultivation for 24 h (data not shown). However, none of them remained motile and flagellated after 48 h, indicating that the bacteria are motile within the intestinal tract and rapidly repress flagella synthesis when grown on agar plates.

It has been assumed that motility enhances the frequency of bacteria-cell interaction and/or provides an additional force for active cell entry. To investigate whether non-invasiveness of the serotype O:3 strains was caused by a reduction of host cell contacts due to amotility, we performed adhesion and invasion assays with or without centrifugation of the bacteria onto host cells (Fig. 3A). When we pre-grew the bacteria at 25°C, adhesion and internalization was slightly increased after centrifugation, but the overall efficiency was still significantly lower compared to YeO:8 8081v. This demonstrated that amotility of the bacteria reduced host cell contact and invasion of YeO:3 grown at 25°C. However, this does not fully explain the observed differences. In this context, we also analyzed host cell adhesion and invasion of bacteria grown at 37°C (Fig. 3B). Without centrifugation, the number of adherent YeO:8 8081v was significantly reduced and no invasion of the bacteria was detectable at 37°C. In contrast, YeO:8 8081v adhered tightly to HEp-2 cells after bacteria were artificially brought into cell contact by centrifugation, but they were not internalized (Fig. 3B). This is consistent with previous studies showing that synthesis of the flagella and the primary internalization factor invasin is repressed at 37°C in Y. enterocolitica 8081v, whereas production of the major adhesion factor YadA is induced at 37°C but not at moderate growth temperatures [15], [41]. As shown in Fig. 3B, pre-growth at 37°C and artificially induced host cell contact led to a significant raise of cell adhesion of all tested O:3 strains. Notably, only under these conditions efficient host cell invasion of YeO:3 strains was as efficient as cell uptake obtained with YeO:8 8081v grown at 25°C (20–30% of adherent bacteria). Since efficient cell adhesion and internalization of YeO:3 strains was only achieved after artificial host cell contact, in all following experiments bacteria were centrifugated onto host cells.

Internalization of Y. enterocolitica O:3 into human epithelial cells

Based on the previous experiments it seemed possible that an additional thermo-regulated internalization mechanism is responsible for host cell invasion at 37°C. To compare the invasion mechanism used by YeO:3 and YeO:8 strains, we monitored cell entry of YeO:8 8081v grown at 25°C and YeO:3 Y1 grown at 37°C into HEp-2 (Fig. 4A) and Caco-2 (data not shown) cells by scanning electron microscopy. We found that adherence and invasion of both Y. enterocolitica serotypes showed very common features and were not cell type specific. After host cell binding, the cell surface in the vicinity of the microbes seems to be slightly drawn down, pseudopodia and lamellipodia are formed and the eukaryotic cell membrane then seems to enclose and surround the bacteria into a membrane-bound vacuole. In contrast, no cell adherence of YeO:3 strain Y1 was observed when grown at 25°C, and only simple attachment, but no formation of membrane protrusions was detectable when YeO:8 8081v was precultivated at 37°C (data not shown). This suggested that the internalization mechanism initiated by Y. enterocolitica serotype O:3 and O:8 strains is similar but expressed at different temperatures.

Expression analysis of Y. enterocolitica O:3 invasin

In order to test this hypothesis, we analyzed the amount of invasin in both Y. enterocolitica serotypes and found that high amounts of the primary invasion factor invasin were present in all tested YeO:3 strains at 25°C and 37°C, whereas in YeO:8 8081v invasin was only detectable at 25°C, but not at 37°C (Fig. 5AB). Production of invasin in YeO:3 strains at 37°C explains why the invasion rate is significantly enhanced at this growth temperature. However, this also raised the question why no internalization of the bacteria was observed when the bacteria were grown at 25°C, although similar amounts of the invasin protein were produced (Fig. 3, 5).

Y. enterocolitica O:3 O-antigen blocks InvA-mediated invasion at 25°C

To decipher the differences in the host cell invasion properties between the Y. enterocolitica O:3 and O:8 serotype, we first performed adhesion and invasion experiments with E. coli K-12 expressing the invA_O:3 and invA_O:8 genes and found a similar ability of both invasin proteins to promote cell attachment (25%) and entry (5%) (data not shown). This led to the hypothesis that a temperature-regulated surface structure might block invasin function of YeO:3 strains at moderate growth temperatures. Indeed, composition of the outer membrane and particularly make-up of LPS was shown to be strongly temperature-dependent in Y. enterocolitica [32]. Both the branched outer core hexasaccharide (OC) and the homopolymeric O-antigen (O-Ag) of the unique YeO:3 LPS are maximally produced below 30°C, whereas only very reduced levels of these LPS components are displayed on the bacterial surface at 37°C [32]. In order to investigate whether they sterically block the access of invasin to host cells, we used different mutant strains of Y. enterocolitica O:3 strain YeO3 deficient in O-Ag formation (YeO3-R2), OC biosynthesis (YeO3-OC), or both (YeO3-OCR) [42]. As shown in Fig. 6A, both O-Ag deficient mutant strains (YeO3-R2, YeO3-OCR) have an increased capacity to interact and enter human epithelial cells, whereas no difference was detectable with the OC knock-out mutant (YeO3-OC). When the adhesion and uptake assays were performed at 37°C, the overall adhesion and invasion levels of the YeO3 wild-type strain were significantly increased and identical to that of YeO:8 8081v grown at 25°C, and no significant differences were observed in the absence of the O-Ag or the OC (Fig. 6A). Notably, differences in host cell interactions did not result from differences in invA or yadA expression as identical amounts of invasin and YadA were detectable in the Y. enterocolitica O:3 wild-type YeO3 and the O-Ag and OC mutants grown at 25°C and 37°C (Fig. 6B). Taken together, these data strongly suggest that the YeO:3 O-Ag reduces host cell interactions at 25°C, most likely through steric hindrance of adhesin/invasin host cell receptor binding. However, this does not seem to be the only reason why YeO3 is less invasive at 25°C than YeO8 8081v, as invasion of the O-Ag mutant strains was still lower compared to invasion of the Y. enterocolitica O:8 strain (Fig. 6A).

Co-expression of invasin and YadA is necessary for efficient invasion at 37°C

Besides invasin, also the virulence plasmid-encoded YadA protein promotes tight adhesion of Y. enterocolitica to host cells [43]. We first investigated expression of the yadA gene in response to temperature and found that similar amounts of YadA are produced in all tested Y. enterocolitica O:8 and O:3 strains at 37°C (Fig. 5B, 6B) whereas no synthesis could be detected at 25°C (data not shown). Furthermore, we analyzed cell adhesion and internalization of Y. enterocolitica O:3 strain Y1 grown at 25°C or 37°C in the presence and absence of invasin or YadA (Fig. 7A), and confirmed production or loss of adhesins in the equivalent Y. enterocolitica strains (Fig. 7B). Deletion of the invA gene had no effect on host cell binding, but eliminated the ability of the YeO:3 strains to invade human epithelial cells independently from growth temperature. This phenotype was fully complemented by an invA expression plasmid. In contrast, loss of YadA had no effect on host cell invasion and cell adherence at 25°C. However, host cell binding and invasion were significantly reduced when yadA-deficient bacteria were grown at 37°C. Overexpression of the yadA gene under control of an inducible promoter (P_BAD) complemented this phenotype and increased cell binding and entry levels at 37°C. Even more strikingly, it promoted highly efficient cell adhesion and invasion of bacteria grown at moderate temperature, similar to YeO:8 8081v (Fig. 7A). Thus, co-expression of both adhesins is required to permit efficient cell binding and internalization of serotype O:3 strains into host cells: YadA is needed to maximize adhesion whereas invasin is necessary to initiate the internalization process.

Analysis of invA expression in Y. enterocolitica O:3

Our previous experiments clearly demonstrated that the absence of YadA results in low invasiveness of YeO:3 strains at 25°C, despite the presence of invasin. Yet, invasin expression at 37°C is a special feature of serotype O:3 strains, as it is not produced in other previously characterized Yersinia strains, e.g. YeO:8 8081v (Fig. 5) [15] and Y. pseudotuberculosis [44]. Therefore, we started to elucidate the molecular mechanisms underlying such differences. First, the invA coding and regulatory region of all Y. enterocolitica O:3 isolates used in this study were sequenced and an IS1667 element inserted at position −143 of the invA promoter was identified (Fig. 8A). To address whether presence of the IS1667 insertion is restricted to strains of the same geographic region isolated over a relatively short timeframe, we also sequenced the invA locus of 22 additional Y. enterocolitica O:3 isolates collected from all over the world between 1973 and 2008 (Table S1). All tested isolates contained the IS1667 element at the same position within the invA regulatory region. To test the influence of the inserted IS element, we compared the activities of the invA promoter of YeO:8 8081v (P_invO:8) and YeO:3 Y1 wild-type (P_invO:3) or after deletion of the IS1667 insertion (P_invO:3ΔIS). We found that integration of the mobile element is accompanied with a much stronger expression of the invA promoter. As shown in Fig. 8B, expression of the P_invO:3ΔIS::luxCDABE and the P_invO:8::luxCDABE fusions were very similar and significantly lower than P_invO:3::luxCDABE expression at 37°C. This result is consistent with a western blotting analysis showing that invasin production is considerably higher in the YeO:3 strains than in YeO:8 strain 8081v at 37°C (Fig. 5). As the luxCDABE reporter generates a non-linear and often stronger signal than the relative change in transcription, we also performed a quantitative RT-PCR analysis and observed a 6.5-fold reduction of relative invA mRNA levels in the ΔIS1667 mutant YE15 compared to the wild-type strain (Fig. S3).

To find out whether higher activation of the invO:3 promoter was due to the insertional inactivation of inhibitory sequences (e.g. H-NS binding sites) or to the presence of specific IS sequences different portions of the invA upstream region were deleted and transcription of the P_invO:3::luxCDABE fusion in the Y1 wild-type strain was analyzed. High expression of the P_invO:3::luxCDABE fusion was obtained with deletion constructs harboring sequences upstream of position −448, whereas P_invO:3 promoter activity was severely reduced with the fusions starting at or downstream from position −248 (Fig. 8C). This demonstrated that the P_invO:3 activity cannot solely be caused by insertional inactivation of inhibitory sequences, and indicated that an IS-encoded function contributes to P_invO:3 activation. In fact, insertion of the IS1667 sequences from position −448 and −144 upstream of the promoterless luxCDABE operon resulted in strong expression of the fusion construct, indicating that an additional promoter (P_IS1667) oriented outward of the IS element drives invA_O:3 expression (Fig. 8B). In fact, primer extension analyses revealed a strong IS-encoded promoter (P_IS1667) with a −35 region located upstream and the −10 region downstream of position −248. P_IS1667 initiated transcription from position −219 with respect to the transcriptional start site of a second promoter (P_invA) located within the invA regulatory region (Fig. 8D, S4). P_invA was equal to the invA promoter of Y. enterocolitica O:8 [15] and exhibited a similar activity when the inserted IS1667 element was deleted (Fig. 8B).

Since the IS1667 is inserted into the 3′-end of the binding site I of the transcriptional activator protein RovA (Fig. 8A) [45], [46], we also analyzed whether invA expression in Y. enterocolitica O:3 strain Y1 is still dependent on RovA. We found that invA mRNA levels and the activity of all highly activated P_invO:3::luxCDABE fusions starting from position −1830, −1169 and −448 were significantly reduced in the absence of the rovA gene, demonstrating that strong enhancement of invA expression by the IS-encoded promoter still requires the function of the transcriptional activator protein (Fig. 8C, S3).

Previous footprint analysis revealed that RovA interacts with two distinct binding sites of the Y. pseudotuberculosis invA promoter [46], and sequence homology as well as RovA band shift analysis indicated that similar binding sites are also recognized by RovA in the invA regulatory region of YeO:8 8081v [45]. RovA-binding site I was partially destroyed by the insertion of the IS1667 element in the invA_O:3 promoter (Fig. 9A). However, band shift analysis with purified recombinant RovA and different DNA fragments of the invA promoter region demonstrated that RovA still interacts specifically with RovA sequences upstream of the IS1667 element containing major parts of binding site I (Fig. 9B). Interestingly, RovA was also found to specifically interact with fragments harboring the 3′-end (−342 to −146) of the integrated mobile element, although a slightly higher concentration was required for RovA-DNA complex formation. This demonstrated that this portion of the IS1667 element includes sequences, which are also preferentially recognized by RovA.

It is very likely that RovA is needed to alleviate H-NS-mediated repression at sites located downstream of the IS1667 insertion (Fig. 9A) to permit maximal transcription of the invA promoter. To test this hypothesis, we also studied the interaction of H-NS with different fragments of the invO:3 promoter region. As shown in Fig. 9C, H-NS was able to preferentially interact with a fragment harboring the 3′-portion of the IS1667 element (−342 to −146), but the affinity was slightly lower compared to H-NS binding to the invA promoter fragment (−72 to +103). This strongly suggests that RovA is still required to eliminate H-NS mediated repression to allow optimal expression of invasin by the P_IS1667 and the P_invO:3 promoter.

Enhanced RovA production in Y. enterocolitica O:3 strains

Requirement of RovA for invA transcription in Y. enterocolitica O:3 at 37°C was unexpected as it has been shown that rovA expression in Y. enterocolitica O:8 and Y. pseudotuberculosis strains is strongly thermoregulated and only expressed at moderate temperatures [44], [47]. The RovA protein was found to act as a thermosensor which undergoes a conformational change upon a temperature shift from 25°C to 37°C. This thermo-induced conformational change reduces the DNA binding activity of the regulatory protein and renders it more susceptible to proteolysis by the Lon protease [18]. As a result, RovA activation of invA expression is abolished at 37°C. Although RovA was shown to activate invA expression in Y. enterocolitica O:3 (Fig. 8C), invasin expression does not appear to be strongly temperature-regulated compared to other Yersinia strains (Fig. 5, 6B [15], [44]).

To better understand the different control mechanisms, rovA expression in the different Y. enterocolitica isolates was analyzed. We found that all YeO:3 isolates produced very high levels of RovA at 25°C and 37°C; whereas no RovA was detected at 37°C in other Yersinia strains, e.g. YeO:8 strain 8081v and Y. pseudotuberculosis (Fig. 5, data not shown [44], [47]). Expression analysis of the P_rovAO:3::lacZ and P_rovAO:8::lacZ fusions revealed that both rovA promoters are not auto-activated and are either not or only very weakly dependent on the temperature (Fig. 10A, S6). Next, we addressed whether thermo-sensing and proteolysis varies between the RovA_O:8 and RovA_O:3 proteins. We introduced low-copy plasmids carrying the rovAO:3 gene of YeO:3 Y1 or the rovAO:8 gene of YeO:8 8081v into a Y. enterocolitica O:3 rovA mutant strain (YE12) and compared RovA levels after growth at 25°C and 37°C (Fig. 10B). Almost identical levels of the RovA proteins were detected at 25°C. However, significantly lower amounts of the RovA_O:8 protein were visible at 37°C, while RovA_O:3 concentrations remained almost the same (Fig. 10B). This strongly suggested that post-transcriptional mechanisms controlling RovA levels must be different in YeO:3 strains. To test this hypothesis, we sequenced the rovA locus of all 49 available Y. enterocolitica O:3 strains (Table S1). We found that the rovA genes of 45 strains, including all isolates tested in this study vary from rovA of other Y. enterocolitica serotypes by a single point mutation in codon 98, resulting in a P98S change in the amino acid sequence of the translated regulatory protein. To find out whether this substitution affects function of RovA as a thermosensor, we overexpressed and purified RovA of YeO:8 8081v and YeO:3 Y1 and compared their DNA-binding capacity at 25°C and 37°C (Fig. S5). However, interaction of both RovA variants with DNA fragments of the invA regulatory region was still temperature-dependent. Significantly more of both RovA proteins was required at 37°C for RovA-DNA complex formation, indicating that the thermosensing function is not severely affected by the P98S exchange. Next, we addressed thermo-dependent susceptibility of the RovA variants to degradation by the Lon protease. To this aim, we reintegrated a copy of the rovA_O:3 or rovA_O:8 gene into the genome of a rovA deficient YeO:3 strain (YE12) and performed stability assays. Identical amounts of RovA_O:3 were still visible 90 min after protein biosynthesis was stopped (Fig. 10C). In contrast, the RovA_O:8 protein was rapidly degraded at 37°C, and significantly lower amounts of the regulatory protein were detectable 90 min after cessation of protein synthesis.

Influence of higher RovA and invasin levels in YeO:3 on invasion and virulence

To test the effect of the IS1667 insertion in the invA promoter and the more stable RovA_O:3(S98) variant on host cell invasion, we compared the amount of produced invasin and RovA in YeO:3 strains YE13 (rovA_O:3), YE14 (rovA_O:8) and YE15 (P_invO:3ΔIS) (Fig. 11A) and investigated the efficiency of these bacteria to enter HEp-2 cells (Fig. 11B). High levels of invasin were detectable in YE13, whereas the instable RovA variant and deletion of the IS1667 element produced lower amounts of invasin, leading to a significant reduction of invasiveness into human epithelial cells.

It was previously shown that invasin and RovA are important to invade the intestinal epithelium by Y. enterocolitica O:8 early after infection. The rovA-deficient mutants were found to be attenuated in the ability to reach and/or replicate in the deeper tissues and organs and induce a milder inflammation of the Peyer's patches [48], whereas the LD₅₀ values of the wild-type and the invA mutant were essentially identical but the colonization of the host tissues was delayed [4]. In order to determine whether higher invasin and RovA levels in Y. enterocolitica O:3 also affect pathogenesis, we tested the virulence of wild-type and mutant strains in the murine infection model. First, single strain infections were performed and bacterial colonization of Peyer's patches (PPs), mesenteric lymphnodes (MLNs), liver and spleen was assessed. Since only minor differences could be highlighted (data not shown), we performed co-infection experiments to determine whether presence of the wild-type affects the ability of the mutants to colonize tissues in a single host. This minimizes inherent inter-animal biological variations and can expose even subtle differences of the biological fitness and virulence, e.g. in the kinetics of infection. BALB/c mice were orally infected with 5×10⁸ bacteria in an inoculum comprised of an equal mixture of (i) the parental Kan^S wild-type strain Y1 (rovA_O:3(S98)) and the Kan^R mutant strain YE14 (rovA_O:8(P98)) or (ii) Y1 and YE15 (P_invO:3ΔIS) harboring a stable vector which only differs in its antibiotic resistance cassette to establish the ability to discriminate strains. Three days after infection, mice were dissected and the numbers of bacteria present in the PPs, MLNs, liver or spleen were determined (Fig. 12). The results of the infection showed that both, the parental (YE13 rovA_O:3(S98)) and the rovA_O:8(P98) mutant strain (YE14) are capable of establishing an infection, but considerably higher numbers of bacteria encoding the less stable RovA_O:3(P98) variant from YeO:8 (YE14) were recovered from all dissected tissues. About 2- to 10-fold more bacteria of this strain were isolated from the lymphatic tissues or the organs (Fig. 12A) compared to the parental strain YE13 (rovA_O:3(S98)). Also comparison of the relative virulence ratio (Fig. 12B) and calculation of the competitive index of the mutant relative to the wild-type strain (Fig. 12C) indicated that higher concentrations of RovA during mouse infections at 37°C are disadvantageous for the colonization and multiplication of YeO:3 in the organs. In contrast, significantly lower numbers of strain YE15 lacking the IS1667 element in the invA promoter region were isolated. About 10–20 times less bacteria were recovered from the PP and MLNs (Fig. 12A). The difference in the dissemination of the bacteria was even more striking. The IS1667 deletion strain YE15 was strongly attenuated in its ability to reach deeper tissues. Only in some occasions it reached the liver and spleen, but the bacterial load of the mutant in the liver and spleen was always significantly lower compared to wild-type (Fig. 12). In summary, these data strongly indicates that high invasin expression levels during the course of an infection combined with a fine-tuned control of the virulence regulator RovA are advantageous for YeO:3 virulence in mice.

Discussion

The ability of Y. enterocolitica to bind and invade into host cells is essential for pathogenesis and persistance in its human host. Results of the present investigation highlight important differences in the adhesion properties between serotype O:3 strains (responsible for more than 70% of human yersiniosis cases) and other Y. enterocolitica serotypes, e.g. serotype O:8, whose pathogenicity has been extensively investigated. Comparative analysis of cell binding properties demonstrated that the same repertoire of virulence factors is implicated in host cell binding in the serotype O:3 isolates, but their interplay and expression profile in response to environmental signals is significantly different from O:8 strains (Fig. 13).

We show that synthesis of the primary internalization factor invasin is highly activated and nearly constitutive in all tested Y. enterocolitica O:3 strains. This is in contrast to O:8 serotypes in which invasin synthesis is repressed at 37°C due to H-NS mediated silencing and rapid degradation of the invA activator protein RovA. Interestingly, a previous study also reported that invA expression of a serotype O:9 strain was higher than in serotype O:8, but it was still significantly reduced at 37°C [49]. Constitutive expression of the invA gene in the O:3 strains was acquired by an IS1667 insertion into the invA regulatory region harbouring RovA and H-NS binding sites. Gene activation by transposons has been described for other genetic systems but the induction mechanism of the Y. enterocolitica O:3 invA gene seems distinct from previously reported systems. Transposable elements usually activate gene expression by replacing a negative regulatory element or through introduction of promoter elements [50], [51]. One of the best-characterized examples of transposon-mediated gene activation is the beta-glucoside (bgl) operon of E. coli. This system is usually repressed but can be activated by IS insertions up- or downstream of the promoter in either orientation relieving H-NS repression [52], [53]. However, deletion analysis revealed that transposon-mediated invA activation in Y. enterocolitica O:3 is not solely due to disruption of the inhibitory H-NS binding sites, but also requires an IS-specific activating element. One recent study revealed a novel transposon-mediated gene activation mechanism. An IS5 insertion at a single site and in only one orientation was found to activate expression of the glpFK operon in a crp background [54]. A short sequence at the 3′ end of the IS5 transposon, including a permanently bent polyA-tract and an IHF binding site, was shown to be required for glpFK induction. This shows that unique sequences within a mobile element can act as an enhancer or gain an activator binding function sufficient to activate close promoters. In this study we found that IS1667-promoted activation of invA expression in Y. enterocolitca O:3 at 25°C and 37°C is largely dependent on the presence of an IS1667-generated promoter and alternative RovA (activator) and H-NS (silencer) binding sites. RovA of YeO:8 was previously shown to activate invA expression only at moderate temperatures through antirepression of H-NS-mediated silencing [45]. A temperature upshift to 37°C, however, results in a conformational change within RovA that strongly reduces the DNA-binding capacity of the regulator. It has been previously shown that the apparent dissociation constant (K_d) of the thermoregulated RovA protein of Y. pseudotuberculosis is about four-fold increased upon a temperature shift from 25°C to 37°C [18]. Furthermore, it was found that the temperature upshift renders the RovA protein more susceptible to degradation by the Lon and ClpP proteases [18]. Comparable studies with the RovA protein of YeO:8 8081v demonstrated similar properties and identical function as an intrinsic thermosensor (F. Uliczka, unpublished data). Here, we found that a single proline to serine exchange at position 98 (P98S) increases the stability of YeO:3 RovA without affecting the thermosensing ability of the protein. As a consequence, significantly higher RovA concentrations are present within the bacteria and this is sufficient to compensate for the thermo-induced reduction of RovA DNA binding. As YeO:3 strains originate mainly from boars and pigs with a higher body temperature of about 39°–40°C, a more temperature-stable RovA variant might be advantageous for persistence in these animals. According to our proposed structure model of RovA [55] the amino acid P98 is located in a surface exposed loop structure and is as such easily accessible for the proteases. How the P98S mutation affects proteolytic degradation is not yet clear. However, comparative CD spectroscopy of purified RovA_O:8(P98) and a RovA_O:3(S98) variant of Y. pseudotuberculosis indicated that no major structural changes are induced by this amino acid substitution (N. Quade, unpublished results). Furthermore, proteolysis is drastically reduced but not completely blocked by the P98S mutation as a slightly higher concentration of the regulatory protein was detected in a Yersinia lon mutant strain.

In summary, a more stable RovA variant (RovA_O:3(S98)) and an IS1667 insertion in the invA promoter region, providing an additional promoter followed by slightly weaker RovA and H-NS binding sites, allow high expression levels of invasin in YeO:3 strains at 37°C. How these different properties influence pathogenesis is not fully clear, but first experiments addressing host cell invasion and colonization of YeO:3 in the mouse model revealed that loss of the IS1667 element reduced host cell entry and had a severe effect on the infection process in mice. Colonization of the PPs and the MLNs by YeO:3 strain YE15 (P_invO:3ΔIS) was significantly reduced and only occasionally these bacteria were able to reach deeper organs in co-infection experiments. This indicates that high levels of invasin are more advantageous and/or important for YeO:3 to initiate a successful infection than for YeO:8 in mice. In fact, a YeO:8 8081v invA mutant strain shows a delayed but still efficient colonization of deeper tissues [4], [56].

In contrast to invasin, loss of the RovA regulator in YeO:8 8081v leads to a 70-fold increase of the LD₅₀ and causes a much more severe alteration of the infection kinetics, e.g. penetration of the Peyer's patches and mesenterial lymph nodes was much more reduced, and dissemination into liver and spleen was abolished [56]. Interestingly, significantly higher numbers of bacteria could be detected in lymphatic tissues and organs of mice when the unstable variant RovA_O:3(S98) was expressed by YeO:3. This strongly suggests that elevated RovA levels, although they lead to higher amounts of invasin are disadvantageous for the colonization of the organs in mice. Microarray analysis to define the RovA regulon of Y. enterocolitica in YeO:8 revealed 40 genes to be activated and 23 repressed by RovA [57]. Among the RovA-repressed loci are several metabolic genes, e.g. permeases for glutamine, glutamate and aspartate) and their upregulation due to reduced RovA levels at 37°C might be important for the biological fitness and survival in host tissues during infection in mice. A more stable but still thermo-sensitive RovA variant, as found in YeO:3 strains (RovA_O:3(P98)), would allow similar regulatory control over virulence and metabolic genes in pigs and boars with a higher body temperature (39°C–40°C). In order to test whether the IS1667 insertion in the invA promoter region and the RovA_O:3(S98) variant reflects an optimal adaptation to these host organisms we are currently establishing a pig infection model.

Although high levels of invasin are produced by YeO:3 strains at moderate growth temperatures, cell invasion was either not initiated or very inefficient when the bacteria were pregrown at 25°C. This is in strong contrast to other Y. enterocolitica serotypes or Y. pseudotuberculosis isolates which enter host cells with their highest efficiency when cultured at moderate temperatures. Previous analyses showed that induced flagellar-dependent motility is required for efficient invasion of YeO:8, but flagella production of this pathogen is repressed at 37°C [34]. Flagella are needed to ensure migration of the bacteria to host cells, but are not essential for the invasion process once the bacteria contact the mammalian cells. Motility assays and electron microscopy revealed that flagellated and motile strains of Y. enterocolitica O:3 strains can be isolated from the intestinal tract of a mouse, but they rapidly loose their motility and become aflagellated during growth under standard laboratory conditions. As a result, YeO:3 strains are less invasive than other motile serotypes in vitro, but cell entry could be improved upon artificial host cell contact by centrifugation.

However, when the bacteria were pregrown at 25°C, YeO:3 uptake after host cell contact is still less efficient compared to YeO:8 or other serotypes, indicating that other factors repress invasin-mediated internalization at moderate temperatures or enhance cell entry at 37°C. Y. enterocolitica isolates grown at room temperature generally express LPS with O-ag, whereas only very small amounts of O-ag are present in bacteria grown at 37°C [33], [58]. The O-ag of YeO:8 is required for full virulence and plays a major role in pathogen-host interplay by affecting the expression and function of other Yersinia virulence factors, e.g. absence of the O-ag reduced invA expression and internalization into HeLa cells [31]. In contrast, O-ag deficient YeO:3 rough mutants are more efficiently internalized by human epithelial cells. Furthermore, no reduction of invA expression was observed in the rough mutants at 37°C when O-ag expression is fully repressed. Unlike other Yersinia serotypes and other Gram-negative bacteria, the YeO3 O-ag forms a long homopolymer that is linked together with the OC hexasaccharide to the inner core forming a unique branched LPS structure. Its formation was previously shown to prevent proper function of some small size outer membrane proteins. For instance, O-ag was shown to inhibit serum resistance indirectly by masking the adhesin Ail from complement regulator C4bp binding [59]. Therefore, reduced O-ag density in YeO:3 at 37°C is very likely diminishing sterical hindrance thus allowing better access and host cell receptor binding by surface adhesins such as invasin and YadA (Fig. 13).

In fact, besides invasin, also production of the adhesin YadA is required to promote efficient uptake of YeO:3. The virulence plasmid encoded trimeric YadA protein is highly and exclusively expressed at 37°C, and forms a capsule-like, fibrillar matrix covering the bacterial surface [60]. YadA of Y. enterocolitica O:8 strains has been shown to promote tight binding to extracellular matrix proteins such as collagen and laminin, but it does not contribute to epithelial cell entry compared to invasin [19], [61]. In fact, at 37°C when YadA is highly expressed but no or only very low levels of invasin are produced by YeO:8, no internalization of the bacteria is initiated (Fig. 3B, 6A). Internalization of YeO:3 at 37°C also seems to be exclusively mediated by invasin as an invA mutant is unable to enter host cells. Yet, YadA synthesis is not dispensable, as its absence in a yadA mutant or during growth at 25°C results in a significantly lower cell adhesion and uptake rate even in the presence of high amounts of invasin, whereas yadA expression by an inducible promoter at 25°C leads to strong adhesion and efficient invasion of YeO:3 similar to YeO:8. YadA seems to be required to guarantee tight and efficient host cell binding which then in turn leads to a more efficient invasin-mediated uptake. Both invasin and YadA promote direct or indirect binding to beta 1 integrins [13], [62]. High affinity binding and ligand-induced beta 1-integrin-clustering by invasin are required for efficient uptake by this host cell receptor family [63], [64]. However, invasin of Y. enterocolitica does not contain a self-association domain mediating receptor-clustering and uptake in contrast to invasin of Y. pseudotuberculosis [65]. It is therefore tempting to speculate that co-expression of the somewhat longer cell surface adhesin YadA which promotes binding to ECM molecules bound to beta 1 chain integrins promotes or enhances intimate direct interaction of invasin and subsequent internalization (Fig. 13).

In summary, results in the present investigation provide evidence that even small variations between virulence factors and regulators are responsible for the substantial difference in host cell interactions of Y. enterocolitica serotype O:3 in comparison to other Y. enterocolitica serotypes. Serotype O:3 specific variations in the surface molecule expression pattern imply that this Y. enterocolitica subspecies varies in its dynamic capacity to adapt to changing environments and individual niches within the host. A particular repertoire of host interaction genes may confer a survival advantage or pathogenic potential in a specific microenvironment. Thus, an individual subspecies may be better adapted for survival in a particular host or host site, e.g. human gastrointestinal tract or oral cavities of swine (e.g. tongue and tonsils).

Materials and Methods

Ethics statement

All animal work was performed in strict accordance with the German regulations of the Society for Laboratory Animal Science (GV-SOLAS) and the European Health Law of the Federation of Laboratory Animal Science Associations (FELASA). The protocol was approved by the Niedersächsisches Landesamt für Verbraucherschutz und Lebensmittelsicherheit: animal licensing committee permission no. 33.9.42502-04-055/09. All efforts were made to minimize suffering.

Bacterial strains, cell culture, media and growth conditions

The strains used in this study are listed in Table 1. Overnight cultures of E. coli were routinely grown at 37°C, Yersinia strains were grown at 25°C or 37°C in LB (Luria-Bertani) broth. The antibiotics used for bacterial selection were as follows: ampicillin 100 µg/ml, chloramphenicol 30 µg/ml, kanamycin 50 µg/ml, gentamicin 50 µg/ml and tetracycline 10 µg/ml. For infection experiments, bacteria were grown at 25°C or 37°C, washed and diluted in PBS prior to infection.

Human HEp-2 cells were cultured in RPMI 1640 media with GlutaMAX (Invitrogen) supplemented with 7.5% newborn calf serum (Sigma Aldrich) at 37°C in the presence of 5% CO₂. Human Caco-2 cells were grown in DMEM/HAM's F-12 (Biochrom) supplemented with 10% FBS Superior (Biochrom).

DNA manipulations and construction of plasmids

All DNA manipulations, PCR, restriction digestions, ligations and transformations were performed using standard techniques as described previously [66], [67]. Plasmids used in this study are listed in Table 1, and primers are given in Table S2.

Plasmids pFU49 (invA_O:3) and pFU182 (invA_O:8) were constructed by amplification of the invA gene from genomic DNA of YeO:3 Y11 and YeO:8 8081v with primers II40/II42 and the PCR-derived fragments were subsequently integrated into the SacI/SalI sites of pBAD33. For the overexpession of RovA_O:8 the rovA gene was amplified from genomic DNA of YeO:8 8081v with primers II417/II418 and the generated fragment was inserted into the NcoI/XhoI sites of pET28a, generating pFU156. Plasmid pFU157 was obtained by QuikChange mutagenesis of pFU156 using primer II375/II376. Plasmid pFU199 was constructed by inserting a hns⁺_O:3 fragment amplified with primers II726/II727 into the EcoRI/SalI sites of pASKIBA43+. For the construction of pFU220 a BamHI/SalI fragment of pFU188 containing the yadA gene was integrated into pBAD33. pFU188 was obtained by insertion of a PCR fragment amplified with primers II517/II518 from genomic DNA of YeO:3 Y11 into the NcoI/SalI sites of pBAD/Myc-HisA.

Plasmids pFU170 and pFU171 encoding the P_invAO:8::luxCDABE and P_invAO:3::luxCDABE reporter fusions were generated by insertion of a PCR fragment amplified with primers II177/II178 from genomic DNA of YeO:8 8081v or YeO3 Y11 in the BamHI/SalI sites of pFU175. To construct plasmid pFU172, carrying the P_{invAO:3 ΔIS}::luxCDABE fusion, two PCR fragments amplified with primer pairs II177/II179 and II180/II178 were first ligated with their blunt ends and cloned into the BamHI/SalI sites of luxCDABE fusion vector pFU175. Plasmids pFU194–198 were constructed to analyse the effect of promoter P_invAO:3 truncations. This was accomplished by separate cloning of five DNA fragments amplified with primers II542–546 and II178 from genomic DNA of YeO:3 Y11 into the BamHI/SalI sites of pFU175. Plasmids pFU201 and pFU202 carry the invAO:3 promoter region from position −248 to −146 and from −448 to −146, respectively, fused to the luxCDABE operon. For their construction PCR fragments were amplified with primer pairs II570/II543 and II571/II543, respectively, and integrated into the BamHI/SalI sites of pFU175. The P_rovA::lacZ fusions plasmids pFU129 and pFU130 were constructed by insertion of rovA promoter fragments, amplified with primer pair II260/I277 from genomic DNA of YeO:8 strain 8081v or YeO:3 strain Y11, into the BamHI/SalI sites of pFU109.

Following plasmids were engineered for the construction of rovA, invA and yadA mutant strains of Y. enterocolitica. For rovA mutagenesis, plasmid pFU167 was constructed by amplification of sacB with primers II421/II422 from pJE4 and integration into the AvrII/NotI sites of pFU102. pFU102 was constructed by insertion of three PCR-derived fragments into the SpeI/NotI sites of pFU100: (i) a SpeI/SacI fragment containing 179 bp of the rovA regulatory region amplified with primers II171/II172, (ii) a SacI/AatII fragment encoding the chloramphenicol resistance gene of pZA31 luc, and (iii) a AatII/NotI containing 119 bp of the downstream region of rovA amplified with primers II173/II174. For the invA mutagenesis, plasmid pFU213 was constructed by insertion of the SacI/AatII fragment encoding the kanamycin resistance gene of pZS*24MCS into pFU114. The plasmid pFU114 was constructed by insertion of an ‘invA’ fragment into the SalI/NotI sites of pFU100. The PCR fragment contained base pairs 40–339 of the invA coding region, amplified from genomic DNA of YeO:3 Y11 with primer pairs II211/II212 which introduce stop codons at the 5′ and 3′ end in the open reading frame of the ‘invA’ fragment. For yadA mutagenesis, plasmid pFU187 was used. This plasmid was engineered by the insertion of three PCR fragments into the SpeI/NotI sites of pFU167: (i) a SpeI/SacI fragment which contained 150 bp of the yadA regulatory region amplified from genomic DNA of YeO:3 Y11 with primer pair II513/II514 (ii) a SacI/AatII fragment of pFU32 encoding the tetracycline resistance gene, (iii) and a AatII/NotI fragment containing the last 81 bp of the yadA gene plus 69 bp of the yadA downstream region amplified from genomic DNA of YeO:3 Y11 with primer pair II515/II516.

For deletion of the IS1667 element in the invAO:3 regulatory region, we used pFU190. Plasmid pFU190 was created by the insertion of three fragments. Two fragments starting from position −1887 to −1627 and −249 to −1 of the invA promoter region were amplified with primer pairs II519/II522 and II523/II524, respectively, and ligated at their blunt ends. The resulting XhoI/NotI fragment was ligated with the SpeI/XhoI fragment from pFU32 harboring the tetracycline resistance cassette and was inserted into the SpeI/NotI sites of pFU167.

Plasmids pFU184 and pFU185 were used for chromosomal integration of a rovA wild-type and a rovA_S98P mutant copy. Both plasmids were constructed by insertion of the SacI/AvrII fragment harboring the R6K ori and the mobRP4 mobilization region from pFU100 into pFU119 and pFU138, respectively. For the generation of pFU119 rovA_O:3 including its regulatory region was amplificated from genomic DNA of YeO:3 strain Y11 with primer pair II260/II226 and cloned into the BamHI/NotI sites of pFU109. pFU138 was obtained by QuikChange mutagenesis (Stratagene) of pFU119 using primer II377/II378. All clones were confirmed by sequencing (GATC, Konstanz, Germany).

Construction Y. enterocolitica mutant strains

To construct the rovA, invA, and yadA mutants, the suicide plasmids carrying an internal fragment of invA with integrated stop codons (pFU213), or the insertion mutations rovA::Cm^R (pFU167) or yadA::Tet^R (pFU187) were propagated in E. coli S17-1 λpir and introduced by mobilization into YeO:3 strain Y1 and Y11. Transconjugants were selected on Yersinia selective agar (Oxoid) supplemented with antibiotics, selecting for the resistance of the plasmids. Since the suicide vectors cannot replicate in the YeO:3 strains, the obtained colonies are the result of plasmid integration into the Yersinia chromosome at regions of homology. The recombination event yielded merodiploid strains, which includes a wild-type and a mutant copy. Spontaneous second site recombinants where the integrated suicide vector and the wild-type copy of the gene were eliminated were isolated by selecting fast growing transconjugants on 10% sucrose plates. The rovA gene of YeO:3 (rovA_O:3) and YeO:8 (rovA_O:8) were introduced into the ΔrovA strain YE12 by conjugation. Loss of the gene function in resulting mutant strains YE1 (ΔrovA), YE12 (ΔrovA), YE18 (ΔyadA) and YE21 (ΔinvA) and regain of RovA production in strains YE13 (rovA_O:3) and YE14 (rovA_O:8) was verified by PCR and western blotting analysis. Deletion of the IS1667 element in P_invAO:3 was achieved by conjugation of plasmid pFU190 into YeO:3 strain Y1 as described above. All deletions and reintegration were verified by PCR.

Quantitative real-time PCR

Quantitative RT-PCR was performed in triplicate with independent RNA preparations using a Rotor-Gene Q thermo cycler (Qiagen). RNA was prepared using the RNeasy Mini Kit (Qiagen) according to the manufacturer's protocol. 1 µg total RNA was taken for cDNA synthesis using the QuantiTect Reverse Transcription Kit (Qiagen) according to the manufacturer's instructions. For quantitative RT-PCR, reagents from Qiagen QuantiTect SYBR Green PCR KIT (Qiagen) were used. Gene specific-primers used for qRT-PCR amplification are listed in Table S2 and were designed to produce a 120–150 bp amplicon. The amount of PCR product was quantified by measuring fluorescence of SYBR Green dye. Reported gene expression levels were normalized to levels of the 5S rRNA. Standard curves were detected during every run for each gene tested and established by comparing transcript levels in serial dilutions of total RNA from a control sample.

Primer extension analysis to determine the transcriptional start sites of the invA and the IS1667-specific promoter

Primer extension analysis was performed to determine the transcription start points of the invA gene in strain Y1. Y. enterocolitica Y1 was grown in LB at 25°C to an OD₆₀₀ of 3.0 (stationary phase). Total RNA was extracted of the samples using the SV total RNA purification kit (Promega) as described by the manufacturer. Annealing was performed with 20 µg extracted RNA and the 5′-Dig-labelled oligonucleotides (primer III94 for the IS1667 specific promoter, primer III91 for the invA promoter) in 20 µl of 1× First Strand Buffer (Invitrogen) by slow cooling of the sample (0.01°C/sec) including 8 mM dNTPs and 5× FS Buffer (Invitrogen). 200 U Superscript II reverse transcriptase (Invitrogen) was added and incubated for 1 h at 42°C. The size of the Dig-labelled reaction products was determined on a denaturing 4% DNA sequencing gel by a detection procedure as described [68].

Luciferase and beta-galactosidase assays

Optical density (OD₆₀₀) of three independent cultures of the bacteria harboring the different luciferase reporter plasmids was determined and diluted to an OD₆₀₀ of 0.1 to monitor growth of the bacteria at indicated growth conditions (complex media, 25°C and 37°C). In parallel, bioluminescence was detected in non-permeabilized cells with a Varioskan Flash (Thermo Scientific) using the SkanIt software (Thermo Scientific). Bioluminescence was measured for 1 s every 30 min and is given as relative light units (RLU/OD₆₀₀) from three independent cultures performed in duplicate. Beta-galactosidase activity was determined as described [44]. The activities were calculated as follows: beta-galactosidase activity OD₄₂₀ • 6.75 OD₆₀₀⁻¹ • Δt (min)⁻¹ • vol (ml)⁻¹.

Purification of Y. enterocolitica RovA and H-NS

RovA proteins were overexpressed in E. coli BL21 CodonPlus (DE3)-RIL, H-NS was expressed in E. coli KB4. Overnight cultures of E. coli strains, harbouring the plasmids pFU156 (rovA_O:8-his₆), pFU157 (rovA_O:3-his₆) or pFU199 (his₆-hns) were diluted 1∶100 and grown at 37°C in LB medium for 2 h. Subsequently, protein synthesis was induced with 100 µM IPTG (pFU156, pFU157) or 200 µg/l AHT (pFU199) and grown for 4 h. Bacteria overexpressing His-tagged RovA proteins were purified as described [55].

Gel electrophoresis, preparation of cell extracts and western blotting

For the analysis of invA and rovA expression bacteria were grown under environmental conditions as described. The optical density of the cultures was adjusted and a 1 ml aliquot was withdrawn from each culture. The cells were collected by centrifugation, and resuspended in 100 µl sample buffer (100 mM Tris-HCl pH 6,8, 2% SDS, 10% glycerol, 3% DTT, 0.001% bromophenol blue) and analyzed by gel electrophoresis and western blotting. For the immunological detection of the InvA, YadA and RovA proteins, the cell extracts were separated on 10% or 15% SDS-polyacrylamide gels, and the proteins were separated by electrophoresis and transferred onto an Immobilon membrane (Millipore). Identity and expression of the adhesins were confirmed by westernblotting analysis using polyclonal antibodies against the Y. enterocolitica invasin or the Y. pseudotuberculosis RovA and YadA protein, and a second goat alkaline-phosphate antibody (Sigma) using 5-bromo-4-chloro-3-indoylphosphate (XP) and nitroblue tetrazolium (Boehringer Mannheim) as substrates.

In vivo stability analysis of RovA

Protein biosynthesis of bacterial cultures in exponential phase at 37°C was stopped by adding 50 µg/ml gentamycin and 50 µg/ml tetracycline. Samples were taken at indicated time points.

Gel retardation assays

Binding of RovA to defined PCR fragments carrying different portions of the invA regulatory region was carried out in a 20 µl reaction mixture containing increasing amounts of purified RovA protein (0.5–1.5 µg) and 80 ng of DNA. The reaction buffer contained 10 mM Tris-HCl, pH 7.5, 1 mM EDTA, 50 mM NaCl, 5 mM MgCl₂, 5 mM dithiothreitol (DTT) and 5% glycerol. The reaction mixture was incubated for 20 min at room temperature or at 37°C and separated on polyacrylamide gels as described [44]. PCR fragments encoding the invA promoter fragments a, b and c were amplified with primer pairs II519/II551, II546/II178 and II558/II559, and the csiD promoter fragment was produced by PCR with primer pairs 131/132.

Motility assays

A 2 µl aliquot of an overnight culture grown at 25°C in LB medium was spotted onto semisolid agar plates containing 0.35% agar to evaluate motility [69]. The capacity of YeO:3 Y1 and YeO:8 8081v to spread was monitored after 48 h at 25°C and 37°C.

Electron microscopy

YeO3 Y1 and YeO8 8081v grown at 25°C and 37°C overnight were fixed in growth medium with 1% formaldehyde. For transmission electron microscopy thin carbon support films were prepared by sublimation of carbon on freshly cleaved mica. Using 300 mesh copper grids, the samples were negatively stained with 2% (w/v) aqueous uranylacetate, according to the method of [70], and examined in a transmission electron microscope (TEM910, Zeiss, Germany) at an acceleration voltage of 80 kV at calibrated magnifications. Images were recorded digitally with a Slow-Scan CCD camera (ProScan 1024×1024, Scheuring, Germany) with ITEM software (Olympus Soft Imaging Solutions, Münster, Germany). Images were corrected for brightness and contrast applying Adobe photoshop CS3.

For field emission scanning electron microscopy glass coverslips samples were fixed with a solution containing 5% formaldehyde and 2% glutaraldyhde in cacodylate buffer (0.1 M cacodylate, 0.01 M CaCl₂, 0.01 M MgCl₂, 0.09 M sucrose pH 6.9). Dehydration was carried out in a graded series of acetone (10%, 30%, 50%, 70%, 90%, 100%) on ice for 15 min for each step. Samples were then critical-point dried with liquid CO₂ (CPD 030, Balzers Union, Liechtenstein) and covered with a gold film by sputter coating (SCD 040, Balzers Union, Liechtenstein). For examination in a field emission scanning electron microscope (DSM 982 Gemini, Zeiss, Germany), an Everhart Thornley SE detector was used with the inlens SE detector in a 50∶50 ratio at an acceleration voltage of 5 kV.

Cell adhesion and invasion assay

For cell adhesion and uptake assay 5×10⁴ HEp-2 cells were seeded and grown overnight in individual wells of 24-well cell culture plates. Cell monolayers were washed three times with PBS and incubated in binding buffer (RPMI 1640 medium supplemented with 20 mM HEPES (pH 7.0) and 0.4% BSA before the addition of bacteria. Approximately 5×10⁵ bacteria were added to the monolayer and incubated without or after centrifugation of the bacteria onto the monolayer at 22–25°C to prevent bacterial internalization and 37°C to test for cell binding and invasion as described [62], [71]. 30 min post infection, the cells were washed extensively with PBS. The total number of host cell-associated bacteria was determined by cell lysis using 0.1% Triton X-100 and plating on bacterial media. Bacterial uptake was assessed 30 min after infection as the percentage of bacteria, which survived killing by gentamicin, as described [63]. For each strain, the relative level of bacterial adhesion and uptake was determined by calculating the number of colony-forming units relative to the total number of bacteria introduced onto monolayers. Number of invaded bacteria is given relative to the number of cell-bound bacteria. The experiments were routinely performed in triplicate.

Mouse infection

Bacteria used for oral infection were grown overnight in LB medium at 25°C, washed and resuspended in PBS. Female BALB/c mice 6–8 weeks old were purchased by Janvier. Groups of 7–10 animals were pretreated with desferal 24 h prior infection as described previously [72]. Subsequently, mice were orally infected with Y. enterocolitica strains Y1, YE15 or YE14 in single infection and co-infection experiments using a ball-tipped feeding needle. 5×10⁸ bacteria of each strain were administered orogastrically. In co-infection experiments, mice were orally infected with an equal mixture of 5×10⁷ (low dose) or 5×10⁸ (high dose) bacteria of Y. enterocolitica strains Y1 and YE14, or Y1 and YE15. For discrimination of strains Y1 and YE15 low-copy vectors pFU99 and pFU109 with different antibiotic resistance cassettes were introduced in Y1 and Y15, respectively. Presence of these vectors had no effect on Yersinia fitness and virulence and they were maintained in all bacteria recovered from host tissues throughout a five days time course of infection (F. Uliczka, unpublished results). Three or five days after infection, mice were euthanized by CO₂. Peyer's patches, mesenteric lymph nodes, liver and spleen were isolated. The ileum was rinsed with sterile PBS and incubated with 100 µg/ml gentamicin in order to kill bacteria on the luminal surface. After 30 min, gentamicin was removed by extensive washing with PBS for three times. Subsequently, all organs were weighed and homogenized in sterile PBS at 30.000 rpm for 30 sec using a Polytron PT 2100 homogenizer (Kinematica, Switzerland). The numbers of bacteria were determined by plating three independent serial dilutions of the homogenates on LB plates with and without antibiotics. The colony forming units (cfu) were counted and are given as cfu per g organ/tissue. The competitive index relative to wild-type strain Y1 was calculated as described by Monk et al. 2008 [78].

Supporting Information

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