|Home | About | Journals | Submit | Contact Us | Français|
Pathogenic yersiniae (Yersinia pestis, Y. pseudotuberculosis, and Y. enterocolitica) harbor a 70-kb virulence plasmid (pYV) that encodes a type III secretion system and a set of at least six effector proteins (YopH, YopO, YopP, YopE, YopM, and YopT) that are injected into the host cell cytoplasm. Yops (Yersinia outer proteins) disturb the dynamics of the cytoskeleton, inhibit phagocytosis by macrophages, and downregulate the production of proinflammatory cytokines, which makes it possible for yersiniae to multiply extracellularly in lymphoid tissue. Y. enterocolitica serotype O:8 belongs to the highly mouse-pathogenic group of yersiniae in contrast to Y. enterocolitica serotype O:9. However, there has been no systematic study of the contribution of Yops to the pathogenicity of Y. enterocolitica O:8 in mice. We generated a set of yop gene deletion mutants of Y. enterocolitica O:8 by using the novel Red cloning procedure. We subsequently analyzed the contribution of yopH, -O, -P, -E, -M, -T, and -Q deletions to pathogenicity after oral and intravenous infection of mice. Here we showed for the first time that a ΔyopT deletion mutant colonizes mouse tissues to a greater extent than the parental strain. The ΔyopO, ΔyopP, and ΔyopE mutants were only slightly attenuated after oral infection since they were still able to colonize the spleen and liver and cause systemic infection. The ΔyopO mutant was lethal for mice, whereas ΔyopP and ΔyopE mutants were successfully eliminated from the spleen and liver 2 weeks after infection. In contrast the ΔyopH, ΔyopM, and ΔyopQ mutants were highly attenuated and not able to colonize the spleen and liver on any of the days tested. The ΔyopH, ΔyopO, ΔyopP, ΔyopE, ΔyopM, and ΔyopQ mutants had only modest defects in the colonization of the small intestine and Peyer's patches. The ΔyopE mutant was eliminated from the small intestine 3 weeks after infection, whereas the ΔyopH, ΔyopP, ΔyopM, and ΔyopQ mutants continued to colonize the small intestine at this time.
Yersiniae that are pathogenic to humans include Yersinia pestis, Y. pseudotuberculosis, and Y. enterocolitica. Y. pestis is the cause of bubonic plague, which is transmitted by fleas, whereas Y. enterocolitica and Y. pseudotuberculosis cause self-limited food-borne gastrointestinal disease in humans. In the mouse model of infection, however, both Y. enterocolitica and Y. pseudotuberculosis cause systemic disease. Common to all of these species is the presence of a 70-kb virulence plasmid that harbors a type III secretion system (TTSS) and several secreted and translocated proteins called Yersinia outer proteins (Yops) (reviewed by Cornelis ). This plasmid-encoded TTSS enables yersiniae to survive and proliferate extracellularly in host lymphatic tissues. Y. enterocolitica and Y. pseudotuberculosis both translocate a set of at least five effector proteins (YopH, YopO/YpkA, YopP/J, YopE, and YopM), whereas Y. enterocolitica is known to translocate a sixth effector called YopT (35). Four of the above-mentioned Yops (YopH, YopE, YopT, and, YopO/YpkA) disturb cytoskeletal dynamics and thereby inhibit phagocytosis by polymorphonuclear leukocytes and macrophages (12, 23, 28, 49). YopH is a phosphotyrosine phosphatase (61) that dephosphorylates focal adhesion kinase (Fak), paxillin, Fyn-binding protein (FYB), p130cas, and SKAP-HOM, thereby disrupting focal adhesions (2, 10, 11, 16, 29, 46, 47), and suppresses the oxidative burst of macrophages (12, 47). YopH has been shown to contribute not only to evasion of the innate immune response but also to the adaptive immune response by impairing T- and B-cell activation (1, 60). YopE is a GTPase-activating protein that acts preferentially on Rac GTPases, which may explain the YopE-associated effect of actin stress fiber destruction (9, 44, 50). YopT is a cysteine protease that preferentially inactivates RhoA GTPases by cleaving at the C-terminal geranylgeranyl-cysteine residue (52, 62). YopO (YpkA in Y. pseudotuberculosis) is an autophosphorylating serine/threonine kinase that interacts with RhoA, Rac and actin (6, 22, 62). YopP/J induces apoptosis of macrophages and inhibits activation of the transcription factor NF-κB, thereby inhibiting tumor necrosis factor alpha and interleukin-8 release by macrophages and epithelial cells (14, 19, 20). YopM is a leucine-rich repeat protein that traffics to the nucleus of infected cells (54), but its target and function are as yet unknown. Recently, it was shown that YopM forms a protein complex with the two cellular kinases PRK2 and RSK1 (39). YopQ (YopK in Y. pseudotuberculosis) is not one of the translocated effector proteins but has been shown to control the translocation of Yop effectors into eukaryotic cells with a yopK mutant hypertranslocating Yops and inducing a larger YopB-dependent pore in eukaryotic cell membranes (33).
Virulence of Yersinia yop mutants has been previously studied mostly in Y. pseudotuberculosis. It is, however, not possible to generally extrapolate these results to Y. enterocolitica since many differences in virulence factor profile and clinical manifestations exist between the two species. Mutations in yopH, ypkA, yopJ, yopE, yopM, and yopK of Y. pseudotuberculosis serotype III have been shown to result in various degrees of attenuation (13, 15, 24, 27, 34, 37, 38, 42). In most cases, the 50% lethal dose was determined in order to assess virulence. Several studies also analyzed colonization of mouse tissue after oral infection (9, 26, 27, 34, 42, 55). However, comparison of data is difficult because different inbred mouse strains, different strains of Yersinia, and different infection doses and routes of application were used.
The influence of the complete set of Yops on virulence of Y. enterocolitica in the mouse model has been only partially studied (35, 43) with Y. enterocolitica of serotype O:9. This serotype is only weakly pathogenic for mice (due to lack of the high pathogenicity island encoding the biosynthesis and uptake of the siderophore yersiniabactin [ybt] which contributes to mouse virulence), and therefore mice have to be pretreated with an iron chelator such as desferrioxamine, which not only promotes growth of yersiniae by iron delivery via ferrioxamine uptake but also leads to immunosuppression of the host (5). We generated here a set of yop deletion mutants of Y. enterocolitica of the highly pathogenic O:8 serotype WA-314 (biotype 1B) by the recently reported Red recombination procedure (18) and studied the pathogenicity of these mutants and the course of colonization of the small intestine (SI), Peyer's patches (PP), liver, and spleen over 3 weeks after intravenous and oral infection of C57BL/6 mice.
The bacterial strains and plasmids used in the present study are listed in Table Table1.1. Bacteria were cultured aerobically in Luria-Bertani (LB) broth or on LB agar plates (Difco Laboratories, Detroit, Mich.) at 27°C (Yersinia spp.) or 37°C (Escherichia coli). Antibiotics were used at the following concentrations: kanamycin, 25 μg/ml; nalidixic acid, 60 μg/ml; and chloramphenicol, 20 μg/ml.
Plasmid DNA was isolated with Qiagen kits (Hilden, Germany) according to the manufacturer's recommendations. Restriction enzyme digestions, recovery of DNA fragments from agarose gels, ligations, and transformations were performed as previously described (3). Enzymes and deoxynucleoside triphosphates were purchased from Invitrogen (Karlsruhe, Germany). High-fidelity polymerase was obtained from Roche (Mannheim, Germany). Oligonucleotides were synthesized by Thermo (Ulm, Germany).
We generated stable Y. enterocolitica Yop mutants by using the λ phage recombinases Redα and Redβ as previously described for E. coli (18). Recombinases were expressed directly in Yersinia. For this purpose, we transformed WA-314 with plasmid pKD46 harboring recombinases redα and redβ, as well as redγ, an inhibitor of bacterial exonucleases. Yersiniae were grown overnight at 27°C, diluted 1:100, and grown to exponential phase in LB medium containing 0.1% arabinose to induce the expression of recombination functions. Yersiniae were made electrocompetent and frozen at −80°C. Recombination fragments consisting of an antibiotic resistance gene with its own promoter, flanked by 50-nucleotide (nt) homology arms, were generated by PCR. The 3′-end 21 nt of each primer were designed to amplify the kanamycin resistance (Kanr) cassette from pACYC177 (forward, 5-TCACTGACACCCTCATCAGTG-3′; reverse, 5′-CGTCAAGTCAGCGTAATGCTC-3′) or the chloramphenicol resistance (Cmr) cassette from pACYC184 (forward, 5′-TGACGGAAGATCACTTCGCAG-3′; reverse, 5′-TTGAGAAGCACACGGTCAC-3′), whereas the 5′ end of each primer contained the 50-nt homology arms. These were designed so that the entire coding region of each yop gene (yopH, -O, -P, -E, and -T) would be replaced by the antibiotic resistance marker. Homology arms were derived from the sequence of pYVa127/90 (GenBank accession number NC_004564) (25). The ΔyopQ mutant used for virulence experiments harbors the first 50 amino acids of YopQ. The ΔyopM mutant was constructed by ligating a PstI-restricted 1.2-kb Kanr cassette cut from pUK4k into the NsiI site of the yopM gene, which was cloned into the suicide vector pGPCAT. Mutagenesis was performed as previously described (58). WA-C(pYV::CM) was constructed by inserting a Cmr cassette amplified from pACYC184 into the noncoding region of the pYV plasmid, upstream of yadA, by the Red cloning procedure. This strain was shown to be as virulent as the unmarked parental strain WA-314 (results not shown). All mutated pYV constructs were transferred to a plasmidless WA-C strain. All strains were passaged through mice before virulence experiments were performed by intraperitoneal infection with 108 CFU and reisolation of yersiniae from the peritoneum after 20 h.
Secretion of Yop proteins was induced as previously described (57). Yersiniae were grown overnight in LB medium at 27°C, diluted 1:40 in brain heart infusion broth (Difco), and incubated for 2 h at 37°C. Yop expression and/or secretion was induced by the addition of EGTA (5 mM) for Ca2+ chelation, MgCl2 (15 mM), and glucose (0.2%). Bacteria were grown at 37°C for 2 to 3 h and centrifuged (10,000 × g, 15 min), and proteins were precipitated from the culture supernatant with trichloroacetic acid. Released proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) (36) on an 11.5% polyacrylamide gel and then stained with Coomassie blue. Immunoblotting was performed as described previously (31) with nitrocellulose sheets (Schleicher & Schuell). Blocking was performed overnight with 5% bovine serum albumin in phosphate-buffered saline (PBS) at 4°C. Polyclonal rabbit anti-YopO, anti-YopQ, and anti-YopT (1:5,000) antisera, as well as a horseradish peroxidase-conjugated secondary antirabbit antibody (Sigma) diluted 1:5,000, were used for immunostaining.
Six- to eight-week-old female C57BL/6 mice (Harlan, Winkelmann, Germany) were infected with 108 CFU orally or 4 × 104 CFU intravenously from frozen stock suspensions. Stock suspensions were prepared by growing bacteria to stationary phase in LB medium at 27°C, followed by freezing in 15% glycerol. After appropriate dilutions, bacteria were washed twice with PBS, and mice were fed 50 μl by using a microliter pipette, or 100 μl was injected into the lateral tail vein. Mice were subjected to fasting 16 h prior to oral infection. The actually administered dose was determined by plating serial dilutions on Mueller-Hinton agar for 36 h at 27°C. Mice were sacrificed by CO2 asphyxiation. Liver, spleen, and PP were aseptically removed and homogenized in 5 ml (liver) or 1 ml (spleen and PP) PBS. PP were washed to remove loosely attached bacteria by rinsing them with 2 ml of PBS. The SI was washed with 5 ml of ice-cold PBS. To determine the numbers of CFU/organ, serial dilutions of homogenates were plated on Yersinia selective CIN agar (BD Biosciences, Heidelberg, Germany). P values were determined by using a two-tailed, unpaired Student t test. P values of <0.05 were considered significant. For the competition experiment, a two-tailed paired Student t test was used.
Yersinia yop mutants were generated by replacing the coding region of each yop by a Kanr cassette. This was accomplished by Redα- and Redβ-mediated homologous recombination between the pYV plasmid and a PCR product consisting of the Kanr resistance gene flanked by 50-nt homology arms. Correct replacement of the respective yop genes by the Kanr cassette was verified by PCR and SDS-PAGE of secreted Yop proteins and Western blotting (Fig. (Fig.1).1). To rule out any unwanted recombination in the chromosome due to the action of Redα and Redβ, we transferred all mutated plasmids to the previously pYV-cured strain WA-C. Furthermore, we checked that no unwanted recombination in the mutant pYV plasmids had taken place by restriction endonuclease digestion of the resulting Δyop-pYV plasmids with HindIII and BamHI (results not shown). Two of the mutants (ΔyopQ and ΔyopM) generated by replacement of the entire coding region with a Kanr cassette turned out to be deregulated when grown at 37°C (temperature-sensitive phenotype) and consequently unable to colonize any mouse tissue after oral infection. Therefore, to perform virulence studies, we generated another ΔyopQ mutant by Red cloning, sparing the first 50 amino acids of YopQ. This mutant did not show a growth deficit at 37°C. For yopM we used a mutant that we had already constructed by the suicide vector approach. This mutant harbors a 1.2-kb Kanr cassette at nt 661, expresses a truncated version of YopM of ~25 kDa (verified by Western blotting), and shows Ca2+- and temperature-dependent growth like that of the wild type.
Groups of six C57BL/6 mice were orally infected with 108 CFU of each Δyop mutant (WA-C(pYVΔYop) and WA-C(pYV::CM). The course of colonization was determined by counting the surviving bacteria in the liver, spleen, PP, and SI on days 2, 5, 7, 12, and 21 postinfection by plating tissue homogenates (Fig. (Fig.22 and and3).3). Two days after oral infection, all mutants (ΔyopH, ΔyopO, ΔyopP, ΔyopE, ΔyopM, ΔyopT, and yopQ) and WA-C(pYV::CM) were able to efficiently colonize the SI and PP, with ΔyopH, -O, -P, -E, -M, and -Q mutants showing only moderate defects in colonizing these tissues. The course of infection with WA-C(pYV::CM), as well as the ΔyopO, ΔyopP, ΔyopE, and ΔyopT mutants, was progressive, with bacteria disseminating systemically and forming abscesses in livers and spleens by day 5. By this time all mice infected with these mutants showed severe signs of illness. The ΔyopH, ΔyopM, and ΔyopQ mutants, on the other hand, were highly attenuated and were not able to significantly colonize spleens and livers on any of the days tested (limit of detection of 10 CFU in the spleen and 50 CFU in the liver). By day 7, the ΔyopT, ΔyopO, ΔyopE, and ΔyopP mutants showed the highest colony counts in spleens and livers, with most mice infected with WA-C(pYV::CM), ΔyopT, and ΔyopO mutants dying between days 7 and 12 due to systemic infection and high bacterial load in organs (Fig. (Fig.3).3). The ΔyopE and ΔyopP mutants were, however, successfully eliminated from spleens and livers by day 12. Furthermore, ΔyopP, ΔyopE, ΔyopM, and ΔyopQ mutants were still able to colonize the SI and PP by this time. The ΔyopH mutant was able to colonize only the SI but had been eliminated from the PP by this time. At 3 weeks after infection, ΔyopH, ΔyopM, and ΔyopQ mutants were able to colonize the lumen of the SI only, whereas the ΔyopP mutant continued to colonize both the SI and the PP. To demonstrate that attenuation of our mutants was not due to polar effects caused by the Kanr cassette, we complemented the most highly attenuated mutant (ΔyopH) with a low-copy plasmid (pACYC184) harboring yopH and sycH under their natural promoters (57). At 5 days after oral infection, this strain was able to colonize the spleens and livers of infected mice to an extent comparable to WA-C(pYV::CM) (Fig. (Fig.44).
Groups of five C57BL/6 mice were infected with 4.5 × 104 CFU of the Δyop mutants and WA-C(pYV::CM). Surviving bacteria in livers and spleens were determined on days 2 and 4 postinfection (Fig. (Fig.5).5). WA-C(pYV::CM) showed high colony counts in spleens and livers on day 2 (6.53 ± 0.40 and 4.88 ± 0.37 log CFU) with infection progressing by day 4 (8.33 ± 0.54 and 5.73 ± 0.32 log CFU). The ΔyopH mutant was the most highly attenuated mutant, with a 2,100-fold reduction in CFU compared to WA-C(pYV::CM) by day 2. The colony counts were 100-fold lower for ΔyopQ and 13-fold lower for ΔyopM, whereas the ΔyopE and ΔyopP mutants (4.7-fold and 2-fold, respectively) were not dramatically attenuated compared to the parental strain (P > 0.05). The ΔyopT mutant, on the other hand, colonized the spleen to a sevenfold-greater extent on day 2 than did WA-C(pYV::CM). By day 4, infection had progressed for the WA-C(pYV::CM), ΔyopO, ΔyopT, ΔyopM, ΔyopE, and ΔyopP mutants, showing 63-, 229-, 18-, 17-, 4.3-, and 4-fold-higher CFU counts, respectively, in the spleen than on day 2, whereas the CFU counts in the spleens of mice infected with the ΔyopH mutant dropped 40-fold. By day 4 the colony counts in spleens were 219,000-fold lower for the ΔyopH mutant than for WA-C(pYV::CM), 6,300-fold lower for the ΔyopQ mutant, 50-fold lower for the ΔyopM mutant, and 63-fold lower for the ΔyopE and ΔyopP mutants. The ΔyopO mutant showed slightly fewer CFU in the spleen (2.7-fold) but more CFU in the liver (3.2-fold), which was significant only for the liver. The ΔyopT mutant showed higher CFU counts in spleens (1.4-fold) and livers (28-fold) than WA-C(pYV::CM), values that were statistically significant only for livers (P < 0.05). Generally, the CFU counts of the yop mutants and WA-C(pYV::CM) in the livers of infected mice were 10- to 100-fold lower than the CFU counts in the spleens except for the ΔyopH and ΔyopQ mutants on day 4, which showed comparable numbers of bacteria in the liver and spleen.
The oral and intravenous infections suggested that the ΔyopT mutant was slightly more virulent than the wild-type strain. To confirm this, we infected six mice with an equal mixture (108 CFU) of WA-C(pYV::CMΔYopT) and WA-C(pYV::CM) by the intravenous route. Two days later, the mice were killed, and serial dilutions of organs were plated on kanamycin (for selection of the ΔyopT mutant) and chloramphenicol [for selection of WA-C(pYV::CM)] plates. The ΔyopT mutant showed a mean log of 4.23 ± 0.99 CFU in the liver, whereas WA-C(pYV::CM) showed a mean log of 3.05 ± 1.03 CFU. Therefore, the ΔyopT mutant outcompeted WA-C(pYV::CM) by 1.18 log CFU (P = 0.0075). No such difference could be detected for the spleens of mice, with the ΔyopT mutant showing a mean log of 6.61 ± 0.36 CFU and WA-C(pYV::CM) showing a mean log of 6.49 ± 0.34 CFU.
The objective of this study was to systematically analyze the contribution of seven Yops of Y. enterocolitica O:8, one of the highly virulent serotypes of biotype IB (New World strains), to virulence by using the same inbred mouse strain, the same route of application, and the same dose of bacteria. Although several studies have dealt with the effects of Yops on virulence, most of these were performed for Y. pseudotuberculosis serotype III, which differs considerably in virulence factor repertoire (e.g., lacking yersiniabactin) and clinical manifestations from Y. enterocolitica. This is exemplified by one study showing that even a plasmidless Y. pseudotuberculosis strain is able to multiply in the spleen after intravenous infection or to survive in human serum, whereas plasmid-cured Y. enterocolitica is rapidly eliminated from this organ or killed by serum (53, 59). Most importantly for the present study, Y. enterocolitica harbors the TTSS effector YopT, which is usually absent in Y. pseudotuberculosis (35), and several differences in a multitude of other virulence factors exist between the different Yersinia strains, e.g., YopP from Y. enterocolitica O:8 is substantially more efficient in suppressing the NF-κB pathway and mediating apoptosis than serotype O:9 (51). Invasin-mediated uptake efficiency in cell culture is much higher for Y. pseudotuberculosis than for Y. enterocolitica (21, 40). YadA and its collagen-binding potential are required for virulence in Y. enterocolitica but not in Y. pseudotuberculosis (45, 56). Furthermore, differences in serum resistance between the two species have been detected (59), and it has been reported that Y. pseudotuberculosis is more resistant to bactericidal cationic peptides (8) and shows increased outer membrane permeability to hydrophobic agents compared to Y. enterocolitica (7). It is therefore not justified to generally extrapolate mouse virulence studies obtained with Y. pseudotuberculosis to Y. enterocolitica.
The study of virulence in the mouse infection model with a naturally high-pathogenicity-island-negative Y. enterocolitica of serotype O:9 and O:3 is further complicated by the fact that mice have to be pretreated with desferrioxamine B (DFO) to achieve mouse virulence, and this pretreatment may influence pathogenicity because of the immunosuppressive effect of DFO (4). The virulence of yopQ and yopM (43) mutants in the mouse model was previously studied by using Y. enterocolitica O:9. Both mutants were shown to be attenuated after intravenous infection of mice pretreated with DFO. Both mutants were able to colonize spleens and livers of Swiss mice for at least 4 days at reduced levels compared to the wild-type strain. We were able to confirm these results here and extend them to the oral infection model, showing for the first time that both of these mutants are highly attenuated and able to colonize only the SI and PP but are not able to disseminate to the spleens and livers of orally infected mice. ΔyopQ and ΔyopM mutants were able to colonize PP for 2 and SI for 3 weeks but the numbers were somewhat lower than for WA-C(pYV::CM). These oral infections are consistent with studies of a yopK mutant in Y. pseudotuberculosis (34). YopQ fine-tuning of translocation or gating of the YopB-induced pore might be essential for effective immunosuppression of the host and systemic spread of yersiniae as proposed by Holmström et al. (33). Oral infections with ΔyopM mutants have not been performed previously. Together with the intravenous infections, our results indicate that YopM and YopQ are mainly involved in the establishment of a systemic infection in mice.
The virulence of ΔyopH, ΔyopO, ΔyopP, and ΔyopE mutants has been previously studied only for Y. pseudotuberculosis. The most striking difference between the virulence of our mutants and that of Y. pseudotuberculosis is that our ΔyopE mutant is only slightly attenuated after oral infection and caused systemic disease with regular seeding of yersiniae to spleens and livers. Furthermore, our ΔyopE mutant was able to colonize the SI and PP at somewhat reduced levels until day 12 postinfection. Y. pseudotuberculosis yopE mutants, on the other hand, were reported to be highly attenuated, being cleared from PP within 4 days and not able to reach the spleens of orally infected mice (34). These differences could be due to the use of a yadA yopE double mutant in that study (34). Another study using Y. pseudotuberculosis showed a markedly reduced ability of yopE mutants to colonize spleens of mice but only minor defects in colonizing the SI and PP (38). Possibly, the additional presence of YopT in Y. enterocolitica could also account for the more virulent phenotype of our yopE mutant since both of these Yops act on Rho GTPases and are involved in the inhibition of phagocytosis. Presumably, a ΔyopT ΔyopE double mutant of Y. enterocolitica is comparable to a yopE mutant of Y. pseudotuberculosis.
Our ΔyopO and ΔyopT mutants behaved most like WA-C(pYV::CM) after oral and intravenous infections, and in fact most mice succumbed to oral infection with these mutants at around day 7 just like the parental strain. For a yopO mutant, this is consistent with a recent study with Y. pseudotuberculosis (38) but contrasts with another (27) in which a ΔyopO mutant failed to cause a systemic infection. The mutant used in the latter study, however, also harbored a mutation in yadA, which could have had an effect on colonization of the spleen. There is only scarce evidence for the role of YopT in animal models, with one preliminary study showing that a yopT mutant was not affected in its capacity to colonize PP on day 2 after oral infection (35). Surprisingly, our yopT mutant was not attenuated and even showed higher colonization of mouse tissues after oral and intravenous infection than WA-C(pYV::CM). This is a surprising finding in light of the fact that YopT and YopO have a strong influence on phagocytosis resistance in cell culture models (28). YopO binds RhoA and Rac and YopT modifies RhoA and presumably Rac, which may also change binding properties to YopO. Possibly, YopT is redundant in this animal model, and its functions are taken over by other Yops, such as YopO and YopE. Another possibility is that the functions of these effector proteins become apparent only after several weeks of infection, when the adaptive immune system becomes effective. Since C57BL/6 mice succumb to infection after 1 week, it is not possible to study these effects in this model. We are therefore generating double mutants for yopT and other yop genes to test this hypothesis.
Our yopP mutant colonized gut tissues, as well as spleens and livers, at reduced levels but was not impaired in its ability to cause systemic disease, with bacteria regularly colonizing the livers and spleens of all mice after oral infection. By day 12 most mice had eliminated bacteria from spleens and livers, but colonization of gut tissues continued for at least 3 weeks. The role of yopJ in virulence has been previously studied only for Y. pseudotuberculosis. One study claims yopJ to be dispensable for virulence (27), and another shows that a yopJ mutant is highly attenuated, with only two of three PP and one of five spleens being colonized after oral infection (42). These differences could be due to the different Yersinia species used, the different mouse strains used, or different doses of applied bacteria.
Our ΔyopH mutant was by far the most attenuated mutant in both oral and intravenous infections. ΔyopH mutants were only slightly deficient in colonizing the SI and PP initially and were not able to disseminate and cause systemic disease. ΔyopH mutants were eliminated from the PP by day 12, earlier than the other surviving yop mutants, but colonization of the gut lumen continued for at least 3 weeks. Intravenous infections showed that the ΔyopH mutant initially implants into spleens and livers, but colony counts dramatically decrease between days 2 and 4. This indicates that YopH plays important roles in PP, as well as during the systemic stage of disease.
In summary, the ΔyopH, ΔyopO, ΔyopP, ΔyopE, ΔyopM, and ΔyopQ mutants had only modest defects in colonization of the SI and PP. This is consistent with results obtained for Y. pseudotuberculosis (38) and indicates that no single effector Yop is absolutely necessary for colonizing the SI or translocating to the underlying PP. YopH, YopQ, and YopM of Y. enterocolitica are important virulence factors for inducing systemic disease in mice, whereas YopO, YopP, and YopE are dispensable for yersiniae to reach the spleen and liver. The presence of YopT on the other hand even seems to slightly decrease virulence of Y. enterocolitica in this model.
We thank Laryssa Teplytska for excellent technical assistance.
This study was supported by Deutsche Forschungsgemeinschaft DFG (SFB 1887 and Graduiertenkolleg “Infektion und Immunität”). J.H. and H.R. were supported by the Deutsche Forschungsgemeinschaft (priority program “novel vaccination strategies”; HE1297/9-2 and RU838/1-2).
Editor: J. B. Bliska