The RNA-binding protein CsrA plays a central role in positively regulating virulence factors in Erwinia amylovora

The GacS/GacA two-component system (also called GrrS/GrrA) is a global regulatory system which is highly conserved among gamma-proteobacteria. This system positively regulates non-coding small regulatory RNA csrB, which in turn binds to the RNA-binding protein CsrA. However, how GacS/GacA-Csr system regulates virulence traits in E. amylovora remains unknown. Results from mutant characterization showed that the csrB mutant was hypermotile, produced higher amount of exopolysaccharide amylovoran, and had increased expression of type III secretion (T3SS) genes in vitro. In contrast, the csrA mutant exhibited complete opposite phenotypes, including non-motile, reduced amylovoran production and expression of T3SS genes. Furthermore, the csrA mutant did not induce hypersensitive response on tobacco or cause disease on immature pear fruits, indicating that CsrA is a positive regulator of virulence factors. These findings demonstrated that CsrA plays a critical role in E. amylovora virulence and suggested that negative regulation of virulence by GacS/GacA acts through csrB sRNA, which binds to CsrA and neutralizes its positive effect on T3SS gene expression, flagellar formation and amylovoran production. Future research will be focused on determining the molecular mechanism underlying the positive regulation of virulence traits by CsrA.

. Alignment of deduced amino acids of CsrA and secondary structure of csrB from Erwinia amylovora. (A) Alignment of deduced amino acids of CsrA (accession # CBJ47311 and NP_417176) from E. amylovora and Escherichia coli; and RsmA (accession #AAG04294) from Pseudomonas aeruginosa PAO1, and schematic map of the secondary structure of CsrA based on Schubert et al. 56 . Identical residues (*), conserved (:) and semi-conserved (.) substitutions are shown as underneath symbols. (B) Predicted secondary structure of csrB sRNA using the mfold program; (C) Gene expression of csrB and csrA by semi-quantitative PCR in wild type and the csrB and csrA mutants in MBMA medium. RT-minus indicates that no mRNA was added.
bases downstream of EAM_2713 gene and 79 bases upstream of EAM_2712 gene ( Supplementary Fig. S1). The non-coding csrB mRNA transcript is 455 nucleotides long and contains 31 GGA motifs, which are essential for CsrA binding 46,47 . The RNA folding prediction tool M-Fold predicted that the E. amylovora csrB RNA forms 18 loops, which could potentially sequester CsrA (Fig. 1B) 47 . Analysis of the upstream sequence of csrB showed that, starting 165 bases from the transcription start site, it contains 18 bp GacA binding site, TGTAAGAGATCGCTT GTA (underlined are conserved), indicating that csrB might be regulated by GacA (GrrA) 48,49 . An integration host factor (IHF)-binding site (TATCATCTGGTTA) in the upstream region of the rsmB sRNA was recently reported in E. amylovora 50 , and IHF was required for optimal GacA binding to and transcriptional activation of csrB in E. coli and S. enterica 51 .
Semi-quantitative PCR was used to determine if CsrA or csrB affect each other's RNA levels (Fig. 1C). As expected, corresponding PCR products were not detected in both mutant strains. The csrA RNA levels were not changed in the csrB mutant as compared to the wild type (WT) strain. In contrast, the csrB RNA levels were decreased about ∼ 60% in the csrA mutant relative to that of the WT strain (Fig. 1C). These results indicate that the csrB RNA may not be stable without CsrA protein, suggesting that CsrA is required for the csrB RNA accumulation, or that CsrA might indirectly stimulate csrB transcription by positively activating GrrA in a feedback regulation 25,26,52 . Growth defect in the csrA mutant is independent from glycogen accumulation. During construction of the E. amylovora csrA mutant, we observed that the mutant grows very slowly in LB medium. Therefore, we evaluated the growth rate of the csrA and csrB mutant strains in both LB and MBMA media ( Supplementary Fig. S2). The growth rate of the csrB mutant strain was similar to that of the WT in LB medium, while growth of the csrB mutant was slightly increased in MBMA medium ( Supplementary Fig. S2A,B). However, growth of the csrA mutant was greatly reduced compared to the WT in LB and MBMA medium, respectively (Supplementary Fig. S2A,B).
Since CsrA suppresses glycogen synthesis in E. coli, the excessive accumulation of glycogen impairs growth of a csrA deletion mutant and a glgCAP/csrA double mutation could restore the growth of the csrA mutant 28 . Therefore, we examined if a glgCAP mutation in E. amylovora could also restore the growth of the csrA mutant. Growth of the glgCAP mutant was similar to the WT in both media, whereas growth of the csrA/glgCAP double mutant only partially restored the growth of the csrA mutant in both media ( Supplementary Fig. S2C,D). These results suggest that glycogen accumulation may not be responsible for the slow growth of the csrA mutant in E. amylovora.
We also determined whether CsrA-csrB regulates glycogen accumulation in E. amylovora. WT, glg-CAP, csrA, and csrB mutants as well as the csrB complementation strain did not accumulate glycogen ( Supplementary Fig. S3A) 13 . However, the csrA complementation strain showed increased glycogen accumulation, suggesting that in contrary to E. coli, E. amylovora CsrA protein positively regulates glycogen synthesis. In addition, these results further confirmed that the growth defect of the csrA mutant may not be due to increased glycogen accumulation.
CsrA and csrB sRNA inversely regulate motility. We have previously reported that mutations on grrS /grrA gene exhibit increased motility compared to the WT strain 6,13 . Measurements of the diameters of the movement circles showed that the csrB mutant was hyper-motile similar to that of grrA mutant ( Fig. 2A,B). In contrast, the csrA mutant was non-motile and remained restricted to the plating spot similar to the flhDC mutant ( Fig. 2A,B). Complementation for the csrB and csrA mutants restored the motility to the WT levels ( Fig. 2A). These results indicated that CsrA and csrB sRNA are positive and negative regulators of motility, respectively.
CsrA and csrB sRNA inversely regulate amylovoran production and amylovoran biosynthesis gene expression. We have previously reported that the GrrS/GrrA system negatively regulate amylovoran production in vitro 6,13 . The amount of amylovoran produced by the csrB mutant was ten folds higher than that of the WT after 24 h and similar to that of the grrA mutant (Fig. 3A), whereas the csrA mutant did not produce any amylovoran (Fig. 3A), which is similar to those of the rcsB and ams mutants 5,6,14 . Complementation of the csrB and csrA mutants partially restored amylovoran biosynthesis, producing approximately 0.31 and 0.15 units of OD 600, respectively, as compared to 0.11 units for the WT. Consistent with amylovoran production, relative gene expressions of amsG (first gene of the amylovoran biosynthesis operon) and rcsA (a rate limit regulatory gene of amylovoran biosynthesis) in the csrB and grrA mutants were 4-7 and 2.5-3.5 fold higher, respectively, while their expressions were down-regulated 3.5 and more than 10 fold in the csrA mutant, respectively, as compared to the WT in vitro (Fig. 3B). Similarly, relative expression of amsG and rcsA genes in the csrA mutant was down-regulated 3.7 and 3.1 fold, respectively, as compared to the WT in vivo (Fig. 3C). In contrast, rcsA and amsG gene expression was increased by 2.2 and 1.5 fold in vivo in the csrB and grrA mutants as compared to the WT (Fig. 3C). These results indicated that CsrA is a positive regulator of rcsA gene expression and amylovoran production, while csrB negatively regulates expression of rcsA and amylovoran production.
Mutation in csrA, but not csrB, renders E. amylovora non-pathogenic and abolishes its ability to elicit HR in tobacco. We then determined the ability of the csrA and csrB mutants in causing disease on immature pear fruits. For the csrA mutant, no symptoms were developed on immature pears, whereas complementation of the csrA mutant developed symptoms similar to that of the WT and the csrB mutant, but to a lesser degree (Fig. 4A). In addition, the csrA mutant was not able to elicit HR in tobacco, whereas WT, the csrB and complementation strains did ( Supplementary Fig. S3B). These results demonstrated that CsrA, but not csrB, is required for causing disease and for eliciting HR in non-host tobacco.
In order to determine whether inability of the csrA mutant to cause disease is due to its ability in survival in planta, bacterial growth in pears for the csrA and csrB mutants were determined (Fig. 4B). At one day post inoculation (DPI), population of the WT, the csrB mutant, the csrB and csrA complementation strains increased from 4 log CFU/g tissue to 6.2, 5.4, 5.1, and 6.9 log CFU/g tissue, respectively. At two and three DPI, the population of these strains reached similar level, between 8-9 log CFU/g tissue. However, population of the csrA mutant decreased at one DPI, but gradually increased to 3.2 log CFU/g tissue at three DPI, which was about 6 log difference from that of the WT strain, but similar to the dspE and T3SS island deletion mutants 6,11 . This result indicated that the csrA mutant is able to survive in planta, but could not cause disease.
Expression of T3SS genes is abolished in the csrA mutant, but increased in the csrB mutant. To assess the role of CsrA and crsB on the expression of T3SS genes, we compared the relative expression of T3SS regulatory (rpoN, yhbH, hrpS, and hrpL) and dspE effector gene in grrA, csrB and csrA mutants to those of the WT. Expression of rpoN and yhbH was not affected in the csrB and grrA mutants under both in vitro and in vivo conditions, while expressions of hrpL and dspE were increased by 2.5-3 and 2.2 folds in vitro, and 1.5-2.5 and 2.5-2.8 folds in vivo, respectively (Fig. 5A,B). Expression of hrpS was not affected in the csrB mutant, but increased about 2.5 fold in the grrA mutant (Fig. 5A,B). In the csrA mutant, expression of rpoN and yhbH was down regulated by two folds under both in vitro and in vivo conditions; whereas expression of hrpS was down regulated by five and more than 10 folds under in vivo and in vitro conditions, respectively. Furthermore, hrpL and dspE expression was completely abolished in csrA mutant under both conditions. These results confirmed that T3SS gene expression is negatively regulated by csrB sRNA and positively regulated by CsrA.
Moreover, abundance of HrpA protein in WT and three mutants grown in HMM medium was detected by Western blot (Fig. 5C). Only approximately 2.5% protein signals were detected in the csrA mutant, but about 151 and 115% of protein signals were detected in the grrA and csrB mutants, respectively, as compared to that of the WT strain (Fig. 5C). These results indicate that CsrA is required for T3SS protein accumulation.
We also confirmed the relative expression of the csrA and csrB genes under the same condition. As expected, csrA and csrB expression was not detected in the csrA or csrB mutants, respectively (Fig. 5A,B). Expression of csrB was not detected in the csrA or grrA mutant strains (Fig. 5A,B), confirming the semi-quantitative PCR results that

Discussion
The GrrS/GrrA-csrB-CsrA system, composed of a two-component system, a non-coding small regulatory RNA csrB and a small RNA-binding protein CsrA, is a global dual regulatory system in many pathogenic and saprophytic bacteria [54][55][56] . Under certain environmental conditions, GrrS/GrrA system specifically activates the expression of csrB sRNA, which acts as a "molecular sponge" and binds to CsrA, thus sequestering and antagonizing its function 16,47,53,54 . The CsrA protein, which acts as a translational regulator, binds to target gene mRNA, either altering their translation or stability 17,19 . In this study, our results revealed a similar regulatory system exists in E. amylovora, and we have provided undeniable evidence that CsrA plays a central role in positively regulating virulence factors, while GrrS/GrrA-csrB act as a negative regulators, the latter antagonizing the positive role of CsrA. However, it remains to be determined whether the positive regulatory effect of CsrA on various virulence traits is direct or indirect. As a global regulator, the GrrS/GrrA-csrB-CsrA system conveys pleiotropic effects on multicellular behavior, survival and virulence of various organisms, including glycogen accumulation, secondary metabolism, motility, EPS and enzyme production, T3SS and virulence 17,19,54,57 . As a dual regulator, this system acts as either negative or positive regulator depending on organisms or individual phenotype. However, the global effects of GrrS/GrrA were shown to be mediated by exclusively through its control over transcription of sRNAs in P. aeruginosa, E. coli and S. enterica 51,53 . Optimal GrrA binding to and transcription activation of csrB requires IHF in both E. coli and S. enterica 51 . In E. amylovora, mutation of GrrA/GrrS and csrB resulted in identical phenotypes, and expression of csrB also required IHF 13,50 , suggesting that the global effect of GrrS/GrrA might also be exclusively through control over the expression of csrB sRNA. Furthermore, the CsrA-csrB system in E. amylovora works very similarly to those reported in P. aeruginosa, where RsmA acts as a central positive regulator and the GrrS/GrrA-rsmB acts as a negative regulator 31 ; contrary to those reported in other pseudomonads or in closely-related soft rot pathogens such as Pectobacterium and Dickeya 21,44 . Moreover, a csrA/glgCAP double mutant could not restore the slow growth of the csrA mutant in E. amylovora as it does in E. coli 28 , which may be due to that in E. amylovora, glycogen accumulation appears to be mainly regulated by another global regulator, the EnvZ/OmpR system 13 .
CsrA-mediated negative posttranscriptional regulation normally involves CsrA protein binding to the 5' UTR or initially translated region of target mRNAs, which contains multiple CsrA-binding sites (GGA) and one overlapping with SD sequence 47 . Bound CsrA thus represses translation by competing with ribosome binding, leading to destabilization of the target mRNAs 17,46 . CsrA also can activate translation or stabilize target mRNAs by enhancing ribosome binding or by protecting the transcripts from RNase E-dependent degradation 36,37 . In E. amylovora, CsrA positively regulates motility as reported in E. coli and P. aeruginosa; and in contrast to those in Pectobacterium wasabiae and P. carotovorum 38,58,59 . It has been reported that CsrA in E. coli binds to two sites of the flhDC leader sequence and stabilizes the flhDC transcript by masking of the RNase E cleavage sites and protecting the transcript from degradation 37 . It is most likely that E. amylovora CsrA utilizes a similar mechanism to stabilize and protect the flhDC transcripts, which needs to be further proven. Besides motility, CsrA also positively regulates both amylovoran production and T3SS in E. amylovora. The key question remaining is the underlying molecular mechanism of how CsrA positively regulates these virulence traits in E. amylovora. In E. amylovora, amylovoran biosynthesis is positively regulated by the RcsBCD phosphorelay system and RcsA, the rate limiting factor 5,60 ; whereas GrrS/GrrA, EnvZ/OmpR, Lon protease, global regulator H-NS, and orphan protein AmyR (YbjN) are all known negative regulators of amylovoran production 5,13,14,60-63 . H-NS binds to the promoter of rcsA and suppresses its expression; whereas the RcsA protein is subject to Lon-dependent degradation. Additionally, AmyR/YjbN was characterized as a novel negative regulator of EPS production in both E. coli and E. amylovora and may act as a protein stabilizer 62,63 . Recent studies have shown that both lon and ybjN mRNA could be co-purified with CsrA protein in E. coli 32 , but CsrA only bound to the coding sequence of lon mRNA 33 . In this study, expression of rcsA gene was almost abolished in the csrA mutant. Therefore, further studies are needed to determine the molecular targets of CsrA in regulating amylovoran production.
In E. amylovora, transcription of the T3SS genes is positively activated by (p)ppGpp-mediated alternative sigma factor cascade, including the master regulator HrpL, alternative sigma factor RpoN, enhancer binding protein (EBP) HrpS, ribosome-binding protein YhbH, IHF, transcriptional factor DksA and (p)ppGpp biosynthesis proteins RelA and SpoT 7,8,10,64 ; whereas GrrS/GrrA and EnvZ/OmpR systems negatively regulates T3SS gene expression 13 . In P. carotovorum, expression of hrpL is positively regulated by GacA/GacS-rsmB system, while . Relative gene expression of selected genes was calculated by the 2 −ΔΔCt method, utilizing the 16S rRNA as endogenous control and compared to wild type strain. Fold changes were the result of the mean of three replicates. Each experiment was performed at least two times with similar results. Error bars indicate standard deviations. (C) Accumulation of HrpA protein is controlled by CsrA. Abundance of HrpA-His6 protein in WT, the grrA, csrA, and csrB mutant strains was detected by western blot using anti-histidine protein antibody after grown in hrp-inducing minimal medium (HMM) at 18 °C for 6 h. Relative protein abundance was calculated using ImageJ software by utilizing the average pixel value of the signals and utilizing the WT sample as 100%. Cropped blot was displayed and full length blot was presented in Supplementary Fig. S4  RsmA negatively controls its expression 43 . Positive regulation of T3SS by RsmA is also reported in P. aeruginosa, X. campestris and X. citri 30,31,40,41 . It has been reported that RsmA activates T3SS by stabilizing the 5′ UTR of HrpG mRNA in Xanthomonas, suggesting that RsmA may regulate T3SS gene expression through HrpG, the master regulator of T3SS 30 . In addition, (p)ppGpp-mediated stringent response and CsrA regulons shared extensive overlap, suggesting that regulatory interaction exists between CsrA and (p)ppGpp-mediated stringent response regulatory system 17,32 . Therefore, CsrA -dependent control of T3SS gene expression via major transcription regulatory factors might be a conserved feature among pathogenic bacteria 19 . In this study, our results showed that CsrA is required for expression of T3SS genes in E. amylovora, including rpoN, yhbH, hrpS and hrpL regulatory genes, suggesting that these major regulatory genes might be potential targets of CsrA in E. amylovora. Additionally, a lon mutation in P. syringae increases the stability and accumulation of HrpR, another EBP similar to HrpS 65,66 . Therefore, future studies are needed to uncover the molecular mechanisms as how CsrA positively regulates T3SS in E. amylovora.
Based on our results and previous reported data 7-10,13,14,50,60 , we proposed the following working model as how the GrrS/GrrA-csrB-CsrA system might regulate virulence traits in E. amylovora (Fig. 6). In E. amylovora, the T3SS is activated by (p)ppGpp-mediated RpoN-HrpL sigma factor cascade; whereas amylovoran biosynthesis is positively regulated by the RcsABCD TCST system. In addition, the global GrrA/GrrS TCST along with integration host factor (IHF) specifically regulates the expression of csrB sRNA, which acts as a "sponge" to antagonize the effect of CsrA 13,25,[49][50][51]53 . As discussed above, CsrA is a positive regulator of motility in E. amylovora possibly by stabilizing and protecting flhDC transcript from RNase E degradation as previously reported 37 . However, the targets of CsrA in positively regulating T3SS and amylovoran biosynthesis remain unknown. Currently, we are focusing on uncovering the underlying molecular mechanism of CsrA as a central positive regulator of virulence factors in E. amylovora.
Generation of single and double mutants by λ-Red recombinase cloning. E. amylovora mutant strains were generated using λ phage recombinase method as describe previously 6,68 . Briefly, overnight cultures of E. amylovora strains harboring pKD46 were inoculated in LB broth containing 0.1% arabinose and grown to exponential phase (OD 600 = 0.8). Cells were harvested, made electrocompetent and stored at − 80 °C. These cells were electroporated with recombination fragments of cat or kan genes with their own promoter. Cat and kan fragments were obtained by PCR amplification from pKD32 or pKD13 plasmids, respectively, flanked by a 50-nucleotide homology from the target genes. To confirm csrA, csrB, and glgCAP mutations, PCR amplifications from internal cat or kan primers to the external region of the target genes were performed. The coding region of the csrA, csrB, and glgCAP genes was absent from the corresponding mutant strains, except for the first and last 50 nucleotides. Construction of the csrA and csrB complementation plasmids. For complementation of the mutant strains, the genomic region containing the promoter and gene sequence of csrA and csrB were PCR amplified, gel purified and cloned into pGEM-T-easy vector according to manufacturer's instructions (Promega, WI). Plasmid DNA purification, PCR amplification of genes, isolation of fragments from agarose gels were performed using standard molecular procedures 69 . Plasmid verification was performed by sequencing at the UIUC Core Sequencing Facility. Final plasmids were designated as pCsrA and pCsrB and transformed by electroporation into corresponding mutant strains.
Motility assay. Bacterial strains were grown overnight in LB with appropriate antibiotics, harvested by centrifugation and washed three times with PBS. Bacterial suspensions were adjusted to an OD 600 equal to 1.0, and 5 μ L drops were placed onto the center of agar plates (10 g tryptone, 5 g NaCl, 3 g agar per liter) as previously described 14 . Plates were incubated at 28 °C and movement diameters were measured after 48 h post inoculation. The experiments were performed in triplicate and repeated at least three times. CPC assay to determine amylovoran concentration. Amylovoran concentration of the WT, mutant and complementation strains was quantitatively determined by the cetylpyrimidinium chloride (CPC) method as previously described 70 . Briefly, overnight cultures of bacterial strains were harvested by centrifugation and washed three times with PBS. Five mL MBMA medium supplemented with 1% sorbitol were inoculated to a final OD 600 of 0.2 and incubated at 28 °C with shaking. After 24 h, 1 mL of each culture was centrifuged at 7,000 rpm for 10 min and 50 μ L of CPC at 50 mg mL −1 was added to the supernatant. After 10 min of incubation, the turbidity of the suspension and cell density was determined by measuring OD 600 . Amylovoran was determined by normalizing the OD 600 of the suspension to a cell density of 1.0. Each experiment was performed in triplicate and repeated at least three times.

RNA isolation.
Bacterial strains grown overnight in LB media with appropriate antibiotics were harvested by centrifugation and washed three times with 0.5X PBS before inoculating 5 mL of MBMA medium supplemented with 1% sorbitol. For hrp-inducing conditions, bacterial cells were washed three times with HMM before inoculated 5 mL of medium to a final OD 600 = 0.2. After 18 h incubation for MBMA at 28 °C or 6 h incubation for HMM at 18 °C, 2 mL of RNA protect reagent (Qiagen) was added to 1 mL of bacterial cell culture mixed by vortex and incubated at room temperature for 5 min. Cells were harvested by centrifugation and RNA was extracted using RNeasy ® mini kit (Qiagen) according to the manufacturer's instructions. DNase I treatment was performed in column before elution and RNA was quantified using Nano-drop ND100 spectrophotometer. For in vivo conditions, overnight cultures of bacterial strains were harvested by centrifugation, washed three times and suspended in PBS. Immature pear fruits were cut in half and inoculated with bacterial suspensions. After 6 h incubation at 28 °C in a moist chamber, bacterial cells were collected by washing pear surfaces with RNA protect reagent (Qiagen) 2:1 with water and total RNA was extracted as described above.
Reverse transcription quantitative real-time PCR (qRT-PCR). One microgram of total RNA was reverse transcribed using Superscript III reverse transcriptase (Invitrogen, Carlsbad, CA) following the manufacturer's instructions. One μ L of cDNA was used as template for qPCR performed using the ABI 7300 System (Applied Biosystems, Foster City, CA). Power SYBR ® Green PCR master mix (Applied Biosystems) was used to detect gene expression of selected genes with primers designed using Primer3 software. qPCR amplifications were carried out at 50 °C for 2 min, 95 °C for 10 min, followed by 40 cycles of 95 °C for 15 s and 60 °C for 1 min. Dissociation curve analysis was performed after the program was completed to confirm amplification specificity. Three technical replicates were performed for each biological sample. Relative gene expression levels were calculated with the 2 −∆∆Ct method using the 16s rRNA (rrsA) as endogenous control and wild type as reference value.
Semi-quantitative RT-PCR. Total RNA from MBMA medium was extracted and reverse transcribed as described above. PCR reactions were performed on 10 ng of cDNA using csrA-rt and csrB-rt and 16S-rt primers listed in Table S1. RNA samples were used as template for RT-minus controls. PCR amplification was carried out at 94 °C for 2 min, followed 20 cycles of 94 °C for 30 s, 60 °C for 30 s and 72 °C for 30 s. PCR products were separated on an ethidium bromide pre-stained 1% agarose gel, and visualized in a Molecular Imager ® Gel Doc ™ XR System (Bio-Rad).
Virulence assays on immature pear fruits. Virulence assays were performed as described previously 11,12 .
Briefly, overnight cultures of E. amylovora WT, mutants and complementation strains were harvested by centrifugation and suspended in 0.5x PBS. Immature pear fruits (Pyrus communis L. cv. 'Bartlett') were surface sterilized with 10% bleach, pricked with a sterile needle and inoculated with 2 μ L of 100 X dilution of bacterial suspensions at OD 600 = 0.1. Inoculated pears were incubated at 28 °C in a humidity chamber and disease symptoms were recorded after 4 and 7 days post inoculation. The experiment was performed in triplicate at least three times. For bacterial population studies, pears were inoculated as described above and the tissue surrounding the inoculation site was excised with a cork borer no.4 and homogenized in 1 mL of 0.5x PBS. Bacterial growth within the pear tissue was monitored after 1, 2 and 3 days post inoculation by dilution plating on LB with appropriate antibiotics 11,12 . For each time point and strain tested, fruits were assayed in triplicate. The experiment was performed three times.
Western blot. E. amylovora cells grown in HMM at 18 °C for 6 h were harvested, and equal amount of cell lysates was separated by sodium dodecyl sulfate polyacrylamide gels 8 . Proteins were transferred to polyvinylidene fluoride membrane (Millipore) and blocked with 5% milk in phosphate-buffered saline (PBS). To detect HrpA-6His, membranes were probed with rabbit anti-His antibodies (GeneScript, Piscataway, NJ) that were diluted to 1.0 μ g/ml with PBS containing 0.1% Tween 20 (PBST). Immunoblots were then developed with horseradish peroxidase-linked anti-rabbit IgG antibodies (Amersham Biosciences) diluted 1: 10,000 in PBST, followed by enhanced chemiluminescence reagents (Pierce). Images of the resulting blots were acquired using ImageQuant LAS 4010 CCD camera (GE Healthcare). The experiment was performed at least three times.
Statistical analysis. One-way ANOVA and Student-Newmans-Kleus test (p = 0.05) was used to analyze the data. For WT, mutants and complementation strains, changes marked with the same letter did not differ significantly (P < 0.05).