An easy, simple inexpensive test for the specific detection of Pectobacterium carotovorum subsp. carotovorum based on sequence analysis of the pmrA gene
© Kettani-Halabi et al.; licensee BioMed Central Ltd. 2013
Received: 21 September 2012
Accepted: 23 July 2013
Published: 29 July 2013
The species Pectobacterium carotovorum includes a diverse subspecies of bacteria that cause disease on a wide variety of plants. In Morocco, approximately 95% of the P. carotovorum isolates from potato plants with tuber soft rot are P. carotovorum subsp. carotovorum. However, identification of this pathogen is not always related to visual disease symptoms. This is especially true when different pathogen cause similar diseases on potato, citing as an example, P. carotovorum, P. atrosepticum and P. wasabiae. Numerous conventional methods were used to characterize Pectobacterium spp., including biochemical assays, specific PCR-based tests, and construction of phylogenetic trees by using gene sequences. In this study, an alternative method is presented using a gene linked to pathogenicity, in order to allow accuracy at subspecies level. The pmrA gene (response regulator) has been used for identification and analysis of the relationships among twenty nine Pectobacterium carotovorum subsp. carotovorum and other Pectobacterium subspecies.
Phylogenetic analyses of pmrA sequences compared to ERIC-PCR and 16S rDNA sequencing, demonstrated that there is considerable genetic diversity in P. carotovorum subsp. carotovorum strains, which can be divided into two distinct groups within the same clade.
pmrA sequence analysis is likely to be a reliable tool to identify the subspecies Pectobacterium carotovorum subsp. carotovorum and estimate their genetic diversity.
Pectobacterium carotovorum subsp. carotovorum (P. carotovorum subsp. carotovorum) is a plant-pathogenic enterobacterium which belongs to the soft-rot group of Pectobacterium. It has the ability to cause serious damage worldwide on a numerous types of plants in field and storage stage . In Morocco, approximately 95% of the P. carotovorum isolated from potato plants with tuber soft rot are P. carotovorum subsp. carotovorum. This bacteria produce a wide variety of plant cell wall-degrading enzymes, causing maceration of different plant organs and tissues [1, 3]. Many of its virulence genes have been identified, including genes encoding degradative enzymes, diverse regulatory systems, and the type III secretion system . Pectobacterium spp. is a complex taxon consisting of strains with a range of different phenotype, biochemical, host range and genetic characteristics. Several methods were used to characterize this taxon, including biochemical assays and construction of phylogenetic trees by using gene sequences. For example, Toth and his collaborators [4–8] have shown that there are five major clades of Pectobacterium (formerly E. carotovorum): atrosepticum, betavasculorum, carotovorum, odoriferum, and wasabiae. Their analysis did not include P. brasiliensis which form individual clade . Recently, other authors [10, 11] were interested in molecular typing methods. These methods are increasingly used in the analysis of P. carotovorum subsp. carotovorum relatedness in order to identify their transmission routes and to assess its biodiversity. They have demonstrated a high diversity of polymorphism between these subspecies.
To survive, colonize and cause disease, plant-pathogenic bacteria modulate expression of their genes often using two-component signal transduction systems (TCS). These systems typically consist of two conserved components, a sensor histidine kinase and a response regulator . P. carotovorum subsp. carotovorum employs different two-component systems for controlling production of virulence determinants [13–16]. PmrA-PmrB is one example of TCS for plant pathogenic bacteria, which affects production of extracellular enzymes, virulence and bacterial survival in potato tubers as well as in Arabidopsis leaves and generally in planta. The main target genes of this TCS encode products with sequence similarity to DNA binding response regulators and autophosphorylatable histidine kinases.
The pmrA locus is required for resistance to the cationic peptide antibiotic polymyxin B and to other plant-derived antimicrobial peptides in Pectobacterium. It controls the production of proteins that mediate the modification of the lipopolysaccharide (LPS) core and lipid A [17–19]. The changes in LPS structure leads to reduction of the negative charges at cell surface and hence altered interactions with iron and cationic peptides . This gene was found in almost all Enterobacteriaceae. In P. carotovorum subsp. carotovorum, pmrA gene encodes a protein of 222 amino acid (aa) that reveals 59.7% of identity to pmrA of Salmonella and BasR of E. coli. Its inactivation in P. carotovorum subsp. carotovorum does not reduce the maceration ability of the bacterium on potato tuber but nevertheless remains essential for survival under adverse environmental conditions [16, 20, 21]. Phylogenies built with single genes have been used already to examine the relationships of the plant-pathogenic enterobacteria [22–25]. In this study, pmrA sequence analysis was used to identify the Pectobacterium carotovorum subsp. carotovorum and to estimate their genetic diversity. In addition, in at least one other system, this analysis was better correlated with Enterobacterial Repetitive Intergenic Consensus PCR (ERIC-PCR) assays and phylogenies built from 16S rDNA genes .
Results and discussion
Strains used in this study
P. carotovorum subsp. carotovorum
Our pmrA gene sequence analysis, linked to pathogenicity studies, could be used to identify and monitor the diversity of the P. carotovorum subsp. carotovorum subspecies.
Sample handling and isolate bacteria
During the years 2003 to 2011, different potato fields and the most important potato storages were controlled in Morocco and several samples were collected from plants with soft rot disease. Nutrient agar, King’s B agar, Crystal Violet Pectate (CVP) and LPGA medium (5 g/L yeast extract, 5 g/L peptone, 5 g/L glucose 15 g/L agar) were used to isolate the suspected bacteria. The 29 strains used in this study are isolated from different geographic Moroccan regions and had been stored in 20% glycerol at −20°C [2, 30]. Table 1 shows the strains whose sequences were determined in this study and the reference strains used for comparison when phylogenetic trees were constructed. Table 1 includes the strain designations and the GenBank accession numbers for the pmrA sequences.
Biochemical and physiological tests
In order to identify Pectobacterium spp., the strains were grown at 27°C for 24 h on agar plates and they were tested for Gram staining, catalase, oxidase, nitrate production, reductase activity, pectinolytic activity on Sutton medium, and absence pigmentation of the strains in the King B medium (Difco) . Identification of confirmed Pectobacterium spp. isolates to species and subspecies was conducted on the basis of biochemical tests (indole production from tryptophan, lecithinase activity and acid production from α-methyl glucoside, trehalose, sorbitol, melibiose, lactose). All tests were carried out at 27°C for 24 h and compared with the standard strains (see Additional file 1 Table S1 for the fourteen strains used only in this study) [2, 10].
DNA extraction and PCR amplification
Bacterial cultures from frozen stocks were grown onto LPGA medium and suspended in sterile H2O. The concentration was adjusted to 108 CFU.ml-1. DNA was extracted from bacterial suspension as described by Terta et al. . The precipitated DNA then was quantified using a NanoDrop 8000 spectrophotometer (Thermo Scientific, Wilmington, DE, USA), adjusted to 100 ng.μl-1 and stored at 4°C. All PCR amplifications were performed using the following primers: pmr A F0145 (5’-TACCCTGCAGATGAAATTATTGATTGTTGAAGAC-3’) and E2477 (5’-TACCAAGCTTTGGTTGTTCCCCTTTGGTCA-3’) as described by Hyytiäinen et al. 2003 . A 25 μl PCR mix contained: 1 μl DNA, 0.5 U Taq DNA polymerase, 2.5 μl 10 × PCR buffer, 2.5 mM each of dNTPs, 2.5 mM MgCl2, 0.5 μM of each primer. DNA amplification was performed on Veriti® Thermal Cycler (Applied Biosystems) under the following conditions: 5 min at 94°C for initial denaturation, 35 cycles of 1 min at 94°C for, 1 min at 55°C and 2 min 72°C, followed by a final elongation step of 10 min at 72°C. PCR products (6 μl) were separated by gel electrophoresis in 1.8% agarose gels in TBE buffer. Following staining with ethidium bromide, the gels were viewed and photographed under UV Transilluminator. Fragment sizes were determined by comparison to a 100 bp DNA Ladders.
Sequencing of pmrA and phylogenetic analysis
The PCR-amplified fragments of pmrA were purified and the sequencing reactions were performed with a Big-Dye Terminator v3.1 (Applied Biosystems). The pmrA sequences which we determined and the sequences of the reference strains of members of the family Enterobacteriaceae obtained from the GenBank databases were analyzed. The pmrA sequences were first aligned by using the Clustal W program , and then the alignments were corrected by hand. Evolutionary trees for the data set were inferred by using the Neighbor-Joining program of MEGA [31, 33]. The stability of relationships was assessed by performing bootstrap analyses of the Neighbor-Joining data based on 500 resamplings. The entire sequences corresponding to positions 4317866-4318532 of the reference sequence of the subspecies.
Nucleotide sequence accession numbers
The pmrA sequences which we determined have been deposited in the GenBank database under the accession numbers shown in Table 1.
This work was supported by the Agronomic Research for Development Project PRAD N° 07-07 and the “Agence Universitaire de la Francophonie” (AUF).
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