- Research article
- Open Access
Complete genome sequence of the fire blight pathogen Erwinia pyrifoliae DSM 12163T and comparative genomic insights into plant pathogenicity
© Smits et al; licensee BioMed Central Ltd. 2010
- Received: 2 June 2009
- Accepted: 4 January 2010
- Published: 4 January 2010
Erwinia pyrifoliae is a newly described necrotrophic pathogen, which causes fire blight on Asian (Nashi) pear and is geographically restricted to Eastern Asia. Relatively little is known about its genetics compared to the closely related main fire blight pathogen E. amylovora.
The genome of the type strain of E. pyrifoliae strain DSM 12163T, was sequenced using both 454 and Solexa pyrosequencing and annotated. The genome contains a circular chromosome of 4.026 Mb and four small plasmids. Based on their respective role in virulence in E. amylovora or related organisms, we identified several putative virulence factors, including type III and type VI secretion systems and their effectors, flagellar genes, sorbitol metabolism, iron uptake determinants, and quorum-sensing components. A deletion in the rpoS gene covering the most conserved region of the protein was identified which may contribute to the difference in virulence/host-range compared to E. amylovora. Comparative genomics with the pome fruit epiphyte Erwinia tasmaniensis Et1/99 showed that both species are overall highly similar, although specific differences were identified, for example the presence of some phage gene-containing regions and a high number of putative genomic islands containing transposases in the E. pyrifoliae DSM 12163T genome.
The E. pyrifoliae genome is an important addition to the published genome of E. tasmaniensis and the unfinished genome of E. amylovora providing a foundation for re-sequencing additional strains that may shed light on the evolution of the host-range and virulence/pathogenicity of this important group of plant-associated bacteria.
- Genomic Island
- Fire Blight
- rpoS Gene
- Flagellar Gene
- T6SS Gene Cluster
Fire blight caused by the enterobacterium Erwinia amylovora, a quarantine pathogen in Europe, is the most important global threat to pome fruit production (i.e., apple, pear) and to a wide-variety of Rosaceae (Maloideae), including amenity and forest species . E. amylovora is native to the North Eastern USA, and it was the first phytopathogenic bacterium described (see ). This invasive pathogen was first introduced into the UK in the late 1950s and has spread across Europe over the past three decades, with continuing advance eastward that threatens the native origin of apple in Central Asia . Fire blight symptoms include recurvature of shoots (shepherd's crook), necrosis, ooze, and cankers. The pathogen can enter through nectaries, hydathodes and wounds resulting in blossom, shoot or rootstock blight syndromes . E. amylovora growth is highly dependent on weather conditions, which has been used to develop disease forecasting models, and it is passively vectored by flower-foraging insects . Epidemics can develop rapidly and result in death of individual plants or entire orchards within a single season, leading to severe economic losses . E. amylovora has poor ecological fitness away from host or surrogate plants .
Erwinia pyrifoliae is a newly described pathogen, closely related to the main fire blight pathogen E. amylovora. E. pyrifoliae is primarily a pathogen of Asian or Nashi pear (Pyrus pyrifolia) and is considered to have a restricted geographic distribution in East Asia (Korea and Japan) [6–8]. Monitoring to detect E. pyrifoliae is rarely conducted, although a quantitative PCR method based on differential 16S rRNA and 16S-23S ITS sequences [9, 10] has recently been developed; thus the precise distribution of this pathogen is somewhat uncertain. E. pyrifoliae causes fire blight disease symptoms essentially indistinguishable from those of E. amylovora infection. Limited host germplasm screening with E. pyrifoliae strains indicates a slightly wider host-range than originally thought, with virulence observed on selected commercial pear (Pyrus communis) and apple (Malus domestica, 'Idared') varieties . The level of virulence on non-Asian pear hosts is markedly lower than that typically observed in E. amylovora, suggesting that important genetic differences remain to be elucidated.
In contrast to the considerable genetic information available for E. amylovora [11, 12], relatively little is known about the genetic basis of virulence and environmental fitness in E. pyrifoliae . As for E. amylovora, E. pyrifoliae intra-species genotypic diversity appears low, with strain differences primarily observed in plasmid content . Thus far, only minor genetic differences have been found between E. pyrifoliae and E. amylovora [13, 15].
The objectives of our work were to sequence the complete genome of the type strain of E. pyrifoliae, strain DSM 12163T, and then compare it to the recently sequenced genome of the non-pathogenic pome fruit epiphyte, E. tasmaniensis Et1/99 . Identifying differential sequences among these related bacteria may provide useful insights into host-pathogen interactions that could eventually be exploited for fire blight control.
General genome description
General features of the genome of E. pyrifoliae DSM 12163T.
Sequencing coverage (454)
Sequencing coverage (Solexa)
Calculated copy number/cell
Annotation was completed using the genome annotation system GenDB , and manually optimized. In total, 4,038 open reading frames (ORFs) were predicted. The chromosome contains seven rRNA operons, and 74 tRNAs, which falls within the range observed for most free-living enterobacterial genomes. Several low G+C regions indicated the presence of horizontally acquired sequences. Inspection of some of these indicated the presence of several prophages in the chromosome.
Earlier reports identified four plasmids in a large group of E. pyrifoliae strains, including strain DSM 12163T [18, 19]. Recently, the complete sequences of plasmids pEP36 and pEP2.6 from E. pyrifoliae Ep1/96 were published . These two plasmids were found to be present in the genome of E. pyrifoliae DSM 12163T with slightly differing sizes (35901 bp and 2610 bp, respectively). We sequenced and annotated two additional small plasmids of sizes 4,960 bp (pEP5) and 3,070 bp (pEP3).
From the coverage of the individual plasmids, it is possible to estimate the copy number of each plasmid in E. pyrifoliae DSM 12163T (Table 1). According to this calculation, plasmid pEP36 and pEP5 are present in 5-6 copies per cell, while the small plasmids pEP3 and pEP2.6 have a medium copy number ranging from 18-20 copies per cell. This explains the high yield of plasmids reported in earlier studies, whereas it is more difficult to obtain plasmid pEA29 from E. amylovora present at approximately two copies per cell (T.H.M. Smits and B. Duffy, unpublished data).
rpoS RNA polymerase sigma factor deletion
During genome assembly, it was observed that E. pyrifoliae DSM 12163T has a 140 bp deletion in the rpoS gene (EPYR_03050), when compared to the E. amylovora OT1 or E. tasmaniensis Et1/99 rpoS gene sequence. This 140 bp deletion results in a frameshift and a coding interruption after the RpoS subregion 1.2 . After this deletion, the remaining sequence of the rpoS gene resumes in a different frame, starting from subregion 2.4 in RpoS . This deletion thus encompasses a highly conserved region that putatively interacts with the core RNA polymerase.
Type III secretion system operons
Type III secretion systems (T3SSs) are widely distributed among proteobacterial pathogens of plants, animals, and humans, and constitute a fundamental virulence determinant . In other bacteria, T3SSs were found to be critical for the establishment of non-pathogenic host-relationships with plants [26, 27] and insects . Mutations or absence of T3SS genes interfere or abolish bacterial-host interaction . Generally, genes encoding elements of the T3SS machinery are conserved among bacterial species, but each system includes specific effectors targeting respective hosts. Proteins secreted by the Hrp complex of E. amylovora and other plant pathogenic bacteria are required for virulence on susceptible host plants and for the elicitation of a hypersensitive response in resistant or non-host plants [25, 30].
The genome of E. pyrifoliae DSM 12163T contains two distinct T3SSs. One T3SS is closely related to the hrp/dsp cluster of E. amylovora, while the second T3SS is more similar to the inv/spa cluster of Salmonella typhimurium . The h ypersensitive r esponse and p athogenicity related region (hrp) of E. pyrifoliae DSM 12163T is composed of 25 genes (EPYR_03319-EPYR_03343) organized in four operons encoding the T3SS machinery. The number and the arrangement of these genes are similar to the known hrp pathogenicity island found in E. amylovora , except for the absence of ORFU1 and ORFU2 which are located between the hrpA and hrpS genes in E. amylovora. Both ORFU1 and ORFU2 are also absent in the genome of E. tasmaniensis Et1/99 .
The genomic arrangement of the hrp region in E. pyrifoliae DSM 12163T is identical to the T3SS arrangement found in E. pyrifoliae strain WT3 . In E. pyrifoliae DSM 12163T the hrp region is bordered by the h rp e ffector and e licitors region (HEE, EPYR_03311-EPYR_03318) and the H rp-a ssociated e nzymes (HAE, EPYR_03344-EPYR_03349) region. Both regions are organized identically as in E. amylovora , while the HAE region is missing from the genome of the non-pathogenic E. tasmaniensis Et1/99 . The HEE region includes the harpin genes hrpN and hrpW, dspA/E encoding a secreted effector essential for E. amylovora virulence , and the chaperone genes orfA, orfB, orfC, and dspB/F. The HAE region includes hrp-associated systemic virulence genes (hsvABC), the gene hrpK encoding for a putative type III translocator , and two genes encoding proteins of currently unknown function.
Type VI secretion system
T6SS gene clusters have recently been found to be widespread among pathogenic and non-pathogenic Gram-negative bacteria . Bacteria living in close association with eukaryotic cells are purported to use the T6SS as a mechanism for maintaining pathogenic or symbiotic interactions with their hosts. T6SS gene clusters consist of a set of 14 currently recognized core genes and conserved genes that vary in composition between species . Two putative effector proteins in the human pathogen Vibrio cholerae, Hcp (haemolysin co-regulated protein) and Vgr (Val-Gly repeats), are secreted by a T6SS . In the plant pathogenic bacterium Pectobacterium atrosepticum SCRI1043 (syn. Erwinia carotovora subsp. atroseptica), vgr and hcp genes are up-regulated when this pathogen is grown in the presence of potato extract, suggesting a potential role in virulence . Two mutants, each defective in a gene of the T6SS gene cluster, showed reduced virulence compared to wild-type P. atrosepticum in potato tuber and stem virulence bioassays . In the pea symbiont Rhizobium leguminosarum, a locus linked to the T6SS was discovered that negatively affects pea nodulation .
The Hcp encoded in the T6SS cluster of E. pyrifoliae DSM 12163T is 91.9% identical to its ortholog in E. tasmaniensis Et1/99. Apart from this hcp gene, E. pyrifoliae DSM 12163T possesses two additional hcp genes on the plasmids pEP3 and pEP5 (Fig. 2). The Hcp proteins encoded on the E. pyrifoliae DSM 12163T plasmids are more related to each other (82.5% identity) than to the Hcp proteins of the large chromosomal T6SS clusters. The related enterobacterium Serratia proteamaculans 568 has a similar gene organization for its T6SS (Fig. 5A), but has no additional genes downstream of hcp1, an additional hcp gene (hcp2), and only one vgrG gene. In comparison, Hcp1 is more closely related to the Hcp genes of E. pyrifoliae DSM 12163T and E. tasmaniensis Et1/99 than to Hcp2. The P. atrosepticum SCRI1043 T6SS gene cluster is completely different from that in E. pyrifoliae DSM 12163T regarding its organization [37, 43].
A second set of designated T6SS-related genes was found in the genomes of E. pyrifoliae DSM 12163T (EPYR_02109-EPYR_02113) and E. tasmaniensis Et1/99 (ETA_18657-ETA_18659) (Fig. 5B) which are absent in S. proteamaculans 568. In E. pyrifoliae DSM 12163T, three putative core genes (EPYR_02109, EPYR_02110/02111, EPYR_02113) and one conserved gene were found (EPYR_02112), while in E. tasmaniensis Et1/99 one of these core genes was absent. Genes in this second set show low homology to each other and to the large T6SS clusters. A frameshift in COG3523 (EPYR_02110/02111) within this T6SS cluster of E. pyrifoliae DSM 12163T was identified which leads to an early stop-codon in the gene. It can be deduced that this gene cluster is inactivated, and prone to mutations and deletions.
Two sets of genes encoding for flagellar assembly and chemotaxis related proteins were found in the genome of E. pyrifoliae DSM 12163T. One set is tightly clustered (EPYR_00976-EPYR_01028) and the encoded proteins show higher identity with the corresponding proteins of Salmonella and Escherichia spp. than with those of E. tasmaniensis Et1/99 . This suggests that the entire region was acquired as a genomic island via horizontal genetic transfer. Only the right boundary of the genomic island is found in E. pyrifoliae DSM 12163T, as discernible by a reduced G+C-content bordered by an IS2-type integrase (EPYR_01040) flanking smpB (EPYR_01041), a gene also found the E. tasmaniensis Et1/99 genome (ETA_09720). The left border of the genomic island does not display distinctive insertion features. The first upstream-gene with high homology to E. tasmaniensis Et1/99 is tsx (EPYR_00974), which matches a gene that encodes a nucleoside-specific channel-forming protein in E. tasmaniensis Et1/99 (ETA_09440). Notably, in E. tasmaniensis Et1/99 the region included between ETA_09440 and ETA_09720 contains quorum-sensing genes expRI which are absent in E. pyrifoliae DSM 12163T.
A second complete set of flagellar genes is present but split among different clusters in the genome of E. pyrifoliae DSM 12163T (EPYR_01609-EPYR_01614, EPYR_01651-EPYR_01668, EPYR_02267-EPYR_02282, EPYR_02322-EPYR_02336). This second set closely resembles the flagellar genes found in E. tasmaniensis Et1/99 and appears to be ancestral in E. pyrifoliae DSM 12163T. Compared to the acquired flagellar assembly apparatus, the native gene cluster contains two extra genes (EPYR_01615 and EPYR_02267) encoding FliZ, a putative alternative sigma factor regulatory protein and the putative CheV chemotaxis signal transduction protein, respectively.
Metabolism of sorbitol has been described as a contributing virulence factor in E. amylovora  on pome fruits which utilize sorbitol as a primary carbon storage compound . The genome of E. pyrifoliae DSM 12163T contains a complete sorbitol gene cluster (EPYR_00602-EPYR_00606), and the organism is able to utilize sorbitol as a sole carbon source . The non-pathogenic E. tasmaniensis Et1/99 lacks a sorbitol gene cluster in its genome , and may thus be disadvantaged in competitive interactions in environments rich in sorbitol. The exact role of sorbitol utilization in virulence is unresolved, since sorbitol content in apple trees has no specific effect on fire blight disease severity . Associations between sorbitol and fire blight  suggest rather an osmotic-potential effect which could be due to various carbon compounds. Transgenic apple trees with down-regulated sorbitol synthesis compensate by increasing production of other sugars (i.e., sucrose, glucose) , and both of these are also substrates for E. pyrifoliae and E. amylovora which carry the respective metabolic genes.
A second EPS produced by E. amylovora strains, levan, is also reported to contribute to virulence . E. pyrifoliae DSM 12163T does not have levan biosynthetic genes and does not produce levan, which has also been reported to be lacking in the related fire blight Erwinia sp. from Japan . It is proposed that the lack of levan may contribute to the restricted host-range in these species compared to E. amylovora, although levan biosynthesis in vitro has been reported in non-pathogenic E. tasmaniensis Et1/99.
Quorum-sensing (QS) refers to the ability of bacteria to regulate gene expression in accordance with the presence of extracellular signalling molecules, or autoinducers (AI), that are produced in a cell density-dependent manner . Two principal QS systems are known in Gram-negative bacteria and are defined by the chemical nature of the AI involved .
The AI-1 system utilizes N-acyl homoserine lactones (AHLs), produced by the LuxI family of proteins, as signal molecules. This system was first described in the marine bacterium Vibrio fisheri , where it controls bioluminescence production. Above a certain concentration, the secreted AHL binds the LuxR receptor and the resulting complex activates target gene transcription by binding a specific promoter site (lux box). Several AHLs have since been described in a wide-variety of Gram-negative pathogenic and non-pathogenic bacteria, differing principally in the N-acyl side chain moiety of the AHLs, with each unique AHL signal controlled by its own pair of luxRI gene orthologs .
In E. pyrifoliae, proteins encoded by one gene set (EPYR_02385-EPYR_02386) have low sequence identity with the autoinducer biosynthetic and receptor proteins PhzI/PhzR of Pseudomonas chlororaphis (22 and 26% respectively) and ExpI/ExpR of P. atrosepticum SCRI 1043 (17% and 22%). However, EPYR_02386 also shows 45% identity with the DNA-binding transcriptional activator SdiA, which regulates cell division in Escherichia coli and S. typhimurium , and which is known to respond to AHLs generated by other microbial species. For SdiA, no cognate gene encoding a corresponding signal-generating enzyme is present in either E. coli or in S. typhimurium . Thus, SdiA may have a similar activity/non-activity in E. pyrifoliae and other Erwinia species.
Given the very low identity of EPYR_02385 to known AHL synthesis protein and the failure of E. pyrifoliae DSM 12163T to induce a positive reaction in AHL-biosensors Chromobacterium violaceum CV026 and Agrobacterium tumefaciens NTL/pZLR4 (data not shown), it is hypothesized that the gene set composed of EPYR_02385 and EPYR_02386 contributes to production and detection of a yet unknown extracellular signal not obviously related to known QS signals.
A second QS system, based on production of an AI-2 signal molecule and controlled by the LuxS protein, is also widespread among Gram-negative and Gram-positive bacteria , and putatively involved in cross-species bacterial communication . LuxS, a S-ribosylhomocysteine lyase, is however also known to be a central component of the activated methyl cycle (AMC), a metabolic cycle responsible for recycling methionine and generation of the major methyl donor S-adenosyl-L-methionine (SAM) in bacterial cells [60, 61]. It is thus critical that the decision of whether or not the AI-2 system is present in certain species is not only based on the presence of luxS, but also on presence and functionality of the genes coding for the AI-2 receptors . E. pyrifoliae DSM 12163T has a functional luxS gene (EPYR_03027) but it lacks orthologs for both of the two known AI-2 receptors: the LuxPQ-receptor of Vibrio harveyi  and the Lsr ABC-transporter of Salmonella typhimurium . Thus, as in E. amylovora Ea273 , which also carries luxS but lacks AI-2 receptors, this gene probably has a metabolic rather than QS role in E. pyrifoliae.
Iron uptake determinants
Iron is an essential nutritional factor for plant pathogenic bacteria, which have high-affinity iron acquisition systems in order to supply this need . Iron regulation of a wide range of genes is coordinated by Fur (encoded by EPYR_02663), which specifically regulates biosynthesis and uptake of iron-affinity siderophores . The genome of E. pyrifoliae DSM 12163T contains four TonB-dependent receptor genes, one of which is also a putative copper receptor (oprC; EPYR_01920).
Another TonB-dependent receptor gene (EPYR_03492) encodes an ortholog of the E. amylovora ferrioxamine-receptor FoxR . The gene product is directly involved in uptake of ferrioxamines into the periplasm. In E. amylovora, foxR mutants retain ability to synthesize desferrioxamine E, but lose their ability to utilize this as an iron substrate, are impaired in growth under iron-limited conditions such as found on flower surfaces, have reduced virulence, and are less resistant to plant defence responses [67, 68]. Adjacent to foxR, E. pyrifoliae also has a biosynthetic gene cluster dfoJAC (EPYR_03489-EPYR_03491) containing an ortholog of dfoA, one of the biosynthetic genes for desferrioxamine in E. amylovora CFBP1430 , indicating that E. pyrifoliae DSM 12163T synthesizes desferrioxamine E and has an iron-acquisition system similar to E. amylovora . In E. pyrifoliae DSM 12163T, a ferrihydroxamate TonB-dependent receptor and ABC transport system fhuACDB; EPYR_00903-EPYR_00906) is also present, which may contribute to uptake of ferrihydroxamate siderophores (Stockwell et al. 2008).
A fourth TonB-dependent receptor (EPYR_01969) found in E. pyrifoliae DSM 12163T is predicted to belong to the Transport Classification DataBase (TCDB; http://www.tcdb.org/) group TC 1.B.14.2.-, which consists primarily of heme and porphyrin uptake systems. An inactivated homolog of the TonB-dependent receptor yncD (EPYR_02731-EPYR_02732) is also present in the E. pyrifoliae DSM 12163T genome, but is inactivated by frameshifts. The ent-fep-fec gene cluster encoding enterobactin biosynthesis and transport in many Enterobacteriaceae, is absent in the genome of E. pyrifoliae DSM 12163T, as has been observed for E. tasmaniensis Et1/99 .
Comparative genomics to non-pathogenic Erwinia tasmaniensis Et1/99
The difference in genome size between E. pyrifoliae DSM 12163T and E. tasmaniensis Et1/99 is largely due to the insertion of mobile genetic elements in E. pyrifoliae DSM 12163T. At least three regions contain phage genes, indicating insertion of prophages or remnants thereof. Additionally, a large number of genomic islands have inserted into the genome of E. pyrifoliae DSM 12163T, as indicated by the large number of possibly active or inactivated transposases identified. Of the remaining areas, two regions encode restriction systems and one cluster carries a complete additional set of flagellar genes (EPYR_00976-EPYR_01028; see above).
In contrast, E. tasmaniensis Et1/99 contains a large number of fimbrial gene clusters spread across the chromosome that are lacking in E. pyrifoliae DSM 12163T. Additionally, the nas/nir cluster is present in E. tasmaniensis but absent in E. pyrifoliae DSM 12163T, which explains the inability of E. pyrifoliae to generate nitrite from nitrate [7, 19]. We observed that the chromosome of E. tasmaniensis Et1/99 encodes part of the central region of E. pyrifoliae plasmid pEP36 carrying the thiOSGF and the betB genes, but not the entire plasmid. E. tasmaniensis Et1/99 also carries genes for the ferric citrate uptake system fecRABCDE and for achromobactin uptake, which are all lacking in E. pyrifoliae DSM 12163T. From the alignment (Fig. 7), it was observed that E. pyrifoliae DSM 12163T contains the same set of T6SS genes as found in E. tasmaniensis Et1/99 but not previously reported. The incomplete inv/spa T3SS cluster, located close to the mutS gene in E. tasmaniensis Et1/99 (Fig. 4), is absent in E. pyrifoliae DSM 12163T.
Overall, the large-scale analysis of genomic differences between E. pyrifoliae DSM 12163T and E. tasmaniensis Et1/99 does not clearly reveal why E. pyrifoliae and not E. tasmaniensis is pathogenic. Mutational analysis of different genomic features is needed to determine their role in pathogenicity compared with non-pathogenic E. tasmaniensis. Our results also suggest that comparison of the genome sequences of E. pyrifoliae and E. amylovora, and different strains within each species, could reveal host-range determinants.
Compared to E. amylovora, the genome of E. pyrifoliae DSM 12163T encodes many of the same virulence factors, including two T3SSs, sorbitol metabolism, exopolysaccharides, and desferrioxamine biosynthesis. However, in E. pyrifoliae levan production and a third T3SS cluster are absent. Whether these factors contribute to the reduced host-range of this pathogen remains to be elucidated. Comparison to the genome of the non-pathogenic E. tasmaniensis Et1/99 indicated an additional flagellar gene cluster, absence of AHL biosynthesis genes, and a modified range of iron acquisition systems which may play a role in pathogenicity. As more of the species that have been identified with fire blight-like symptoms or as epiphytes on Rosaceae [9, 13, 18, 36, 71–77] are sequenced and can be compared on a whole-genome scale, further clues to the evolution and origin of necrotrophic Erwinia, and insights into host-pathogen interactions, can be anticipated.
Genomic DNA was isolated using the Wizard Genomic DNA Purification Kit (Promega, Madison WI, USA). Whole-genome sequencing was performed by GATC (Konstanz, Germany) using both a 454 GS-FLX and a Solexa sequencer.
Overview of sequence data for the genome of E. pyrifoliae DSM 12163T.
Total sequence output
Average read length
Coverage (4 Mb)
No. of contigsa
No. of contigs > 500 bp
A total of 4,835,468 high-quality filtered sequence reads with an average read length of 36 bp were generated by Solexa sequencing (Table 2). Average coverage was equivalent to 43.5×. Reads were assembled using the E. pyrifoliae Ep1/96 chromosome, plasmid pEP36 and pEP2.6. All reads were additionally de novo assembled using the program EDENA  with manually optimized settings. This yielded 3,162 contigs (N50 = 22,267; mean length = 1,206; maximum length = 12,612; minimum length = 100). The assembled contigs were aligned to the sequence using the SeqMan program of the LASERGENE package (DNASTAR, Madison, WI, USA).
Assembly of the E. pyrifoliae DSM12163T genome sequence was done in two steps. For the chromosome, GenBank accession FP236842 was used as reference. The sequences for plasmids pEP36 and pEP2.6 (AY123045, AY123048) were published , and used as a template for assembling these sequences. In a first step, the longer pyrosequencing reads were mapped to the available references using Roche's gsMapper application. When both sequence coverage and quality indicated a difference between the two strains with high confidence, the reference sequence was modified to reflect this change. Afterwards, both 454 and the shorter Solexa reads were mapped to the modified sequences with several custom scripts. In most cases, the Solexa reads supported the information from the 454 sequences and in some cases the Solexa data could be used to close gaps in the references where no 454 data was available. Based on the mapping information from both 454 and Solexa reads, contigs were created where coverage was high enough and at least 75% of all mapped reads agreed about a base for a given position. When no consensus base could be determined, an 'N' was inserted.
The reference sequence was also used as a template for the previously assembled contigs using SeqMan. Most contigs aligned to the template, and the non-aligned contigs were mainly due to false assembly in an earlier phase and could be resolved by realignment. The leftover contigs were checked by BlastN versus the template, and two contigs that were not covered by any part of the template were extended by several rounds of assembly versus the 454 reads until they were closed. This assembly was then confirmed by assembly using the Solexa reads, and by shifting the zero-point in the newly assembled plasmid sequences (pEP5 and pPE3).
Genes were predicted using a combined strategy  based on the CDS prediction programs Glimmer  and Critica . Subsequently, the potential function of each predicted gene was automatically assigned using the GenDB annotation pipeline . The resulting genome annotation was curated manually, and metabolic pathways were identified using the KEGG pathways  tool in GenDB.
Routine sequence manipulations were done using several subroutines of the LASERGENE package. Whole-genome comparisons were done using the progressive alignment option of the Mauve comparison software (Version 2.0 ).
For the detailed analysis of the E. pyrifoliae DSM 12163T genome sequence, the Transport Classification DataBase (TCDB) http://www.tcdb.org/ was used for improving the automated annotation of transporters. For comparative classification of the T3SS effectors, the Pseudomonas syringae Hop database http://pseudomonas-syringae.org/Hop_database.xls was blasted on protein level versus the annotation of the E. pyrifoliae DSM 12163T genome.
The genome sequence of E. pyrifoliae DSM 12163T has been deposited at EBI and received the accession numbers EMBL:FN392235 (chromosome), EMBL:FN392238 (pEP36), EMBL:FN392239 (pEP5), EMBL:FN392237 (pEP3) and EMBL:FN392236 (pEP2.6).
This work was supported by the Swiss Secretariat for Education and Research (SBF C07.0038) and the Swiss Federal Office for Agriculture (BLW Fire Blight Research - Pathogen). It was conducted within the European Science Foundation research network COST Action 864.
- Duffy B, Schärer H-J, Bünter M, Klay A, Holliger E: Regulatory measures against Erwinia amylovora in Switzerland. EPPO Bull. 2005, 35: 239-244. 10.1111/j.1365-2338.2005.00820.x.View ArticleGoogle Scholar
- Bonn WG, Zwet van der T: Distribution and economic importance of fire blight. Fire blight the disease and its causative agent, Erwinia amylovora. Edited by: Vanneste JL. 2000, Wallingford, UK CAB International, 37-53. full_text.View ArticleGoogle Scholar
- Jock S, Donat V, López MM, Bazzi C, Geider K: Following spread of fire blight in Western, Central and Southern Europe by molecular differentiation of Erwinia amylovora strains with PFGE analysis. Environ Microbiol. 2002, 4 (2): 106-114. 10.1046/j.1462-2920.2002.00277.x.PubMedView ArticleGoogle Scholar
- Thomson SV: Epidemiology of fire blight. Fire blight the disease and its causative agent, Erwinia amylovora. Edited by: Vanneste JL. 2000, Wallingford, UK CAB International, 9-36. full_text.View ArticleGoogle Scholar
- Johnson KB, Stockwell VO: Management of fire blight a case study in microbial ecology. Annu Rev Phytopathol. 1998, 36: 227-248. 10.1146/annurev.phyto.36.1.227.PubMedView ArticleGoogle Scholar
- Geider K, Auling G, Jakovljevic V, Völksch B: A polyphasic approach assigns the pathogenic Erwinia strains from diseased pear trees in Japan to Erwinia pyrifoliae. Lett Appl Microbiol. 2009, 48: 324-330. 10.1111/j.1472-765X.2008.02535.x.PubMedView ArticleGoogle Scholar
- Kim W-S, Gardan L, Rhim S-L, Geider K: Erwinia pyrifoliae sp. nov., a novel pathogen that affects Asian pear trees (Pyrus pyrifolia Nakai). Int J Syst Bacteriol. 1999, 49: 899-906.PubMedView ArticleGoogle Scholar
- McGhee GC, Schnabel EL, Maxson-Stein K, Jones B, Stromberg VK, Lacy GH, Jones AL: Relatedness of chromosomal and plasmid DNAs of Erwinia pyrifoliae and Erwinia amylovora. Appl Environ Microbiol. 2002, 68 (12): 6182-6192. 10.1128/AEM.68.12.6182-6192.2002.PubMed CentralPubMedView ArticleGoogle Scholar
- Kim W-S, Hildebrand M, Jock S, Geider K: Molecular comparison of pathogenic bacteria from pear trees in Japan and the fire blight pathogen Erwinia amylovora. Microbiology. 2001, 147: 2951-2959.PubMedView ArticleGoogle Scholar
- Lehman SM, Kim W-S, Castle AJ, Svircev AM: Duplex real-time polymerase chain reaction reveals competition between Erwinia amylovora and E. pyrifoliae on pear blossoms. Phytopathology. 2008, 98 (6): 673-679. 10.1094/PHYTO-98-6-0673.PubMedView ArticleGoogle Scholar
- Eastgate JA: Erwinia amylovora the molecular basis of fireblight disease. Mol Plant Pathol. 2000, 1 (6): 325-329. 10.1046/j.1364-3703.2000.00044.x.PubMedView ArticleGoogle Scholar
- Oh C-S, Beer SV: Molecular genetics of Erwinia amylovora involved in the development of fire blight. FEMS Microbiol Lett. 2005, 253: 185-192. 10.1016/j.femsle.2005.09.051.PubMedView ArticleGoogle Scholar
- Triplett LR, Zhao Y, Sundin GW: Genetic differences between blight-causing Erwinia species with differing host specificities, identified by suppression subtractive hybridization. Appl Environ Microbiol. 2006, 72 (11): 7359-7364. 10.1128/AEM.01159-06.PubMed CentralPubMedView ArticleGoogle Scholar
- Shrestha R, Lee SH, Kim JE, Wilson C, Choi S-G, Park DH, Wang MH, Hur JH, Lim CK: Diversity and detection of Korean Erwinia pyrifoliae strains as determined by plasmid profiling, phylogenetic analysis and PCR. Plant Pathol. 2007, 56: 1023-1031. 10.1111/j.1365-3059.2007.01679.x.View ArticleGoogle Scholar
- Shrestha R, Tsuchiya K, Baek SJ, Bae HN, Hwang I, Hur JH, Lim CK: Identification of dspEF, hrpW and hrpN loci and characterization of the hrpNEp gene in Erwinia pyrifoliae. J Gen Plant Pathol. 2005, 71: 211-220. 10.1007/s10327-005-0191-6.View ArticleGoogle Scholar
- Kube M, Migdoll AM, Müller I, Kuhl H, Beck A, Reinhardt R, Geider K: The genome of Erwinia tasmaniensis strain Et1/99, a non-pathogenic bacterium in the genus Erwinia. Environ Microbiol. 2008, 10 (9): 2211-2222. 10.1111/j.1462-2920.2008.01639.x.PubMedView ArticleGoogle Scholar
- Meyer F, Goesmann A, McHardy AC, Bartels D, Bekel T, Clausen J, Kalinowski J, Linke B, Rupp O, Giegerich R: GenDB - an open source genome annotation system for prokaryote genomes. Nucleic Acids Res. 2003, 31: 2187-2195. 10.1093/nar/gkg312.PubMed CentralPubMedView ArticleGoogle Scholar
- Maxson-Stein K, McGhee GC, Smith JJ, Jones AL, Sundin GW: Genetic analysis of a pathogenic Erwinia sp. isolated from pear in Japan. Phytopathology. 2003, 93 (11): 1393-1399. 10.1094/PHYTO.2003.93.11.1393.PubMedView ArticleGoogle Scholar
- Rhim S-L, Völksch B, Gardan L, Paulin J-P, Langlotz C, Kim W-S, Geider K: Erwinia pyrifoliae an Erwinia species different from Erwinia amylovora causes a necrotic disease of Asian pear trees. Plant Pathol. 1999, 48: 514-520. 10.1046/j.1365-3059.1999.00376.x.View ArticleGoogle Scholar
- Fu J-F, Chang H-C, Chen Y-M, Chang Y-S, Liu S-T: Sequence analysis of an Erwinia stewartii plasmid, pSW100. Plasmid. 1995, 34 (2): 75-84. 10.1006/plas.1995.9999.PubMedView ArticleGoogle Scholar
- Lonetto M, Gribskov M, Gross CA: The s70 family sequence conservation and evolutionary relationships. J Bacteriol. 1992, 174 (12): 3843-3849.PubMed CentralPubMedGoogle Scholar
- Anderson M, Pollitt CE, Roberts IS, Eastgate JA: Identification and characterization of the Erwinia amylovora rpoS gene RpoS is not involved in induction of fireblight disease symptoms. J Bacteriol. 1998, 180: 6789-6792.PubMed CentralPubMedGoogle Scholar
- Andersson RA, Kõiv V, Norman-Setterblad C, Pirhonen M: Role of RpoS in virulence and stress tolerance of the plant pathogen Erwinia carotovora subsp. carotovora. Microbiology. 1999, 145: 3547-3556.PubMedView ArticleGoogle Scholar
- Mukherjee A, Cui Y, Ma W, Liu Y, Ishihama A, Eisenstark A, Chatterjee AK: RpoS (Sigma-S) controls expression of rsmA a global regulator of secondary metabolites, harpin and extracellular proteins in Erwinia carotovora. J Bacteriol. 1998, 180: 3629-3634.PubMed CentralPubMedGoogle Scholar
- Hueck CJ: Type III protein secretion systems in bacterial pathogens of animals and plants. Microbiol Mol Biol Rev. 1998, 62 (2): 379-433.PubMed CentralPubMedGoogle Scholar
- Freiberg C, Fellay R, Bairoch A, Broughton WJ, Rosenthal A, Perret X: Molecular basis of symbiosis between Rhizobium and legumes. Nature. 1997, 387: 394-401. 10.1038/387394a0.PubMedView ArticleGoogle Scholar
- Göttfert M, Röthlisberger S, Kündig C, Beck C, Marty R, Hennecke H: Potential symbiosis-specific genes uncovered by sequencing a 410-kilobase DNA region of the Bradyrhizobium japonicum chromosome. J Bacteriol. 2001, 183 (4): 1405-1412. 10.1128/JB.183.4.1405-1412.2001.PubMed CentralPubMedView ArticleGoogle Scholar
- Dale C, Young SA, Haydon DT, Welburn SC: The insect endosymbiont Sodalis glossinidius utilizes a type III secretion system for cell invasion. Proc Natl Acad Sci USA. 2001, 98 (4): 1883-1888. 10.1073/pnas.021450998.PubMed CentralPubMedView ArticleGoogle Scholar
- Alfano JR, Collmer A: Type III secretion system effector proteins double agents in bacterial disease and plant defence. Annu Rev Phytopathol. 2004, 42: 385-414. 10.1146/annurev.phyto.42.040103.110731.PubMedView ArticleGoogle Scholar
- Jock S, Kim W-S, Barny M-A, Geider K: Molecular characterization of natural Erwinia pyrifoliae strains deficient in hypersensitive response. Appl Environ Microbiol. 2003, 69 (1): 679-682. 10.1128/AEM.69.1.679-682.2003.PubMed CentralPubMedView ArticleGoogle Scholar
- McClelland M, Sanderson KE, Spieth J, Clifton SW, Latreille P, Courtney L, Porwollik S, Ali J, Dante M, Du F: Complete genome sequence of Salmonella enterica serovar Typhimurium LT2. Nature. 2001, 413: 852-856. 10.1038/35101614.PubMedView ArticleGoogle Scholar
- Oh C-S, Kim JF, Beer SV: The Hrp pathogenicity island of Erwinia amylovora and identification of three novel genes required for systemic infection. Mol Plant Pathol. 2005, 6 (2): 125-138. 10.1111/j.1364-3703.2005.00269.x.PubMedView ArticleGoogle Scholar
- Shrestha R, Lee SH, Cho S, Lim CK, Hong S, Cho JM, Hwang I, Hur JH, Kim W-S: The hrp genes cluster in Erwinia pyrifoliae and determination of HR active domain in HrpNEp protein. Acta Hort. 2008, 793: 221-230.View ArticleGoogle Scholar
- Boureau T, ElMaarouf-Bouteau H, Garnier A, Brisset M-N, Perino C, Pucheu I, Barny M-A: DspA/E, a type III effector essential for Erwinia amylovora pathogenicity and growth in planta, induces cell death in host apple and nonhost tobacco plants. Mol Plant-Microbe Interact. 2006, 19 (1): 16-24. 10.1094/MPMI-19-0016.PubMedView ArticleGoogle Scholar
- Petnicki-Ocwieja T, van Dijk K, Alfano JR: The hrpK operon of Pseudomonas syringae pv. tomato DC3000 encodes two proteins secreted by the type III (Hrp) protein secretion system HopB1 and HrpK, a putative type III translocator. J Bacteriol. 2005, 187 (2): 649-663. 10.1128/JB.187.2.649-663.2005.PubMed CentralPubMedView ArticleGoogle Scholar
- Bocsanczy AM, Beer SV, Perna NT, Biehl B, Glasner JD, Cartinhour SW, Schneider DJ, DeClerck GA, Sebaihia M, Parkhill J: Contributions of the genome sequence of Erwinia amylovora to the fire blight community. Acta Hort. 2008, 793: 163-170.View ArticleGoogle Scholar
- Boyer F, Fichant G, Berthod J, Vandenbrouck Y, Attree I: Dissecting the bacterial type VI secretion system by a genome wide in silico analysis what can be learnt from available microbial genomic resources?. BMC Genomics. 2009, 10: 104-10.1186/1471-2164-10-104.PubMed CentralPubMedView ArticleGoogle Scholar
- Bingle LEH, Bailey CM, Pallen MJ: Type VI secretion a beginner's guide. Curr Opin Microbiol. 2008, 11 (1): 3-8. 10.1016/j.mib.2008.01.006.PubMedView ArticleGoogle Scholar
- Pukatzki S, Ma AT, Sturtevant D, Krastins B, Sarracino D, Nelson WC, Heidelberg JF, Mekalanos JJ: Identification of a conserved bacterial protein secretion system in Vibrio cholerae using the Dictyostelium host model system. Proc Natl Acad Sci USA. 2006, 103 (5): 1528-1533. 10.1073/pnas.0510322103.PubMed CentralPubMedView ArticleGoogle Scholar
- Mattinen L, Nissinen R, Riipi T, Kalkkinen N, Pirhonen M: Host-extract induced changes in the secretome of the plant pathogenic bacterium Pectobacterium atrosepticum. Proteomics. 2007, 7: 3527-3537. 10.1002/pmic.200600759.PubMedView ArticleGoogle Scholar
- Liu H, Coulthurst SJ, Pritchard L, Hedley PE, Ravensdale M, Humphris S, Burr T, Takle G, Brurberg M-B, Birch PRJ: Quorum sensing coordinates brute force and stealth modes of infection in the plant pathogen Pectobacterium atrosepticum. PLoS Pathog. 2008, 4 (6): e1000093-10.1371/journal.ppat.1000093.PubMed CentralPubMedView ArticleGoogle Scholar
- Roest HP, Mulders IHM, Spaink HP, Wijffelman CA, Lugtenberg BJJ: A Rhizobium leguminosarum biovar trifolii locus not localized on the Sym plasmid hinders effective nodulation on plants of the pea cross-inoculation group. Mol Plant-Microbe Interact. 1997, 10 (7): 938-941. 10.1094/MPMI.1922.214.171.1248.PubMedView ArticleGoogle Scholar
- Bell KS, Sebaihia M, Pritchard L, Holden MTG, Hyman LJ, Holeva MC, Thomson NR, Bentley SD, Churcher LJC, Mungall K: Genome sequence of the enterobacterial phytopathogen Erwinia carotovora subsp atroseptica and characterization of virulence factors. Proc Natl Acad Sci USA. 2004, 101 (30): 11105-11110. 10.1073/pnas.0402424101.PubMed CentralPubMedView ArticleGoogle Scholar
- Aldridge P, Metzger M, Geider K: Genetics of sorbitol metabolism in Erwinia amylovora and its influence on bacterial virulence. Mol Gen Genet. 1997, 256 (6): 611-619. 10.1007/s004380050609.PubMedView ArticleGoogle Scholar
- Teo G, Suzuki Y, Uratsu SL, Lampinen B, Ormonde N, Hu WK, DeJong TM, Dandekar AM: Silencing leaf sorbitol synthesis alters long-distance partitioning and apple fruit quality. Proc Natl Acad Sci USA. 2006, 103 (49): 18842-18847. 10.1073/pnas.0605873103.PubMed CentralPubMedView ArticleGoogle Scholar
- Duffy B, Dandekar AM: Sorbitol has no role in fire blight as demonstrated using transgenic apple with constitutively altered content. Acta Hort. 2008, 793: 279-283.View ArticleGoogle Scholar
- Suleman P, Steiner PW: Relationship between sorbitol and solute potential in apple shoots relative to fire blight symptom development after infection by Erwinia amylovora. Phytopathology. 1994, 84: 1244-1250. 10.1094/Phyto-84-1244.View ArticleGoogle Scholar
- Kim W-S, Schollmeyer M, Nimtz M, Wray V, Geider K: Genetics of biosynthesis and structure of the capsular exopolysaccharide from the Asian pear pathogen Erwinia pyrifoliae. Microbiology. 2002, 148: 4015-4024.PubMedView ArticleGoogle Scholar
- Bernhard F, Schullerus D, Bellemann P, Geider K, Nimtz M, Majerczak DR, Coplin DL: Genetics and complementation of DNA regions involved in amylovoran synthesis of Erwinia amylovora and stewartan synthesis of Erwinia stewartii. Acta Hort. 1996, 411: 269-274.View ArticleGoogle Scholar
- Coplin DL, Majerczak DR, Bugert P, Geider K: Nucleotide sequence analysis of the Erwinia stewartii cps gene cluster for synthesis of stewartan and comparison to the Erwinia amylovora ams cluster for synthesis of amylovoran. Acta Hort. 1996, 411: 251-257.View ArticleGoogle Scholar
- Gross M, Geier G, Rudolph K, Geider K: Levan and levansucrase synthesized by the fireblight pathogen Erwinia amylovora. Physiol Mol Plant Pathol. 1992, 40 (6): 371-381. 10.1016/0885-5765(92)90029-U.View ArticleGoogle Scholar
- Pierson LS, Wood DW, Pierson EA: Homoserine lactone-mediated gene regulation in plant-associated bacteria. Annu Rev Phytopathol. 1998, 36: 207-225. 10.1146/annurev.phyto.36.1.207.PubMedView ArticleGoogle Scholar
- Miller MB, Bassler BL: Quorum sensing in bacteria. Annu Rev Microbiol. 2001, 55: 165-199. 10.1146/annurev.micro.55.1.165.PubMedView ArticleGoogle Scholar
- Nealson KH, Hastings JW: Bacterial bioluminescence its control and ecological significance. Microbiol Rev. 1979, 43 (4): 496-518.PubMed CentralPubMedGoogle Scholar
- Lerat E, Moran NA: The evolutionary history of quorum-sensing systems in bacteria. Mol Biol Evol. 2004, 21 (5): 903-913. 10.1093/molbev/msh097.PubMedView ArticleGoogle Scholar
- Wang X, de Boer PAJ, Rothfield LI: A factor that positively regulates cell division by activating transcription of the major cluster of essential cell division genes of Escherichia coli. EMBO J. 1991, 10 (11): 3363-3372.PubMed CentralPubMedGoogle Scholar
- Michael B, Smith JN, Swift S, Heffron F, Ahmer BMM: SdiA of Salmonella enterica is a LuxR homolog that detects mixed microbial communities. J Bacteriol. 2001, 183 (19): 5733-5742. 10.1128/JB.183.19.5733-5742.2001.PubMed CentralPubMedView ArticleGoogle Scholar
- Xavier KB, Bassler BL: Interference with AI-2-mediated bacterial cell-cell communication. Nature. 2005, 437: 750-753. 10.1038/nature03960.PubMed CentralPubMedView ArticleGoogle Scholar
- Winans SC: Bacterial esperanto. Nat Struct Biol. 2002, 9 (2): 83-84. 10.1038/nsb0202-83.PubMedView ArticleGoogle Scholar
- Winzer K, Hardie KR, Williams P: LuxS and autoinducer-2 their contribution to quorum sensing and metabolism in bacteria. Adv Appl Microbiol. 2003, 53: 291-396. full_text.PubMedView ArticleGoogle Scholar
- Rezzonico F, Duffy B: Lack of genomic evidence of AI-2 receptors suggests a non-quorum sensing role for luxS in most bacteria. BMC Microbiol. 2008, 8: 154-10.1186/1471-2180-8-154.PubMed CentralPubMedView ArticleGoogle Scholar
- Reading NC, Sperandio V: Quorum sensing the many languages of bacteria. FEMS Microbiol Lett. 2006, 254 (1): 1-11. 10.1111/j.1574-6968.2005.00001.x.PubMedView ArticleGoogle Scholar
- Taga ME, Miller ST, Bassler BL: Lsr-mediated transport and processing of AI-2 in Salmonella typhimurium. Mol Microbiol. 2003, 50 (4): 1411-1427. 10.1046/j.1365-2958.2003.03781.x.PubMedView ArticleGoogle Scholar
- Rezzonico F, Duffy B: The role of luxS in the fire blight pathogen Erwinia amylovora is limited to metabolism and does not involve quorum sensing. Mol Plant-Microbe Interact. 2007, 20 (10): 1284-1297. 10.1094/MPMI-20-10-1284.PubMedView ArticleGoogle Scholar
- Expert D: Withholding and exchanging iron interactions between Erwinia spp. and their host plants. Annu Rev Phytopathol. 1999, 37: 307-334. 10.1146/annurev.phyto.37.1.307.PubMedView ArticleGoogle Scholar
- Dellagi A, Brisset M-N, Paulin J-P, Expert D: Dual role of desferrioxamine in Erwinia amylovora pathogenicity. Mol Plant-Microbe Interact. 1998, 11 (8): 734-742. 10.1094/MPMI.19126.96.36.1994.PubMedView ArticleGoogle Scholar
- Kachadourian R, Dellagi A, Laurent J, Bricard L, Kunesch G, Expert D: Desferrioxamine-dependent iron transport in Erwinia amylovora CFBP 1430 cloning of the gene encoding the ferrioxamine receptor FoxR. BioMetals. 1996, 9 (2): 143-150. 10.1007/BF00144619.PubMedView ArticleGoogle Scholar
- Expert D, Dellagi A, Kachadourian R: Iron and fire blight role in pathogenicity of desferrioxamine E, the main siderophore of Erwinia amylovora. Fire blight the disease and its causative agent, Erwinia amylovora. Edited by: Vanneste JL. 2000, Wallingford, UK CAB International, 179-195. full_text.View ArticleGoogle Scholar
- Feistner GJ: Proferrioxamine synthesis in Erwinia amylovora in response to precursor or hydroxylysine feeding metabolic profiling with liquid chromatography-electrospray mass spectrometry. BioMetals. 1995, 8 (4): 318-327. 10.1007/BF00141605.PubMedView ArticleGoogle Scholar
- Darling ACE, Mau B, Blattner FR, Perna NT: Mauve multiple alignment of conserved genomic sequence with rearrangements. Genome Res. 2004, 14: 1394-1403. 10.1101/gr.2289704.PubMed CentralPubMedView ArticleGoogle Scholar
- Roselló M, Ferrer S, Llop P, López MM, Christen R, Gardan L: Description of Erwinia piriflorinigrans sp. nov., causal agent of pear blossom necrosis. Acta Hort. 2008, 793: 137-140.View ArticleGoogle Scholar
- Chung YR, Brenner DJ, Steigerwalt AG, Kim BS, Kim HT, Cho KY: Enterobacter pyrinus sp. nov., an organism associated with brown leaf spot disease of pear trees. Int J Syst Bacteriol. 1993, 43: 157-161.View ArticleGoogle Scholar
- Hao MV, Brenner DJ, Steigerwalt AG, Kosako Y, Komagata K: Erwinia persicinus a new species isolated from plants. Int J Syst Bacteriol. 1990, 40: 379-383.PubMedView ArticleGoogle Scholar
- Stockwell VO, Hockett K, Marie C, Duffy B: Pink Erwinia amylovora colony discoloration in diagnostic isolations by co-cultured bacteria. Acta Hort. 2008, 793: 539-542.View ArticleGoogle Scholar
- Jock S, Geider K: Molecular differentiation of Erwinia amylovora strains from North America and of two Asian pear pathogens by analyses of PFGE patterns and hrpN genes. Environ Microbiol. 2004, 6 (5): 480-490. 10.1111/j.1462-2920.2004.00583.x.PubMedView ArticleGoogle Scholar
- Geider K, Auling G, Du Z, Jakovljevic V, Jock S, Völksch B: Erwinia tasmaniensis sp. nov., a non-phytopathogenic bacterium from apple and pear trees. Int J Syst Evol Microbiol. 2006, 56 (12): 2937-2943. 10.1099/ijs.0.64032-0.PubMedView ArticleGoogle Scholar
- Mergaert J, Hauben L, Cnockaert MC, Swings J: Reclassification of non-pigmented Erwinia herbicola strains from trees as Erwinia billingiae sp. nov. Int J Syst Bacteriol. 1999, 49: 377-383.PubMedView ArticleGoogle Scholar
- Hernandez d, François P, Farinelli L, Østerås M, Schrenzel J: De novo bacterial genome sequencing millions of very short reads assembled on a desktop computer. Genome Res. 2008, 18: 802-809. 10.1101/gr.072033.107.PubMed CentralPubMedView ArticleGoogle Scholar
- McHardy AC, Goesmann A, Pühler A, Meyer F: Development of joint application strategies for two microbial gene finders. Bioinformatics. 2004, 20 (10): 1622-1631. 10.1093/bioinformatics/bth137.PubMedView ArticleGoogle Scholar
- Salzberg SL, Delcher AL, Kasif S, White O: Microbial gene identification using interpolated Markov models. Nucleic Acids Res. 1998, 26 (2): 544-548. 10.1093/nar/26.2.544.PubMed CentralPubMedView ArticleGoogle Scholar
- Badger JH, Olsen GJ: CRITICA coding region identification tool invoking comparative analysis. Mol Biol Evol. 1999, 16 (4): 512-524.PubMedView ArticleGoogle Scholar
- Kanehisa M, Goto S, Kawashima S, Nakaya A: The KEGG databases at GenomeNet. Nucleic Acids Res. 2002, 30 (1): 42-46. 10.1093/nar/30.1.42.PubMed CentralPubMedView ArticleGoogle Scholar
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