- freely available
Genes 2012, 3(3), 361-377; doi:10.3390/genes3030361
Published: 4 July 2012
Abstract: The bacterium Xanthomonas campestris pathovar musacearum (Xcm) is the causal agent of banana Xanthomonas wilt (BXW). This disease has devastated economies based on banana and plantain crops (Musa species) in East Africa. Here we use genome-wide sequencing to discover a set of single-nucleotide polymorphisms (SNPs) among East African isolates of Xcm. These SNPs have potential as molecular markers for phylogeographic studies of the epidemiology and spread of the pathogen. Our analysis reveals two major sub-lineages of the pathogen, suggesting that the current outbreaks of BXW on Musa species in the region may have more than one introductory event, perhaps from Ethiopia. Also, based on comparisons of genome-wide sequence data from multiple isolates of Xcm and multiple strains of X. vasicola pathovar vasculorum, we identify genes specific to Xcm that could be used to specifically detect Xcm by PCR-based methods.
The bacterium Xanthomonas campestris pathovar musacearum (Xcm) is the causal agent of banana Xanthomonas wilt (BXW). This disease has devastated economies based on banana and plantain crops (Musa species) in East Africa . Xcm was first described as a wilt-causing pathogen on enset (Ensente ventricosum), a plant closely related to banana that is a staple crop in the highlands of Ethiopia . In 1974 Yirgou and Bradbury  wrote that “Great care should be taken to see that enset wilt does not escape and establish itself on banana in other parts of the world where it could pose a serious problem on this crop”. Ominously, one and a half decades later, a major epidemic of this disease was reported in Uganda . Subsequently it has spread into many banana-growing regions around the Great Lakes in Uganda, Kenya, Tanzania, Democratic Republic of Congo, Rwanda and Burundi [4,5,6,7]. Efforts are underway to tackle this pathogen by a number of different measures including cultural practices  and genetic modification of the crop [9,10].
Although currently classified as a member of the species Xanthomonas campestris, we recently showed that Xcm is more likely to be a strain of the species Xanthomonas vasicola . We previously  generated complete genome sequences for a single isolate of Xcm from banana in Uganda (NCPPB4381) and for a single isolate of X. vasicola pathovar vasculorum (Xvv) that is non-pathogenic on banana and was isolated from sugarcane in Zimbabwe (NCPPB702). These two isolates share identical gyrase B DNA sequences, consistent with their very close evolutionary relationship [11,13].
Differences between these two genome sequences revealed several candidate genes that might play a role in adaptation to the banana host. These may also be useful tools in identifying genes for deployment of disease resistance. Specifically, these included homologues of effectors secreted and translocated by the type III secretion system (T3SS). T3SS effectors have previously been shown to contribute to host-specificity acting as virulence and/or avirulence factors . In common with most previously sequenced Xanthomonas genomes, Xcm encodes homologues of the effectors AvrBs2, AvrGf1, XopF, XopK, XopL, XopN, XopP, XopQ, XopR, XopX and XopZ as well as homologues of XopA, XopB, XopG, XopH, XopI, XopY, XopAA, XopAD, XopAE and XopAK, which are found in some other Xanthomonas species [12,14]. Xcm also encodes homologues of P. syringae effectors HopW1 and HopAF1 and Ralstonia solanacearum putative effector RipT . Xcm encodes two predicted YopJ-like C55 cysteine proteases (RefSeq accessions ZP_06491730 and ZP_06492219) that are absent from Xvv 702. On the other hand, Xvv 702 encodes a close homologue (ZP_06483517) of XopAF (also known as AvrXv3), which is absent from Xcm .
Previous work showed that Xcm is a highly monomorphic pathogen and no specific genetic differences have yet been detected among different isolates using traditional typing and diagnostic methods [13,15]. Affordable complete genome sequencing now makes it feasible to identify cryptic genetic diversity among isolates of a genetically monomorphic pathogen , though this approach is only just starting to be applied to monomorphic phytopathogens .
Here we use genome-wide sequencing to discover a set of single-nucleotide polymorphisms (SNPs) among East African isolates of Xcm. These SNPs have potential as molecular markers for phylogeographic studies of the epidemiology and spread of the pathogen. Our analysis reveals the presence of at least two major sub-lineages of the pathogen; Xcm isolates from Uganda, Kenya, Tanzania and Burundi are genetically distinct from isolates collected in Ethiopia, DR Congo and Rwanda, suggesting that the current outbreaks of BXW on Musa species in the region may have more than one introduction.
2. Results and Discussion
2.1. Genome Sequencing
We used the Illumina GA2x sequencing platform to generate genome-wide sequence data for 13 isolates of Xcm available from the National Collection of Plant Pathogenic Bacteria (NCPPB). We also sequenced a further three African isolates of Xvv, a pathovar that is very closely related to Xcm but non-pathogenic on banana. We also included in our analyses the genome sequence data from Xcm NCPPB4381 and Xvv NCPPB702 that we published previously . Table 1 lists the sequenced isolates and the depth to which each was sequenced. We submitted all raw sequence data to the Sequence Read Archive . Note that another isolate from Tanzania, NCPPB4393, is described in the NCPPB’s catalogue as Xcm, but we previously sequenced its genome and showed that it is actually Xanthomonas sacchari . We generated genome assemblies de novo for NCPPB2005, NCPPB4379, NCPPB4380, NCPPB4384, NCPPB4392, NCPPB4394, NCPPB1326, NCPPB1381 and NCPPB206 using Velvet 1.1.04 . These have been submitted to GenBank  with accession numbers AKBE00000000, AKBF00000000, AKBG00000000, AKBH00000000, AKBI00000000,
|Table 1. Isolates of X. campestr is pv. musacearum (Xcm) and X. vasicola pv. vasculorum (Xvv) subjected to genome-wide sequencing. All Xcm isolates were originally collected from diseased banana plants except for NCPPB2005, which was isolated from Ensete ventricosum. All Xvv isolates were originally collected from sugarcane, except for NCPPB206, which was isolated from maize.|
|Isolate||Source and Date of Isolation||Coverage||SRA Accession|
|Xcm NCPPB2005||Ethiopia 1967||72×||SRR489154.7|
|Xcm NCPPB2251||Ethiopia 1969||13×||SRR494492.2|
|Xcm NCPPB4379||Uganda (Kayunga) 2007||102×||SRR494484.2|
|Xcm NCPPB4380||Uganda (Kiboga) 2007||113×||SRR494485.2|
|Xcm NCPPB4381||Uganda (Luwero) 2007||56×||SRR020203.3|
|Xcm NCPPB4383||Uganda (Wakiso) 2007||11×||SRR494493.2|
|Xcm NCPPB4384||Uganda (Nakaongola) 2007||55×||SRR494488.2|
|Xcm NCPPB4387||D. R. Congo (Kivu province) 2007||13×||SRR494494.1|
|Xcm NCPPB4389||Rwanda (Gisenyi province) 2007||16×||SRR494495.2|
|Xcm NCPPB4392||Tanzania (Muleba district, Kagera region) 2007||72×||SRR494498.3|
|Xcm NCPPB4394||Tanzania (Muleba district, Kagera region) 2007||92×||SRR494489.1|
|Xcm NCPPB4395||Tanzania (Muleba district, Kagera region) 2007||117×||SRR494490.2|
|Xcm NCPPB4433||Burundi 2008||13×||SRR494496.1|
|Xcm NCPPB4434||Kenya (Teso district) 2008||15×||SRR494497.1|
|Xvv NCPPB206||South Africa 1948||70×||SRR494500.3|
|Xvv NCPPB702||Zimbabwe 1959||35×||SRR020202.3|
|Xvv NCPPB1326||Zimbabwe 1962||63×||SRR494491.5|
|Xvv NCPPB1381||Zimbabwe 1962||66×||SRR494499.3|
AKBJ00000000, AKBK00000000, AKBL00000000 and AKBM00000000. The most contiguous of these assemblies was for NCPPB4384. This consisted of 84 scaffolds, of which the 12 longest scaffolds were each at least 154 Kb long and accounted for more than 2.5 Mb; that is the N50 length was 154 Kb for NCPPB4384. The N50 lengths for the other Xcm assemblies were 56 Kb (NCPPB2005), 146 Kb (NCPPB4379), 147 Kb (NCPPB4380), 87 Kb (NCPPB4392) and 151 Kb (NCPPB4394).
2.2. Distinguishing Xcm from Xvv
The currently used method for identifying BXW is by isolation of bacteria from the infected plant and performing fatty acid and metabolic analyses . However, this approach is only appropriate once symptoms become visible, by which time it may be too late to control or eradicate the pathogen. An alternative approach, amenable to the rapid detection and identification of bacterial plant pathogens is the use of the polymerase chain reaction (PCR). A specific assay for detecting Xcm has recently been proposed based on PCR amplification of the hrpB gene . However, this gene is also conserved in Xvv and this assay was unable to distinguish between Xcm and non-banana-pathogenic isolates Xvv NCPPB702 and NCPPB1326 . Another study  generated several PCR primer pairs that were highly specific for Xcm but this study did not utilize Xcm or Xvv genomic sequence but rather used sequences from a range of other xanthomonads and so the candidate primers had to be tested for specificity by trial and error. Another recent study  exploited our previous  Xcm and Xvv draft genome sequence data to rationally design primers specific for Xcm. However, this was based on genome sequence from a single isolate of Xvv and a single isolate of Xcm. Until now, little was known about sequence diversity among isolates. Therefore, we identified a set of genes that are conserved in all of the sequenced isolates of Xcm but are absent from all the sequenced isolates of Xvv and are therefore candidates for use in an Xcm-specific PCR assay. Examples of these genes are listed in Table 2. Note that this list of genes was not generated by aligning assembled genome sequences. We aligned raw unassembled sequence reads against the previously published Xcm NCPPB4381 reference genome sequence  using the Burrows-Wheeler Aligner BWA . This approach has the advantage of avoiding assembly artifacts and problems arising from incomplete assemblies. In our BWA alignments of raw Illumina sequence reads versus the reference genome sequence, the full length of each gene was covered by reads (depth of one or greater) from all our Xcm Illumina sequence datasets. Each of these genes has no matches (i.e., zero depth of) to any sequence reads in our Xvv Illumina datatsets (as judged from the BWA alignments).
|Table 2. Candidate genes for development of an Xcm-specific PCR-based assay. The listed genes conserved in all of the sequenced Xcm isolates but absent from all of the sequenced Xvv isolates. Presence or absence of each gene was assessed based on alignment of Illumina sequence reads from each isolate against the Xcm NCPPB4381 reference genome sequence (RefSeq: ACHT00000000) using BWA .|
|RefSeq Locus tag||Predicted Gene Product|
|XcampmN_010100009057||general secretion pathway protein D|
|XcampmN_010100011643||conjugal transfer relaxosome component TraJ|
|XcampmN_010100011573||Fis family transcriptional regulator|
|XcampmN_010100010849||XRE family transcriptional regulator|
|XcampmN_010100001342||ISXo2 putative transposase|
|XcampmN_010100001332||ABC-type antimicrobial peptide transport system ATPase component|
|XcampmN_010100001327||RND family efflux transporter MFP subunit|
|XcampmN_010100011563||putative DNA methylase|
|XcampmN_010100001337||peptide ABC transporter permease|
|XcampmN_010100013883||restriction endonuclease-like protein|
|XcampmN_010100000225||putative secreted protein|
2.3. The Sequenced Xcm Isolates Comprise a Single Monophyletic Clade
We identified SNPs among the Xcm and Xvv isolates based on BWA  alignments of our Illumina sequence data against the X. oryzae pv. oryzae MAFF 311018 reference genome sequence (RefSeq: NC_007705). Based on nucleotides found at 21,525 polymorphic positions we generated the maximum likelihood phylogenetic tree shown in Figure 1. This clearly groups all of the sequenced Xcm isolates into a single distinct clade that is closely related to but distinct from the sequenced Xvv isolates.
2.4. Xcm Isolates from Uganda, Kenya, Tanzania and Burundi are Genetically Distinct from Isolates from Ethiopia, DR Congo and Rwanda
We next identified SNPs among the Xcm and Xvv isolates based on BWA  alignments of our Illumina sequence data against the Xcm NCPPB4381 reference genome sequence (RefSeq: ACHT00000000). Out of 2,908,042 nt over which there was no ambiguity, 2,907,999 were invariant across all isolates; that is the Xcm genomes shared at least 99.9985% identity. Based on nucleotides found at 243 polymorphic positions we generated the maximum likelihood phylogenetic tree shown in Figure 2. This clearly delineates the Xcm clade into two distinct sub-lineages, I and II. Sub-lineage I include isolates from Ethiopia, DR Congo and Rwanda whilst Sub-lineage II includes isolates from Uganda, Tanzania, Burundi and Kenya. The two sub-lineages are distinguishable from each other by 86 polymorphic positions. These are listed in full in the Supplementary File and in part in Table 3.
|Table 3. Examples of non-silent single-nucleotide polymorphisms that distinguish Xcm sub-lineages I (Ethiopia, DR Congo and Rwanda) and II (Uganda, Kenya, Tanzania, Burundi).|
|RefSeq Accession||Position||I||II||Locus Tag and Predicted Gene Product|
|NZ_ACHT01000013||861||g||c||XcampmN_010100000120 putative ISXo8 transposase|
|NZ_ACHT01000014||6000||a||g||XcampmN_010100000165 putative monovalent cation/H+ antiporter subunit A|
|NZ_ACHT01000034||8898||t||c||XcampmN_010100000807 putative integrase protein|
|NZ_ACHT01000045||1261||a||g||XcampmN_010100001162 bifunctional aspartate kinase/diaminopimelate decarboxylase protein|
|NZ_ACHT01000045||45,548||a||c||XcampmN_010100001377 chemotaxis protein|
|NZ_ACHT01000059||1907||c||t||XcampmN_010100001687 putative sugar transporter component|
|NZ_ACHT01000101||995||g||t||XcampmN_010100003517 soluble lytic murein transglycosylase|
|NZ_ACHT01000104||13,081||t||g||XcampmN_010100003612 GTP-dependent nucleic acid-binding protein EngD|
|NZ_ACHT01000113||10,410||t||g||XcampmN_010100004062 acetyltransferase (GNAT) family protein|
|NZ_ACHT01000242||10,465||a||c||XcampmN_010100007585 dihydrolipoamide acetyltransferase|
|NZ_ACHT01000294||2184||g||t||XcampmN_010100009424 xanthan biosynthesis glucuronosyltransferase GumK|
|NZ_ACHT01000345||1576||t||c||XcampmN_010100010814 cytochrome C peroxidase|
|NZ_ACHT01000402||4858||t||c||XcampmN_010100012145 heavy metal transporter|
|NZ_ACHT01000404||632||g||a||XcampmN_010100012200 tryptophan halogenase|
|NZ_ACHT01000500||23,584||a||g||XcampmN_010100016057 putative polysaccharide deacetylase|
|NZ_ACHT01000520||5360||a||g||XcampmN_010100016692 5-methyltetrahydrofolate-homocysteine methyl transferase|
|NZ_ACHT01000549||7371||a||c||XcampmN_010100018271 two-component system sensor protein|
|NZ_ACHT01000560||4001||t||c||XcampmN_010100018673 exodeoxyribonuclease III|
|NZ_ACHT01000590||927||c||t||XcampmN_010100019303 RNA polymerase sigma factor|
|NZ_ACHT01000626||10,220||t||c||XcampmN_010100019733 putative glutathionylspermidine synthase|
|NZ_ACHT01000634||2345||t||c||XcampmN_010100019848 beta-mannosidase precursor|
|NZ_ACHT01000644||2590||g||a||XcampmN_010100020168 two-component system sensor protein|
|NZ_ACHT01000694||10,665||a||t||XcampmN_010100022153 peptide-acetyl-coenzyme A transporter family protein|
|NZ_ACHT01000720||19,485||t||c||XcampmN_010100023003 drug:proton antiporter (19121–20371)|
The geographic locations of the sequenced Xcm isolates are shown in Figure 3. It has been widely assumed that the outbreaks in Uganda, and subsequent outbreaks in neighboring countries, ultimately originated in Ethiopia, with the pathogen perhaps being inadvertently transmitted via international trade. Consistent with this model, the Xcm isolates from DR Congo and Rwanda do indeed show extremely high levels of genetic similarity to Ethiopian isolate NCPPB2251. However, the isolates from Uganda, Kenya, Tanzania and Burundi show a distinct genotype, characterized by the 86 consistent SNP differences. This is not consistent with a single introduction from Ethiopia into East Africa.
Our data do not exclude the possibility that the current outbreaks can ultimately be traced back to Ethiopia; it is possible that both lineages I and II are endemic there and it is simply by chance that the two available isolates happen to belong to the DR Congo/Rwanda sub-lineage I. There is an urgent need to collect a range of isolates from Ethiopia and survey their genotypes to ascertain the level of genetic diversity in this pathogen’s presumed centre of origin. Genotyping new isolates should be possible and will be expedited by developing these newly discovered SNPs into PCR based molecular markers. Similarly, there is a pressing need to survey genotypes of a much larger collection of isolates from outbreaks in all the banana growing areas to uncover the routes of geographical spread at a much higher degree of resolution. Ideally a survey of genotypes should be conducted on isolates for which precise details are available on the date and the geographic location at which they are collected.
It should also be noted that although we have categorized the isolates according to the country in which they were collected, paths of transmission may be more influenced by geographical boundaries rather than by political ones. For example, although Rwanda shares two of its borders with Uganda and Tanzania it is somewhat isolated from them by lake and forest.
All of the available isolates from Uganda were collected in 2007 from sites in the central region geographically close to Mukono where the disease was first reported and probably all represent the same single outbreak. It would be interesting to compare these with isolates from outbreaks in Kabale (near Rwanda) or Kasese (near DR Congo).
All of the available isolates from Tanzania also belonged to sub-lineage II along with those from Uganda. The disease was reported in Tanzania shortly after it was discovered in Uganda and there has been unconfirmed speculation that it may have been inadvertently carried to Tanzania by banana alcohol traders from the Buganda region, close to where the sequenced Ugandan isolates were collected. Our molecular sequence data are consistent with this but do not provide definitive proof.
Although BXW was reported in DR Congo after it was reported in Uganda, the field pictures first sent to Uganda from DR Congo, showed greater devastation. It is not clear where banana Xanthomonas wilt occurred first: DR Congo or Uganda. There is a lot of movement of people and bananas from Congo to Rwanda and back, conflicts notwithstanding, and so it is perhaps not surprising that we observe isolates from these two countries belonging to the same sub-lineage I. However, the close relationship between an Ethiopian isolate and those in Rwanda and DRC is not so easily explained unless it is by sampling bias or by one-off international travel; if disease spread was primarily determined by movement of local people and bananas between countries, then we would instead expect isolates from Rwanda, Uganda and DR Congo to cluster together.
2.5. Comparison of Xcm Isolated from Enset Versus Xcm Isolated from Banana
Most of the available isolates of Xcm were originally isolated from banana. The exception is NCPPB2005, which was isolated from Ensete ventricosum in Ethiopia in 1967. This isolate clearly falls within Xcm sub-lineage I (Figure 2). This enset-associated isolate differs from the banana-associated isolates NCPPB2251, NCPPB4387 and NCPPB4389 at 67 SNP positions listed in the Supplementary File. Some examples of these differences are listed in Table 4 and include non-silent polymorphisms in several potential virulence genes (e.g., homologues of hrpF and a gene encoding a HopW1 T3SS effector). However, since Xcm is able to infect both banana and enset [2,3] it is not clear whether these differences have any biological significance. It would be interesting to survey a much larger sample of isolates from both banana and enset to search for any significant associations between genotype and host species that might reveal adaptation.
|Table 4. Examples of non-silent single-nucleotide polymorphisms that distinguish NCPPB2251 from banana versus NCPPB2005 from enset.|
|Refseq Accession||Position||NCPPB 2005 (enset)||NCPPB 2251 (Banana)||NCPPB 4389 (Banana)||Locus Tag and Predicted Gene Product|
|NZ_ACHT01000041||15,615||c||t||t||XcampmN_010100000977 hemolysin III|
|NZ_ACHT01000072||4507||a||c||c||XcampmN_010100002109 VirB3 protein|
|NZ_ACHT01000140||1116||c||t||t||XcampmN_010100004536 LacI family transcription regulator|
|NZ_ACHT01000199||8012||g||t||g||XcampmN_010100006143 type III secreted effector HopW1|
|NZ_ACHT01000215||3229||c||t||c||XcampmN_010100006660 HrpF protein|
|NZ_ACHT01000294||31,553||g||a||a||XcampmN_010100009559 MFS transporter|
|NZ_ACHT01000303||7530||a||c||c||XcampmN_010100009850 histidine kinase/response regulator hybrid protein|
|NZ_ACHT01000332||2191||a||g||g||XcampmN_010100010574 putative filamentous hemagglutinin-like protein|
|NZ_ACHT01000360||1961||a||g||g||XcampmN_010100011266 two-component system sensor protein|
|NZ_ACHT01000374||12,027||t||c||c||XcampmN_010100011573 Fis family transcriptional regulator|
|NZ_ACHT01000388||5277||t||g||g||XcampmN_010100011860 AraC family transcriptional regulator|
|NZ_ACHT01000439||5166||c||g||g||XcampmN_010100013743 ECF subfamily RNA polymerase sigma factor|
|NZ_ACHT01000560||2783||c||t||t||XcampmN_010100018663 molybdopterin biosynthesis|
|NZ_ACHT01000668||1036||c||a||a||XcampmN_010100021383 ABC transporter permease|
|NZ_ACHT01000690||6284||t||g||g||XcampmN_010100022008 isocitrate dehydrogenase|
2.6. Loss of Phage-Associated Genes in Some Xcm Isolates
In addition to surveying SNPs, we also searched for loss or gain of genes. By aligning sequence reads against the previously published NCPPB4381 genome assembly and systematically comparing gene-coverage in each of the alignments, we were able to identify a genomic region (GenBank: GG699410.1) that showed differential coverage among different isolates of Xcm (Figure 4). This region shows significant similarity at the amino acid and nucleotide sequence levels to two previously sequenced phage: Xanthomonas phage Cfc1 (RefSeq: NC_001396.1)  and Stenotrophomonas phage phiSHP2 (GenBank: HM150760.1). Specifically, two Tanzanian isolates (NCPPB4392 and NCPPB4395) appear to have completely lost at least 17 genes from this region, while Ethiopian isolate NCPPB2005 has lost 11 of the same genes. Interestingly, another isolate from the same area of Tanzania (NCPPB4394) appears to have these genes intact as do all the Ugandan, Kenyan, Rwandan and Burundi isolates. Furthermore, there is a high concentration of SNPs in this genomic region. Therefore, it seems likely that this genomic region represents the relic of a phage or similar mobile element that is in the process of degenerating, convergently, in some members of both sub-lineages.
2.7. Experimental Validation of Genetic Polymorphisms
One of the major motivations for comparing these genome sequences is to provide a resource for generating molecular markers that can be used epidemiological and biogeographical studies on a much larger panel of isolates without the need for whole-genome sequencing using, for example, the polymerase chain reaction (PCR). Therefore, we used the results of our genome comparisons to design pairs of PCR primers that can be used to distinguish between the two sub-lineages of Xcm (Table 5). A similar approach could also be taken to assay other classes of SNPs identified from the genome sequence data.
To experimentally validate SNPs, we used an approach based on digestion of PCR products with restriction enzymes. Many of the SNPs that we identified are predicted to fall within restriction sites. For example, position 6150 in RefSeq accession NZ_ACHT0100081 is a G that falls within an AluI restriction site (AG↓CT). However, in NCPPB2005 and the other members of sub-lineage I, this G is substituted for an A abolishing the recognition sequence for the AluI restriction enzyme (see Supplementary Files for a figure illustrating this SNP and several others). There are no other AluI sites in the vicinity of this SNP. We generated a pair of primers flanking approximately 250 bp either side of the SNP and amplified this 500 bp sequence by PCR. The two alleles could then be readily distinguished by digestion with AluI (see Figure 5). We used the same approach to design assays for three other SNPs (see Table 5 and Figure 5).
|Table 5. Polymerase chain reaction (PCR) primers used for distinguishing the two sub-lineages by restriction fragment length polymorphisms.|
|Primer Sequences||Target Sequence RefSeq Accession Number and Coordinates||Restriction Enzyme|
3. Experimental Section
Bacterial strains were obtained from the National Collection of Plant Pathogenic Bacteria (NCPPB) at FERA. DNA library preparation and genome sequencing using the Illumina GA2x were performed using standard Illumina protocols as previously described .
For DNA preparation, bacterial strains were grown overnight at 28 °C in 10 mL King Broth shaken at 200 rpm. Cells were harvested by centrifugation and re-suspended in TE buffer (50 mM Tris-HCl, 40 mM EDTA, pH 8.0). Bacterial cells cultured overnight in Kings Broth were pelleted, lysed with 12 µL of 20 mg/mL lysozyme and RNase at 10 mg/mL and incubated at 25 °C for 10 min. Further lysis was done with 17 µL 10% sodium dodecyl sulfate and incubated on ice for 5min. Proteins were dissolved with 170 µL of 8M ammonium acetate, vortexed vigorously for 30 s centrifuged at 4 °C at maximum speed for 15 min. DNA was precipitated with isopropanol and re-dissolved in 100 μL of 10 mM Tris, pH 8.0, and 1 mM Na2EDTA.
DNA amplification was performed in 30 µL reaction volumes containing 3 µL 10X PCR buffer, 1.2 µL of 50mM MgCl2, 2.4 µL of 2.5 mM dNTP, 1.5 µL of 10 µM each primer, 2ng DNA and 1 U recombinant Taq DNA polymerase. Amplification was performed using a thermocycler with initial denaturation (95 °C, 5 min), followed by 35 cycles of denaturation (95 °C, 0.5 min), annealing (60 °C, 0.5 min) and extension (72 °C, 0.5 min), with a final extension (72 °C, 10 min). The amplified products were electrophoretically separated in 4% (w/v) agarose gel at 80 V for 1 h in TAE buffer and visualized with UV light after staining in ethidium bromide (0.5 µg mL).
Amplified DNA fragments were digested with restriction endonucleases (AluI, Fok or NdeI). The restriction analysis was performed with 2.5 U of the endonuclease using the buffer and temperature recommended by the manufacturers (New England Biolabs). Restriction fragments were separated in a 8% (w/v) agarose gel with 100 bp ladder (Promega, G210A) at 100 V for 1 h in TAE buffer and visualized with UV light after staining in ethidium bromide (0.5 µg mL).
We used BWA  to align Illumina sequence reads against a reference genome sequence and used IGV  to visualize the alignments (see Figure 4). We used MEGA5 for phylogenetic analyses. De novo assembly of Illumina sequence reads was performed using Velvet 1.1.04 . We discarded any sequence reads that contained one or more ‘N’ prior to assembly.
We used a very conservative approach to infer SNPs from alignments of Illumina reads against the previously published Xcm NCPPB4381 reference draft genome assembly. To avoid false positives and false negatives, we only used those regions of the Xcm genome with a coverage depth of five or more for every sequenced Xcm genome and where there was at least 95% consensus among the sequence reads within each isolate. Just over 60% of the length (2,908,042 out of 4,782,144 nt) of the Xcm NCPPB4381 genome fulfilled these two criteria. In other words, for 60% of the Xcm genome, there was sufficient quantity and consistency in our data to be almost certain of the sequence in all of the fourteen isolates; for the remaining 40% of the genome, there was some degree of ambiguity in the data for at least one of the isolates.
Phylogenetic relationships were inferred using a maximum likelihood method based on the Tamura-Nei model  conducted using the MEGA5  software package. Bootstrap consensus trees inferred from 500 replicates were taken to represent the evolutionary history of the taxa analyzed. Branches corresponding to partitions reproduced in fewer than 50% bootstrap replicates were collapsed. Initial tree(s) for the heuristic search were obtained automatically as follows. When the number of common sites was <100 or fewer than one quarter of the total number of sites, the maximum parsimony method was used; otherwise the BIONJ method with MCL distance matrix was used. The trees are drawn to scale, with branch lengths measured in the number of substitutions per site. All positions containing gaps and missing data were eliminated.
We have deployed high-throughput whole-genome sequencing to explore genetic diversity among isolates of Xcm, the bacterial pathogen responsible for BXW, which is devastating banana and plantain crops in East Africa and threatens the food security of millions. To understand the evolution and geographical spread of this newly emerging pathogen, we need molecular markers such as SNPs. Given the high degree of genome sequence identity among isolates (99.9985 %), genome-wide sequencing is the only tractable way of discovering sequence polymorphisms and is beginning to be applied to bacterial phytopathogens .
The high degree of sequence similarity among isolates indicates a very recent origin of the pathogen. The molecular markers discovered here enabled us to reconstruct the phylogenetic relationships between Xcm isolates from diverse geographical locations within the known range of the pathogen in Africa. Interestingly, the isolates fell into two major sub-lineages. This may indicate that there have been at least two separate introductions of Xcm into the banana-growing regions around Lake Victoria. This contrasts with the widely held working assumption that Xcm spread from Ethiopia to Uganda and thence subsequently into neighboring countries. This view is largely based on the fact that Xcm was reported in Ethiopia in the late 1960s, then Uganda in 2001 and only later in other African countries (2004: D. R. Congo, 2005: Rwanda and Tanzania, 2006: Kenya and Burundi). However, it is possible that the disease has existed for some time before being officially reported, especially given the armed conflicts in D. R. Congo and Rwanda at the time. An alternative hypothesis is that all outbreaks in the region can be traced back to a single introduction of inoculum that contained some genetic diversity and that some genetic diversity is maintained within the population. Under that scenario, our results could be explained by stochastic effects of sampling error given such a small number of isolates. Therefore, there is a pressing need to collect and genotype many more isolates, including multiple isolates from within single outbreaks. On the other hand, where we have sequenced multiple isolates from a single geographical area (the five isolates from central Uganda and the three isolates from North Western Tanzania), only a single sub-lineage was observed. This would be an unlikely outcome if both sub-lineages were approximately equally abundant at these sites. Therefore, we currently favour the multiple-introduction model until further isolates and genetic data are available.
This study was supported by the National Agriculture Research Organisation, Uganda under the MSI/WorldBank grant 2009. The authors wish to thank Karen Moore and Alex Moorhouse for their invaluable technical assistance with sequencing and Marta De Torres Zabala for expert guidance to A.W. in the laboratory.
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