BMC Plant Biology BioMed Central

Genetic chimerism of Vitis vinifera cv. Chardonnay 96 is maintained through organogenesis but not somatic embryogenesis Abstract Background: Grapevine can be a periclinal chimera plant which is composed at least of two distinct cell layers (L1, L2). When the cell layers of this plant are separated by passage through somatic embryogenesis, regenerated plants could show distinct DNA profiles and a novel phenotype which proved different from that of the parent plant.


Background
Chickpea (Cicer arietium L.) is one of the world's more important but less studied leguminous food crop with over 10 M ha grown across the Americas, the Mediterranean basin, East Africa, the Middle East, Asia and Australia [1]. As a grain legume it plays a significant role in the nutrition of the rural and urban poor in the developing world, as it provides a protein-rich supplement to cerealbased diets particularly of vegetarians and subsistence farmers who cannot afford meat. Despite its economic importance, chickpea productivity has been low because of yield losses to foliar and soil-borne fungal diseases (ascochyta blight, fusarium wilt and botrytis grey mould), insect pests (helicoverpapod borer) and abiotic stresses such as drought, cold and salinity. Sources of resistance and tolerance to these constraints exist in the wild Cicer germplasm yet remain largely unused by conventional breeding programs [2][3][4][5]. Three annual Cicer gene-pools have been defined based on the available hybridization reports, biochemical and molecular diversity analysis [6]: species within the primary gene-pool (C. arietinum, C. reticulatum and C. echinospermum) can be readily crossed usually generating fully fertile progeny; while species within the secondary gene-pool (C. bijugum, C. pinnatifidum and C. judaicum) can be successfully crossed with the cultigen C. arietinum, providing hybrid embryos are rescued. However, the progeny of crosses between primary and second gene-pools are frequently sterile; finally, species within the tertiary gene-pool (C. cuneatum, C. chorassanicum, C. yamashitae and others ) have not yet been successfully crossed with the cultigen Cicer arietinum.
Cultivated chickpea has a relatively low level of diversity, due to a series of bottlenecks caused by restricted distribution of the wild progenitors and the founder effect associated with domestication [7]. In addition, chickpea breeding programs have limited themselves to a small number of cultivated genotypes having sources of biotic stress resistance and abiotic stress tolerance with little or no use of wild species [5]. This has resulted in limited durability of resistances to many of the major pests and diseases, and limited progress in abiotic stress tolerance breeding. Wild germplasm accessions held at the International Centre for Agricultural Research in Dry Areas (ICARDA) in Syria, the International Institute for the Semi-Arid Tropics (ICRISAT) in India and other genebanks in USA, Europe and Australia contain valuable sources of novel genetic variation for improvement of these traits [6]. The wild Cicer species from the secondary gene-pool (particularly C. bijugum, C. pinnatifidum and C. judaicum) are known to possess multiple sources of pest and disease resistance and tolerance to abiotic stresses including drought and cold [7,8].
Where species barriers can be overcome, molecular markers will facilitate rapid and efficient transfer of economically important traits into cultivated breeding pools. This will have the added advantage of broadening the narrow genetic base of this crop and thereby reducing its vulnerability to evolving pest and disease pressures, while simultaneously providing stable increases in yield far beyond the current 0.6% annual improvement [1].
SSR markers remain the marker of choice for marker assisted selection in many breeding programs. However, SSR motifs may evolve too rapidly to be valuable as the sole assay for interspecific diversity analysis. In addition, markers shown to have tight genetic linkage to target genes in interspecific mapping populations may lose their selective power when used in backcross programs based on interspecific derivatives. Thus, there is a need for the development and utilization of gene-based markers that better serve molecular breeding applications and diversity analysis of germplasm.
In this context, the most important criteria for new markers are high reproducibility, detection of co-dominance polymorphism and suitability for rapid large-scale low cost screening. EST-based markers fulfill these criteria and since they are associated with the coding regions of the genome they also enhance molecular germplasm evaluation by capturing variation across transcribed regions and in genes of known function. This potentially resolves the problem of limited genomic coverage suffered by traditional single gene phylogenetic studies [30,31]. Targeted EST development has already begun in chickpea, focusing on ABA-related mechanisms of water-deficit tolerance in epicotyl tissue [32].
Our objective in this study was to increase the public EST resource for chickpea with a particular focus on root tissue, as constitutive drought tolerance mechanisms (such as root system development) are a common target for the crop physiology community [33] and are increasingly identified by genomics studies as important components of stress tolerance mechanisms [32,34]. Thus, an EST library was constructed after SSH of root tissue from two very closely related chickpea (C. arietinum) genotypes the landrace ICC 4958 and the popular local variety Annigeri, both considered to possess important sources of drought tolerance [35,36]. Following sequencing and functional annotation, we have generated over 100 EST markers which we have used in preliminary diversity analysis of wild and cultivated Cicer germplasm.
A summary of the number of EST clones and respective gene contigs classified in various functional categories based on align-ments with public databases Figure 1 A summary of the number of EST clones and respective gene contigs classified in various functional categories based on alignments with public databases. Putative identifications were assigned to 2130 of the 2858 sequences generated from a chickpea root subtractive hybridization library. Percentages indicate the proportion of unigenes from the total number of unigenes identified in whole dataset.

Results and discussion
The SSH process resulted in over 4000 clones expected to be largely associated with ICC 4958 (SSH tester) but could conceivably also include some highly constitutively expressed genes from Annigeri (SSH driver). Typically the cDNA inserts ranged from 0.5-1 kb. All clones were partially or fully sequenced through a single pass read from the 3' end and trimmed of vector and low quality sequences. A length threshold of 170 bp was set in view of the minimum expected size of a functional gene-encoding region (exon) [37]. Removal of short sequences (below 170 bp: largely comprising of problematic repeats and sequences predominantly composed of poly-A) resulted in 2858 high quality EST sequences with an average length of 480 bp all available at the ICRISAT Chickpea EST Database [38].

Analysis of ESTs and assembly of consensus sequences
Gene annotations were based on similarities to either known or putative ESTs in the public databases. All annotations were based on Blast searches, with a score threshold of ≥ 200 for BLASTn. For tBLASTx a score threshold of >100 was set, as these generally had e-values <10 -5 with a minimum of 50% identity over at least 30% of the length of the protein, which are the commonly used thresholds for reliable sequence annotation [39,40]. Tentative functional annotations of EST sequences based on tBLASTx were grouped under 12 general categories based on the biochemical functions of the predicted proteins ( Figure  1). The 2858 sequences were assembled into 210 contigs with 267 ESTs remaining unassociated (singletons). Putative identifications could be assigned to 2179 of the 2858 sequences (76%), representing 73% of the unigenes (178 singletons and 162 contigs), and all of these proteins were represented in other plant species. The 2858 sequences were assembled into 210 contigs with 267 ESTs remaining unassociated (singletons). Assuming that in most cases each contig represents one gene [41] a maximum number of 477 genes are represented in this dataset (available at NCBI: accession numbers CK148643-CK149150). The total length of contigs ranged from 240 to 1291 bases (with an average of 648 bases) while the largest number of ESTs assembled into one contig was 255. EST assembly leading to the generation of tentative consensus (TC) sequences has dramatically reduced the redundancy in this database, as reported elsewhere [42] (see Additional file 1).
Over three quarters of the 210 consensus sequences (77% equivalent to 164 contigs) were found to have significant similarity (tBLASTx >100) to sequences in public databases. Many of these annotations (47 consensus sequences) were validated through comparison with the CDD database using RPS-BLAST which compares a protein query sequence to a position-specific score matrix prepared from the underlying conserved protein domain alignment [43]. Conserved motifs consistent with tBLASTx annotations were identified in 47 consensus sequences providing an additional level of confidence for these assigned gene functions (see Additional file 2).
As expected, we observed a substantial number of the EST contigs and singletons to have no significant homology (NSH: 48 contigs and 89 singletons; 29%) to either nucleotide or protein sequences in public databases at the time of analysis. This compares well to the higher proportion of sequences (44%) reported with little or no homology from chickpea leaf tissue [44]. In addition, a substantial number of ESTs (approximately 19% of the unigenes) were found to have similarity with unannotated hypothetical, putative or unknown proteins contained in the public databases and were, therefore, placed in the unidentified function (UF) class.
otyping [45]. As optimization relies on the sequential investigation of each reaction variable, the process can take a long time, thus the conditions of optimization are rarely identified empirically and individual components are rarely all tested simultaneously. However, Cobb and Clarkson [46] devised a strategy in which the components of a PCR reaction could be tested together using the least number ofexperiments based on the Taguchi principle [47]. We adapted the Cobb and Clarkson [46], 9 reactions of 4 PCR components to a 5 reactions of 5 PCR components, the additional component being enzyme concentration. This further reduced the time and cost of optimization, whilst also minimizing the cost of the PCR screening by also considering enzyme concentration. Final primer (0.15 -0.5 pmol) and Taq DNA polymerase (0.2 -0.5 U) concentrations resulted in a reagent unit cost of US$0.08 per PCR sample. This compares very favorable with other reports of PCR unit costs [48,49]. Clearly DNA extraction costs are an equally important component for molecular breeding programs and can also be greatly reduced as has been reported elsewhere [50]. The primer sequences and optimization parameters of all the polymorphic markers are given in Table 2. Optimization also resulted in fewer spurious amplification products and clearer polymorphic bands amongst the accessions studied ( Figure 2).

EST marker diversity analysis
A total of 106 EST primers were designed, optimized and screened, of which 48 gave good amplification products in ICC 4958 (the SSH tester accession in the EST generation process) while 58 were deemed unsuitable as they either did not produce an amplification product or generated a complex pattern of bands which were difficult to evaluate. Of the 48 primers pairs screened across 1 cul-tivated and 8 wild Cicer species, 44 were polymorphic ( Table 2). A total of 167 polymorphic fragments ranging in size from 200 to >1000 bp was scored on polyacrylamide or agarose electrophoresis gels depending on product size ( Figure 2). The number of alleles detected per primer ranged from 2 -8 with the polymorphic information content (PIC) ranging 0.03 -0.89 (Table 5).
Fourteen of the 106 EST's contained SSR motifs, of which 10 contained perfect trinucleotide repeats. A relatively large proportion of these EST-SSR markers (8) were derived from the no significant homology (NSH) and unknown protein functional (UF) classes, based on sequence comparisons (BLASTn tBLASTx and PSI-BLAST). Markers from these EST classes have readily detected polymorphism in the diverse germplasm tested (PIC 0.20-0.82). Since over 48% of the EST's generated from the chickpea root library fall into NSH and UF classes, these are clearly useful markers with potentially important, yet unknown functions.
The EST data-set generated in this study was used to compute pair-wise genetic distances between species according to Band similarity coefficient and UPGMA clustering. In order to display, with minimal distortion, the genetic relationships between species, a Principle Coordinate Analysis (PCoA) was carried out. The first two dimensions of the PCoA plot indicate the presence of 5 clusters, which account for 20% and 17% of the total variation ( Figure 3). Dollo and polymorphism parsimony analysis (DOLLOP) conducted on this data-set found one most parsimonious tree with 301 steps (Figure 4) corresponding well with the PCoA analysis.
Both PCoA and parsimony analysis provide clear separation of most species. Both analysis grouped C. echinospermum, C. reticulatum and C. arietinum, together. These three species are classified together as the primary gene pool based on crossability studies. Similarly, all previous diversity studies based on allozymes [52], RAPD [16,53], microsatellite [54], ISSR [15,55] and AFLP [17] markers have also grouped C. echinospermum, C. reticulatum and C. arietinum together. The EST-based diversity analysis presented here shows C. arietinum (believed to be the wild annual progenitor [56] of cultivated chickpea) to be slightly distant to C. echinospermum and C. reticulatum but still within the same cluster (best reflected by the PCoA analysis Figure 3). All previous molecular diversity studies have clustered C. bijugum, C. pinnatifidum and C. judaicum together, although sometimes not well differentiated from the primary gene-pool species based on molecular diversity analysis. These three species are commonly considered to represent the secondary gene-pool as they require embryo rescue to recover viable progeny when crossed with the cultigen [6]. Both parsimony and PCoA analyses of the EST data-set clustered C. judaicum, C. pinnatifidum and C. bijugum together. This is in agreement with previous studies which demonstrated the close association of these three species. The current analysis suggests that C. pinnatifidum and C. judaicum are more closely related. This is in agreement with previous reports based on morphology analysis [56], seed storage protein analysis [57] and isozyme analysis [12]. In contrast, ecogeographical studies of the wild Cicer germplasm have suggested that C. judaicum to be quite diverged [7], which may explain the outlying position of one C. judaicum accession studied here (IG 69986) (Figure 4). Most other species generally fall into one of two clusters generally col-lectively referred to as the tertiary gene pool (Figure 3 and Figure 4) from which no viable hybrids have been reported from crosses with the cultigen.
Parsimony analysis grouped C. chorassanicum with C. cuneatum, but placed the C. yamashitae accessions as outliers ( Figure 4). This data supports the tertiary group proposed by Croser et al. [6] to consist of; C. chorassanicum which has never been successfully crossed with cultivated chickpea and C. yamashitae and C. cuneatum which have been crossed with the cultigen but the resultant progeny have failed to flower or proven sterile. However, this is not reflected in the PCoA (Figure 3).
The distribution of accessions from the same species within secondary and tertiary clusters suggests that these two gene-pools may not be as distinct as previously expected. This may indicate that there are some tertiary gene-pool species that might be more readily crossed with the cultigen than their taxonomic classification would otherwise indicate. However, since the current study is based on a limited numbers of accessions for both C. cuneatum and C. yamashitae further research is required to fully define the relationships between these species and the scope of new opportunities for plant breeders.

Conclusion
This is the first report of the use of EST-based markers for estimating genetic distances between annual Cicer species. We report on the development and characterization of 106 EST markers from chickpea sequences with functional annotations or unknown functions, some of which contain SSR motifs. These markers have detected high levels of polymorphism amongst the wild species studied here and initial results indicate that around 20% are polymorphic in intraspecific (C. arietinum) mapping populations, either directly or as cleaved amplified polymorphic sequences (CAPS) based markers [58].
The EST marker-based diversity analysis reported here broadly supports the Cicer taxonomy based on allozymic data and conclusions by Croser et al. [6]. The concurrence of our EST data with that of allozymic studies in particular suggests that many gene-based loci do have a common ancestory across Cicer species, as proposed but not substantiated by Choumane et al. [54]. Clustering patterns based on RAPD, AFLP and ISSR are generally very similar [15,17,55] but are substantially different to those based on the EST marker analysis reported here and the previously reported allozyme-based analyses [59]. This may be a consequence of RAPD, AFLP and ISSR markers sampling fundamentally different regions of the genome (under different evolutionary pressures) as compared with markers based on expressed genes. Unfortunately a detailed comparison of different assays is confounded by the vir- tual absence of common accessions and the adoption of different statistical analyses in each study [6].
The EST database developed in this study provides a preliminary profile of some differentially expressed genes that may be associated with constitutive mechanisms important for stress tolerance and root development in chickpea roots. These include transcripts with putative annotations for proteases, T6P synthase, non-specific lipid transfer proteins, MRP-like ABC transporters, chaperones-HSP70, TCP-1-alpha, bZIP transcription factor, calcium ATPases, protein kinases, MRP4 glutathione-conjugate transporter, glutathione S-transferase, phosphoenol pyruvate carboxylase, S-adenosyl methionine synthetase (see Additional files 1 and 2 for full details). It is envisaged that these differentially expressed genes can be validated by the chickpea community and the most promising ESTs used in candidate gene mapping and allele mining. The resultant annotated EST markers will then be of substantial value for marker-assisted introgression programs based on interspecific crosses using wild Cicer species that harbour agronomically valuable genes.
One of the aims of chickpea breeding is to address the continuing need for cultivars adapted to particular geographical regions or with specific new ideotypes to ensure sustainability and profitability of production. An important means of continuing to achieve such breeding objectives is through the use of novel germplasm [60]. Many breeding programs, in particular those involving rice and wheat, have successfully utilized molecular and statistical approaches in accelerating the introduction of novel genes from wild species through marker accelerated backcross breeding.
The availability of increasing amounts of sequence data in many legume species now offers the potential for routine development of gene-based markers. These provide the ultimate assay (or so-called 'perfect marker') for indirect trait selection and map-based cloning. Combining genebased markers together with highly polymorphic flanking SSR markers will greatly assist in reducing linkage drag and increasing the speed and efficiency of subsequent introgression programs. Finally, molecular genetic diversity analysis based on EST markers may also provide a

Plant material and growth conditions for SSH
Fifteen seeds from each chickpea accession (ICC 4958 and Annigeri) were sterilized with 25% chlorex (v/v) for 10 mins, rinsed twice with sterile distilled water, before placing in pre-sterilized plant pots containing sterilized vertisol. The soil was collected from the field, passed through a 2 mm sieve and autoclaved in plastic bags using a 60 min cycle at 120°C and repeated three times on consecutive days. Seeds were sown immediately after the last autoclave cycle.
Three seeds were sown per pot; the plants were maintained in a Conviron growth chamber (Conviron, Winnipeg, Man.) under optimal physiological conditions for chickpea growth: 25°C day (11 h) and 12°C night (13 h), 455 µmoles m -2 sec -1 illumination intensity, 80% day and 40% night relative humidity, and irrigation as required.
Roots were harvested 28 days after germination (with flowering expected after 30 days). The soil was washed off the roots in running water, the intact whole plant was lifted out of the soil and soil particles were gently rubbed off in running water with gloved hands. The root tissue was subsequently treated with (0.1% v/v) DEPC solution and immersed in sterile Milli Q water, excess water from the roots was blotted onto filter paper and roots were weighed (approx. 2 g), flash frozen in liquid nitrogen and stored at -80°C.

RNA isolation and suppressed subtractive hybridization
The subtraction of the two genomes was achieved through a process of PCR-based suppression of genes common to both genotypes, and genes that are differentially expressed are enriched. As the process is based on PCR, low copy number cDNA can be detected from the tester (ICC 4958). RNA isolation and library construction was carried out by Avestha Gengraine Technologies (Bangalore, India). Total RNA was isolated from the root tissue of ICC 4958 and Annigeri using Trizol reagents (GIBCO-BRL) for RNA isolation, mRNA was purified using Oligotex (Qiagen GmbH, Hilden, Germany).
The suppression subtractive hybridization (SSH) process was carried out using a Clontech PCR-Select cDNA subtraction kit (Clontech INC. USA). Tester (ICC 4958) and driver (Annigeri) cDNA was restricted with RsaI for 90 mins and cDNA from the ICC 4958 was ligated with the required adaptors. Adaptor ligation was confirmed by PCR, followed by one round of over-night hybridisation with Annigeri as the driver and ICC 4958 as the tester. A second round of hybridisation was followed by primary PCR (27 cycles) and secondary PCR (12 cycles) according to the manufacturer's instructions for the PCR-Select. The PCR products of the subtraction were analyzed by gel electrophoresis and cloned using pCR4-TOPO cloning kit (Invitrogen Inc., USA). The cDNA clones were amplified in E. coli DH10B cells by electroporation and insert containing clones were selected by plating on LB agar containing 100 ug/ml ampicillin. Large colony forms were picked and used to regenerate single clone cultures in 96-well microtitre plates. After growth over-night at 37°C, glycerol was added to a final concentration of 15% and cultures were stored at -80°C.

EST sequencing
Cultures of transformed E. coli were grown over-night in 100 ul LB media containing 100 ug/ml ampicillin, the cells were centrifuged and suspended in sterile distilled water, heat denatured for 10 mins at 95°C, 1 ul of supernatant was used for insert amplification with M13 forward and reverse primers. Inserts (5 ul) were separated by electrophoresis on 1.2% agarose gel containing ethidium bromide to confirm amplification of a single insert and for quantification. After SAP/exonuclease I digest, 4 ul of the insert was sequenced using T 7 primer and 1/8 fraction of the recommended volume of dye terminator reagent (Big Dye terminator cycle sequencing kit v2, ABI-Foster City) for cycle sequencing. After removal of dye blobs by ethanol precipitation, DNA sequences were analyzed by capillary-electrophoresis using an Applied Biosystems genetic analyzer model ABI 3700 or ABI 3100.

Sequence analysis for predicting gene function
Base calling was performed using the ABI DNA Sequence Analysis Software (v3.7) or by Chromas v2.2 (Technelysium Pty Ltd. Australia). All sequences were scanned visually for quality of the peak shapes and corresponding base call. Vector sequences were trimmed using Sequencher v.4 (Gene Codes, Ann Arbor, MI) software and low quality bases (quality score <20) were trimmed from both ends of sequences. A total of 4000 sequences were analyzed, only sequences of more than 170 bp with less than 5% ambiguity were processed. The RPS-BLAST outputs were similarly processed using an in-house script, retaining the following information from the top-scoring alignments: gene identifier, description, score and e-value. Each result was manually interpreted and classified according to the biochemical function of the predicted protein.

Plant material and DNA isolation
Fifteen chickpea accessions representing 9 annual Cicer species, including the cultivated species C. arietinum, were used in this study (Table 1). Seeds of these accessions were germinated in Jiffy pots in a growth room and DNA was extracted from 4-5 pinnules of 15-20 day old individual plants with 2% CTAB extraction buffer containing 0.03% mercaptoethanol as described in [50]. DNA concentrations were determined by comparing the sample intensity (1 µl) with that of known amounts of uncut lambda DNA by electrophoresis in 1.2% 'Ready-to-run' agarose gels (Amersham) containing ethidium bromide. DNA was diluted to a working stock concentration of 10 ng/µl and checked before use.

Primer design of EST markers
A total of 106 EST sequences were chosen that represented diverse functional/stress annotations, a selection of which contained SSR motifs. In addition, primers were also designed from a random selection of sequences categorized as having 'no significant homology' (NSH) and 'unknown protein function' (UF) when compared with either nucleotide or protein sequences in public databases.
Primer sequences were designed using Genefisher 1.1 software [65] using the following criteria 57 -63°C melting temperature (Tm), 40-50% GC content, 17-24 bp primer length and the difference in Tm between forward and reverse primer pairs was limited to 2°C. For those EST sequences containing repeat motifs, primers were designed to flank the microsatellite region. Optimal primer pairs were selected using Netprimer, the primer design algorithm which analyzes all possible secondary structures including hairpins, self-dimers and cross-dimers [66]. The Tm and product length of 8 forward and reverse pairs per sequence from Genefisher software were evaluated by Netprimer software for minimal or no secondary structure. All primer and EST sequences are accessible through the ICRISAT Chickpea EST Database [38].

PCR optimization and evaluation
The chickpea accession ICC 4958 (from which the EST sequences were derived) was used as the reference accession for primer optimization. A total of 106 EST primers (synthesized by MWG, Germany) were optimized simultaneously for the following PCR components using a modified (5×5) grid [46]. On this basis initial optimization of the five major components in a PCR (concentrations of primer, template DNA, Mg ++ , dNTP and enzyme) were empirically determined for each primer used in this study (Table 3). Optimal touch-down temperature and number of amplification cycle profiles were also determined for each primer pair (Table 4). This procedure is important to minimize non-specific amplification, maximize data accuracy and minimizes cost.
PCR amplified products with a size range of 200-600 bp were resolved by non-denaturing polyacrylamide gels electrophoresis (6-10% acrylamide/bisacrylamide, 20:1 in TBE). Bands were visualized through a modified silver staining protocol [67] as follows: gels were immersed in water for 3 mins, followed by 20 mins in 0.1% CTAB solution and 0.3% ammonia solution for 15 mins. Silver staining solution was freshly prepared each day, consisting of 0.1 % (w/v) AgNO 3 in 4 mM NaOH solution, 0.5 to 0.6 ml of 25% ammonia was titrated until the cloudy suspension became clear. Gels were gently agitated in the silver nitrate solution for 30 mins, and developed in 1.5% (w/v) sodium carbonate and 0.02% (v/v) formamide solution until bands appeared. The gels were rinsed in water, fixed in 1.5% glycerol solution and documented by scanning. PCR products above 600 bp were resolved by agarose gels electrophoresis (0.8-1%) containing ethidium bromide.

EST marker data collection and analysis
The amplification profile from each EST marker was checked for reproducibility and subsequently scored visually (and independently rescored) for the presence (1) or absence (0) of polymorphic bands. The degree of polymorphism was quantified using the polymorphic information content (PIC) calculator [68] based on the following formula: where Pi is the frequency of an individual genotype.
Pair-wise genetic distances were calculated with NTSYS-pc software version 2.0 [69] as S xy = 1 -(2n xy /n x + n y ) as S xy = 1 -(2n xy /n x + n y ) based on band coefficient [70], where n xy are shared bands amongst the individuals, n x and n y are the number of fragments exhibited by each individual. Distance based on Band coefficient is similar to the genetic distance (GD) formula by Nei and Li [71]: GD = 1 -S xy . The 15 × 15 similarity matrix (based on Band coefficient) was subjected to sequential agglomerative hierar-chical nested (SAHN) clustering using UPGMA (unweighted pair-group method analysis). Principle coordinate analysis based on these distance estimates was performed using NTSYS, using consecutive commands of 'DCENTRE' and 'EIGEN' in order to generate a PCoA plot which is more informative in highlighting differences between major taxonomic groups than dendrogram repre- sentations. Maximum parsimony analysis was conducted using the PHYLIP program Dollo and polymorphism parsimony analysis version 3.63 [72] and the consensus tree viewed in tree view.