- Research article
- Open Access
Phamerator: a bioinformatic tool for comparative bacteriophage genomics
© Cresawn et al; licensee BioMed Central Ltd. 2011
Received: 12 May 2011
Accepted: 12 October 2011
Published: 12 October 2011
Bacteriophage genomes have mosaic architectures and are replete with small open reading frames of unknown function, presenting challenges in their annotation, comparative analysis, and representation.
We describe here a bioinformatic tool, Phamerator, that assorts protein-coding genes into phamilies of related sequences using pairwise comparisons to generate a database of gene relationships. This database is used to generate genome maps of multiple phages that incorporate nucleotide and amino acid sequence relationships, as well as genes containing conserved domains. Phamerator also generates phamily circle representations of gene phamilies, facilitating analysis of the different evolutionary histories of individual genes that migrate through phage populations by horizontal genetic exchange.
Phamerator represents a useful tool for comparative genomic analysis and comparative representations of bacteriophage genomes.
Bacteriophages represent a numerically vast, highly dynamic, evolutionarily ancient, and genetically highly diverse population [1–3]. Phage genomes are typically small compared to those of their bacterial hosts (ranging from a few to several hundred kilobases) and no longer present significant technical challenges to sequence determination . As genomic sequencing approaches get simpler and cheaper, the availability of individual phage isolates for characterization becomes limiting, a need that can be effectively addressed through integrated research-education programs involving undergraduate and high school student investigators [4, 5].
In spite of their relatively small size, phages present significant challenges to accurate genome annotation including gene identification. Two principal issues arise. First, phage genes tend on average to be small (~600 bp), approximately two-thirds the average size of bacterial genes [1, 6]. Many of the genes required for virion structure and assembly are relatively large (tape measure genes can be over 6 kbp long), but those in the non-structural genomic segments are small, often shorter than 100 codons. Secondly, phage genomes are replete with genes of unknown function for which no homologues have been described [7–10].
Mosaic architectures are hallmarks of phage genomes, and individual phages can be considered as particular combinations of interchangeable modules, each of which can be present in two or more different genomic contexts [10, 11]. In some cases, where the recombination events giving rise to these mosaic structures occurred relatively recently in evolutionary time, mosaicism is apparent through nucleotide sequence comparisons [12–14]. When the events occurred in more remote evolutionary times the evidence of common ancestry is usually no longer apparent at the nucleotide level, but often can be revealed from comparison of the predicted amino acid sequences [15–17]. Such comparisons reveal that individual phage genomes are typically constructed from multiple modules - often corresponding to single genes - each of which has a distinctly different phylogeny . As such, accurate compilations of whole genome phylogenies that reflect the evolutionary history of the entire genome are not possible, and reticulate-based representations are needed to capture this evolutionary complexity [16, 18].
The mechanisms giving rise to genome mosaicism are unclear but must accommodate the striking observation that module boundaries correspond closely with gene boundaries, and in some cases, domain boundaries [11, 19]. One model invokes homologous recombination events targeted to short conserved boundary sequences between genes, and there is evidence for this in some phage genomes [20, 21]. However, there are numerous examples where no conserved boundary sequences are evident, raising the possibility that mosaicism results largely from illegitimate recombination events between randomly chosen partners sharing little or no sequence identity [10, 11]. In this second model, correspondence between module and gene boundaries results from the selection for gene function, not from targeting of the recombination events .
Comparison of genomes from phages that infect taxonomically diverse hosts typically provides little information into their evolution because of only very limited similarity at either the nucleotide or amino acid sequence level [4, 11]. Phages of a common host, however, have the advantage that they are more likely to have been in recent genetic communication with each other and to have exchanged modules in recent evolutionary times . Large sets of phage genomes are now available for several hosts including Burkholderia, Bacillus, Enterobacteriaceae, Mycobacteria, Prochlorococcus and Synechococcus, Pseudomonas, and Staphylococcus, although even these can span enormous genetic diversity [1, 6].
A large number of phages that infect Mycobacterium smegmatis mc2155 have been isolated and a comparative analysis of 80 has been described [4, 6, 10, 14]. Although these are genetically diverse, the diversity is heterogeneous, and phages can be grouped into 'clusters' according to their overall nucleotide sequence relationships . Of the 80 published completely sequenced mycobacteriophage genomes, 75 can be grouped into ten major clusters, seven of which can be further subdivided into subclusters according to the extent of the nucleotide similarities . Five of the genomes have no close relatives and are referred to as 'singletons' . Because the currently sequenced mycobacteriophage genomes under-represent the mycobacteriophage population-at-large, these cluster designations will undergo modifications as new genomes are sequenced . There are, however, numerous examples of genes that are shared between phages of different clusters and whose common ancestry is only apparent from amino acid sequence similarity [4, 6, 10]. We have proposed previously  that mycobacteriophage genes related to each other can be grouped into phamilies (phams) and that mosaic relationships can be analyzed and represented using pham-annotated genomes maps and phamily circles that show the patterns of which phages contain members of particular phams. Although manual or semi-automated approaches are applicable when only small numbers of genomes are analyzed , this becomes an impossible task as the number of genomes expands.
We describe here a software program 'Phamerator' that provides bioinformatic tools for both analyzing and representing phage genome mosaicism. The core functionality of Phamerator performs pair wise similarity searches between predicted protein products of a set of phage genomes, and assorts them into phamilies (phams) of related sequences. Genome maps can be displayed that illustrate the relationships between phages at both the nucleotide and amino acid sequence level. Moreover, the evolutionary histories of specific genes can be displayed by phamily circles in which all gene members of particular phams are represented, and for which multiple phams can be compared. We illustrate the utilities of Phamerator using a set of 111 completely sequenced mycobacteriophage genomes, but the program is applicable to any set of phage genomes for which comparative analysis is desired.
Phamerator database architecture
Phamerator is written entirely in the Python computer programming language and makes use of a number of modules, including the Biopython framework for computational biology . Biopython provides a programmatic interface for sequence manipulation, the construction and parsing of files in relevant formats, and access to external command line applications such as those used for sequence alignment. For the latter, Phamerator uses Biopython to interact with local instances of BLASTP and CLUSTALW. Due to the significant computational time required for performing large numbers of sequence alignments, Phamerator employs a distributed processing model that is implemented using Python Remote Objects (Pyro). Phamerator was developed on Ubuntu Linux but should be able to run on any modern UNIX-based operating system.
Use of distributed computing resources
Adding genomes to a large Phamerator database is time-consuming, with the length of time required being proportional to the size of the existing database and the number of genes in the genome to be added. However, the length of time required to perform this operation can be reduced by distributing the required calculations to several computers. The reduction in time required scales approximately linearly with the number of available computers. Communication between computers is achieved using the Python Remote Objects (Pyro) library, and can be distributed to computers on the local network or across the Internet.
Availability and distribution
Phamerator operates using a client/server model. A relational database resides on the server computer and is distributed to client computers when they run the Phamerator client program. This enables all clients to have the performance benefits associated with interacting with data stored on the local computer along with a benefit normally associated with processing data on a server--assurance that the data being used is up-to-date. Because the data files being disseminated are relatively small (approximately 10-100 megabytes), a modest server can handle the load of hundreds of users without performance deterioration.
Phamerator can be downloaded from: http://phamerator.csm.jmu.edu/files/phamerator-current.tar.gz. Further information and installation instructions are provided in Additional Files 1 and 2.
Rationale for Phamerator construction and operations
The pervasive mosaicism of bacteriophage genomes requires bioinformatic tools that can organize and display their complex relationships. Two key questions arise in phage comparative analysis: what are the relationships between genes that are evolutionarily mobile within a given set of phage genomes, and how are they related to genes found in other genomes. Both approaches are complicated by the presence of intragenic mosaicism reflecting distinct evolutionary histories of gene segments [4, 13, 27–29].
Phamerator is a computational tool designed to sort phage genes into phamilies of related sequences using pairwise amino acid sequence comparisons of predicted gene products. Rather than using ortholog identification programs such as HMMER or Pfam  we have employed BLASTP and CLUSTALW to perform pairwise comparisons that are then assembled into phamilies of related proteins. Both of these programs are relatively fast computationally, a critical factor when large numbers of computations are required. For example, in the dataset of 111 phage genomes used here, a total of 1.77 × 108 comparisons must be computed. We note that the use of efficient pairwise BLASTP comparisons to generate families of protein sequences has been described previously .
To identify homologues of previously identified proteins Phamerator performs automated searches of GenBank non-redundant protein sequences, as well as searches for conserved domains in the NCBI conserved domain database using the RPS-BLAST tool. This information can be exported in tabular form, or represented in a whole-genomic context. Details of the Phamerator program are described in the Methods section and an overview of database structure is shown in Figure 1.
The building of phams is strongly influenced by the specific parameters used for amino acid comparisons. In early studies initiated prior to Phamerator development we used a BLASTP cutoff value of 0.001 and a CLUSTALW cutoff of 25% amino acid sequence identity for manual pham building . However, as the number of mycobacteriophage genomes increased and computational processing became essential, it became clear that these largely arbitrarily chosen parameters promoted assembly of many large phams that require time-consuming manual deconvolution . We therefore explored the impact of varying the threshold values for BLASTP and CLUSTALW on pham assembly.
There is also a dramatic change in the size of the largest pham as the threshold level varies from 32.5% to 27.5% (Figure 2A). At 32.5% the largest pham contains 172 members, but increases to 2, 505 at 27.5% (Figure 2A). The size of the largest pham is more stable between 32.3% and 50% identity thresholds and varies from 172 to 53. We interpret these data as indicating that between 50% and 32.5% identity, pham assembly proceeds in a manner that simply reflects the variation in the overall relationships between genes. However, at levels below 32.5%, there is an increasing proportion of phams that are more complex, such that not all pairwise matches within the pham are above the threshold level. One example might be where two genes (e.g. gene A and gene B) have been fused into a single open reading frame (gene C), such that although genes A and C, and gene B and C, both surpass the threshold, the unrelated genes A and B do not (a specific example is phage PBI1 genes 6 and 7, which are fused in phage Gumball to form gene 6). For routine database building purposes where we wish to avoid the assembly of large phams that then warrant subsequent deconvolution, we have chosen to use a 32.5% CLUSTALW threshold, but note that comparison of phams generated with these parameters and those with lower stringencies should be useful in analyzing intragenic mosaic relationships.
One advantage of CLUSTALW as an assembly program is that the threshold values are independent of gene length. Nonetheless, we predict there are instances where large genes may not exceed the CLUSTALW threshold but are evidently homologues because of statistically informative BLASTP scores. We therefore examined the impact of including a BLASTP search along with the CLUSTALW comparison (using a 32.5% cut off value) and varying the BLASTP cut off value (pham membership thus required meeting either the CLUSTALW or the BLASTP thresholds) (Figure 2C, D). As threshold values are made less stringent we observe a reduction in the total number of phams and the number of orphams, and a corresponding increase in mean pham size and the size of the largest pham (Figures 2C, D). Between BLASTP thresholds of 10-50 and 10-20 these is only a modest change in the total pham number (from 2, 757 to 2, 644; ~4% reduction) and number of orphams (from 1, 322 to 1, 260; ~4% reduction), but the size of the largest pham changes from 118 to 198 (68% increase). Upon manual inspection of all phams with 100 or more members at the BLASTP thresholds between 10-50 and 10-20 we see 'false' pham assembly occur as illustrated by joining of a phamily of tape measure proteins with a phamily of lysin proteins, through sharing of small but closely related domains. Nonetheless, inclusion of the BLASTP comparison with a 10-50 threshold joins several lysin phams that are separate when using just the CLUSTALW comparison. We conclude that inclusion of BLASTP contributes rather little to the pham assembly process, but that a combination of a CLUSTALW threshold of 32.5% and a BLASTP cut off of 10-50 offers optimal parameters for this dataset, building phams of homologous proteins while minimizing construction of complex phams in which only segments of the proteins are related to each other.
When these parameters are applied to this dataset, the 111 mycobacteriophage genomes contain a total of 12, 298 genes that assemble into 2, 757 phamilies with a mean size of 4.46 genes/pham; 1, 322 phams are orphams (48%) and the largest pham contains 118 members.
Identification of known homologues and conserved domains
Once a novel genome has been sequenced and annotated, questions about the functions of individual genes encoded within the genome can be addressed. This process is facilitated by analyzing the predicted gene products for the presence of conserved domains. Numerous tools already exist for this purpose, but the NCBI conserved domain database (CDD) aggregates many of them into a single, searchable dataset. These domain databases often use different, complementary techniques such as hidden Markov models or position-specific scoring matrices to define domains and for the matching of novel sequences to existing domain models. To leverage the power of each of these approaches, we have implemented a system in Phamerator whereby phage proteins are used to query CDD, and the results are presented in a searchable database browser in addition to being displayed on genome maps. The latter affords both a global view of the genomes and provides a way to visualize the conservation of specific sequences in the Phamerator dataset with those in other organisms.
An analysis of the distribution of CDD hits among the mycobacteriophage protein sequences reveals that a current search produces a total of 16, 420 matches among the 18, 901 predicted proteins, for an average of 0.87 matches per protein. However, as expected, the distribution of matches is non-random, with only 2, 981 proteins (15.8%) having at least one CDD entry match, with the average number of matches for these proteins being 5.51. While 935 proteins each match a single domain, a single protein, Myrna gp183 (the presumed Lysin A), matches 77 domain models, most of which are aminotransferases. Generally, when numerous matches of a single protein to domains in the CDD are found, it reflects the redundant nature of the CDD dataset, although in some cases it reflects the presence of multiple domains within a single protein.
Computation of nucleotide sequence similarities
Phamerator uses the BLAST "Align Two Sequences" program (bl2seq) to perform pairwise local alignments of whole genome sequences. An E value of 1e-4 was chosen as the BLAST threshold. The alignments are performed between adjacent genomes on the linear genome maps and the results are overlaid on the maps using shading between the genomes to depict the aligned regions. This shading is color-coded according to the E value with violet representing an E value of zero and red an E value equal to the threshold used.
Representation of genome maps
Phamily circle representations of gene phylogenies
Phamily circle diagrams can be generated for individual phams and include the name for each phage in the database positioned around the circumference of a circle, ordered and colored according to cluster and subcluster designation (Figure 8). If a given phage has a gene that is a member of the phamily represented in the diagram, the protein name is included with the phage name. Arcs are drawn between pairs of genomes that contain a gene member of that phamily; relationships derived from CLUSTALW analyses are represented in blue, and BLASTP in red. In the Pham3102 example shown in Figure 8, the phamily of small proteins is present in 33 of the genomes and distributed among several cluster and subclusters. Some of the relationships are shown as blue-only arcs, indicating that the relationships exceed the threshold of 32.5% amino acid sequence identity of the CLUSTALW comparisons but does not meet the E value of 10-50 for the BLASTP comparisons (Figure 8). The gene sequences can be readily exported for each pham and used to construct neighbor-joining trees for comparison with the phamily circles.
An abundance of Orphams
We have explored the use of Phamerator with several other sets of phage genomes including SPO1-like phages of Bacillus subtilis and a group of Streptomyces phages, but we have recently successfully generated a database from 319 genomes, substantially larger than the 111-genomes described here. We recognize that as the number of complete phage genome sequences increases that the computational time required increases as the square of the number of genes, and this could impose considerable limitations. For example, increasing the number of genomes to 1, 000 - not an unreasonable expectation given the advances in DNA sequencing technology - increases the number of pairwise computations to ~1011, a 1000-fold increase in time over the current dataset. However, with recent advances in cloud computing and the availability of massively parallel and multi-core computing systems we anticipate that these demands can be readily met. For example, cloud-computing systems can provide more than a 1000-fold increase in the number of processors at minimal cost. Phamerator will remain a useful tool for comparative phage genome analysis for the next few years. We also note that recent developments in alternative profile-based similarity searches such as HMMERHEAD and HHMER3 http://hmmer.org/ that greatly increase their efficiencies should provide additional Phamerator components [32, 33].
Phamerator provides a simple but useful computational tool for dissecting the genetic relationships among bacteriophage genomes, and displaying them in informative representations. Phamerator is especially useful for analysis of particular sets of phages such as the mycobacteriophages described here, but can be readily expanded to include a broader phage set, in which it is desired to map the horizontal exchange of genes between phage populations (for example, between Streptomyces phages, Propionibacterium acnes phages, Rhodococcus phages, and the mycobacteriophages). Because of its computational intensity, it is less well suited to mapping global genome-scale relationships among large phage genome sets, but other programs have been described for this purpose [34, 35]. The use of a commonplace Biopython framework and MySQL database software should facilitate interaction of the Phamerator database components with other web-based utilities to make this a broadly accessible utility.
This work was supported in part by a grant to the University of Pittsburgh by the Howard Hughes Medical Institute (HHMI) in support of G.F.H. under HHMI's Professors program. Support was also provided by grants from NIH to R.W.H. (GM51975), to G.F.H. (GM093901) and to S.G.C. (AI082527).
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