Genome Sequence of Avery's Virulent Serotype 2 Strain D39 of Streptococcus pneumoniae and Comparison with That of Unencapsulated Laboratory Strain R6

Abstract

Streptococcus pneumoniae (pneumococcus) is a leading human respiratory pathogen that causes a variety of serious mucosal and invasive diseases. D39 is an historically important serotype 2 strain that was used in experiments by Avery and coworkers to demonstrate that DNA is the genetic material. Although isolated nearly a century ago, D39 remains extremely virulent in murine infection models and is perhaps the strain used most frequently in current studies of pneumococcal pathogenesis. To date, the complete genome sequences have been reported for only two S. pneumoniae strains: TIGR4, a recent serotype 4 clinical isolate, and laboratory strain R6, an avirulent, unencapsulated derivative of strain D39. We report here the genome sequences and new annotation of two different isolates of strain D39 and the corrected sequence of strain R6. Comparisons of these three related sequences allowed deduction of the likely sequence of the D39 progenitor and mutations that arose in each isolate. Despite its numerous repeated sequences and IS elements, the serotype 2 genome has remained remarkably stable during cultivation, and one of the D39 isolates contains only five relatively minor mutations compared to the deduced D39 progenitor. In contrast, laboratory strain R6 contains 71 single-base-pair changes, six deletions, and four insertions and has lost the cryptic pDP1 plasmid compared to the D39 progenitor strain. Many of these mutations are in or affect the expression of genes that play important roles in regulation, metabolism, and virulence. The nature of the mutations that arose spontaneously in these three strains, the relative global transcription patterns determined by microarray analyses, and the implications of the D39 genome sequences to studies of pneumococcal physiology and pathogenesis are presented and discussed.

Streptococcus pneumoniae (pneumococcus) is a major human respiratory pathogen that causes several serious diseases, including pneumonia, otitis media (ear infection), sinusitis, meningitis, and septicemia (reviewed in references 81, 112, and 114). Invasive pneumococcal diseases result in high rates of mortality and morbidity, especially among young, elderly, debilitated, and immunosuppressed individuals (54, 55). It is estimated that more than 1 million people die each year from pneumococcal infections worldwide, especially in developing countries (59, 80). In the United States and elsewhere, resistance to a range of antibiotics is increasing at an alarming rate among clinical isolates of S. pneumoniae (6, 60). As part of its life cycle, pneumococcus exists as a commensal bacterium that inhabits and colonizes the nasopharynx of up to 20 and 50% of healthy adults and children, respectively, at any time (81, 113). The transition from commensal bacterium to opportunistic pathogen often occurs after another respiratory tract infection. For example, pneumococcal pneumonia has been a leading secondary infection and cause of death during influenza pandemics (9).

Strains of S. pneumoniae are categorized into serotypes based on the structures of their exopolysaccharide capsules, of which there are more than 85 kinds (35, 117). To date, the complete genome sequences have been determined for only two strains of S. pneumoniae (48, 110), and partial sequences are being determined for other serotype strains that are prevalent as current clinical isolates (see references 20, 28, 42, 104, and 109 and http://genome.microbio.uab.edu/strep/info/ and http://www.sanger.ac.uk/Projects/S_pneumoniae/). The genome sequences of the virulent serotype 4 strain, TIGR4, which is a recent clinical isolate (110), and the avirulent, unencapsulated laboratory strain R6 revealed numerous aspects of the metabolism and genome organization of S. pneumoniae (48, 110). A startling finding from these initial comparisons is the diversity among the genomes of the different serotypes of S. pneumoniae (109). In fact, as many as 10% of the genes may be substantially diverged or absent in comparisons between the genomes of different serotype strains (20, 42, 44, 109). In addition, pneumococcal genomes contain a relatively large number of insertion elements, transposon remnants, and repeat sequences, which suggests that pneumococcal genomes may exhibit considerable plasticity (109). Because of this extreme diversity, it has become imperative to study colonization and virulence in a number of different serotypes of S. pneumoniae, each of which causes a distinct pattern of infection in animal models (16, 44, 88).

The genome sequence of strain R6 was determined because it has become a standard laboratory strain for the study of fundamental cellular processes, such as transformation, cell division, and peptidoglycan biosynthesis (e.g., see references 1, 25, 58, 78, and 84). Strain R6 was derived about 40 years ago from strain R36A (12, 89), which was derived about 60 years ago by Avery and coworkers for the landmark demonstration that DNA is the genetic material (Fig. 1) (8, 12, 76). R36A was, in turn, derived from strain R36, which was derived originally from the clinical serotype 2 isolate D39 (Fig. 1) (8, 12, 76). R36, R36A, and R6 were isolated because they were nonreverting mutants lacking type 2 capsule and were increasingly competent for natural transformation, before the discovery of the competence stimulatory peptide (45). Providing an isogenic avirulent strain for comparison with serotype 2 progenitor D39 was not a goal of these derivations.

FIG. 1.

Pedigree of strains D39 (NCTC), D39 (Lilly), and R6 whose genome sequences are compared in the present study. (The figure was modified from reference 12.) See the introduction and reference 12 for details.

Besides its historical significance, strain D39 has been adopted as a leading model of pneumococcal pathogenesis (e.g., see references 14, 17, 65, 87, 88, and 96). Although strain D39 was isolated from a patient about 90 years ago (Fig. 1), it remains extremely virulent in animal models of infection (e.g., see below and references 14, 16, 17, 87, 88, and 96) and has proven to be highly tractable in genetic mutant constructions (e.g., see references 14, 16, 17, and 96). Aside from a large deletion of part of the capsule (cps) biosynthesis locus, it has often been assumed that the genetic composition of strain D39 and R6 differ by only a limited number of mutations (e.g., see reference 12). However, there is no direct evidence for this assumption, which is partly based on the fact that mutagenesis is not mentioned in the derivation of strains R36, R36A, or R6 (8, 12, 76). It has also been unclear whether pathogenic islands present in strain TIGR4 (110) but absent from strain R6 (48) were lost during derivation and passage. Moreover, not having the genome sequence of the most commonly used strain of S. pneumoniae has hampered the interpretation of physiology and pathogenesis studies.

We report here the sequence of two different isolates of serotype 2 strain D39. One isolate designated as D39 (NCTC) is from the National Collection of Type Cultures (NCTC; United Kingdom) and is currently widely used in studies of pneumococcal physiology and pathogenesis (e.g., see references 16 and 17). According to their records, D39 (NCTC) was deposited in the NCTC collection about 60 years ago (Fig. 1). The second isolate designated D39 (Lilly), which was used previously by this laboratory (96), was obtained from Lilly Research Laboratories, who obtained it from Janet Yother (University of Alabama at Birmingham [UAB]). We do not know the exact propagation history of D39 (Lilly), but the two D39 isolates have been separated in captivity by at least 21 years and possibly longer (Janet Yother, unpublished data). Comparison of the genome sequences of these two D39 isolates with the corrected genome sequence of strain R6 indicates mutations that likely arose separately in each of the three strains compared to the D39 progenitor strain. This analysis shows that the genome of serotype 2 strain D39 has been unexpectedly stable during propagation in captivity and that the genome sequence of strain D39 (NCTC) remains extremely close to that of the deduced D39 progenitor strain. In contrast, there are over 80 mutational differences between strain R6 and the D39 progenitor strain (Fig. 1). One important implication of the present study is that some metabolic relationships observed in laboratory strain R6 may not directly apply to pathogenic strain D39. We also report the occurrence of unusual deletion or insertion mutations of immediately adjacent direct repeat sequences in S. pneumoniae and the sometimes significant effects of seemingly minor mutations on global transcription patterns of these three strains.

MATERIALS AND METHODS

Bacterial strains.

A single-colony isolate of strain R6 was assigned the unique strain designation EL59 (48). This isolate originated from the same stock as the sequenced R6 strain deposited in the American Type Culture Collection (ATCC BAA-255) (48). A single-colony isolate of strain D39 obtained from Lilly Research Laboratories (Eli Lilly and Co., Indianapolis, IN) was assigned the unique strain designation IU1680 and is referred to as D39 (Lilly) herein. A second D39 isolate, NCTC 7466, was purchased from the NCTC (London, United Kingdom). The lyophilized sample of NCTC 7466 was resuspended in brain heart infusion (Bacto BHI; Becton Dickinson) broth upon receipt, spread onto Trypticase soy agar II (modified) (Becton Dickinson) containing 5% (vol/vol) defibrinated sheep blood (TSAII BA) for single-colony isolation, and incubated at 37°C in an atmosphere of 5% CO₂. All colonies were alpha-hemolytic and white, but we observed two colony types: larger, shiny, smooth colonies and smaller, flatter, rough colonies. A representative colony of each type was single colony isolated three times on blood agar plates. The representative smooth colony was assigned the unique strain designation IU1690 and is referred to as D39 (NCTC). D39 (NCTC) and D39 (Lilly), whose genome sequences are reported here, are sensitive to optochin (36) and are positive in Quellung reactions to type 2 capsule antiserum (Statens Serum Institut, Denmark) (36). The representative smaller rough colony (strain IU1691) was optochin sensitive but was negative in the Quellung reaction to antisera against type 2, 3, and 4 capsules. IU1691 had spontaneously lost its ability to synthesize capsule and was not characterized further.

General DNA sequencing strategy.

Previous determinations of the R6 and TIGR4 genome sequences (48, 109, 110) were hampered by the inability to recover random shotgun clones, presumably due to instability or toxicity, and by difficulties in assembling repeat-rich pneumococcal sequences (see reference 109). To avoid these problems, we used the R6 sequence as a blueprint to design PCR primers and performed a PCR walk around the chromosomes of D39 (NCTC) and D39 (Lilly) (see Fig. 2 and below). We spaced PCR primers to synthesize amplicons of about 900 bp with 300-bp overlaps between amplicons. The coverage of the D39 sequence was one to two separate sequence runs for each amplicon from D39 (NCTC) and D39 (Lilly) in regions that exactly matched the previously published R6 sequence (48). In regions that did not match the R6 sequence or that were different between the two D39 strains, we confirmed sequence differences with two to four separate sequence runs from two or more independent amplicons from each strain, and we rechecked the published sequences in these regions of R6 (48) or the cps cluster of D39 (50). Approximately 7,000 PCR primers were generated in this project and are listed in Appendix S1. Automated and manual annotation were performed as described below. The sequence of strain D39 (NCTC) was deposited in GenBank (accession information: s_pneumoniae_d39_1 CP000410), with genes assigned the “SPD” prefix.

FIG. 2.

Primer-walk strategy used to sequence the genomes of strains D39 (NCTC) and D39 (Lilly). Overlapping PCR amplicons were synthesized and sequenced by using primers based on the published sequence of strain R6 (48). See the text for details. The figure is not drawn to scale.

Purification of genomic DNA for sequencing.

D39 and R6 strains were grown exponentially in static BHI broth to an optical density at 620 nm (OD₆₂₀) of ∼0.2 at 37°C in an atmosphere of 5% CO₂. Bacteria were harvested by centrifugation (3,200 × g, 4°C, 10 min). Cells were washed with 1 volume of ice-cold 50 mM Tris-50 mM EDTA (pH 8.0) and then suspended in 1/10 volume of the same buffer. Triton X-100 and sodium dodecyl sulfate were added to the cell suspension at final concentrations of 0.1% (vol/vol) and 0.01% (wt/vol), respectively. Mixtures were incubated at 37°C for 30 min, followed by sequential extraction with buffered phenol, phenol-chloroform-isoamyl alcohol (25:24:1), and chloroform-isoamyl alcohol (24:1). Genomic DNA was precipitated by addition of 1/10 volume of sodium acetate (pH 5.2) and 3 volumes of 100% ethanol. DNA was collected by centrifugation (16,000 × g, 15 min, 4°C). DNA pellets were allowed to air dry and dissolved in TE buffer (10 mM Tris-HCl, 1 mM EDTA [pH 8.0]). Concentrations of DNA were determined by absorption at 260 nm (A₂₆₀).

Generation of PCR amplicons for sequencing.

Primers used for PCR and sequencing were designed by using the Vector NTI program (Invitrogen). Primers were chosen based on a predicted T_m of about 58°C and lack of predicted secondary structure. Primers were synthesized by MWG Biotech, Inc., in a 96-well format. PCRs (25 μl) containing genomic DNA and high-fidelity Pfu polymerase (Stratagene) were performed according to the manufacturer's instructions. The purity of PCR products was evaluated by agarose gel electrophoresis in a 96-comb/well format apparatus (Owl Scientific). PCRs that yielded expected amplicons were purified by using the Wizard MagneSil purification kit (Promega) according to the manufacturer's instructions. Purified PCR amplicons were sequenced directly. A new pair of PCR primers was designed when PCRs failed to generate sufficient amplicon or yielded nonspecific products. For regions that were recalcitrant to amplification by Pfu polymerase, rTth polymerase (Applied Biosystems) was used to generate PCR amplicons.

Sequencing PCR amplicons.

Each sequencing reaction (10 μl) contained 5 μl of purified PCR amplicon, 0.4 μM primer, 1 mM MgCl₂, and 0.75 to 1.0 μl of BigDye terminator mixture (Applied Biosystems). For regions of predicted strong secondary structure, 5% dimethyl sulfoxide (vol/vol [final concentration]) was added to reactions to facilitate polymerase readthrough. Products of sequencing reactions were resolved by capillary electrophoresis on an ABI 3730 DNA Analyzer (Applied Biosystems) located in the Indiana Molecular Biology Institute. Sequence data were analyzed by using the CodonCode Aligner program to determine Phred scores. Regions with low Phred scores (Q < 15; <95% base call accuracy) were discarded and not used in alignments. The published R6 sequence (48) and the type 2 capsule biosynthetic operon (cps) (50) were used in the CodonCode Aligner Program to guide sequence alignments. D39 sequences containing differences from the published R6 and cps sequences or between the two D39 strains were sequenced multiple times to rule out possible PCR-generated errors. The corresponding regions were resequenced from R6 genomic DNA to identify errors in the published R6 sequence (Table 1).

TABLE 1.

Interpretation and summary of sequence changes in D39 (NCTC), D39 (Lilly), and R6 (ATCC)

Sequence change presence in:			Interpretation	Changes
D39 (NCTC)	D39 (Lilly)	R6 (ATCC)		No.	Type
Yesa	Yes	No	Change arose in R6 (ATCC)	81	Seventy-one single-base-pair changes, three small insertions, one large insertion, five small deletions, and one large deletion of part of the cps locus reported previously (50)
Yesb	No	Yes	Change arose in D39 (Lilly)	8	Six single-base-pair changes, one small deletion, and one large deletion
Nob	Yes	Yes	Change arose in D39 (NCTC)	5	Four single-base-pair changes and one small deletion
Yesc	Yes	Yes (resequenced)	Error in published R6 sequence	28	Fourteen in one IS1167 element
Yesd	Yes	NA	Error in published D39 cps sequence	12	One frameshift; eleven single-base-pair changes (six in cps2B)

^aData compiled in Table 2 and Table S1 in the supplemental material.

^bData compiled in Table 4 and Table S2 in the supplemental material.

^cData compiled in Table S4 in the supplemental material.

^dData compiled in Table S5 in the supplemental material.

Annotation. (i) Finding genes.

All candidate genes were identified by using version 3.01 of the Glimmer gene finding system (26, 99; http://www.cbcb.umd.edu/software/glimmer/). The tRNAscan-SE tool (68) was used to identify tRNAs; rRNA genes and other structural RNAs were identified directly from BLAST (4) search results.

(ii) Homology searches.

The translation of each gene prediction was searched against a variety of public and private databases. Blast-Extend-Repraze (BER; http://ber.sourceforge.net) was used to search an internal nonidentical amino acid database constructed from all proteins available from GenBank (http://www.ncbi.nlm.nih.gov), UniProt (http://www.pir2.uniprot.org/), and the Comprehensive Microbial Resource database (http://www.tigr.org/CMR). A multiple alignment of each predicted protein and its BER hits was calculated by using MUSCLE (30). The Pfam (10) and TIGRFAM (41) libraries of hidden Markov models (HMMs) were searched by using programs from the HMMer package (29). Other amino acid sequence signatures, domains, or functional sites were predicted by searching all proteins against the PROSITE database (31). The SignalP (13) and TMHMM (62) algorithms were used to predict putative signal sequences and membrane-spanning domains, respectively. Family prediction was also done by searching (using BLAST) all predicted proteins against version 2 of the NCBI clusters of orthologous genes (COG) database (108). Domain-based paralogous families were built on the basis of HMM hits and homologous regions (detected by using BLAST) not covered by the HMM models.

(iii) Automated annotation.

A computer program developed at The Institute for Genomic Research (TIGR), AutoAnnotate, analyzed the BER and HMM search results and putatively assigned a common name, gene symbol, enzyme commission (EC) number (http://www.expasy.ch/enzyme), and TIGR and gene ontology (GO) (7) role categories in an automated fashion. AutoAnnotate uses a hierarchical approach first by evaluating the isology (sequence similarity) and score of each HMM match, followed by an evaluation of the length and the percent similarity of each BER alignment in order to predict a functional assignment to each gene. If there was a hit to an equivalog-level HMM (41) with a score above the trusted cutoff, the identifying information attached to that HMM (common name, role category, gene symbol, and EC number if applicable) was assigned to the predicted coding region. If no high scoring equivalog-level hit existed, the BER search results were evaluated. The program looked for a full-length match of at least 80% of the length of the subject, with at least 35% identity. If more than one match was found, the program attempted to choose a match with a name that followed TIGR's naming conventions and assigned a TIGR role category. If the chosen BER match was a hypothetical protein from another species or if no pairwise matches met the match criteria, AutoAnnotate went back to the HMM results and looked for nonequivalog hits. If any hits existed, the protein was assigned a family name based on the HMM name. Proteins with a pairwise match to a hypothetical protein from another species, but no HMM hit, were named a “conserved hypothetical protein.” Proteins with no HMM or BER matches remained named “hypothetical protein.”

(iv) Curating gene models.

The results of the homology searches were manually analyzed to curate predicted initiator codons and to identify potential frameshifted genes or genes with introduced stop codons. The assembly sequence was checked against the traces to determine whether frameshift or point mutations were introduced during the closure or assembly process or whether they were authentic. Overlapping genes were manually resolved either by evaluating and editing the initiation codon for each overlap or by retaining the one overlapping gene with sequence similarity to some other protein or domain.

Genes missed by Glimmer were identified by a BLAST search against an internal nonidentical amino acid database of the six-frame translation of regions of the genome where no homology evidence for the existing gene set was present. The output was manually reviewed, and new genes were added to the data set as required.

(v) Manual annotation.

All available evidence for each protein was evaluated by a human curator by using the manual annotation tool Manatee (http://manatee.sourceforge.net). Based on the evidence associated with each protein, the following descriptive information was assigned where appropriate: common name, gene symbol, EC number, TIGR role category, designation of homologous genes in the R6 (48) and TIGR4 (110) genome sequences, and gene ontology (7) terms. Specific functional annotations were assigned based on high-quality matches to experimentally characterized proteins found in the BER results or to equivalog-level HMM matches. Less specific and family level annotations were based on domain, superfamily, or subfamily HMMs or on the presence of specific motifs such as TMHMM or SignalP. In addition, the presence of genes in a putative gene cluster or pathway was important information included in each evaluation.

Determination of the number of repeats in spd0080 (spr0075).

The number of direct repeats in spd0080 (spr0075) was determined by two approaches. First, different pairs of flanking primers (e.g., III-F-036 and III-R-042 in Fig. 3) were used in PCRs containing rTth polymerase to amplify the repeat region. Amplicon sizes were determined by agarose gel electrophoresis relative to a 1-kb molecular weight marker ladder run in parallel (Fig. 3). Second, Southern blots were performed on genomic DNA from strains digested with NheI, which cuts outside of the region containing the direct repeats. Digested DNA was resolved by agarose gel electrophoresis and transferred to Hybond N+ membrane (GE Healthcare) by standard protocols (100). A 294-bp amplicon probe corresponding to an internal region of each repeat was synthesized by PCR using primers III-F-038 and III-R-040. Nonradioactive labeling of the amplicon probe, hybridization to the blots, and signal detection were performed according to instructions provided in the gene image AlkaPhos Direct kit (GE Healthcare).

FIG. 3.

PCR analysis of the repeated region in the spd0080 gene of D39 (spr0075 of R6). Primers III-F-036 and III-R-042 flanking the multiple 456-bp repeats of the SSURE domain (21) were used in PCRs to amplify the region as described in Materials and Methods. Amplification products from strains R6, D39 (Lilly), and D39 (NCTC) are shown next to a 1-kb molecular mass marker ladder (left lane) and the expected sizes of amplicons containing one to eight repeat units. The predominant species indicated repeats of eight or six SSURE units in this gene in R6 or D39, respectively. The faint ladder of bands differing by one repeat unit are likely a PCR amplification artifact and were not observed in Southern blots (see text). The extent to which this region was sequenced is indicated at the bottom of the figure. As was done previously (48), we inserted a placeholder sequence containing the five repeats reported previously for R6 into this region of the D39 genome sequence (see the text).

Microarray analyses.

Bacteria were grown statically in BHI broth at 37°C in an atmosphere of 5% CO₂. Overnight cultures were adjusted to an OD₆₂₀ of ∼0.1 (16-mm tubes) and diluted a further 50-fold into fresh BHI. Growth was monitored by change in OD₆₂₀ as measured in a Spectronic 20 spectrophotometer. Cultures were harvested at an OD₆₂₀ of ∼0.1, and RNA was extracted by a hot lysis-acid phenol protocol, followed by purification using the RNAeasy minikit (QIAGEN) as described previously (96). Thirty micrograms of total RNA was used to synthesize cDNAs for each sample, followed by direct labeling using Cy3- or Cy5-dCTP (GE Healthcare). Synthesis, labeling, hybridization (16 to 18 h at 42°C), and washing protocols were performed as recommended by the microarray manufacturer (see http://www.ocimumbio.com/web/arrays/assets/downloads/manuals/manual_bacteria.pdf). S. pneumoniae R6 microarrays were purchased from MWG Biotech, Inc. (now available from Ocimum Biosolutions). Details of the S. pneumoniae oligonucleotide array are described in GEO platform entry GPL536 (http://www.ncbi.nlm.nih.gov/projects/geo/). Microarray slides were scanned on an Axon GenePix 4200A microarray scanner, and images were analyzed by using GenePix Pro 5.0 software (Molecular Devices). Microarray data were obtained from three independent biological replicates, including one dye swap. The data normalization was performed with GeneTraffic 3.2 software (Iobion Informatics) using the Lowess (subgrid) method. The data were normalized both with or without background subtraction and used to calculate expression ratios. Ratios did not differ significantly with or without background subtraction.

Expression ratios from the three replicates were averaged to obtain the average fold changes expressed in Tables S6 and S7 in the supplemental material. Bayesian P values were calculated by using the Cyber-T Web interface (http://visitor.ics.uci.edu/genex/cybert/) (66). The cutoff for significant changes in relative transcript amounts was set at positive or negative 1.8-fold with a Bayesian P value of <0.001. Intensity data and expression ratio data are deposited in the GEO database (accession no. GSE5375).

Animal models of infection.

Experiments involving murine models of infection were conducted with prior approval by the Bloomington Institutional Animal Care and Use Committee and were performed in strict compliance to the Guide for the Care and Use of Laboratory Animals, prepared by the Committee on Care and Use of Laboratory Animals of the Institute of Laboratory Animal Resources, National Research Council (82). ICR outbred male mice (21 to 30 g; Harlan Sprague) were inoculated by intraperitoneal injection (∼100 CFU in 100 μl), intratracheally (∼2.5 × 10⁶ CFU in 50 μl), or intranasally (10⁵ or 10⁶ CFU in 50 μl) by standard methods published previously (17, 96). Time to moribundity was monitored and recorded, after which animals were sacrificed by CO₂ asphyxiation. Death was not used as an endpoint. Survival curves were analyzed by using GraphPad Prism software and were compared by using the log-rank test. For biophotonic imaging, ICR mice were infected intratracheally with D39 (NCTC) luxABCDE (designated IU1912) or D39 (Lilly) luxABCDE (designated IU1933), which were constructed by transformation with a PCR amplicon containing the Tn4001 luxABCDE cassette synthesized from strain Xen 35 (38, 88). Images of bioluminescent animals were obtained essentially as described previously (87, 88) at approximately 10-h intervals.

RESULTS AND DISCUSSION

Summary of DNA sequence results.

We determined and annotated the genome sequence of the two D39 isolates D39 (NCTC) and D39 (Lilly) (Fig. 1) as described in Materials and Methods. Differences between the sequences of D39 (NCTC) and D39 (Lilly) are described here. We compared the two D39 sequences with the published sequence of strain R6 (Table 1 and see Tables S1 and S2 in the supplemental material). At positions where there were differences among the three sequences, we repeated and confirmed the D39 sequence determinations, and we resequenced these regions in the R6 genome (see Materials and Methods). This analysis revealed 28 sequence errors in the previously published R6 sequence (48) (Tables 1 and S4 in the supplemental material). Fourteen of these errors were in a single IS1167 element and likely arose as an artifact of sequence assembly. We also identified 12 differences that may be errors in the previously published sequence of the capsule (cps) biosynthesis region of strain D39 (Tables 1 and S5). Six of these sequence differences were clustered in the cps2B gene.

By comparing these three closely related sequences, we deduced the likely sequence of the D39 progenitor strain and mutations that arose separately in the D39 (NCTC) and D39 (Lilly) isolates and during the multistep isolation of laboratory strain R6 (Fig. 1). This interpretation indicated that the widely used D39 (NCTC) strain is most closely related to the D39 progenitor strain, with only five mutational differences (Table 1). D39 (Lilly) is also closely related to the progenitor strain with only eight mutational differences, including one large deletion that arose spontaneously during propagation in this laboratory. Therefore, D39 (NCTC) and D39 (Lilly) differ from each other by 13 mutations. In contrast, laboratory strain R6 contains 81 mutational differences compared to the D39 progenitor strain (Table 1). This large number of mutational differences in laboratory strain R6 was unexpected and does not support the commonly held notion that strain R6 was derived from strain D39 through a limited number of mutational events (e.g., see reference 12). These mutations and their possible impacts on physiology and pathogenesis are considered below.

How the unexpectedly large number of mutations arose in strain R6 is unknown. The predecessors of R6 (Fig. 1) were propagated repeatedly in the presence of antibody against serotype 2 capsule to select for the stable loss of capsule biosynthesis (8, 76). It is unknown whether this kind of serial propagation under stress could have led to increased mutagenesis. Alternatively, it is possible that some type of agent-induced mutagenesis was performed during the derivation of R6 from progenitor strain D39. Mutagenesis was not reported in the derivation of strain R6 (Fig. 1) (see references 8, 76, and 89). On the other hand, mutagenesis would have been entirely appropriate given the goals of those earlier experiments, which were to provide a laboratory background for transformation and genetic studies (see the introduction) (8, 76, 89). R6 remains a suitable laboratory strain for basic experiments on fundamental genetic and physiological mechanisms in pneumococcus. However, because laboratory strain R6 contains so many mutations compared to the D39 strain, it cannot be assumed that physiological and metabolic properties studied in strain R6 will extrapolate to pathogenic strain D39. Future experiments aimed at comparing the physiological, metabolic, and pathogenic properties of mutants may best be performed directly in D39 (NCTC) or in an isogenic avirulent derivative of D39 (NCTC). To this end, we have constructed stable unencapsulated mutants of strain D39 (NCTC) [strain IU1824 = D39 (NCTC) Δcps2A′-cps2H′ rpsL41 and strain IU1945 = IU1824 rpsL⁺], which contain the same 7,505-bp deletion within the capsule (cps) biosynthetic region present in R6-related laboratory strains. IU1824 was constructed by using the Janus cassette method for allele replacement (107) and contains the rpsL41 allele, which imparts resistance to streptomycin but does not seem to impair virulence (data not shown; see Materials and Methods). Strain IU1945 is an rpsL⁺ transformant of strain IU1824.

There is another important difference between the D39 strains and laboratory strain R6. PCR analyses showed that both D39 (NCTC) and D39 (Lilly) carry the cryptic pDP1 plasmid (15, 86, 103, 105), whereas laboratory strain R6 does not (data not shown). Thus, the R6 strain has been cured of this plasmid. We sequenced the 3,161-bp pDP1 plasmids from both D39 stains and found the sequence to be identical to that reported previously (86). The cryptic pDP1 plasmid contains seven open reading frames but, aside from a replication protein, the other six putative open reading frames do not show significant homology to other genes, and their functions remain unknown (86). Although the function(s) and selection that maintain the cryptic pDP1 plasmid remain unknown, the replication apparatus of pDP1 has been used to construct shuttle vectors (94).

Besides the large 7,505-bp deletion of the cps2A-cps2H region, there is one other large mutational difference between the genome sequences of the D39 and R6 strains. The spd0080 gene in D39 (spr0075 in R6) encodes a surface protein containing tandem direct repeats of a 456-bp sequence (Fig. 3). The spd0080 (spr0075) gene is conserved in other pneumococcus serotypes, and four repeat units have been reported in this gene for serotype 4 strain TIGR4 (110). The repeated amino acids of this unusual protein constitute SSURE domains that bind to the extracellular matrix protein fibrinogen and may play a role in adhesion to eukaryotic host cells (21). PCR analysis using pairs of different primers flanking the repeat regions showed that both D39 strains contain six copies of the repeat (Fig. 3). In contrast, laboratory strain R6 contains eight copies of the repeat and thus has acquired two additional copies compared to the D39 strains. The eight copies in strain R6 reported here differ from the seven copies reported previously (48). Besides prominent single bands, these PCR analyses revealed a faint ladder of amplicons containing one to more than six repeats (Fig. 3). This ladder, which was used to assign the number of repeats in the prominent amplicons, is likely an amplification artifact that resulted from internal pairing of the repeats during the PCR. Consistent with this interpretation, faint amplicons containing more than six repeats were often observed for the D39 strains (Fig. 3). In addition, Southern blots of genomic DNA were consistent with the presence of six or eight copies of the repeats in D39 or R6, respectively, and did not show ladders of additional bands (data not shown). The exact sequence of the repeat region in spd0080 (spr0075) could not be determined by the primer walk approach or standard sequencing methods. As was done before (48), we inserted a placeholder sequence containing the five repeats used previously for R6 into this region of the D39 genome sequence. The rest of the genome sequence was determined completely for both D39 strains.

Major sequence differences between strains D39 and R6.

The genome sequence of strain R6 has many more mutations compared to the deduced progenitor D39 strain than either of the current D39 isolates (Tables 1 and 2 and see Tables S1 and S2 in the supplemental material). Nevertheless, the synteny between the R6 and D39 progenitor strain is nearly 100% (data not shown), and the vast majority of mutational differences are single-base-pair changes, only three of which result in stop codons (Table 2 and Tables S1 and S3 in the supplemental material). This finding is significant for several reasons. Pairwise comparisons between the R6 and TIGR4 genome sequences revealed ca. 10% differences, including six regions containing insertions or deletions and five regions of different content between conserved flanking sequences (20, 104, 109). It was not entirely clear whether laboratory strain R6 had lost some of these regions during its derivation and cultivation. In fact, aside from the cps deletion, the loss of large pathogenic islands has not occurred in R6 or the two current D39 isolates (Tables 1 and 2 and Tables S1 and S2 in the supplemental material). This observation supports the view that the serotype 2 and 4 strains of pneumococcus have fundamental differences in their genomes that did not arise as a result of cultivation.

TABLE 2.

Sequence changes that arose in strain R6 compared to progenitor strain D39^a

Change category (no. of changes)	Description
Single-base-pair
changesb (71)	Fifty-one missense (two following frameshift mutations); three nonsense; eight intercistronic (some correlated with changes in transcript levels); nine silent
Deletions (6)	ΔC (frameshift); ΔA (intercistronic); ΔA (frameshift); Δ8 bp of adjacent direct repeat (intercistronic); Δ41 bp (intercistronic); Δ7,505 bp that removes part of the capsule biosynthesis (cps) locus (50)
Insertions (4)	Insertion of two 456-bp direct repeat units (912 bp) in spr0075; inversion and insertion of 25-bp internal to cps2A at the junction of cps deletion; insertion of 30-bp adjacent direct repeat (in frame) in pcpA, encoding choline-binding protein; insertion of 2 bp (frameshift)

^aSpecific mutations are listed in Tables S1 and S3 in the supplemental material. R6 has also lost cryptic plasmid pDP1 (see the text).

^bThere were 45 transition mutations: 19 GC to AT (27%) and 26 AT to GC (37%). There were 26 transversion mutations: 7 GC to TA (10%); 10 AT to CG (14%); 7 GC to CG (10%); and 2 AT to TA (3%).

An interesting feature of pneumococcal genomes is the presence of numerous active and inactive IS elements and inverted sequences termed BOX or RUP elements (48, 79, 110). It has been speculated that these repeated sequences may promote genetic rearrangement and genomic plasticity. Comparison between the R6 and D39 progenitor sequence shows that rearrangements and transposition have not occurred in the approximately 70 years since strain R36 was first separated from the progenitor D39 strain (Fig. 1).

Several properties of the mutations that arose in laboratory strain R6 are noteworthy. The mutations result in changes in the amino acid sequences of numerous important proteins that mediate physiological processes, such as murein biosynthesis and transcription regulation, or virulence in the encapsulated D39 strains (Table 3). Very few of these mutated genes are linked directly to competence development (e.g., cinA), and there is no apparent correlation between mutations in competence genes and the increased transformability reported for R6 compared to the D39 progenitor strain (Fig. 1). The transcription patterns discussed below suggest a more complicated correlation at the level of gene expression.

TABLE 3.

Virulence and physiologically important genes with altered sequences in strain D39 compared to strain R6^a

D39 locus tag	Gene	Function	Source or referenceb
SPD_0063	strH	β-N-Acetylhexosaminidase	STM (43)
SPD_0065	bgaC	β-Galactosidase	52
SPD_0080		SSURE fibronectin binding	21
SPD_0081	rr08	Response regulator	63, 111
SPD_0168	ribE	Riboflavin synthesis	71
SPD_0315-SPD_0323	Δcps	Capsule biosynthesis	3, 69
SPD_0336	pbp1A	Penicillin-binding protein transglycosylase/transpeptidase	49, 64, 90
SPD_0479	nusA	Transcription termination/antitermination	18
SPD_0636	spxB	Pyruvate oxidase	STM/experimental (12, 65, 87, 91, 92, 106)
SPD_0660	ftsX	ABC transporter/cell division	102
SPD_0665	pyrDA	Dihydro-orotate dehydrogenase (pyrimidine biosynthesis)	5
SPD_0773	fruA	Fructose PTS	STM (43)
SPD_0854	flpA(pavA)	Fibronectin binding	STM/experimental (47, 64, 95)
SPD_0967	murA1	Homolog of MurA (first step in murein biosynthesis)	19, 70
SPD_1131	carB	Carbamoylphosphate synthase, heavy subunit (pyrimidine biosynthesis)	73
SPD_1337	atpA	Proton-translocating ATPase, F1 α subunit	32
SPD_1346		Hypothetical	STM (43)
SPD_1461	psaB	Manganese transport	Experimental (24, 27, 72, 75, 85)
SPD_1462	psaC	Manganese transport	Experimental (24, 27, 72, 75, 85)
SPD_1512	secA	Preprotein translocase subunit	93
SPD_1671	amiA	Oligopeptide transport	2, 57
SPD_1740	cinA	Competence induced	STM (43)
SPD_1758	rpoC	RNA polymerase β′ subunit	116
SPD_1797	ccpA	Catabolite control	STM/experimental (37, 53)
SPD_1961		Hypothetical (putative transcription regulator)	STM (43)
SPD_1965	pcpA	Choline-binding protein	STM/experimental (43, 101)
SPD_1974		Conserved hypothetical	STM (43)
SPD_1987		Hypothetical (fucolectin-related protein)	STM (43)
SPD_2005	dltA	d-Ala ligase	STM (43)
SPD_2012	glpO	α-Glycerophosphate oxidase	98
SPD_2022	clpC	Stress-related ATPase	Experimental (22, 23, 51, 96, 97)
SPD_2028	cbpD	Murein hydrolase	STM/experimental (, 40, 43, 46, 56)

^aSpecific mutations are listed in Tables S1 and S3 in the supplemental material.

^bEvidence for a role in virulence exists where indicated. STM, signature-tagged mutagenesis.

If mutagenesis was used to generate the R6 strain, interpretation of the distribution of single-base-pair mutations in R6 compared to the D39 progenitor strain becomes problematic (Tables 1 and 2 and Tables S1 and S3 in the supplemental material). Nonetheless, there are two interesting mutational differences. First, there are three separate instances of deletion or insertion of adjacent repeat sequences. These range from an 8-bp deletion in an intercistronic region between manL and adh to two larger insertions in potential virulence factor genes: a 30-bp in-frame insertion in pcpA and insertions of two tandem 456-bp in-frame SSURE domain repeat units in spr0075 (Fig. 3). Deletion and insertion of adjacent repeat sequences such as these likely arise by RecA-independent misalignment mechanisms (reviewed in reference 67). This kind of mutation has not been reported previously for S. pneumoniae and may contribute to the regulation and genetic diversity in this and other bacteria with relatively small genomes (67, 91). Second, of four cases of small deletion or insertion mutations, only one occurred in a homopolymeric run of bases (see Tables S1 and S2 in the supplemental material). Spontaneous deletion and insertion in runs of bases seem to play roles in phase variation phenomena of bacterial pathogens (reviewed in reference 11) and have been reported previously in other serotypes of S. pneumoniae (91). However, they were not prevalent during the derivation of strain R6 from the D39 progenitor strain.

Microarray analyses of transcript amounts in strain D39 (NCTC) compared to R6 were performed for bacteria growing statically in BHI broth in an atmosphere of 5% CO₂ (see Materials and Methods). The D39 and R6 sequences differ mainly by single base substitutions (Tables 1 and 2 and Table S1 in the supplemental material). Therefore, we expected that commercially available microarrays containing 50-mer oligomers based on the R6 sequence would work well for studies of D39 transcription patterns, including transcription of the capsule biosynthesis (cps) genes, which comprise an operon (50) and are partly included on the R6 microarrays. This prediction is confirmed by the comparison in Fig. 4. Most transcript levels were comparable in the two strains grown under these conditions (Fig. 4 and Table S6 in the supplemental material). However, there are some notable differences. As expected, deletion of part of the capsule (cps) region in R6 was reflected in the microarray comparison (Fig. 4). Unexpectedly, mutations in several intercistronic regions in R6 seemed to affect the transcript amounts of adjacent gene clusters, suggesting the cotranscription of genes from possible promoters or regulatory sites in these intercistronic regions (Fig. 4). In addition, the relative transcript amounts of eight competence regulon genes increased in R6 compared to D39 (Fig. 4; see also Table S6 in the supplemental material). However, none of these genes contained mutations in R6 compared to D39, and the mechanism of their induction remains unknown. The increased expression of this set of genes could, in part, contribute to the reported increase in transformability of R6 compared to the D39 progenitor (Fig. 1).

FIG. 4.

Microarray analysis of relative transcript amounts in strains D39 (NCTC) and R6 grown exponentially in BHI. Microarray analyses were performed as described in Materials and Methods. A representative log-scale scatter plot of relative transcript amounts is shown, and fold changes and Bayesian P values for transcripts changing at least 1.9 are listed in Table S6 in the supplemental material. Genes comprising the capsule locus are circled. Symbols indicate coregulated gene clusters as follows: stars, competence-induced genes (cibBC [allolysis], single-strand binding protein [ssb], and cglABCD comYD [peptioglycan-spanning structural proteins]); circles (spd0501 to spd0503; spr0504 to spr0506), genes coregulated with licT (spd0501; spr0504); diamonds (spd0559 to spd0562; spr0562 to spr0565), genes coregulated with ptsN (spd0559; spr0562); squares (spd1958 to spd1961; spr1937 to spr1940), genes coregulated with a BglG-family transcriptional regulator (spd1961; spr1940); triangles (spd1029 to spd1034; spr1052 to spr1057), genes coregulated with an HAD superfamily hydrolase (spd1034; spr1057). IC, mutation in upstream intercistronic region; Pt, point mutation within gene coding sequence. See the text for additional details.

Major sequence differences between two isolates of strain D39.

In contrast to strain R6, there are relatively few mutational changes between D39 (NCTC) and D39 (Lilly) and the deduced D39 progenitor strain (Tables 1 and 4). D39 (NCTC) and D39 (Lilly) contain only five and eight mutational differences, respectively, compared to the D39 progenitor and thirteen mutational differences between themselves. These mutations almost certainly arose spontaneously and reveal the pattern of mutations that arose during repeated culturing of these serotype 2 strains. D39 (NCTC) shows relatively minor changes compared to the D39 progenitor (Tables 1 and 4 and Table S2 in the supplemental material). The single-base-pair change in the IC (spd1248/spd1249 intercistronic region [corresponds to IC spr1274/spr1275 in R6] does not influence the transcript amounts of adjacent genes (see Table S7 in the supplemental material). The lone frameshift mutation is in a hypothetical gene (spd0800; corresponds to R6 spr0806) and results in a carboxyl-terminal truncation of only three amino acids (see Table S2 in the supplemental material). Of the three missense mutations, two are in hypothetical genes (spd1137 [corresponds to R6 spr1161] and spd1751 [corresponds to R6 spr1769]), and one is in a putative regulator of capsule biosynthesis (cpsY) (spd0818 [corresponds to R6 spr0828]) (61). spd1751 (corresponds to R6 spr1769) and cpsY (spd0818) were identified as putative virulence factors in previous STM screens (Table 5) (43). The microarray analyses described below did not detect a relative change in cps transcript amounts between D39 (NCTC) and D39 (Lilly), which contains the cpsY progenitor sequence. Moreover, D39 (NCTC) remains extremely virulent in murine models of infection using intranasal or intraperitoneal inoculation (see below and Materials and Methods), implying that the missense mutations that arose in spd1751 and cpsY in D39 (NCTC) do not strongly affect virulence. Thus, overall, the effects of the mutational changes in D39 (NCTC) seem minimal, and D39 (NCTC) is the serotype 2 isolate of choice for future physiological, genetic, and virulence studies.

TABLE 4.

Sequence changes that arose in strain D39 (NCTC) or D39 (Lilly) compared to progenitor strain D39^a

Strain	Changes
D39 (NCTC)	ΔG (frameshift); three missense mutationsb; one single base change in IC regionb
D39 (Lilly)	Five missense mutationsc; one silent changec; one ΔT (frameshift); one ΔtreP-amiC deletion (7,958 bp) between 14-bp direct repeats (AGTCGCTGTATAAG)

^aSpecific mutations are listed in Table S2 in the supplemental material.

^bThere were three transition mutations: one GC to AT (25%) and two AT to GC (50%). There was one transversion mutation: 1 GC to CG (25%).

^cThere were four transition mutations: two GC to AT (33%) and two AT to GC (33%). There were two transversion mutations: one AT to CG (17%) and one GC to CG (17%).

TABLE 5.

Virulence and physiologically important genes with altered sequences in strain D39 (NCTC) compared to strain D39 (Lilly)^a

D39 locus tag	Gene	Function	Source or referencee
SPD_0133b	cibB	Competence-induced bacteriocin (allolysis)	spr0128 (48; see reference 40)
SPD_0157b	hk07	Histidine kinase	63, 111
SPD_0383b	fabD	Malonyl coenzyme A-acyl carrier protein transacylase	115
SPD_0635b	ctpA	Cation transport	STM (43)
SPD_0636b	spxB	Pyruvate oxidase	STM/experimental (12, 65, 87, 91, 92, 106)
SPD_0800c		Hypothetical	spr0806 (48)
SPD_0818c	cpsY	Capsule regulation	43, 61
SPD_1137c		Hypothetical (ABC transporter)	spr1161 in (48)
SPD_1428b	cmk	Cytidylate kinase	118
SPD_1669b,d (ΔtreP-amiC)	ΔamiD	Oligopeptide transport	STM (43)
SPD_1670b,d (ΔtreP-amiC)	ΔamiC	Oligopeptide transport	STM (43)
SPD_1751c		Hypothetical (putative membrane protein)	STM (43)

^aSpecific mutations are listed in Table S2 in the supplemental material.

^bArose in strain D39 (Lilly) compared to D39 progenitor strain.

^cArose in strain D39 (NCTC) compared to D39 progenitor strain.

^dArose spontaneously during propagation of D39 (Lilly) in this laboratory.

^eEvidence for a role in virulence exists where indicated. STM, signature-tagged mutagenesis.

In contrast, the eight unique mutations in strain D39 (Lilly) compared to the D39 progenitor strain are not as benign as those in strain D39 (NCTC) (Tables 4 and 5 and Table S2 in the supplemental material). Several of these mutational differences are in genes important for virulence identified in previous STM screens in murine models of infection, including genes encoding a putative copper transporter CtpA (Spd0635), pyruvate oxidase SpxB (Spd0636), and oligopeptide transporters AmiC (Spd1670) and AmiD (Spd1669) (Table 5 and Table S2 in the supplemental material). Other sequence differences are in key regulatory and metabolic genes, such as the genes encoding competence-induced bacteriocin CibB involved in allolysis (Spd0133), histidine kinase HK07 (Spd0157), malonyl acyl carrier protein transacylase FabD (Spd0383), and cytidylate kinase Cmk (Spd1428) (Table 5).

Because of these mutational differences, we tested whether D39 (Lilly) was attenuated for virulence compared to D39 (NCTC). Both strains are virulent in an ICR mouse model of infection (see Materials and Methods) (Fig. 5). Intraperitoneal infection of either strain resulted in severe moribundity of mice within 1 day (data not shown). Survival curves after intranasal inoculation with either strain were statistically indistinguishable over 6 days (data not shown). However, survival curves after intratracheal inoculation suggested that D39 (Lilly) is partially attenuated for virulence compared to D39 (NCTC) (data not shown). Monitoring of infection by biophotonic imaging (see Materials and Methods) confirmed this conclusion (Fig. 5). In a typical experiment, comparable infections were confined to the lungs for both strains about 19 h after inoculation (Fig. 5A). By 85 h after inoculation, the D39 (NCTC) strain had spread from the lungs into the bloodstream in most mice and was causing fatal, systemic infection (Fig. 5B, left) (see references 87 and 88). In contrast, the D39 (Lilly) strain often remained confined to the lungs and, in some cases, appeared to be cleared from the lungs (Fig. 5B, right).

FIG. 5.

Biophotonic imaging of ICR male mice (ca. 25 to 30 g) infected with D39 (NCTC) luxABCDE or D39 (Lilly) luxABCDE. Each mouse was infected intratracheally (IT) with 50 μl of buffered saline containing ∼2.5 × 10⁶ CFU of each strain (see Materials and Methods) (96). Bioluminescence was monitored and recorded at various times in separate animals (87, 88). Typical images from 1-min exposures are shown 19 h (A) and 85 h (B) after infection. The mouse in the lower right corner has cleared the D39 (Lilly) infection.

The compilation of the kinds of mutations that arose spontaneously in the two D39 isolates is informative (Table 4). Most of the single base changes are transition mutations, which are nearly evenly distributed between GC→AT and AT→GC changes (Table 4). Both D39 (NCTC) and D39 (Lilly) produce significant amounts of hydrogen peroxide, as reported previously for other pneumococcal strains (12, 92), although D39 (Lilly) produces ∼3-fold less than D39 (NCTC) (S. Ramos-Montanez, unpublished results). Despite this production of hydrogen peroxide, GC→AT mutations, which are indicative of oxidative damage, do not predominate as might have been anticipated from an earlier study of spontaneous mutations that arise in different pneumococcal strains (91). The only large spontaneous deletion found in strain D39 (Lilly) arose between two nontandem 14-bp direct repeats in the treP-amiC region of the chromosome (Table 4 and Table S2 in the supplemental material). PCR analyses of different stocks and derivatives of D39 (Lilly) showed that this deletion arose spontaneously in this laboratory during routine propagation (single colony isolation on TSAII BA, followed by liquid culture in BHI) without obvious selection to replenish frozen stock vials. Deletions between such short nontandem direct repeats have been reported before in pneumococcus (91) and likely arise by a RecA-independent mechanism involving DNA misalignment during replication (67). Finally, the single spontaneous frameshift mutation in D39 (Lilly) again did not occur in a homopolymeric run of bases (Table 4 and Table S2 in the supplemental material) and causes a severe truncation of CtpA, which has been implicated in copper uptake and virulence (34, 43).

The 13 mutational differences between D39 (NCTC) and D39 (Lilly) caused marked changes in relative transcript amounts when the strains were grown exponentially in BHI (Fig. 6 and Table S7 in the supplemental material). In fact, there are about as many transcripts with changed relative amounts in D39 (NCTC) compared to D39 (Lilly) as there are in D39 (NCTC) compared to R6 (compare Fig. 4 and 6). Three regulatory patterns can be discerned in the comparison between transcript amounts in D39 (NCTC) and D39 (Lilly). The deletion in D39 (Lilly) of the amiCDEF operon (Fig. 6), which encodes an oligopeptide transporter (Table 5), may be linked to the increase in expression of the ilvBNC operon in D39 (Lilly) compared to D39 (NCTC) (Fig. 6 and Table S7 in the supplemental material). The ilvBNC operon, which mediates the biosynthesis of isoleucine and valine from pyruvate (83), is likely a member of the CodY regulon in S. pneumoniae (39) and may also be regulated by attenuation (77; http://cmgm.stanford.edu/∼merino/streptococcus_pneumoniae_R6/indice_alpha.html). In D39 (NCTC) growing in BHI, the intact AmiABCDEF transporter likely increases the intracellular concentration of isoleucine compared to D39 (Lilly). Branched-chain amino acids are the corepressors of CodY that presumably lead to repression of ilvBNC transcription in D39 (NCTC) relative to D39 (Lilly).

FIG. 6.

Microarray analysis of relative transcript amounts in strains D39 (NCTC) and D39 Lilly) grown exponentially in BHI. Microarray analyses were performed as described in Materials and Methods. A representative log-scale scatter plot of relative transcript amounts is shown, and the fold changes and Bayesian P values for transcripts changing at least 1.8-fold are listed in Table S7 in the supplemental material. Symbols are as follows: squares (spd1664 to spd1670), genes partially or completely deleted in D39 (Lilly); circles (spd0404 to spd0408), ilvBNC gene cluster likely regulated to compensate for deletion of amiCDEF; stars, ciaRH two-component signal transduction system; triangles, genes regulated in a “cia-on” mutant (74).

A second transcription pattern is the increased expression of the CiaRH two-component regulatory system in D39 (NCTC) compared to D39 (Lilly) (Fig. 6). We do not know the basis for this increase in CiaRH transcript amounts and whether it is somehow linked to deletion of amiCDEF in D39 (Lilly). Nevertheless, the increased transcription of ciaRH likely leads to a “Cia-on” state (74), the hallmarks of which include relative increases or decreases in the transcript amounts of malPM, axe1, spd0913 (corresponds to R6 spr0931), and htrA or comCD, respectively, in D39 (NCTC) compared to D39 (Lilly) (Fig. 6). Finally, we observed increased relative transcript amounts of the malXCD operon in D39 (NCTC) compared to D39 (Lilly) (Fig. 6). We do not know the basis of this increase, but it could be related to the increased expression of malPM in the “Cia-on” state in D39 (NCTC).

Further insights into pneumococcal physiology, metabolism, and virulence.

As noted above, the overall genome structure appears to have been remarkably stable for virulent serotype 2 D39 strains, which have been maintained in captivity for nearly a century. Although D39 and R6 have the capacity for genetic plasticity (48, 110), major deletions and rearrangements have not occurred in these strains during cultivation, and the D39 strains have maintained their extreme virulence in murine models of infection (Fig. 5) (see Materials and Methods) (96). The D39 genome sequences reported here confirm several previous conclusions that were tentatively based on the genome sequence of laboratory strain R6 (48, 110). Notably, major differences in the genetic complements of D39 and TIGR4 were confirmed, such as the presence of a single sortase gene in D39 compared to four sortase genes in TIGR4 (48, 109, 110). Indeed, D39 and TIGR4 contain significant genetic differences that contribute to the different diseases that they cause in infection models (see the introduction). An unusual process confirmed by the D39 sequences is the devolution of amino acid biosynthetic and transposase genes in serotype 2 pneumococcus. The D39 and R6 sequences contain four truncated amino acid biosynthetic genes, serB, metY, leuD, and leuA, which mediate serine, methionine, and leucine biosynthesis. Other members of these key pathways, such as serA, are already missing from the genome, and it appears that the remaining genes in these pathways exist as inactive remnants. Likewise, there are many (>30) inactive transposase gene remnants in the D39 chromosome. In summary, the genome sequence of strain D39 should significantly increase our understanding of pneumococcal physiology, pathogenesis, and evolution; help in the interpretations of previously performed experiments; and allow the design of future studies, including swapping pathogenic islands between different pneumococcal serotype strains.

ADDENDUM IN PROOF

The difference in the sequence of the dltA gene in strains D39 and R6 (Table 3) was recently independently confirmed by M. Kovacs, A. Halfmann, J. Fedtke, M. Heintz, A. Peschel, W. Vollmer, R. Hakenbeck, and R. Bruckner (J. Bacteriol. 188:5797-5805, 2006). They show that the mutation in strain R6 inactivates dltA (d-alanine ligase), resulting in sensitivity to cationic antimicrobial peptides. The 12 differences in the sequence of the cps (capsule biosynthesis) region reported in Tables 1 and S5 have been confirmed as sequencing errors in a previous paper (50; F. Iannelli, personal communication). Corresponding corrections have been made by F. Iannelli to GenBank file AF026471.