- Research article
- Open Access
Intragenic tandem repeat variation between Legionella pneumophila strains
© Coil et al; licensee BioMed Central Ltd. 2008
Received: 22 April 2008
Accepted: 10 December 2008
Published: 10 December 2008
Bacterial genomes harbour a large number of tandem repeats, yet the possible phenotypic effects of those found within the coding region of genes are only beginning to be examined. Evidence exists from other organisms that these repeats can be involved in the evolution of new genes, gene regulation, adaptation, resistance to environmental stresses, and avoidance of the immune system.
In this study, we have investigated the presence and variability in copy number of intragenic tandemly repeated sequences in the genome of Legionella pneumophila, the etiological agent of a severe pneumonia known as Legionnaires' disease. Within the genome of the Philadelphia strain, we have identified 26 intragenic tandem repeat sequences using conservative selection criteria. Of these, seven were "polymorphic" in terms of repeat copy number between a large number of L. pneumophila serogroup 1 strains. These strains were collected from a wide variety of environments and patients in several geographical regions. Within this panel of strains, all but one of these seven genes exhibited statistically different patterns in repeat copy number between samples from different origins (environmental, clinical, and hot springs).
These results support the hypothesis that intragenic tandem repeats could play a role in virulence and adaptation to different environments. While tandem repeats are an increasingly popular focus of molecular typing studies in prokaryotes, including in L. pneumophila, this study is the first examining the difference in tandem repeat distribution as a function of clinical or environmental origin.
Variable number tandem repeats (VNTRs) are increasingly widely used as molecular markers in prokaryotes. More recently, attention has turned towards examining the possible functional significance of these tandem repeats, especially that of microsatellites, which are often found outside coding regions, [1–7]. Moreover, the biological significance of intragenic tandem repeats, located within coding regions, has been demonstrated for particular genes [8–11]. With the explosion of available bacterial genomic sequences it has become clear that most, if not all, bacterial genomes contain a considerable number of intragenic tandem repeats [12, 13]. The finding that intragenic tandem repeats are so widespread in prokaryotes suggests that the few cases documented so far may be only the tip of the iceberg and that some of the many uncharacterized tandem repeats in bacteria possibly play functional roles in pathogenesis and/or in adaptation to environmental stresses.
Here we have investigated the presence and distribution of tandemly repeated sequences in the genome of the opportunistic pathogen, Legionella pneumophila, the etiological agent of Legionnaires' disease. This microorganism flourishes naturally in fresh water environments, but is also frequently found in artificial water systems, which are considered the main source of Legionella infections in humans . The L. pneumophila species comprises over 15 serogroups, of which serogroup 1 is responsible for the majority of human infections. While these Gram-negative bacteria can multiply free-living in culture, it is now widely accepted that intracellular replication in amoebic hosts such as Acanthamoeba, Naegleria, or Hartmanella is essential for the propagation and dissemination of L. pneumophila . Industrial settings, altered lifestyle, and a growing number of elderly and immunocompromised individuals have led to an increase in number of reported L. pneumophila infections, which occur following inhalation of contaminated aerosols. When L. pneumophila reach the lungs, they are ingested by alveolar macrophages wherein they replicate and which they finally destroy. Ultimately host cell lysis and cell death, as well as the extracellular or surface-associated action of bacterial degradative enzymes, result in damage of lung tissue. L. pneumophila infections end in an acute and severe, often fatal, pneumonia, if not quickly and correctly diagnosed.
Two recent studies have examined tandem repeats in L. pneumophila as a way to discriminate between closely related strains. However, these studies have not differentiated between intergenic and intragenic repeats [16, 17]. In addition, researchers studying individual virulence factors in L. pneumophila have noted the presence of repeats in these genes, and have suggested possible functional roles for the repeats [18, 19]. In this study, we have identified and characterized the tandem repeat variations between 115 strains of L. pneumophila serogroup 1, collected from a wide variety of environments and patients.
Origin of bacterial strains and growth conditions
Lab strains 130 b (Klaus Heuner, University of Wurzburg, Germany), Corby (K. Heuner), Lens (Carmen Buchreiser, Institut Pasteur, and CNRS URA, France), and Paris (C. Buchreiser), were obtained from the indicated labs and the Philadelphia strain was obtained from the American Tissue Culture Collection (ATCC). Strains S03, S1, S18, S3, S32, S66, S71, and S88 were isolated via filtration and selective plating from natural water sources collected at different sites throughout Belgium (kind gift of Dr. Priscilla Declerck, Katholieke Universiteit Leuven, Belgium)(unpublished). Strains IMC 1, 5, 16, and 23 were isolated from water taps, air conditioning units, and incubators in a pediatric hospital in Portugal (kind gift of Dr. Milton S. da Costa, University of Coimbra, Portugal) . The 12 "LEA/LE" strains were isolated and serotyped in our laboratory from heat or acid treated swimming water samples (natural and manmade) collected throughout Belgium (kind gift of Dr. Rudy Calders, Provincial Institute for Hygiene, Antwerp, Belgium). The 18 "L" strains were isolated from various manmade environmental water sources (cooling towers, air conditioning units, pipes, irrigation hydrants, showers, water tanks, and fountains) in Spain (kind gift of Dr. Fernando Gonzalez Candelas, University of Valencia, Spain) [21, 22]. Strains MGAS-357, MGAS-637, and MGAS-670 were isolated from sputum samples of sporadic clinical infection cases in Belgium (kind gift of Dr. Jan Verhaegen, University Hospital Gasthuisberg, Belgium)(unpublished). Strain HRD-4 was isolated from a sputum samples in Portugal (Dr. Milton S. da Costa)(unpublished). Strains give the "BEL" designation were isolated from sputum samples of clinical infections during three different outbreaks of Legionella in Belgium (kind gift of Dr. Marc Struelens, Free University of Brussels, Belgium)(unpublished). Strains ITA-5 and ITA-12 represent two unrelated community-acquired Legionella infections from Italy (kind gift of Dr. Isabella Marchesi, University of Modena and Reggio Emilia, Modena, Italy)( and unpublished). The 33 "HL" and 6 "LG" strains were isolated from sporadic, epidemic, and endemic patient infections throughout France (National Reference Center on Legionellae, Lyon, France) ([24, 25] and unpublished). The 17 "hot springs" strains (ALF, ED, IZ, NMEX, SG) were isolated from boreholes and hot spring runoffs in Portugal and the U.S.A. with a median temperature of 42°C (Dr. Milton S. da Costa)[26, 27].
Unless otherwise described, all established L. pneumophila strains were grown at 37°C and 5% CO2 in buffered yeast extract broth containing α-ketoglutarate (BYE-α) or on buffered charcoal yeast extract broth plates containing α-ketoglutarate (BCYE-α) and supplemented with L-cysteine and ferric pyrophosphate . All strains were stored as glycerol stocks at -80°C and thawed fresh for genomic DNA isolations. For "stress" experiments, cultures of the Philadelphia strain were grown on BCYE-α plates (replated every 3–4 days) at 27°C, 37°C (without CO2), 37°C (with CO2) and 42°C (without CO2) for three months. This work was carried out with permission of the K.U. Leuven Biosafety Council and according to the EU directive 93/88 and 90/219/EC.
Genomic DNA isolation
Strains were grown overnight in a 5 ml culture of BYE-α. Genomic DNA was isolated from 1 ml of this culture using a Wizard® Genomic DNA Purification Kit (Promega) according to the manufacturer's recommendations. The integrity of the DNA was assessed by agarose gel electrophoresis.
PCR and sequencing
PCR primers were designed using the Primer3 software  and chosen based on regions of high similarity (if possible) between the published Philadelphia, Lens, and Paris strain sequences (see Additional File 1). PCR was performed using SuperTaq DNA polymerase (HT Biotechnology) in 50 μl reaction volumes. Initial denaturation at 94°C for 2 min was followed by 30 cycles of denaturation at 94°C for 30 s, annealing at 45°C for 45 s, and elongation at 72°C for 2 min. The final extension step was 2 min at 72°C. Products were visualized on 1% agarose gels for initial characterization. For sequencing the repeat regions directly, a larger portion of the gene was amplified from each strain and the repeat region was sequenced by VIB Genetic Service Facility, Antwerp, Belgium. Repeats were counted from these sequences using "Tandem Repeats Finder". Sequence-based typing of all strains except for L430–L2006 was performed using the seven gene method as previously described [31, 32]. Strains L430–L2006 were already typed using the older six gene method [21, 22].
In silico screening of the Legionella pneumophila genome for intragenic tandemly repeated sequences
Genes containing intragenic tandem repeat arrays in the Philadelphia strain
Length of repeat (bp)
Hsp60, 60 K H eat s hock p rotein
Cop per efflux A TPase copA2
TPR repeat protein
TPR repeat protein
TPR repeat protein
Transmembrane Tfp pilus assembly protein FimV
TPR repeat protein
TPR repeat protein
30S Ribosomal protein S1
Arginine 3rd transport system periplasmic binding protein ArtJ
UV B-r esistance protein UVR8
TPR repeat protein, protein-protein interaction
UVB-resistance protein UVR8
Leucine rich repeat protein family
Ankyrin repeat family protein
TPR domain protein
ATP-dependant DNA helicase RecG
Enh anced entry protein EnhC
Tail fiber protein SclB (collagen-like)
Functional categorization of genes containing tandem repeats
Subcellular localization of proteins containing tandem repeats
L. pneumophila Philadelphia proteome (n = 2941)
Proteins containing repeats (n = 23)
31.1% (n = 915)
21.7% (n = 5)
18.2% (n = 534)
0% (n = 0)
0.8% (n = 22)
21.7% (n = 5)
1.8% (n = 53)
4.3% (n = 1)
1.2% (n = 36)
8.7% (n = 2)
46.9% (n = 1381)
43.4% (n = 10)
PCR characterization of repeat variability between strains
In order to determine if a particular repeat was "polymorphic" or "monomorphic", we screened a panel of 47 different L. pneumophilia serogroup 1 strains by PCR using primers designed to flank the 26 repeat regions described above. These strains included common lab strains, clinical isolates and environmental isolates (see Methods). Of the 26 repeats, 7 were found to be polymorphic (LPG1038, LPG1299, LPG1555, LPG2224, LPG2416, LPG2644, LPG2793). At the sequence level, the internal conservation of these polymorphic repeats was, on average, higher than that of the monomorphic repeats (unpaired t-test, p-value .0021), as observed previously . Genes LPG1299, LPG2644, and LPG2793 correspond to the previously characterized VNTR markers Lpms35, Lpms31, and Lpms3 respectively . Of the genes that were polymorphic, LPG1038, LPG1555, LPG2224, LPG2416, and LPG2793 each possessed only 2 or 3 alleles whereas LPG1299 possessed 22 alleles. The repeat region for gene LPG2644 possesses 12 alleles and more data about LPG2644 and its encoded protein will be described in detail elsewhere (Vandersmissen, L., Coil, D.A., De Buck, E., Lammertyn, E., Anné, J. submitted for publication).
Patterns of repeat variation
These 7 repeats were further examined in an additional 106 strains, for a total of 153 strains, divided into four strain groups: lab strains (n = 5), environmental strains (n = 59), clinical strains (n = 65), and hot springs strains (n = 24). However, lab strains were not considered for any subsequent statistical analyses. We next performed sequence-based typing on all 153 strains in order to examine the relatedness of the strains. Strains were excluded if they were collected from the same site and possessed both the same SBT type and the same pattern of tandem repeat variation. This resulted in the removal of 38 strains from our analysis, leaving 42 environmental strains, 51 clinical strains, and 17 hot springs strains for a total of 115 strains (see Additional File 2).
Comparison of average tandem repeat copy number between strain types
Average number of repeats
Hot springs (H)
Student t-test p-values
E versus C
E versus H
C versus H
Stability of repeat number
Most tandemly repeated sequences are known to be able to mutate at a faster rate than non-tandemly repeated sequences (for a recent review, see ). Therefore, we were interested in examining the stability of these repeats over time, to ensure that our data do not simply represent a "snapshot" in time of repeat copy number in these strains. We began by serially passaging identical cultures of the Philadelphia strain at various temperatures for three months (see Methods). At the end of this period, we measured the repeat copy number in each of the 26 candidate repeat arrays and found that none of them had varied over this time span (data not shown). Because two of the 23 candidate genes are involved in UVB resistance (Table 1) we also examined the stability of these two repeats under repeated exposure to UV light. Plates of Philadelphia strain were exposed to varying lengths (30, 60, 120, 240 seconds) of UVB radiation just after streaking at each passage (~ every 3 days). While there was a noticeable effect on survival of the bacteria, after 10 generations no changes in repeat number were observed for either LPG1976 or LPG2224 (data not shown).
While bacteria in general appear to have a large number of tandem repeats, the possible phenotypic effects of intragenic repeats are only beginning to be examined. Evidence exists from other organisms that variable number tandem repeats are involved in the evolution of new genes, gene regulation, adaptation, resistance to environmental stresses, and avoidance of the immune system. In this work, we have investigated the presence and variability in copy number of tandemly repeated sequences in the genome of L. pneumophila, an important human pathogen and model for the study of host-pathogen interactions. We have identified 23 genes containing tandem repeats and determined that seven of them exhibited variability in repeat copy number between strains.
More importantly, we have demonstrated that the distribution of repeat variation is significantly non-random in L. pneumophila and therefore may have functional implications. Our results suggest that the number of intragenic tandem repeats found within most genes varies as a function of strain origin. Six of the seven genes examined display distinctive differences between the three groups of strains examined (environmental, clinical, and hot springs). In particular, four genes exhibit significant differences in repeat copy number between environmental and clinical samples. Moreover, for three of the four genes, the distribution of repeat copy number is also significant between clinical samples and hot springs samples, further highlighting the potential significance of the higher repeat copy number found in clinical samples for these genes.
One possible complication with an experiment of this nature is the rate of change of repeat copy number. While a variety of studies have been undertaken examining the mechanism and stability of tandem repeats, none of them addressed intragenic tandem repeats in particular and most have focused on smaller microsatellites (1–6 bp) . In our hands, none of these larger repeats changed in copy number through multiple generations under a variety of conditions. While these conditions do not accurately substitute for a competitive natural environment, these experiments do suggest that intragenic repeat number is reasonably stable over time.
The four genes which exhibit significant differences in repeat copy number between environmental and clinical samples are of particular interest from a clinical perspective since tandem repeats in these genes could play roles in the pathogenesis of L. pneumophila. LPG1038 is annotated as "vrrb" in the published sequence, however we have been unable to verify any nucleotide or protein homology with the "variable region with repetitive sequence B" (vrrb) gene from Bacillus anthracis . Furthermore, BLAST searches with this sequence do not produce any significant hits other than those from the published L. pneumophila sequences. It is therefore possible that this gene may represent a novel virulence factor in which tandem repeats could play a functional role. LPG1299 is homologous to the fimV gene described in Pseudomonas aeruginosa . This gene is thought to be involved in twitching motility, possibly through the remodeling of the peptidoglycan layer to enable assembly of type IV pili. Twitching motility is known to be important in the virulence of P. aeruginosa, however it has not yet been described in L. pneumophila. LPG2416 is a gene of unknown function but contains an ankyrin repeat sequence, thought to mediate protein-protein interactions , and which have been recently demonstrated to play a role in the manipulation of L. pneumophila host physiology and infection [37, 43, 44]. Lastly, LPG2793 encodes an effecter of the Icm/Dot type IV secretion system and is known to play a role in the release of L. pneumophila from a protozoan host [45, 46].
Overall, our results provide a detailed examination of variable intragenic tandem repeat distribution as a function of strain origin. These data suggest a potential functional role of tandem repeats in adaptation to different environments. Current work is focused on understanding the exact role that intragenic tandem repeats play in particular genes.
We would like to thank Dr. Isabelle Henry for help with data analysis and for critical review of the manuscript. DAC is supported by a BOF fellowship (KU Leuven Onderzoeksfonds PDM/F/07/038). This work was further financed by grants OT/05/62 from KU Leuven Onderzoeksfonds and G.0289.06 from Research Foundation – Flanders (FWO).
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