Genomic island excisions in Bordetella petrii
© Lechner et al; licensee BioMed Central Ltd. 2009
Received: 28 November 2008
Accepted: 18 July 2009
Published: 18 July 2009
Among the members of the genus Bordetella B. petrii is unique, since it is the only species isolated from the environment, while the pathogenic Bordetellae are obligately associated with host organisms. Another feature distinguishing B. petrii from the other sequenced Bordetellae is the presence of a large number of mobile genetic elements including several large genomic regions with typical characteristics of genomic islands collectively known as integrative and conjugative elements (ICEs). These elements mainly encode accessory metabolic factors enabling this bacterium to grow on a large repertoire of aromatic compounds.
During in vitro culture of Bordetella petrii colony variants appear frequently. We show that this variability can be attributed to the presence of a large number of metastable mobile genetic elements on its chromosome. In fact, the genome sequence of B. petrii revealed the presence of at least seven large genomic islands mostly encoding accessory metabolic functions involved in the degradation of aromatic compounds and detoxification of heavy metals. Four of these islands (termed GI1 to GI3 and GI6) are highly related to ICEclc of Pseudomonas knackmussii sp. strain B13. Here we present first data about the molecular characterization of these islands. We defined the exact borders of each island and we show that during standard culture of the bacteria these islands get excised from the chromosome. For all but one of these islands (GI5) we could detect circular intermediates. For the clc-like elements GI1 to GI3 of B. petrii we provide evidence that tandem insertion of these islands which all encode highly related integrases and attachment sites may also lead to incorporation of genomic DNA which originally was not part of the island and to the formation of huge composite islands. By integration of a tetracycline resistance cassette into GI3 we found this island to be rather unstable and to be lost from the bacterial population within about 100 consecutive generations. Furthermore, we show that GI3 is self transmissible and by conjugation can be transferred to B. bronchiseptica thus proving it to be an active integrative and conjugative element
The results show that phenotypic variation of B. petrii is correlated with the presence of genomic islands. Tandem integration of related islands may contribute to island evolution by the acquisition of genes originally belonging to the bacterial core genome. In conclusion, B. petrii appears to be the first member of the genus in which horizontal gene transfer events have massively shaped its genome structure.
The enormous impact of horizontal gene transfer (HGT) on the evolution of bacterial species has only been recognized during the past years . Among the mobile genetic elements involved in HGT genomic islands are of particular relevance since they can comprise large genomic regions encoding accessory factors required by the bacteria to thrive in specific environments. For example, many virulence related factors of pathogenic bacteria are encoded on so-called pathogenicity islands, while metabolic islands frequently encode factors required for detoxification of poisonous compounds or for the utilization of specific carbon sources such as aromatic compounds [2, 3].
The genus Bordetella harbours several important pathogens infecting humans and various animals. While B. pertussis and B. parapertussis are etiological agents of whooping cough in man, B. bronchiseptica and B. avium can cause respiratory infections in various mammalian species and birds, respectively . B. petrii was the first Bordetella species isolated from the environment, while all other Bordetella species so far could only be found in obligate association with host organisms . Phylogenetically, B. petrii appears to be closely related to a common ancestor of the pathogenic Bordetellae and links the genus with other environmental bacteria of the genera Achromobacter and Alcaligenes [5, 6]. B. petrii was repeatedly isolated from contaminated soil [7, 8]. However, recently, several isolates from clinical specimens associated with bone degenerative disease or cystic fibrosis were found to be closely related to B. petrii, although the underlying etiology is not clear in any of the cases [9–11]. The pathogenic Bordetellae encode a multitude of virulence factors including several toxins and adhesins . The evolutionary origin of these factors is unclear, since in contrast to many virulence genes of other pathogens they are not located on mobile genetic elements such as pathogenicity islands or prophages. In fact, so far only few presumptive horizontal gene transfer events are known among the pathogenic members of the genus, e.g. a 66 kb island encoding iron transport genes that presumably has been exchanged between B. pertussis and B. holmesii, a pathogenic species mainly found in immunocompromised individuals . A prevalent feature in the evolution of virulence in this genus is reductive genome evolution, since strains specialized on particular host organisms such as the exclusive human pathogen B. pertussis have presumably evolved from a B. bronchiseptica-like ancestor. Specialization to a single host was accompanied by a massive genome size reduction. In agreement with this assumption, B. pertussis harbors numerous pseudogenes and virtually all B. pertussis genes have counterparts in B. bronchiseptica .
The remaining genomic islands, GI4, GI5, and GI7, encode type IV secretion systems probably involved in conjugal transfer . GI4 has very pronounced similarities with Tn4371 of Ralstonia oxalatica and other bacteria including Achromobacter georgiopolitanum and encodes metabolic functions involved in the degradation of aromatic compounds . GI5 and GI7 encode a phage P4 related integrase and genes involved in metabolism of aromatic compounds or in detoxification of heavy metals. Finally, there is a region on the B. petrii genome (termed GI in ) which is characterized by a low GC content, but does not have other characteristic features of a genomic island thus possibly being a remnant of a former mobile element. GI encodes metabolic functions for the degradation of phthalate and protocatechuate .
In the present study we characterize these putative genomic islands and show that most of them are in fact active, at least in terms of excision from the chromosome. We show that these elements are responsible for the genomic instability of B. petrii observed during long term growth in vitro.
Results and discussion
Long term survival of B. petrii in river water and appearance of phenotypic variants
B. petrii was the first Bordetella species isolated from the environment, i.e. from a river sediment. The analysis of its survival capacity in river water revealed a high survival rate and nearly no decay in viability during a period of 38 weeks, while under the same experimental conditions viability of a B. bronchiseptica strain declined rapidly and no viable bacteria could be detected in the water samples after about three weeks (data not shown). The short survival time of B. bronchiseptica is somewhat surprising, since in a previous study it was shown to persist for more than 20 weeks in lake water . A possible explanation for this may be that different B. bronchiseptica strains were used in these studies. However, the direct comparison of B. bronchiseptica and B. petrii demonstrates that B. petrii has a much more pronounced capacity to survive in river water for a prolonged time period which is in agreement with its original isolation from river sediment. Interestingly, after about 20 days of the survival experiment stable phenotypic variants of B. petrii with differing colony morphology regarding colour and colony size appeared when the bacteria were plated on LB agar plates (data not shown). In this study, three of these variants (named f, g, k) were further characterized. All of these variants showed virtually identical growth characteristics at 37°C in liquid LB medium, while two of them (f, k) showed a markedly impaired growth capacity at 15°C as compared to the wild type strain and to variant g (data not shown).
Genome rearrangements involving the genomic islands of B. petrii
Characterization of spontaneous B. petrii variants using a DNA microarray
Predicted genomic islands (GI)
Genes present or absent in the variants g, f, and k
Presence of GI in the variants
GI (Bpet0187 – Bpet0310)
Bpet0187 – Bpet0310
GI1 (Bpet1009 – Bpet1275)
Δ Bpet1009 – Bpet1287
GI2 (Bpet1288 – Bpet1437)
Bpet1288 – Bpet1437
GI3 (Bpet1438 – Bpet1545)
Δ Bpet1438 – Bpet1545
GI4 (Bpet2166 – Bpet2216)
Bpet2166 – Bpet2216
GI5 (Bpet3699 – Bpet3770)
Δ Bpet3699 – Bpet3779
GI6 (Bpet4174 – Bpet4316)
Δ Bpet4174 – Bpet4315
GI7 (Bpet4544 – Bpet4630)
Bpet4544 – Bpet4630
The comparison of the deleted genes of the variants with those which according to the annotation are encoded on the GIs revealed a perfect congruence of the predicted island borders and the microarray data in the case of GI3, while the extent of the deletions and therefore the sizes of these elements differed from the bioinformatic prediction in the case of GI1, GI5 and GI6 . According to these data, GI1 appears to comprise additional 12 genes (Bpet1267–1287), GI5 additional 9 genes (Bpet3771–3779), and GI6 appears to lack one gene (Bpet4316) (Table 1). These data were further corroborated by a series of Southern blot experiments with probes specific for the respective genes, the results of which matched perfectly with the microarray data (data not shown).
Definition of the borders of the genomic islands of B. petrii
PCR detection of excised circular intermediates of the genomic islands GI1 to GI7
Primer combinations used
Size of the expected PCR product [bp]
PCR product obtained
For GI2 we obtained a PCR product demonstrating the involvement of the direct repeats directly flanking the island at sequence positions 1,350,146 and 1,493,541. Since GI2 is not directly associated with a tRNA gene it appears likely that it has integrated in the left repeat of GI3 at sequence position 1,493,541, which was generated by the previous insertion of GI3 in the respective tRNA gene (tRNA-11). For GI3 we obtained the expected data which also correspond to the microarray results described above. Moreover, we obtained evidence that the clc-like elements GI1–GI3 can excise together in different combinations: GI2–GI3 and GI1–GI2–GI3. Therefore, these islands appear to be able to excise independently from each other, but also in various combinations thereby potentially forming composed transmissible elements. In the case of the fourth clc-like element, GI6, the microarray data revealed the presence of the Bpet4316 gene in the chromosome even after excision of the element. This is surprising, since the direct repeat sequence which should be the target for the GI6 integrase lies beyond this gene. Thus, the Bpet4316 gene should be located within the excised region. Curiously, the PCR experiments aiming in the detection of circular intermediates showed that the Bpet4316 gene is also part of the circular excised form of this element. This suggests a duplication of the Bpet4316 gene during excision by an unknown mechanism.
In the case of GI4 and GI7 we obtained PCR products providing evidence for excised circular intermediates which perfectly match the previous bioinformatical predictions based on the detailed sequence analysis about the size of these islands. In contrast, in case of GI5 we were not able to detect a circular intermediate neither with the originally predicted borders nor with the additional genes suggested by the microarray experiments (Bpet3771–3779), although the microarray data of the phenotypic variants f, g, and k definitely revealed the deletion of this element from their genomes.
As shown above, we were able to detect circular intermediates of most genomic islands by PCR amplification, although the microarray experiments with the phenotypic variants clearly demonstrated the deletion events. Possible explanations for this fact could be that the excised islands are diluted during growth of the bacteria since they cannot replicate. Moreover, the experimental protocols for the two methods are different and PCR amplification is much more sensitive as compared to cy3/cy5 labeling by Klenow polymerisation.
Stability of genomic island GI3
Transfer of genomic island GI3 to Bordetella bronchiseptica
The data presented here underline the previous notion of a highly mosaic genome of B. petrii. By microarray analysis of spontaneous phenotypic variants of B. petrii and by direct detection of excised circular intermediates of the B. petrii GIs we show that all of them are active at least in terms of excision. We provide evidence that the adjacent integration of highly related elements may enable these elements to pick up additional genomic material placed between the integration sites thereby leading to an increase in the size of the islands. Moreover, the adjacent placement of islands encoding highly similar integrases and attachment sites may also lead to the formation of novel huge composite islands. For ICE-GI3 we show that without selective pressure this island is lost from the bacterial population. Moreover, we show that this island is self transmissible and can be transferred to another Bordetella species, B. bronchiseptica. Therefore, the evolution of B. petrii involved massive horiztonal gene transfer, while in the classical pathogenic Bordetella species only very few examples of HGT have been reported, e.g. the horizontal transfer of insertion elements, the acquisition of an genomic region encoding an iron uptake system in B. holmesii and, possibly, the inactivation of the genes encoding adenylate cyclase toxin in a specific B. bronchiseptica lineage by a horizontally acquired gene cluster encoding peptide transport genes [12, 23, 24]. This may indicate that their unique habitat due to an obligate host association has dramatically limited the impact on horizontal gene transfer for the pathogenic Bordetellae once they had acquired their capacity to infect and to persist exclusively in vertebrate hosts.
Bacterial strains and growth conditions
In this study B. petrii DSM12804, the type strain of the species , B. bronchiseptica BB7866 , and B. bronchiseptica PS2, carrying a TnphoA insertion in the genome, conferring kanamycine resistance , were used. B. petrii was routinely grown in LB broth, while B. bronchiseptica strains were cultured on BG-agar plates or in SS-liquid medium, as previously described . If necessary, antibiotics were added to the culture media in the following concentrations: tetracycline, 12.5 μg/ml; kanamycine, 50 μg/ml. Conjugation experiments were carried out by filter mating as described previously . The long time survival experiments were carried out as described by Preston and Wardlaw . For this purpose sterile filtered river water from the river Main was inoculated with bacteria B. bronchiseptica BB7866 and B. petrii (2,000 CFU/ml), respectively, and incubated at 37°C. Samples were taken at different time intervals up to 263 days after inoculation and bacterial number was counted by plating out serial dilutions of the bacteria.
Molecular genetic tools
DNA manipulations including cloning, restriction analysis, DNA-sequence analysis, preparation of genomic DNA, Southern blots were carried out according to standard procedures. In all cases, chromosomal DNA used for PCR reactions or for whole genome hybridization analyses was purified from bacterial cultures inoculated from single colonies on agar plates. Pulsed field electrophoresis was carried out with the BioRad CHEF-DRII system as described previously .
B. petrii DNA microarray specifications and hybridization conditions
Sixty-mer oligonucleotides sequences were designed as described previously using OligoArray2.0. Lyophilised 5'-aminated oligonucleotides (Sigma Aldrich) were then resuspended in SciSPOT AM 1× buffer at 20 μM final concentration before being spotted on aldehyde coated Nexterion slides AL (Schott) using QArray2 (Genetix) spotter. Slides were then incubated at room temperature in a humidity chamber (> 90% relative humidity) and then in an oven at 120°C during 1 hour. Slide surface was then blocked twice for 2 min in 0.2% SDS solution, then twice for 2 min in RNase-DNase free water. The slides were then incubated at room temperature during 15 min in 125 mM NaBH4 prepared extemporally in a 3:1 (vol/vol) PBS:Ethanol mixture. The slides were then rinsed twice for 2 min in 0.2% SDS, then twice for 2 min in RNase-DNase free water and dried before hybridisation.
Genomic DNA extraction and labelling
Genomic DNA used for the microarray experiments was prepared by using the Genomic-tip 100/G anion exchange columns (Qiagen), following the manufactor's recommendation. 20 μg of the genomic DNA was digested with MboI restriction enzyme (2 U/μg, Fermentas) at 37°C for 2 hours and complete restriction was confirmed by agarose gel electrophoresis. The fragmented genomic DNA was purified with phenol-chloroform-isoamyl alcohol (25:24:1). Aliqouts of 2 μg of genomic DNA were labelled using the Amersham Nick Translation Kit N5500 (GE Healthcare) in the presence of 91.3 μM dATP, 91.3 μM dGTP, 91.3 μM dTTP, 26.1 μM dCTP, and 33 μM Cy3-dCTP or Cy5-dCTP. Cy-labelled dCTP was obtained from Perkin-Elmer. After incubation at 15°C in the dark for 4 hours, the labelled genomic DNA was purified using the QIAquick Spin PCR Purification Kit (Qiagen).
Microarray hybridisation and data analysis
Genomic DNA from the reference strain B. petrii DSM 12804 was hybridised against each B. petrii variant (g, k, f) in a dye-swap experimental design. Labeled genomic DNA was resuspended in 480 μl of hybridisation buffer containing 40% deionised formamide, 5× Denhardt's solution, 50 mM Tris pH 7.4, 0.1% SDS, 1 mM Na pyrophosphate, and 5× SSC, denatured at 95°C for 3 min and hybridised to the B. petrii microarray for at least 12 hours at 52°C. After hybridisation the microarrays were washed for 5–8 min at 42°C with wash buffer (2× SSC, 0.2% SDS), in 0.5× SSC for 10 min and in 0.05× SSC for 5 min at room temperature. A last rinse was carried out in 0.01× SSC for 30 sec before the microarrays were dried by centrifugation for 5 min at 200 g. The arrays were scanned using an Innoscan 700 (Innopsys) microarray scanner, and analyzed with ImaGene 8.0.0 (BioDiscovery). Normalisation of the data was carried out with R Project for Statistical Computing http://www.r-project.org. The following genome typing analysis was performed with the program GACK http://falkow.stanford.edu/whatwedo/software.
Determination of circular intermediates of the genomic islands by PCR
Oligonucleotides used in this study
5'-TAC GGA CCT TCT CGG CGG-3'
5'-GAC CCA AGG CAA GAC GCT G-3'
5'-ATT ACC CGC ATT CCC TTG TTG-3'
5'-TCG TTG ACC TCG CTC CTC CA-3'
5'-TAC GAC AGT TGA CCA CAG TTG-3'
5'-CTC TGC CGT CCC TCC TTG-3'
5'-TCA AGA CCA TCG TAT AGC GG-3'
5'-AGG TCT AGG AAA ACT GGG CGA ATC-3'
5'-GTA TTC CTG TGC CTA GAT TGG-3'
5'-TCA GCC CCA GCA ACT ATC C-3'
5'-ATG AAC ACC CGG CGA CCC-3'
5'-GAG CTA ACC TAC TGT CCC AT-3'
5'-GTT TTG GGA TGT TTT GAA GCG TG-3'
5'-CGG TCG AAG AAG CCA GCA GT-3'
5'-GAT AGG GTT CGC TCA CAC GGC-3'
5'-CTC CTC CAG CAA CAA TAC GG-3'
5'-TTG AGA CGA CTA TGA ACC CAG-3'
5'-CGC CCA TTG CCA CGA CCG-3'
5'-GAC GGC GGC CGC ATC TGG CAA AGC-3'
5'-ATA CTA GTC ATC GCG TGA TCC TCG CGA A-3'
5'-ATG AAT TCA ATA CGC CCG AGA CCC GCG-3'
5'-CAT CTC GAG AAA ACG GTG AAG GCC AGC-3'
5'-CCG TCT CCA ATC CCA AGG C-3'
5'-CTG GAA CAA GAA GGC CG C-3'
Construction of a B. petrii strain harbouring a tetracycline resistance gene in GI3
The insertion of a tetracycline resistance cassette in the genomic island GI3 was performed by homologous recombination using a tetracycline resistance cassette derived from the cloning vector pBR322 flanked by B. petrii derived sequences. Briefly, for this purpose two DNA fragments derived from the intergenic region of the B. petrii genes Bpet1523 and Bpet1524 encoded on GI3 were amplified using the PCR primer pairs Tet1/Tet2 and Tet3/Tet4 (Table 3) which harboured restriction sites for Not I and Bcu I (Tet1/Tet2) and for Eco RI and Xho I (Tet3/Tet4), thereby providing suitable ends for ligation with the tetracycline gene cassette. The tetracycline gene was ligated with the amplified DNA fragments and cloned into pBluescript KS cut with Not I and Xho I. The plasmid harbouring the tetracycline cassette was then purified and electroporated into B. petrii according to standard procedures using a Micropulser (BioRad, Germany). Bacteria were then plated on LB agar plates containing tetracycline to select for integration of the tetracycline cassette into the genome. Resulting clones were checked by Southern blotting and PCR analysis for proper integration of the resistance cassette at the desired position on GI3. The resulting strain B. petrii GI3::tetR was used for conjugation experiments and for the analysis of island stability. These experiments were carried out as described previously . Briefly, overnight cultures (15 h, 37°C) of the strain were diluted 1:100 in 30 ml of LB broth. Bacteria were incubated at 37°C and samples were taken during the late lag, mid-log, early stationary, and late stationary phases. The identification of spontaneously arising tetracycline sensitive clones was performed by plating out serial dilutions on LB agar plates with and without tetracycline.
We thank Dagmar Beier for critically reading this manuscript. This work was supported by a grant of the Deutsche Forschungsgemeinschaft within the priority research programme SFB479/A2.
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