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Journal of Bacteriology, June 2008, p. 4084-4087, Vol. 190, No. 11
0021-9193/08/$08.00+0     doi:10.1128/JB.00065-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Mobilization of the incQ Plasmid R300B with a Chromosomal Conjugation System in Salmonella enterica Serovar Typhi {triangledown}

Stephen Baker,1,2* Derek Pickard,1 Sally Whitehead,1 Jeremy Farrar,2 and Gordon Dougan1

The Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire, United Kingdom,1 Oxford University Clinical Research Unit, Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam2

Received 13 January 2008/ Accepted 27 March 2008


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ABSTRACT
 
Salmonella pathogenicity island 7 (SPI-7) in Salmonella enterica serovar Typhi appears to be related to other genomic islands. Evidence suggests that SPI-7 is susceptible to spontaneous circularization, loss, and transposition. Here, we demonstrate that a region within SPI-7 has the ability to mobilize the small incQ plasmid R300B.


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TEXT
 
Examples of conjugation systems encoded on the chromosomes of enteric bacteria by conjugative transposons are limited to only a few examples and include CTnR391 from Proteus rettgeri and CTnscr94 from Salmonella enterica serovar Senftenberg (5, 10). Salmonella pathogenicity island 7 (SPI-7) is a 134-kbp genomic island that is situated between two partially copied tRNApheU genes on the chromosome of Salmonella enterica serovar Typhi (11). The original annotation of S. enterica serovar Typhi CT18 predicted that SPI-7 contained multiple regions that constituted a classical pathogenicity island (9). These regions include the locus for the production and exportation of the Vi capsule and the genes responsible for the expression of a type IVB pilus, which aids attachment to human epithelial cells (13).

Modular in structure, SPI-7 appears to have evolved via a series of several independent horizontal gene transfer events. This theory is supported by the truncated nature of corresponding islands in Salmonella enterica serovars Paratyphi C and Dublin and the plethora of genes on SPI-7 from S. enterica serovar Typhi that appear to be involved in recombination (11). On closer examination, SPI-7 contains several modules containing hypothetical genes that are not involved in pathogenicity but that may be involved in the transfer of the element. Evidence demonstrates that not only is SPI-7 capable of inserting into a different tRNAphe site, but in some S. enterica serovar Typhi strains, SPI-7 is susceptible to spontaneous excision and deletion (3, 8). Furthermore, it has been shown that SPI-7 belongs to a family of genomic islands, including pKLC102 from Pseudomonas aeruginosa and HAI2 from Erwinia carotovora (2, 6) (Fig. 1). Therefore, SPI-7 has many of the attributes generally associated with conjugative transposons. However, the mobilization of the element or smaller plasmids by conjugative transfer has not been demonstrated.


Figure 1
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  		FIG. 1. Alignment of SPI-7 from S. enterica serovar Typhi with HAI2 from Erwinia carotovora subsp. atroseptica SCRI1043. Schematic representation of a pairwise alignment of SPI-7 from S. enterica serovar Typhi CT18 with HAI2 from Erwinia carotovora subsp. atroseptica SCRI1043. Regions of significant amino acid homology are represented by gray bars. The arrows represent the coding sequences, and the colors of the arrows correspond to the predicted functions: blue, mob; yellow, pil; and purple, tra (Table 1). The gene names correspond to the gene names in the respective genome sequences. The numbers at the top and bottom of the figure correspond to the coordinates within the respective genomes (left and right) and the approximate sizes of the compared fragments that have been calculated (center). Also highlighted are the locations of the constructed mutations in SPI-7, {Delta}pilS, {Delta}pilV, {Delta}1, {Delta}2, and {Delta}3.

We hypothesized that SPI-7 could behave like other conjugative transposons and had the ability to transfer to a suitable recipient. To add greater insight into the functions of some of the hypothetical genes and regions within SPI-7, we reannotated by PSI-BLAST the coding sequences between STY4521 and STY4597, encompassing approximately 62 kbp of DNA sequence (Fig. 1). First, it was apparent that there was bias toward the coding sequences on the leading strand (Table 1 and Fig. 1), which is a common feature of plasmids. Second, many of the hypothetical genes encoded on SPI-7 demonstrated similarity to genes from plasmids and other genomic islands, many of which appeared to have a role in plasmid replication or conjugative transfer.


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  		TABLE 1. PSI-BLAST results of hypothetical regions of SPI-7 in S. enterica serovar Typhi CT18a

Preliminary conjugative transfer experiments demonstrated that SPI-7 containing a kanamycin determinant could not be transferred from S. enterica serovar Typhi into a Salmonella enterica serovar Typhimurium recipient or an SPI-7-negative S. enterica serovar Dublin strain. However, we were able to transfer the 8,684-bp incQ plasmid, R300B, from S. enterica serovar Typhi BRD948 into a tetracycline-resistant S. enterica serovar Typhimurium recipient, albeit at a low transfer rate (~3 in 108 recipient cells).

Using the lambda red recombinase system described by Datsenko and Wanner (4), we constructed five individual S. enterica serovar Typhi BRD948 mutations by the insertion of a chloramphenicol resistance determinant (Fig. 1). Two of the mutations were gene specific and located within the pil region. The interrupted genes included the major pilin gene (pilS) and a gene adjacent to a shufflon which mediates bacterial self-association (pilV) (7); these mutations were named {Delta}pilS and {Delta}pilV, respectively. The remaining three mutations encompassed several genes each and were in the region of SPI-7, containing the majority of the genes that we hypothesized to be involved in the conjugative transfer. This region included homologues to the conjugative transfer genes traC and traG. The mutations were named {Delta}1, {Delta}2, and {Delta}3, and the fragments removed by each deletion were 4,694 bp, 6,698 bp, and 6,999 bp, respectively (Fig. 1). The chloramphenicol resistance determinant was removed using pCP20, thus making the mutations nonpolar. All mutations were checked by PCR for the correct deletions, and all strains were transformed with R300B. R300B has an active oriT and the relaxosomal genes required for conjugation; however, it is non-self-transmissible and requires a donor mating pair formation for mobilization (12).

Conjugation experiments were performed by mixing mid-log-phase cultures of the various donors with an S. enterica serovar Typhimurium recipient harboring a tetracycline resistance determinant. The S. enterica serovar Typhimurium recipient alone acted as the negative control. The bacterial cultures were washed in 10 mM MgSO4 and injected through a 0.45-µm nitrocellulose filter. The filters were placed on minimal medium plates and incubated at 37°C overnight. Filters were removed and grown in Luria-Bertani medium without selection for 2 h. The bacterial cultures were pelleted via centrifugation, and transconjugants were selected on Luria-Bertani medium supplemented with 150 µg/ml of streptomycin and 100 µg/ml of tetracycline. Conjugation was initially confirmed by antibody agglutination and plasmid extraction on the transconjugants. Experiments were conducted on three separate occasions, each consisting of three replicates.

The results of the conjugative transfer of R300B into the various strains are shown in Fig. 2. The pilS and pilV mutations did not significantly reduce the mobilization rate of R300B from the S. enterica serovar Typhi donor to the S. enterica serovar Typhimurium recipient. However, {Delta}1, {Delta}2, and {Delta}3 all diminished the detectable level of conjugative transfer of R300B by over 10-fold. The conjugation rates of {Delta}1, {Delta}2, and {Delta}3 were significant (P < 0.05) by Student's t test with respect to S. enterica serovar Typhi BRD948.


Figure 2
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  		FIG. 2. Graph showing the number of transconjugants obtained after mating S. enterica serovar Typhi BRD948, {Delta}pilS, {Delta}pilV, {Delta}1, {Delta}2, and {Delta}3 (all containing R300B) with S. enterica serovar Typhimurium. Transconjugants for each experiment were selected on medium containing tetracycline and streptomycin, where S. enterica serovar Typhimurium alone acted as a negative control for each experiment. The data presented are background-corrected mean averages of the results from three experiments, each containing three replicates (i.e., nine replicates in total). Significant P values (P < 0.05) determined by Student's t test calculated by comparing data from S. enterica serovar Typhi BRD948 with the corresponding experimental strain are demonstrated.

The acquisition and maintenance of elements like SPI-7 may present a dramatic change in the phenotype of the bacteria, which can aid pathogenesis, transmission, or survival. Indeed, the gain of large fragments of DNA which aid the lifestyle of S. enterica serovar Typhi has been well documented (1). However, the mechanisms of acquisition and dissemination of such genomic islands are poorly understood and difficult to examine under laboratory conditions. Here we have demonstrated that SPI-7 contains a functional conjugation system that permits the transfer of a small incQ plasmid. We were, however, unable to detect the conjugation of the whole island into suitable recipients under these conditions, which suggests that this ability may have been lost since the original acquisition of SPI-7. These data add insight into the mechanics of how such elements are acquired and how related genomic islands may be able to be mobilized between strains or act as donor systems for the movement of other small pieces of horizontally transferred DNA.


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ACKNOWLEDGMENTS
 
This work was funded by the Wellcome Trust, 215 Euston Road, London NW1 2BE, United Kingdom.


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FOOTNOTES
 
* Corresponding author. Mailing address: Oxford University Clinical Research Unit, Hospital for Tropical Diseases, 190 Ben Ham Tu, Quan 5, Ho Chi Minh City, Vietnam. Phone: (84-8) 9 241 761. Fax: (84-8) 9 238 904. E-mail: sbaker{at}oucru.org Back

{triangledown} Published ahead of print on 4 April 2008. Back


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Journal of Bacteriology, June 2008, p. 4084-4087, Vol. 190, No. 11
0021-9193/08/$08.00+0     doi:10.1128/JB.00065-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Meyer, R. (2009). The R1162 Mob Proteins Can Promote Conjugative Transfer from Cryptic Origins in the Bacterial Chromosome. J. Bacteriol. 191: 1574-1580 [Abstract] [Full Text]  

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