A mariner-Based Transposition System for Listeria monocytogenes

Construction of mariner-based transposon delivery vectors.

The plasmids and primers used for construction of a mariner delivery vector for L. monocytogenes are listed in Tables 1 and 2, respectively. pPL2 (17) and pDG780 (12) were digested with SacI and XhoI, and the gram-positive kanamycin (kan) resistance cassette from pDG780 was ligated into pPL2 to create pMC14. The gram-positive chloramphenicol acetyltransferase gene (cat) from pPL2 was amplified by PCR with primer pair Marq155/156 and ligated into pCR2.1-Topo (Invitrogen) to create pMC1. pMC1 was digested with BamHI and ligated into the BglII site of pMMOrf (15) between the 5′ and 3′ Himar1-inverted terminal repeats (ITR), creating pMC3. The Himar1 transposase gene (tpase) (16) was amplified by PCR from pNF1100 (provided by Nancy Freitag) with primer pair Marq188/234. The promoter regions of the Bacillus subtilis CU1065 (provided by John Helmann) mrgA and katA genes were amplified by PCR, using primer pairs Marq247/248 and Marq249/250, respectively. P_mrgA, P_katA, and tpase PCR fragments were digested with BamHI, and each promoter was individually ligated to tpase. The P_mrgA-tpase and P_katA-tpase ligation products were amplified by PCR with primer pairs Marq247/188 and Marq249/188, respectively. The P_mrgA-tpase and P_katA-tpase PCR products and pMC14 were digested with KpnI and SphI. The pMC14 fragment comprising P4oriT, p15Aori, gram-negative cat, and gram-positive kan genes was ligated with P_mrgA-tpase and P_katA-tpase, respectively. The ITR-cat-ITR fragment from pMC3 was ligated at the KpnI and XhoI sites, and the gram-positive cat gene was later replaced by ermC. This replacement was done by amplifying ermC from pPL3e (10) with primer pair Marq205/206, digesting the PCR products and vector with NdeI, and replacing the cat gene between the ITR with ermC. Last, the temperature-sensitive origin of replication pE194ts ori in pKSV7 (22) was amplified by PCR, using primer pair Marq194/195, digested with KpnI, and ligated into each vector, creating pMC38 (P_mgrA) and pMC39 (P_katA) (Fig. 1). The vectors are 8,172 bp (pMC38) and 8,297 bp (pMC39), and the transposon itself is 1,395 bp.

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FIG. 1.

Physical map of the mariner-based transposon delivery vectors pMC38 and pMC39. The vectors comprise the Escherichia coli p15A low-copy-number replication origin (5), the RP4 ori for conjugative transfer (20), the pE194ts gram-positive temperature-sensitive replication origin (11, 25), a gram-negative chloramphenicol resistance gene (cat) (5), a gram-positive noninducible erythromycin resistance gene (ermC) (25) flanked by the 29-bp ITR of the Himar1 mariner (15), a gram-positive kanamycin resistance gene (kan) (12) as a screening marker for loss of the plasmid, and the Himar1 mariner transposase gene (tpase) (16). The indicated restriction sites represent those used for cloning, but they are not necessarily unique. Gm⁻, gram negative.

The Himar1 transposase and the ITR sequences are the only two factors required for transposition; thus, successful expression of the transposase in L. monocytogenes is the key element. In our initial constructs, the L. monocytogenes p60 (pMC25) and actA (pMC30) promoters were used to direct transcription of the transposase gene. This approach failed, as the entire plasmid invariably integrated into the chromosome. However, when we used B. subtilis to evaluate the efficiency of transposition with these same vectors, we obtained a very low level of plasmid retention (data not shown). We reasoned that the Listeria species promoters were responsible for mediating plasmid integration into the chromosome of L. monocytogenes and sought to use two B. subtilis σ^A-dependent promoters (P_mrgA and P_katA) with no sequence similarity to the Listeria genome (6). This approach was very successful.

Evaluation of the mariner-based transposon delivery vector.

pMC38 and pMC39 were preferentially transferred into L. monocytogenes strain 10403S by electroporation, as the efficacy of transfer by conjugation was very low. Transformants were selected at 30°C on brain heart infusion (BHI) plates supplemented with erythromycin at 5 μg/ml. Individual colonies were grown overnight in BHI with erythromycin and kanamycin (10 μg/ml) at 30°C with shaking. The cultures were diluted 1/200 in broth with erythromycin, grown for 1 h at 30°C with shaking, and then shifted to 40°C for about 6 h until the optical density at 600 nm was between 0.3 and 0.5. Aliquots of the culture were plated on BHI agar supplemented with erythromycin and incubated at 40°C. Individual colonies were picked and plated in parallel on BHI agar supplemented with either erythromycin or kanamycin to evaluate the rate of plasmid retention. The rate of plasmid retention was calculated by dividing the number of kanamycin-resistant colonies (due to plasmid retention) by the number of erythromycin-resistant colonies (total number of mutants with the plasmid or with the transposon only). The same procedures were used to evaluate the Tn917-based transposition system, Tn917-LTV3 (4), except that 1 μg/ml erythromycin plus 25 μg/ml lincomycin were used for selection of transposon mutants and 12.5 μg/ml tetracycline was used to evaluate plasmid retention.

In general, we obtained 10-fold-more mutants with the mariner-based vectors than with the Tn917-based vector (Table 3). Plasmid retention was less than 2.5% for the mariner-based vectors, whereas it was more than 50% with the Tn917-based vector. Therefore, by comparing the numbers of transposon insertion mutants (colonies that have lost the plasmid) generated by the two systems, we estimated that the efficiency of transposition of the mariner-based vectors was more than 20-fold higher than that of the Tn917-based vector.

To evaluate the randomness of transposition, we arbitrarily picked 100 erythromycin-resistant colonies from one library, performed Southern blot analysis, and identified the sites of transposon insertion. For Southern blot analysis, a 400-bp fragment within the ermC gene was amplified from pMC38 by PCR, using primer pair Marq206/254. The probe was labeled with alkaline phosphatase, using the AlkaPhos Direct labeling system from Amersham Biosciences. Of the 100 mutants, 84 had a single transposon insertion, whereas 16 had two-to-three insertions (data not shown). To identify the sites of transposon insertion, we initially performed arbitrary PCR to amplify the DNA sequences flanking the transposon (8). DNA was amplified from either end of the transposon with a series of two rounds of PCR with Taq polymerase in the first round and Expand High Fidelity polymerase (Roche) in the second round. In each round, a transposon-specific primer and an arbitrary primer were used. The arbitrary primers Marq207 and Marq208 were previously identified as ARB1B and ARB2 by Garsin et al. (8). The approximate locations of transposon-specific primers are illustrated in Fig. 1. In the first round, DNA fragments from the left and right ends of the transposon were amplified with primer pairs Marq207/255 and Marq207/269, respectively. For the second round, 5 μl of a 1/25 dilution from the first round of PCR was used in a 20-μl reaction. DNA fragments from the left and right ends of the transposon were amplified with primer pairs Marq208/256 and Marq208/270, respectively. The PCR products were sequenced, using primers Marq257 and Marq271 for the left and right ends of the transposon, respectively. The Biotechnology Research Center of Cornell University performed the sequencing with an Applied Biosystems automated 3730 DNA analyzer. The ListiList website (http://genolist.pasteur.fr/ListiList/ ) was used for sequence analysis.

Readable sequencing results were obtained from 77 transposon insertion mutants, including one pair of siblings and a series of three genes that were hit twice. For the 77 mutants, 36 insertions were in positive-strand open reading frames, 29 in negative-strand open reading frames, and 12 in intergenic regions (Fig. 2). The mutants distributed evenly along the L. monocytogenes genome, and there was no bias in terms of the transposon orientation. We further aligned all the insertion sites, and no sequence specificity beyond the known requirement of the dinucleotide TA was found (data not shown).

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FIG. 2.

Locations of 77 sequenced Himar1 insertions in the chromosome of L. monocytogenes. The bars located outside the circle indicate transposons that were oriented in the same direction as the positive strand, whereas the bars located inside the circle indicate transposons that were oriented in the opposite direction. Each quarter of the chromosome is identified with the approximate base pair, except for bp 1, which is identified by an arrow.

Taken together, these results show that the newly designed mariner delivery vectors are powerful genetic tools to study L. monocytogenes. The mariner-based system outachieves the Tn917-based system in the following aspects: transposition efficiency, randomness, and a low rate of plasmid retention. The temperature-sensitive replicon (pE194ts ori) and the noninducible erythromycin resistance gene (ermC) are common to many gram-positive bacteria. We believe that this mariner-based system will be a great tool for the entire community of scientists working with L. monocytogenes and other low-GC gram-positive bacteria.