Development of multiple strain competitive index assays for Listeria monocytogenes using pIMC; a new site-specific integrative vector
© Monk et al; licensee BioMed Central Ltd. 2008
Received: 14 March 2008
Accepted: 13 June 2008
Published: 13 June 2008
The foodborne, gram-positive pathogen, Listeria monocytogenes, is capable of causing lethal infections in compromised individuals. In the post genomic era of L. monocytogenes research, techniques are required to identify and validate genes involved in the pathogenicity and environmental biology of the organism. The aim here was to develop a widely applicable method to tag L. monocytogenes strains, with a particular emphasis on the development of multiple strain competitive index assays.
We have constructed a new site-specific integrative vector, pIMC, based on pPL2, for the selection of L. monocytogenes from complex samples. The pIMC vector was further modified through the incorporation of IPTG inducible markers (antibiotic and phenotypic) to produce a suite of four vectors which allowed the discrimination of multiple strains from a single sample. We were able to perform murine infection studies with up to four EGDe isolates within a single mouse and showed that the tags did not impact upon growth rate or virulence. The system also allowed the identification of subtle differences in virulence between strains of L. monocytogenes commonly used in laboratory studies.
This study has developed a competitive index assay that can be broadly applied to all L. monocytogenes strains. Improved statistical robustness of the data was observed, resulting in fewer mice being required for virulence assays. The competitive index assays provide a powerful method to analyse the virulence or fitness of L. monocytogenes in complex biological samples.
Historically, the measurement of bacterial virulence has involved the use of infection models to access the ability of a pathogen to cause disease. One widely used method is the LD50 assay, which is defined as the number of bacteria required to kill 50% of the infected hosts. This method yields valuable data pertaining to the cumulative, absolute virulence of the bacterium, which can theoretically be compared between laboratories. But as detailed by Beuzón and Holden , it is a crude method as it does not relay information on the infection kinetics. Also, if the deletion of a gene does not increase the LD50, it does not necessarily mean that the gene product does not play a role in the virulence of the bacterium. If two or more strains (e.g. wild type to mutant or independent isolates) could be compared within a single host, the kinetics of infection could be monitored, which could expose subtle differences. Intra-animal experiments would help to minimise inherent inter-animal biological variation and also improve the identification of mutations or isolates with reduced competitive fitness within the host . This form of assay has been termed a "competitive index" and is becoming an increasing popular method to examine bacterial virulence [3–5]. One crucial factor is to establish the ability to discriminate strains, without adversely impacting on the natural fitness of the organism.
Listeria monocytogenes is a foodborne pathogen, which can cause fatal infections in a susceptible host . In humans, the initial step of gastrointestinal invasion is mediated via the interaction of a bacterial cell surface exposed protein, Internalin A (InlA), with the host cell surface ligand, E-cadherin . Subsequent intracellular replication and spread can lead to systemic disease. While the mouse is a poor model of listerial gastrointestinal disease due to the limited affinity of InlA for murine E-cadherin, the tools required for systemic proliferation are functional once the gastrointestinal tract is bypassed via intravenous or intraperitoneal injection . Identification and assessment of genes required for the virulence of L. monocytogenes has been greatly helped by the sequencing of multiple genomes [9, 10]; however, functional post genomic analysis requires the development of improved techniques for the discrimination of virulence potential. LD50 measurements are still widely used, but for the reasons described above, competitive indices could provide a more elegant alternative. Even though competitive index assays have been previously applied to L. monocytogenes [11–13], these are not broadly applicable and have inherent limitations (see Discussion section).
Here, we have established a method to stably tag L. monocytogenes strains and assess their competitive fitness in complex samples. Through the development of a new site-specific integrative vector, pIMC, we have produced four derivatives with different IPTG inducible antibiotic and phenotypic markers for their subsequent discrimination from complex samples.
Construction of pIMC
Development of in vivo multiple competitive index assay
Comparative analysis of virulence potential is a cornerstone in understanding the ability of a pathogen to cause disease and in determining the relative contribution of putative virulence factors. We applied pIMC to establish a widely applicable method to evaluate virulence potential during mixed infections, in the form of a competitive index (CI) . To exploit the high level of chloramphenicol resistance of pIMC, which allows selection from complex samples, we subcloned three IPTG-inducible antibiotic resistance markers ermAM (EryR), aphA3 (KanR), tetM (TetR) and an IPTG-inducible phenotypic marker, gusA (Gus) into pIMCa (see Material and Methods). These markers enable strains to be distinguished directly from each other by antibiotic selection or through X-gluc hydrolysis (leading to a blue colony colour). These plasmids were electroporated into EGDe and the resultant strains were evaluated in vitro for growth rate and in vivo for virulence. No differences in growth rate were observed between the strains when grown in BHI (data not shown).
Virulence comparison of different L. monocytogenes strains
Our prior experience with the pPL2 plasmid [15, 16] indicated that the chloramphenicol resistance expressed was relatively low, therefore we were unable to directly select L. monocytogenes out of complex samples. This could be due to the inducible nature of gram-positive cat genes as described by Lovett . To circumvent the requirement for induction of cat expression, we remodelled pPL2 to decrease plasmid size and exchange the inducible cat promoter for a highly expressed constitutive version. This increased the MIC of the new vector, pIMC, ten-fold compared to pPL2. The improved selection allows the isolation of tagged L. monocytogenes from complex environments such as intestinal contents or food samples. Further development of pIMC involved the creation of a suite of four vectors with diverse antibiotic and phenotypic markers to allow the discrimination of individual L. monocytogenes isolates. These were used to establish a competitive index assay to compare the relative fitness of L. monocytogenes strains. The tags did not compromise the fitness of the transformed strains as determined by growth in complex media and by the maintenance of an initial infection ratio through out a three day time course in Balb/c mice. The method established allows the direct discrimination of strains without post-enumeration manual scoring, such as PCR or replica plating [17, 18]. The introduction of post enumeration scoring can introduce bias in the discrimination of bacteria, as only a small sample size is processed per organ. When samples can be directly enumerated, larger numbers can be analysed and the introduction of human error reduced. Also, the IPTG inducible promoter should help to decrease any potential consequences of marker expression during competitive growth.
We also observed improved statistical robustness when analysing data from competitively infected mice. We found that ratios were maintained throughout the course of infection (Fig 2b), suggesting that, as observed with Salmonella typhimurium , true replication of the inoculum occurs rather than clonal expansion. The statistical significance was especially evident when data from the third day post infection was analysed (Fig 3a). Large differences in the CFU counts isolated from individual livers and spleens were observed due to inherent variation in the infection process and animal-animal variability. However, analysis of the ratio of strains demonstrated improved statistical validity (Fig 3b). For the experiment reported in Fig 3, 15 mice were used, whereas traditionally 45 mice would have been required if each strain were analysed individually. Therefore, using mixed infections, fewer mice are required to produce better results, a powerful demonstration of the 'reduce and refine' principles.
Competitive index assays for L. monocytogenes have previously been described by two research groups. Auerbuch et al  established a strain of L. monocytogenes (10403S) tagged with Tn917 (EryR), which mimics wild type 10403S infections. This has been widely applied by researchers using the 10403S strain [19–22]. However, the assay developed is only applicable to 10403S, requires further analysis post enumeration (i.e. patching of colonies) and only allows the comparison of wild type to a second unmarked strain. In 2006, a fluorescence based method for the discrimination of L. monocytogenes strains was established in a replicative plasmid system . A total of five fluorescent proteins were shown to be functional, with three suitable for simultaneous use to distinguish strains (due to emission spectra). While the tagging method is non-invasive, prolonged incubation is required for chromophore maturation and in the absence of selective pressure, significant and variable plasmid loss was observed, depending on the fluorescent marker used . The authors also describe difficulty in discriminating large virulence attenuations due to the non-selective nature of the marker.
From the comparison of three commonly used laboratory strains of L. monocytogenes, we observed distinct differences in the kinetics of infection. Upon re-examination of the sequence of the inlB gene from F2365, it was shown to encode a nonsense mutation leading to premature stop codon in the gene . This may help to explain the impaired ability to establish infection within the liver compared to the 10403S and EGDe, as InlB plays an important role in liver colonization .
We have applied the competitive index experiments to in vivo experiments, but it equally could be used in vitro to examine growth or survival within both sterile and complex systems. Additionally, we envisage the use of internal controls in experiments, such as the comparison of mutant, wild type and complemented mutant, or the dual tagging of a wild type and two separate mutants in murine or tissue culture assays (e.g. adhesion, invasion and/or intracellular multiplication). We acknowledge that problems may be encountered in certain situations when comparing multiple strains in a single host, e.g. if a molecule involved in quorum sensing complemented a virulence defect or when the route of infection can be hijacked by a defective competing strain . Nonetheless, we believe our protocol displays significant advantages over previously described methods and provides an additional tool for use in infection biology.
We have established a method for the comparison of the relative fitness of L. monocytogenes strains utilising a novel, stable integrative plasmid, pIMC, based on the pPL2 phage integrase plasmid. This method allows for the selection and discrimination of up to four isolates from complex samples, without the requirement for post-enumeration processing. There were no detrimental effects on virulence or growth rate of the L. monocytogenes strains due to tag expression, as demonstrated by systemic spread in a BALB/c mouse model similar to that seen with a wild type strain. The utility of the method was demonstrated through the direct comparison of virulence of three commonly used L. monocytogenes strains (EGDe, 10403S and F2365). The data yielded improved statistical robustness when the ratios were examined rather than the cumulative CFU counts from spleens and livers. EGDe was shown to predominate in the liver and spleen by day three of infection compared to the other two strains. F2365 exhibited similar kinetics to 10403S in spleen replication but was significantly impaired in the ability to replicate within the liver when compared to both strains.
Strains, Antibiotics and Reagents
Plasmids, Strains and Oligonucleotides
Temperature sensitive plasmid for the delivery of Tn917. 11 kb. EryR KanR.
Lactococcal beta-glucuronidase (gusA) transcriptional fusion vector. 4.6 kb. CmR.
Site-specific Listerial integrative vector. High-level CmR from Phelp driven expression. 4.6 kb. CmR.
Site-specific Listerial integrative vector. High level IPTG controlled gene expression. 7.5 kb. KanR.
Site-specific Listerial integrative vector. IPTG controlled expression of aphA-III ex pTV1-OK. CmR
 This study
Site-specific Listerial integrative vector. IPTG controlled expression of gusA ex pNZ272. CmR
 This study
Site-specific Listerial integrative vector. IPTG controlled expression of ermAM ex pTV1-OK. CmR
 This study
Site-specific Listerial integrative vector. IPTG controlled expression of tetM ex CH919. CmR
 This study
Wild type 1/2a strain. Genome sequenced.
Wild type 1/2a strain. Genome sequenced. Broad Institute (MIT).
Wild type 4b strain. Genome sequenced.
EGDe transformed with pIMC3kan integrated at the tRNAARG.
EGDe transformed with pIMC3gus integrated at the tRNAARG.
EGDe transformed with pIMC3ery integrated at the tRNAARG.
EGDe transformed with pIMC3tet integrated at the tRNAARG.
10403S transformed with pIMC3ery integrated at the tRNAARG.
F2365 transformed with pIMCtet integrated at the tRNAARG.
Wild type Escherichia coli. Used for routine cloning.
MG1363 Lactococcus lactis subsp. lactis containing Tn919.
108 Phelp B REV
181 CAT C FWD
203 MCS FWD
204 MCS REV
205 Back FWD
206 Phelp A FWD
209 CAT D REV
211 Back REV
373 gusA FWD
374 gusA REV
385 aphA3 FWD
386 aphA3 REV
387 ermAM FWD
388 ermAM REV
408 tetM FWD
409 tetM REV
Construction of pIMC: a site specific integrative plasmid
The site-specific integrative listeriophage vector, pPL2, was modified by spliced overlap extension (SOE) PCR to incorporate constitutive chloramphenicol selection and decrease vector size. Initially three fragments were amplified: (A) pBluescriptII KS (+) multiple cloning site (MCS) including T3 and T7 promoter primer binding sites (IM203/204) (B) the pPL2 backbone from 1100 to 4585 ([GenBank:AJ417449]) (IM205/211) and (C) the Phelp promoter (from pPL2lux-Phelp)  fused to chloramphenicol acetyltransferase (cat) gene from pNZ8048  by SOE PCR (IM181/209 and IM206/108). Phelp is a chimeric construct containing an optimized consensus lactococcal promoter PCP25  joined to the 5' UTR of the L. monocytogenes hlyA gene . The MCS of pBluescriptII KS (+) was joined to the backbone (1100 bp end) of pPL2 to remove both cat genes. The Phelp-cat amplimer was joined to the backbone (4585 end) of the previous PCR product. The PCR product for pIMC (4581 bp) was gel extracted and phosphorylated with T4 polynucleotide kinase (New England Biolabs). The product was ligated with LigaFAST rapid DNA ligation system (Promega) for 30 min at 22°C, transformed into DH10B with selection on LBA containing Cm at 10 μg/ml. A single clone of pIMC was fully sequenced and deposited under the accession number: [EMBL:AM940001]. The plasmid schematic (Fig 1a) was drawn with the online plasmid drawing tool  and exported as an .svg file on an iBook (Apple) from the Opera web browser into Adobe Illustrator CS2 (Adobe) for further manipulation as an .svg file.
Competitive index assay constructs
The pIMK3 is a kanamycin version of pIMC  which contains the gram-positive functional rrnB transcription termination sequence up stream (Aat II/Sac I) of an IPTG inducible promoter (Sac I/Nco I). Located downstream of the IPTG inducible promoter is the highly expressed repressor, Phelp-lacI (Sal I/Kpn I). The above Aat II/Kpn I region was subcloned from pIMK3 into pIMC, producing pIMCa. The genes for antibiotic markers tetM from CH919 genomic DNA , ermAM from pTV1-OK , aphA3 from pTV1-OK  and the phenotypic marker gusA from pNZ272  were cloned as Nco I/Pst I fragments into pIMK3 and confirmed phenotypically in E. coli. The marker and promoter were then subcloned as Sac I/Pst I fragments into the corresponding sites of pIMCa, yielding pIMC3ery, pIMC3gus, pIMC3kan and pIMC3tet. Constructs were transformed into L. monocytogenes generating strains: EGDe::pIMC3ery, EGDe::pIMC3gus, EGDe::pIMC3kan, EGDe::pIMC3tet, 10403S::pIMC3ery and F2365::pIMC3tet. The production of these constructs took advantage of the high-level CAT expression from pIMC to facilitate in vivo selection (from faecal/intestinal samples) and allow the discrimination of genotypes by inducible marker expression, when used in co-culture experiments.
Competitive index assay experiments
Overnight cultures of the tagged strains were washed three times with PBS and diluted back to an OD600 nm of 0.1 (1× 108 cfu/ml) (Biophotometer, Eppendorf). Cultures were then subsequently mixed at ratios of 1:1:1:1, 83.3:13.2:2.75:0.75. (EGDe::pIMC3gus, EGDe::pIMC3tet, EGDe::pIMC3ery and EGDe::pIMC3kan, respectively) or 1:1:1 (EGDe::pIMC3kan, 10403S::pIMC3ery and F2365::pIMC3tet, respectively) and diluted 1:500 to obtain 2 × 105 cfu/ml. Fifteen specific-pathogen free female BALB/c mice (aged 6–8 weeks; Harlan) were intravenously inoculated via tail vein with 100 μl of diluted cells. The inoculum was enumerated on the following BHI based agars (A) BHI only (B) Cm 7.5 + 1 mM IPTG + X-gluc (C) Cm 7.5 + 1 mM IPTG + Kan (D) Cm 7.5 + 1 mM IPTG + Erm (E) Cm 7.5 + 1 mM IPTG + Tet. For the comparison of EGDe, 10403S and F2365, X-gluc containing agars were omitted. In preliminary experiments the incorporation of IPTG, X-gluc and Cm was shown not to impact on the recovery of L. monocytogenes from organ homogenates (data not shown). On days 1, 2 and 3 post infection, five mice from each group were sacrificed and spleens and livers aseptically removed. The organs were homogenized in 5 ml of PBS, serially diluted and enumerated on the agars described above. For the comparison of EGDe, 10403S and F2365 agar (B) was omitted.
The comparison of the tagged strains' ability to compete within a mouse was determined as follows: the CFU per organ from each strain within a single mouse was divided by the cumulative total of the four strains (addition of each single count) to obtain a ratio of each strain per organ. This ratio was divided by the initial ratio of the inoculum to obtain a relative virulence ratio (RVR). A RVR score of 1 denotes no change the ability to compete, e.g. for the comparison of EGDe, 10403S and F2365 the RVR scores were represented relative to EGDe (set as 1), thus obtaining a competitive index (CI) value. All procedures involving animals complied with relevant legislation and were approved by the animal ethics committee at University College Cork.
Statistical analysis (One sample T-test, Microsoft Excel) was applied to the raw CFU and RVR counts through the calculation of CFU or ratio difference (e.g. strain 1 to strain 2, strain 1 to strain 3 and strain 2 to strain 3) per organ (n = 5). A Microsoft Excel spreadsheet is attached for the calculation of the RVR and subsequent one sample T-test of CFU and RVR (additional files 1, 2 and 3). Competitive index was calculated relative to EGDe with the RVR of 10403S and F2365 per organ divided by the RVR of EGDe (additional file 3). The average CI from 5 organs is presented in Fig 3c.
We would like to thank Paddy O'Reilly and Michelle Cronin for supplying strain CH919 and plasmid pNZ272, respectively. The authors would like to acknowledge the funding received from the Irish Government under the National Development Plan 2000–2006 and the funding of the Alimentary Pharmabiotic Centre by the Science Foundation of Ireland Centres for Science Engineering and Technology (CSET) programme.
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