A multi-host approach to identify a transposon mutant of Pseudomonas aeruginosa LESB58 lacking full virulence
Pseudomonas aeruginosa is an opportunistic bacterial pathogen well known to cause chronic lung infections in individuals with cystic fibrosis (CF). Some strains adapted to this particular niche show distinct phenotypes, such as biofilm hyperproduction. It is necessary to study CF clinical P. aeruginosa isolates, such as Liverpool Epidemic Strains (LES), to acquire a better understanding of the key genes essential for in vivo maintenance and the major virulence mechanisms involved in CF lung infections. Previously, a library of 9216 mutants of the LESB58 strain were generated by signature-tagged mutagenesis (STM) and screened in the rat model of chronic lung infection, allowing the identification of 163 STM mutants showing defects in in vivo maintenance.
In the present study, these 163 mutants were successively screened in two additional surrogate host models (the amoeba and the fruit fly). The STM PALES_11731 mutant was the unique non-virulent in the three hosts. A competitive index study in rat lungs confirmed that the mutant was 20-fold less virulent than the wild-type strain. This study demonstrated the pertinence to use a multi-host approach to study the genetic determinants of P. aeruginosa strains infecting CF patients.
KeywordsPseudomonas aeruginosa Cystic fibrosis Lung infection Virulence factors LESB58 Rat Dictyostelium discoideum Drosophila melanogaster
Liverpool Epidemic Strain
phosphate buffered saline
revolutions per minute
reverse transcription quantitative polymerase chain reaction
tryptic soy broth
type three secretion system
Pseudomonas aeruginosa is one of the most common pathogenic bacteria causing lung infections among cystic fibrosis (CF) patients . P. aeruginosa infecting CF patients undergo microevolution: mucoid strains, which also express lower levels of virulence factors such as type three secretion system (TTSS) effectors, are favored. Those are the CF-adapted P. aeruginosa strains [2, 3].
The Liverpool Epidemic Strain (LES) B58 (LESB58) is one of those strains found in chronic CF lung infections and one of the first P. aeruginosa strains identified as epidemic among CF patients . The phenotypic features of LES include biofilm hyperproduction and resistance to several clinically useful antibiotics .
Pseudomonas aeruginosa studies classically use the strain PAO1, originally isolated from a human wound . However, knowing that CF-adapted strains have unique phenotypes, it is necessary to use CF-adapted strains such as LESB58 to explore genes involved in the virulence and the in vivo maintenance of P. aeruginosa in CF lungs.
To determine which genes are the most important for LESB58’s pathogenicity, signature-tagged mutagenesis (STM) was used to create 9216 mutants. In a screening for the survival of the STM mutants in the rat model of chronic lung infection, 163 mutants had a growth defect in vivo, suggesting subdued virulence .
In the present study, we performed additional screening of the 163 mutants, this time using successively the amoeba Dictyostelium discoideum and the fly Drosophila melanogaster as two other surrogate host models. The rat, the amoeba and the fly are three very different model hosts in the study of bacterial virulence and served respectively as a chronic lung infection model , a phagocyte model , and a systemic infection model . We were able to identify that the STM PALES_11731 mutant was the only one that was defective in all three hosts.
Materials and methods
Dictyostelium discoideum predation assay
Bacterial lawns were prepared by suspending bacteria in lysogeny broth (LB) (OD595 of 2) and spreading 300 μL of this suspension on a SM 1/5 Petri dish . D. discoideum DH1-10 cells routinely grown at 21 °C in HL5 medium supplemented with 15 μg/mL of tetracycline were used as a host . Cells were washed and resuspended in HL5 without tetracycline, counted using a haemocytometer, and serial dilutions were performed to obtain: 3000, 1000, 300, 100, 30 or 10 cells/5 μL. These dilutions were spotted (5 μL drops) on the dried bacterial lawn and the Petri dishes were incubated at room temperature (21–23 °C) for 6 days.
Fly pricking assay
Adult female flies aged of 7 ± 2 days were pricked according to a modified previously published protocol . Bacterial cells were grown in tryptic soy broth (TSB) and diluted to an OD600 of 0.2 in a sterile solution of 10 mM MgSO4 supplemented with 100 μg/mL ampicillin. The flies were anesthetized using CO2 and pricked in the dorsal thorax using a 23S gauge Hamilton needle dipped in the appropriate bacterial suspension. For each strain tested, at least 30 flies were infected. The flies were separated into groups of 10 in vials containing 5% sucrose solidified with 1.5% agar. At least 10 control flies were also pricked with a solution of 10 mM MgSO4 supplemented with 100 μg/mL ampicillin. The flies were kept at 25 °C and 65% humidity. Fly survival was recorded daily and survival data was compiled and analyzed with Kaplan-Meier survival curves. The log-rank (Mantel–Cox) test was used to assess significance between the curves.
Competitive index in rat model
Agar beads were prepared according to a modification of a previously described method [8, 14]. The STM PALES_11731 mutant (tagged with tetracycline resistance within mini-Tn5 transposon) and the wild-type LESB58 were grown separately in TSB. Overnight cultures were sedimented by centrifugation (3000×g, 10 min), washed twice with 1 mL of phosphate buffered saline (PBS), and added to 9 mL of 2% agar, prewarmed to 48 °C. A mixture of equal counts of wild-type and mutant cells was added to 200 mL heavy mineral oil at 48 °C with rapid stirring on a magnetic stirrer in a water bath for 5 min at room temperature, followed by 10 min without stirring. The oil-agar mixture was centrifuged (3000×g, 20 min) to sediment the beads and washed twice with PBS. The preparations, containing beads of 100–200 µm in diameter, were used as inocula for animal experiments. The number of bacteria in the beads was determined by homogenizing the bacterial bead suspension and plating 10-fold serial dilutions on Mueller–Hinton agar (MHA) and MHA supplemented with 45 µg/mL tetracycline.
Six Sprague–Dawley rats were anaesthetized using isofluorane (2% of respiratory volume) and inoculated by intubation using a venous catheter 18G and syringe (1-cc Tuberculin) with 120 µL of a suspension of agar beads-embedded bacteria containing approximately 2 × 107 colony-forming units (CFU)/injection. 7 days later, the bacteria were extracted from the infected rat lungs and counted using MHA for the total bacterial number of LESB58 wild-type cells and STM mutant cells or with MHA with 45 µg/mL tetracycline for STM mutant selection.
The in vivo competitive index (CI) was determined as the CFU output (in vivo) ratio of the STM PALES_11731 mutant in comparison to the wild-type strain, divided by the CFU input ratio of mutant to wild type [15, 16]. The final CI was calculated as the geometric mean of the individual animals’ CI.
Results and discussion
Reduced virulence of LESB58 mutants in Dictyostelium discoideum
Identification of the STM PALES_11731 mutant with the Drosophila systemic model
The STM PALES_11731 mutant is strongly attenuated in the chronic lung infection model
Potential consequences of the transposon insertion in the STM PALES_11731 mutant
Genotyping  of the STM PALES_11731 mutant revealed that the mini-Tn5-tet transposon was inserted in the 3′ region of gene PALES_11731 (yfgM), 10 nucleotides before the end of the gene’s sequence (Additional file 1: Figure S1). PALES_11731 codes for YfgM, an ancillary SecYEG translocon subunit  for which the exact function remains unclear. The insertion introduces a stop codon and the last two amino acids of the translated protein are missing (Additional file 1: Figure S2). The predicted structure of the protein suggests that the mutation does not clearly affect the YfgM function. In Escherichia coli, an inactivation of yfgM increases the bacteria sensitivity to acidity . The STM PALES_11731 mutant resistance to acid stress was, however, the same as for the wild-type strain (Additional file 1: Table S2), supporting the idea that YfgM is still functional.
Polar effects are frequently observed in transposon mutagenesis. The mutated operon contains nine genes and the transposition in yfgM, the seventh, could have silenced the two downstream genes. RT-qPCR confirmed that there was no significant transcription defect of these genes (Additional file 1: Figure S3). The following phenotypic tests were performed to confirm this result.
The eighth gene of the operon is PALES_11741 (bamB, previously named yfgL), coding for the outer membrane protein assembly factor BamB (YfgL). In Salmonella enterica, bamB was found to be necessary for the expression of the TTSS , a major virulence mechanism for many bacteria, including P. aeruginosa [24, 25, 26]. We tested the TTSS expression of the STM PALES_11731 mutant but no significant difference with the wild type could be observed (Additional file 1: Figure S4).
It was demonstrated that a bamB mutant in reference strain PAO1 is highly sensitive to antibiotics (especially those targeting cell wall synthesis) and lysozymes . Therefore, we tested the resistance of the STM PALES_11731 mutant to piperacillin (a β-lactam antibiotic), tobramycin (an aminoglycoside antibiotic) and lysozymes. There was no significant difference with the wild type (Additional file 1: Figure S5). This is an additional indication that bamB might not be affected by the transposition in the STM PALES_11731 mutant.
The ninth gene of the operon is engA (also known as der), coding for the GTP-binding protein EngA (GTPase Der). This protein plays an essential role in ribosome biogenesis and its inactivation causes growth defects, especially at cold temperatures . Considering this, we compared the STM PALES_11731 mutant and the wild type growth in different conditions. LB medium, a not-restrictive medium, was chosen as it is the most commonly used on P. aeruginosa. SM 1/5 medium, a diluted low-nutrient medium, was also tested. This medium was used for the amoeba predation assay at 21–23 °C. In LB medium at 37 °C, the wild-type strain, but not the STM PALES_11731 mutant, formed floating aggregates resembling biofilm. Since the usual biofilm definition implies an adhesion to a surface, we can refer to these unattached structures as biofilm-like structures (BLSs) . This phenomenon caused variability in the growth curve measurements, but could be inhibited by the addition of Mg2+. Growth in LB medium supplemented with MgCl2 confirmed the absence of a growth defect for the STM PALES_11731 mutant (Additional file 1: Figure S6). The mutant growth was also comparable to the wild-type LESB58 in SM 1/5 medium at 21 °C (Additional file 1: Figure S7), which shows that engA is likely expressed in the mutant strain. These results also indicated that the STM PALES_11731 mutant defect in virulence is not due to an inherent growth defect.
The highly reduced virulence of the STM PALES_11731 mutant is likely multifactorial
The absence of a BLS formation for the STM PALES_11731 mutant, despite a similar-to-the-wild-type adhered biofilm formation (Additional file 1: Figure S8), cannot itself completely explain the multi-host lack of virulence in the mutant. The amoeba predation assay was performed in a condition in which the wild-type strain does not form BLSs (Additional file 1: Figure S7). However, there was a clear lack of resistance to phagocytosis of the mutant compared to the wild-type strain (Fig. 1). Thus, there must be one or several other virulence mechanisms defective in the mutant to explain its weak resistance to amoeba predation.
Future studies will be necessary to fully understand the impact of the mini-Tn5-tet transposon insertion in the operon containing yfgM. Considering the broad virulence defect of the STM PALES_11731 mutant, this operon appears to play a key role in LESB58 virulence.
Because the transposon did not appear to have an impact on the expression of any of the analyzed genes, it was not possible to link the lack of virulence of the STM PALES_11731 mutant with a specific gene.
CGT, ED, RCL and SJC conceived and designed the experiments. CGT, IKI, GF, VD and SGET performed the experiments. All authors analyzed and interpreted the data. CGT, IKI, ATV, ED, RCL and SJC contributed to the writing and editing of the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request.
Consent for publication
Ethics approval and consent to participate
All of the experimental studies conducted on animals were evaluated and approved by the Université Laval Ethics Committee.
CGT received scholarships from the Institut universitaire de cardiologie et de pneumologie de Québec. This work was supported by the Canadian Institutes of Health Research (CIHR) under Grant MOP-142466 to ED; by the Natural Sciences and Engineering Research Council of Canada under Grant RGPIN-2014-04595 to SJC; and by Cystic Fibrosis Canada under Grant 2610 to RCL. RCL is also funded by a CIHR-Joint Programming Initiative on Antimicrobial Resistance team grant, by Genome Québec and by Genome Canada. ED holds the Canada Research Chair in Sociomicrobiology. SJC is a research scholar of the Fonds de Recherche du Québec-Santé.
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