Engineered live bacteria could provide a new modality for treating lung infections, a major cause of mortality worldwide. In the present study, we engineered a genome-reduced human lung bacterium, Mycoplasma pneumoniae, to treat ventilator-associated pneumonia, a disease with high hospital mortality when associated with Pseudomonas aeruginosa biofilms. After validating the biosafety of an attenuated M. pneumoniae chassis in mice, we introduced four transgenes into the chromosome by transposition to implement bactericidal and biofilm degradation activities. We show that this engineered strain has high efficacy against an acute P. aeruginosa lung infection in a mouse model. In addition, we demonstrated that the engineered strain could dissolve biofilms formed in endotracheal tubes of patients with ventilator-associated pneumonia and be combined with antibiotics targeting the peptidoglycan layer to increase efficacy against Gram-positive and Gram-negative bacteria. We expect our M. pneumoniae-engineered strain to be able to treat biofilm-associated infections in the respiratory tract.
Respiratory diseases are among the top ten causes of death worldwide. Efforts to develop new therapeutics against respiratory tract infections are growing, especially given the mounting concern about antibiotic-resistant bacteria and the paucity of new antibiotics1. Moreover, antibiotic therapies eliminate beneficial lung microbes and can lead to the persistence of pathogenic, resistant strains2. Approximately 65–80% of human infections are associated with biofilms3,4,5,6. They are especially frequent in pulmonary chronic diseases7,8, including cystic fibrosis (CF)9, chronic obstructive pulmonary disease8 and non-CF bronchiectasis, as well as in acute airway infections, such as ventilator-associated tracheobronchitis (VAT) and ventilator-associated pneumonia (VAP)10,11. Biofilms are an ancestral bacterial survival strategy against environmental stress that consists of complex and dynamic structures formed by aggregates of microorganisms embedded in a polymeric matrix, which confers tolerance to antimicrobials12,13 and allows them to evade host defense mechanisms14. Thus, biofilms can cause recurrent, device-associated chronic infections. As a result, the effective minimum bactericidal concentrations of antibiotics for biofilm eradication in vivo are relatively high and can cause adverse effects, such as renal and/or hepatic injury15. Moreover, many of the lung pathogenic bacterial strains are resistant to antibiotics.
Biofilm formation is especially problematic with the use of endotracheal tubes (ETTs) in patients who require invasive mechanical ventilation (MV) in intensive care units (ICUs). VAT and VAP are estimated to occur in 9–27% of all patients receiving MV16. For patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) who receive MV, the incidence rates of VAP/VAT are higher than usual and exceed 50% overall17. Moreover, the mortality rate in VAP patients with COVID-19 was higher than in those with influenza or without viral infection18,19 and even higher when associated with P. aeruginosa biofilms20,21. Until now, most interventions aimed at reducing lung biofilms, including aerosolized antibiotics, have failed or require further investigation22.
Engineered bacteria that are genetically modified to treat diseases—which are classified as live biotherapeutic products—could offer effective therapeutic formulations with fewer adverse effects23,24,25,26,27,28,29,30,31,32,33,34. Most bacterial vectors have been designed to treat gut diseases, with a few targeting diseases affecting other organs. Examples include an engineered strain of Lactobacillus reuteri that decreases high blood levels of phenylalanine in a homozygous PAHenu2 (phenylketonuria) mouse model25 and an engineered strain of Lactobacillus spp. or Saccharomyces cerevisiae designed to immunize against HIV in the gut27 and the cervicovaginal mucosa35,36. However, no bacterial chassis has so far been described for the treatment of lung diseases37.
The site of action of a bacterial therapeutic affects the choice of species38. Ideally, the selected bacterium should be naturally present in the organ to be treated, to ensure its survival and limit spreading to other organs. For example, the Escherichia coli Nissle 1917 strain was engineered to treat P. aeruginosa infections in the gut39, yet it cannot be used to treat respiratory infections because the respiratory tract is not its natural niche. M. pneumoniae is the causative agent of atypical pneumonia and other extrapulmonary pathologies in humans. Compared with other bacterial chassis, M. pneumoniae has the following advantages for treatment of lung infections: (1) it has a small genome (816 kbp); (2) it is a mild pathogen that can be eliminated with available antibiotics; (3) it is a bacterium for which more quantitative and extensive datasets are available40,41,42,43,44,45; (4) it has reduced metabolic and genetic networks46, which reduce the risk of unwanted interference of the engineered circuits; (5) as it lacks a cell wall, it does not trigger a strong inflammatory response and can be combined with antibiotics that attack the peptidoglycan layer present in cell walls of pathogens (as shown in the present study); (6) its main antigens and virulence factors are well characterized44,47,48,49; (7) genetic tools are available to engineer its genome and to obtain an attenuated strain50,51,52; (8) some M. pneumoniae strains, including M129, have a negligible rate of recombination, thereby reducing the risk of horizontal transfer; (9) its UGA codon encodes for tryptophan instead of a translation stop, providing an intrinsic biocontainment mechanism; and (10) it can be grown in a defined, synthetic, serum-free medium to upscale its good manufacturing practice-compliant production53.
We used an engineered, attenuated version of M. pneumoniae M129 strain as a bacterial chassis to treat/prevent infectious lung diseases caused by P. aeruginosa. We first characterized in vivo the safety of use and survival of different attenuated M. pneumoniae M129 strains in mouse lungs, to define the optimal chassis. We then engineered this nonpathogenic chassis by introducing two optimized genetic systems: one that combines biofilm dispersal activities (the glycoside hydrolases PelAh54 and PslGh55 and the A1-II′ alginate lyase56) and another that implements antimicrobial activity (pyocin L1 (ref. 57) or pyocin S5 (ref. 58)) against biofilms formed by P. aeruginosa. We validated the activity of the engineered chassis strain in vitro, ex vivo and in vivo. We showed that the engineered strain can reduce an acute P. aeruginosa infection in the murine model, thereby improving mouse survival, dissolve biofilms formed in vivo on ETTs in patients with VAP and be combined with antibiotics targeting the bacterial cell wall. Thus, it represents a promising alternative modality for preventing or treating biofilm-associated diseases and eradicating bacterial antibiotic resistance.
Delivery and clearance of M. pneumoniae strains in murine lung
We first studied the survival of the M. pneumoniae wild-type (WT) strain in lungs. CD1 mice were inoculated intratracheally (i.t.) or intranasally and the bacterial load was determined in lung and bronchoalveolar lavage fluid (BALF) at 2 d postinfection (d.p.i.) (Extended Data Fig. 1a). As the highest bacterial load was detected in lung samples via the intratracheal route, we used intratracheal administration for the remaining experiments. In lungs, the bacterial load decreases at 4 d.p.i. and 14 d.p.i. compared with 2 dpi (2 and 4(log10), respectively) (Extended Data Fig. 1b,c), indicating that M. pneumoniae is cleared at 14 d.p.i.
Next, we sought to engineer an improved M. pneumoniae strain by removing pathogenic genes. The following genes have been suggested as being responsible for M. pneumoniae pathogenesis: mpn372 which encodes the community-acquired respiratory distress syndrome toxin48,59; mpn133 which encodes a lipoprotein with cytotoxic nuclease activity49; mpn453 which encodes the P30 adhesin protein60; and mpn051 which encodes the glycerol-3-phosphate dehydrogenase/oxidase (GlpD or GlpO)47. We previously showed that the Δmpn051 strain grows poorly in vitro46, because the GlpD enzyme is needed for M. pneumoniae to use phosphatidylcholine as a carbon source in the lungs61. Also, recently we showed that an M. pneumoniae strain harboring deletions in the mpn372 and mpn133 genes (CV2 strain) was attenuated in a mammary gland infection model62. As attenuation can differ in the respiratory tract, and other factors such as adhesion could affect virulence, we characterized the deletion of mpn453 as an additional gene to be removed to obtain an attenuated lung chassis. In the present study, we observed that the nonadherent Δmpn453 strain has a significant reduction of colony-forming units (c.f.u.) recovered at 2 or 4 d.p.i. in mouse lungs compared with the WT strain (Extended Data Fig. 1b), suggesting that attachment to the epithelium is critical for maintenance of M. pneumoniae in the lung. Thus, as a compromise between attenuation and maintenance in lungs, we selected, as an attenuated chassis for lung therapy, the CV2 strain, which harbors deleted mpn372 and mpn133 genes and WT mpn453 and mpn051 genes.
We tested the potential of lung colonization of the CV2 chassis compared with the WT strain by infecting animals i.t. with 1 × 107 c.f.u.(Extended Data Fig. 1c and Table 1). We obtained similar bacterial counts for WT and CV2 strains at 2, 4 and 14 d.p.i., indicating that deletion of mpn372 and mpn133 genes did not affect the CV2 capability of colonizing the lung.
Lung lesions and inflammatory response induced by the CV2 strain
To compare the response induced by CV2 and WT strains, we inoculated mice with a dose of 1 × 107 c.f.u. and then analyzed lungs at 2, 14 and 45 d.p.i. We determined the bacterial load in the lung tissue by quantifying the colony-forming units. In addition, lesions and immune response were evaluated by histopathology and cytokine profile, respectively. Of note, we found no statistical differences in the recovered colony-forming units between strains at different days postinfection and in different lung lobes (Extended Data Fig. 2a). This result showed a homogeneous distribution of the M. pneumoniae strain when inoculated i.t. and corroborated that deletion of genes in the CV2 strain did not affect its lung survival rate.
We then evaluated pulmonary lesions by histopathological analyses of three major lung lobes (right cranial, right middle and left lobe) using five parameters: (1) presence of peribronchial/peribronchiolar inflammatory infiltrate (%); (2) intensity of peribronchial/peribronchiolar inflammatory infiltrate; (3) intensity of bronchial/bronchiolar luminal exudate; (4) presence of perivascular inflammatory infiltrate (%); and (5) interstitial pneumonia intensity63. Based on these parameters, and as previously described62,63, a final total score of up to 26 points was calculated as a global indicator of the lung lesion (Fig. 1a,b, Extended Data Fig. 2b and Supplementary Table 1). More details on the scoring system are given in Methods.
At 2 d.p.i., the total score indicated significantly milder lesions in the CV2 mice compared with the WT infected group (5.8 and 12.1 average points, respectively), with less peribronchiolar and perivascular inflammation and markedly less interstitial inflammation. At 14 d.p.i., the CV2 group showed no significant differences compared with the phosphate-buffered saline (PBS) control group, whereas the WT had remnant tissue injuries related to peribronchiolar, perivascular and interstitial inflammation (score of 6 in the WT versus 1.7 in CV2). At 45 d.p.i., the analyses indicated resolution of lung lesions in both CV2 and WT administered groups (except for perivascular infiltrate, which, although statistically not significant, was still high).
We next studied the induced inflammatory response by evaluating the expression of inflammatory markers in lungs by reverse transcription quantitative PCR (RT–qPCR; Fig. 1c, Extended Data Fig. 2c and Supplementary Table 2). The following panel of genes was analyzed: il1b, il6, il12a, il23a, ifng, tnf, ccl2, ccl3 and cxcl1. We did not observe a significant induction of the il1b, il6, il12a and il23a genes by WT and CV2 (Extended Data Fig. 2c). In general, the response of the remaining markers was not high, although differences between CV2 and WT were observed. At 2 d.p.i., the WT strain induced expression of the inflammatory markers tnf, cxcl1, ccl3, ccl2 and ifng compared with the PBS control mice, whereas CV2 did not induce any marker compared with WT mice. At 14 and 45 d.p.i., and in agreement with the histopathological analysis, the inflammatory response in both WT and CV2 lungs decreased to levels observed in PBS control mice (Fig. 1c).
Taken together, these results demonstrated that CV2 was attenuated in the lungs compared with the WT M. pneumoniae strain, underscoring it as a strong candidate for further engineering as a chassis to treat respiratory diseases.
Engineering an M. pneumoniae strain to dissolve P. aeruginosa biofilms
To introduce properties into our chassis to treat pulmonary infectious diseases, we designed and characterized an optimal genetic system for dispersing P. aeruginosa biofilms, which is one of the main pathogenic bacteria causing VAP. As the P. aeruginosa biofilm is mainly composed of the polysaccharides Pel, PsI and alginate, we engineered the WT strain with a genetic cassette expressing three different enzymes that target these three polysaccharides, namely: the glycoside hydrolases PelAh64 and PslGh55, and the A1-II′ alginate lyase56, fused to a peptide for secretion (MPN142_OPT)62 (European patent 16706622.4; Supplementary Table 3). First, we confirmed the expression of PelAh, PslGh and A1-II′ in the cell lysate and supernatant of CV2_HA by mass spectroscopy (MS; Supplementary Table 4). We then tested the antibiofilm activity of the supernatants of the different M. pneumoniae strains expressing either single enzymes or some of the possible combinations of enzymes against P. aeruginosa by Crystal Violet assay. We found that the M. pneumoniae strain engineered with a combination of the three enzymes showed the best dispersal activity against biofilms formed by P. aeruginosa strains SAT290 and PAO1 (Fig. 2a,b). We obtained similar results when using Alcian Blue as an alternative biofilm-staining method (Extended Data Fig. 3a). Hence, we included PelAh, PslGh and A1-II′ in the attenuated CV2 strain, CV2_HA. Finally, we confirmed the antibiofilm activity of CV2_HA in a panel of clinical P. aeruginosa strains (Fig. 2c). These results demonstrated that the M. pneumoniae strain CV2, which expresses and secretes the glycoside hydrolases PelAh and PslGh and the A1-II′ alginate lyase, degrades P. aeruginosa biofilms in vitro.
Addition of antimicrobial activity to CV2_HA
The ideal engineered M. pneumoniae strain to treat VAP should combine biofilm dispersal and antimicrobial activity. To introduce antimicrobial activity, we engineered CV2_HA to express the bacteriocin pyocin L1 (CV2_HA_P1), which was previously shown to kill some P. aeruginosa strains, including PAO1 (ref. 57). First, we confirmed the capacity of the cell-free supernatant of CV2_HA_P1 to dissolve biofilms formed by two different P. aeruginosa strains by Crystal Violet (Fig. 3a) and also the colony-forming unit count (Extended Data Fig. 3b). Then, we characterized the antimicrobial properties of CV2_HA_P1 on four different P. aeruginosa strains. We found that CV2_HA_P1 inhibited the growth of PAO1 and showed moderate activity against NCTC13437 and BAA-2113 strains but not against the Boston 41501 strain (Fig. 3b and Extended Data Fig. 3c). To diversify the antimicrobial spectrum, we expressed pyocin S5 (ref. 55) instead of pyocin L1, which led to growth inhibition of the P. aeruginosa Boston strain (Extended Data Fig. 4a).
These results demonstrated that (1) the strain CV2_HA_P1 displayed both antibiofilm and antimicrobial activities against P. aeruginosa and (2) the antimicrobial activity of the engineered M. pneumoniae can be modulated to act against specific P. aeruginosa strains by introducing different antimicrobial pyocins.
Effects of CV2_HA_P1 in ETTs from VAP patients
As M. pneumoniae lacks a cell wall, we speculated that it could be used in combination with antibiotics targeting the peptidoglycans of the cell wall of both Gram-positive and Gram-negative bacteria. To test this hypothesis, we evaluated the effect on the growth of M. pneumoniae and different P. aeruginosa strains of antibiotics commonly used in clinics (Table 2 and Extended Data Fig. 4b). As expected, we found that no antibiotics that target the cell wall killed the CV2_HA strain, whereas all the antibiotics were active against most P. aeruginosa strains (Table 2). Of note, although the antibiotics did not dissolve P. aeruginosa biofilms to any significant degree, incubation with the CV2_HA_P1 strain effectively dissolved the biofilm (Extended Data Fig. 4c).
To evaluate the efficacy of our CV2_HA_P1 strain in dissolving in vivo-formed biofilms, we treated sections of ETTs obtained from VAP patients receiving mechanical ventilation in the ICU (see Methods). After a median of 11 d of MV, P. aeruginosa biofilms were observed on the ETTs, with bacterial loads of approximately 2.57 (2.20–4.81) log10(c.f.u. ml−1). The P. aeruginosa strains in the ETTs showed resistance to meropenem (100%), imipenem (100%), aztreonam (100%), amikacin (66%) and ciprofloxacin (33%), but were susceptible to colistin, piperacillin/tazobactam, tobramycin and ceftazidime. Multilocus sequence-type analysis of P. aeruginosa identified the ST109 and ST259 strains, which are allocated to the clonal complexes 253 and 2044. Complex 253 was previously identified from patients on the ICU65 and the complex 2044 was found in patients with bronchiectasis.
We included 14 of the 16 ETT sections in the final analysis, distributed as follows in each treatment group: control (n = 3), ceftolozane/tazobactam (C/T) (n = 4), CV2_HA_P1 (n = 4) and CV2_HA_P1 + C/T (n = 3; Fig. 4a); the remaining two samples were discarded because no P. aeruginosa counts could be obtained due to overgrowth of Proteus spp. After a 24-h incubation, the P. aeruginosa load showed significant differences between the control and the treated groups (Fig. 4b): ETT biofilms treated with antibiotics reduced the P. aeruginosa load and this reduction was even more substantial with the CV2_HA_P1 alone or in combination with the C/T antibiotics. These results demonstrate that CV2_HA_P1 has broad-spectrum activity against biofilms formed by different multidrug-resistant P. aeruginosa clinical strains.
Efficacy of CV2_HA_P1 in a murine lung infection model
To study the efficacy of CV2_HA_P1 in vivo, we first tested its toxicity by inoculating mice with 1 × 108 c.f.u. and analyzing lungs at 2, 14 and 45 d.p.i. by histopathology and cytokine measurement (Extended Data Fig. 5 and Supplementary Tables 5 and 6).
At 2 d.p.i., the same bacterial load was recovered in lungs of WT and CV2_HA_P1 strains; however, the CV2_HA_P1 lungs showed significantly fewer alterations compared with the WT group (P < 0.05). At 14 and 45 d.p.i., no colony-forming units were detected in CV2_HA_P1 lungs and the total score of the histopathology was not significantly different from the PBS controls; in stark contrast, WT infected lungs still presented tissue lesions (Extended Data Fig. 5a–c and Supplementary Table 5). Study of inflammation markers corroborated the resolution of lesions and the attenuation of the engineered CV2_HA_P1 strain (Extended Data Fig. 5d and Supplementary Table 6).
Next, we established a murine model of acute lung infection using PAO1. We immunosuppressed mice with cyclophosphamide and inoculated i.t. different amounts of the P. aeruginosa PAO1 strain (n = 8 mice for each group). Mouse survival, body weight and clinical conditions were assessed at different time points (Extended Data Fig. 6a–d). Mice infected with doses >1 × 104 c.f.u. had to be sacrificed or died at 12 h post-inoculation (h.p.i.); mice infected with 5 × 103 and 1 × 104 c.f.u. survive until 18 h.p.i. (Extended Data Fig. 6b), at which point the clinical score was 4 (Extended Data Fig. 6c; see Methods), and mice infected with 1 × 103 c.f.u. survived until 24 h.p.i. with a final clinical score of 2 and died by 48 h.p.i. Based on these results, we decided to use an inoculum of 1 × 103 c.f.u. per mouse of PAO1, which ensured lung colonization of the infected mice without treatment and survival for a longer period, thereby allowing the therapeutic effect of our chassis to be monitored.
Next, we studied the efficacy of CV2_HA_P1 in reducing the PAO1 load in the established lung infection model (Fig. 5a). We infected mice with the PAO1 strain, 1 × 103 c.f.u. per mouse (as described above), and treated them at 2 h.p.i. with different amounts (1 × 107 or 1 × 108 c.f.u.) of CV2_HA_P1, CV2 or PBS. All mice in the groups survived to 26 h.p.i., at which point they showed decreased body weight and clinical score 2, but no other signs of clinical deterioration. After sacrifice at 26 h.p.i., we counted the bacterial burden in the lungs. CV2 and CV2_HA_P1 colony-forming units were detected in the lungs (Extended Data Fig. 7), indicating that M. pneumoniae can colonize the lungs in the presence of a more severe pathogenic bacterium such as P. aeruginosa. The mean burden of PAO1 in the PBS control was 1 × 106 c.f.u. per g of lung tissue. Mice treated with CV2_HA_P1 at 1 × 108 c.f.u. had a significant reduction in the PAO1 load in the lungs compared with the PBS or CV2 control (reduction of 3.65log10 and 4.39log10, respectively; Fig. 5b). CV2 did not significantly reduce the PAO1 burden in the lungs compared with vehicle or pretreatment control groups at any time. We also studied the histopathology of the lungs at this timepoint. In agreement with the reduction of the PAO1 load, we observed that the total score of lung lesions was significantly lower in the lungs of mice treated with CV2_HA_P1 compared with the controls (Fig. 5c), with less perivascular inflammation and markedly less parenchymal pneumonia. Inflammation markers were also reduced in the lungs of CV2_HA_P1 mice compared with the CV2 group (Fig. 5d). These data indicated that CV2_HA_P1 treatment reduced the PAO1 lung infection in an in vivo model of acute pneumonia.
To study the effect of the CV2_HA_P1 therapy beyond 26 h.p.i., we next analyzed the survival of the mice over days after infection with PAO1 (Fig. 5e). About 50% of mice infected with PAO1 and treated with CV2_HA_P1 survived up to 8 d.p.i. (with a median of 7 d.p.i.), whereas mice treated with the CV2 or PBS control had a median survival of 2 d.p.i. Moreover, histology of mice with PAO1 infection that survived to the 8-d.p.i. timepoint revealed substantially fewer lung alterations in the CV2_HA_P1 group than in the CV2 or PBS control groups (Fig. 5f). These data indicated that CV2_HA_P1 treatment reduced PAO1 lung infection and increased mouse survival.
We also studied the efficacy of CV2_HA_P1 as a prophylactic treatment against PAO1 infection (Extended Data Fig. 8a). We inoculated mice with a mix of M. pneumoniae (WT_HA_P1 or CV2_HA_P1; doses 1 × 105 or 1 × 107 c.f.u., respectively) and PAO1, and we studied the progression of PAO1 infection up to 8 d.p.i. M. pneumoniae colony-forming units in the lungs were recovered from all groups (Extended Data Fig. 8b). PAO1 colony-forming units were significantly reduced in the lungs of mice treated with 1 × 107 c.f.u. of WT_HA_P1 or CV2_HA_P1 strains compared with nontreated control mice (Extended Data Fig. 8c).
Taken together, these results demonstrated that our engineered M. pneumoniae strain CV2_HA_P1 was efficient in treating acute PAO1 infections in a mouse model.
Lung infections, one of the major causes of human mortality, represent an untapped target for bacterial therapeutics. In the present study, we have shown that an engineered strain of the genome-reduced human lung bacterium M. pneumoniae (CV2) is attenuated in the lung and can be used to treat respiratory diseases associated with biofilm formation, such as VAP. The CV2 strain produces mild lesions in the acute phase of the lung infection that are resolved, avoiding chronic damage to the lung tissue, having an attenuated inflammation response and being removed spontaneously from the mouse lung after 4 d.p.i.
To demonstrate the potential use of our chassis to treat infectious lung diseases, we introduced genes to dissolve biofilms made by P. aeruginosa and to kill this bacterium. The biofilm matrix of P. aeruginosa PAO1 comprises DNA, proteins and the polysaccharides Pel and Psl54,55,56; alginate is also a main component of the biofilm of mucoid P. aeruginosa strains12,56. PelAh and PslGh have been reported as optimal enzymes for degradation of Pel and Psl exopolysaccharides, respectively55,64. The alginate lyase enzyme AI-II′, with both poly(M) and poly(G) activities, is effective against biofilms of P. aeruginosa mucoid strains56. We found that the strain expressing the three enzymes (CV2_HA) was effective in dissolving biofilms formed by different mucoid strains of P. aeruginosa. As it was previously reported that combining dispersal and antimicrobial activities could enhance biofilm degradation56,62, we engineered M. pneumoniae to express active pyocin L1 and pyocin S5. Both pyocins were active and specific for the target strains. We decided to use the M. pneumoniae strain expressing pyocin L1 (CV2_HA_P1), which proved to have an effective antimicrobial activity against P. aeruginosa PAO1 infection (which we used in the in vivo mouse infection model). We demonstrated the efficacy of our CV2_HA_P1 strain in dissolving biofilms on ETTs from patients in ICU who had received MV for long periods. We also observed that we could rescue the efficacy of standard-of-care antibiotics that were not efficient because of biofilm when combined with CV2_HA_P1, which opens the way for synergistic combinations.
In a mouse model of acute P. aeruginosa PAO1 infection, CV2_HA_P1 treatment eliminated the infection at 26 h.p.i. and increased the survival rate of the treated mice. No adverse clinical symptoms were observed related to body weight loss, fever, piloerection or respiratory distress, suggesting that treatment with CV2_HA_P1 at a high single dose was effective without toxicity for up to 8 d.p.i. In addition, CV2_HA_P1 showed a prophylactic effect against P. aeruginosa biofilm in vivo, expanding its potential clinical applications.
In conclusion, we have provided evidence that a lung biotherapeutic bacterial strain is effective against biofilm-associated infections in the respiratory tract. We envision that our CV2 chassis could be adapted for the treatment of other infectious and noninfectious lung diseases that require continuous local delivery of therapeutic molecules.
Medium and strain growth conditions
Liquid Hayflick complete medium was prepared by mixing 800 ml of noncomplete medium A (20 g of PPLO broth (Difco, catalog no. 255420), 30 g of Hepes (100 mM final), 25 ml of 0.5% phenol red solution (Sigma-Aldrich, catalog no. P3532)), 200 ml of heat-inactivated horse serum (Life Technologies, catalog no. 26050088), 20 ml of sterile filtered 50% glucose and 1 ml of a 100-mg ml–1 stock of ampicillin (final concentration 100 µg ml–1, ampicillin sodium salt; Sigma-Alrich, catalog no. A9518). Solid Hayflick 1% agar plates were prepared by mixing 800 ml of noncomplete medium A with 10 g of Bacto Agar (BD, catalog no. 214010) and adding 200 ml of heat-inactivated horse serum, 20 ml of sterile filtered 50% glucose and 1 ml of a 100-mg ml–1 stock of ampicillin (final concentration 100 µg ml–1).
For P. aeruginosa growth curves, strains were grown overnight in Tryptic Soy Broth (TSB) medium at 37 °C with shaking. The next day, the cultures were diluted in TSB to absorbance at 600 nm (OD600) = 0.1, and 200 µl was added to 96-well plates and grown at 37 °C with shaking in a TECAN plate reader. Growth was measured as an increase in OD600, with values taken every 20 min up to 48 h. For M. pneumoniae growth curves, strains were inoculated in Hayflick medium in a T75-cm2 flask and grown at 37 °C. After 3 d, cells were scraped from the flasks and resuspended in 1 ml of Hayflick medium. The cell suspension was then diluted 1:200 and 200 µl of this suspension was added to 96-well plates and incubated on static conditions at 37 °C in a TECAN plate reader. Growth was measured as an increase of the ratio between absorbance at 430 nm and 560 nm, with values at 430 nm and 560 nm taken every 2 h for 4 d.
All plasmids generated in this work were assembled following the Gibson method63. When required, IDT Incorporation performed gene synthesis. Oligonucleotides were synthesized by Sigma-Aldrich. Gene amplifications were carried out with Phusion DNA polymerase (Thermo Fisher Scientific). A description of the plasmids is available in Supplementary Table 3. The final sequence of all the plasmids was checked by Sanger sequencing (Eurofins Genomics).
Generation of M. pneumoniae mutant strains
The mutant strain Δmpn453 and CV2 (double mutant carrying deletions in both mpn133 and mpn372) genes were constructed in previous work62. M. pneumoniae strains with genetic platforms were generated by transforming the CV2 and WT strains with vectors described in Supplementary Table 3 by electroporation. After pulsing, cells were selected in T75-cm2 flasks containing 25 ml of plain Hayflick medium with selective antibiotics (tetracycline, 2 μg ml–1, gentamicin, 100 μg ml–1, or chloramphenicol, 20 μg ml–1).
Protein quantification by MS
For the proteome samples of different mutant strains, M. pneumoniae strains were grown to the exponential phase of growth. After a medium sample of 2 ml was removed, cells were washed 3× with PBS and collected in 1 ml of PBS by scraping. Cell samples were centrifuged at 14,000g for 15 min and the pellet was resuspended in 50 µl of 6 M urea (in 200 mM ammonium bicarbonate). The medium samples were centrifuged at 14,000g and then passed over a 0.1-μm filter. The 800-μl sample was concentrated to 50 μl using 3K MWCO columns, and 75 μl of urea in 200 mM ammonium bicarbonate was added to a final concentration of 6 M urea. After 15 min of sonication, all samples were quantified using bicinchoninic acid and then processed for MS. Samples were analyzed by tandem MS combined with liquid chromatography. Briefly, in solution digestion samples were reduced with dithiothreitol (30 nmol, 1 h, 37 °C) and alkylated in the dark with iodoacetamide (60 nmol, 30 min, 25 °C). The resulting protein extract was first diluted 1:3 with 200 mM NH4HCO3 and digested with 1 µg of LysC (Wako, catalog no. 129–02541) overnight at 37 °C and then diluted 1:2 and digested with 1 µg of trypsin (Promega, catalog no. V5113) for 8 h at 37 °C. The tryptic peptides were then first acidified and desalted with a MicroSpin C18 column (The Nest Group, Inc.). Samples were analyzed using an LTQ-Orbitrap Velos Pro mass spectrometer coupled to an EASY-nLC 1000 (Thermo Fisher Scientific). The sample was loaded on to the 2-cm Nano Trap column (inner diameter 100 μm, 5-μm C18 particles; Thermo Fisher Scientific) and separated by reversed-phase chromatography using a 25-cm column (inner diameter 75 μm, 1.9-μm C18 particles; Nikkyo Technos Co., Ltd.). Chromatographic gradients started at 93% buffer A and 7% buffer B with a flow rate of 250 nl min−1 for 5 min and gradually increased to 65% buffer A and 35% buffer B in 120 min. After each analysis, the column was washed for 15 min with 10% buffer A and 90% buffer B. Buffer A is 0.1% formic acid in water and buffer B 0.1% formic acid in acetonitrile. The mass spectrometer was operated in positive ionization mode with nanospray voltage set at 2.1 kV and source temperature at 300 °C. Before the analysis, we performed external calibration of the Fourier transform with Ultramark 1621 and internal calibration with the ion signal of the poly(siloxane) background (m/z 445.1200). For the MS scans, the data-dependent acquisition (DDA) mode was set at a resolution of 60,000, m/z range 350–2,000 and detected in the Orbitrap (automatic gain control (AGC) = 1 × 106 and dynamic exclusion of 60 s). The top 20 most intense ions were selected for collision-induced dissociation fragmentation with normalized collision energy of 35% in each cycle of DDA analysis. For the injection, we selected AGC to 1 × 104, 2.0-m/z isolation window, 10 ms of activation time and 100 ms of maximum injection time. Xcalibur software v.2.2 was used for data acquisition. To eliminate sample residues and ensure the stability of the equipment, we analyzed digested bovine serum albumin (New England Biolabs) between samples66. Proteome Discoverer (Thermo Fisher Scientific) software and Mascot67 and search engine (Matrix Science) were used for the analysis of the acquired spectra. The data were searched against an M. pneumoniae database plus a list of common contaminants68 (87,070 entries) and all the corresponding decoy entries. A precursor ion mass tolerance of 7 p.p.m. was used for MS1 level for peptide identification, using trypsin as the enzyme and allowing up to three missed cleavages. For MS2 spectra, ion mass tolerance was established at 0.5. We used oxidation of the methionine and amino-terminal protein acetylation as variable modifications, and carbamidomethylation on cysteine as a fixed modification. The false discovery rate in peptide identification was set to a maximum of 5%.
The ‘precursor ion area detector’ node from Proteome Discoverer (v.2.0) was used for peptide quantification. The obtained values were used to calculate the protein top three areas with the unique peptide for protein ungrouped (Supplementary Table 4). The raw proteomics data have been deposited to the PRIDE69 repository with the accession no. PXD037233.
In vitro biofilm degradation assay
M. pneumoniae was grown in a T25-cm2 flask for 3 d with 5 ml of Hayflick medium without antibiotics and then the conditioned supernatant was filtered with 0.33-µm sterile syringe filters. P. aeruginosa strains were grown overnight in Erlenmeyer flasks (20 µl stock in 20 ml of TSB) at 37 °C on shaking at 600 r.p.m., and then diluted to an OD600 of 0.15 in TSB. Diluted Pseudomonas culture (100 µl) was then added in triplicate to sterile 96-well, polystyrene microtiter plates. Cells were incubated statically at 37 °C for 24 h to allow for biofilm formation. Biofilms were washed with PBS the following day to remove nonadherent cells and TSB medium. Treatments of 50–100 µl of M. pneumoniae-conditioned filtered medium were added to the wells (using triplicates or more) and plates were incubated at 37 °C for 4 h. After incubation, wells were washed with PBS, stained with 150 µl of 0.1% (w:v in water) Crystal Violet (Sigma-Aldrich) for 10 min, or with 150 µl of 0.1% (w:v in 3% acetic acid) Alcian Blue (Sigma-Aldrich), and washed 3× with PBS. The dye was solubilized by addition of 100 μl of 95% (v:v) ethanol and incubated for 10 min. Absorbance was measured at 595 nm (for Crystal Violet) or 620 nm (for Alcian Blue) using a TECAN plate reader.
To measure the impact of M. pneumoniae supernatants on the number of PAO1 cells, biofilms were formed in 96-well plate and treated as described above. After incubation, supernatants were removed and the attached cells were recovered in 200 µl of PBS, serially diluted, seeded on Pseudomonas agar plates and incubated at 37 °C for 24 h. The colony-forming units were counted in two independent experiments with three technical triplicates each.
In vitro antimicrobial activity test
The antimicrobial activities of the supernatant of M. pneumoniae strains expressing pyocins were tested in a growth curve. M. pneumoniae was grown in a T25-cm2 flask to confluence (3–4 d at 37 °C, 5% CO2) with 5 ml of Hayflick medium without antibiotics, and then the supernatant medium was filtered with 0.33-µm sterile syringe filters. P. aeruginosa strains were grown overnight in Erlenmeyer flasks (20 µl of stock in 20 ml of TSB) at 37 °C with shaking and then diluted to an OD600 of 0.1 in TSB. Diluted Pseudomonas culture (180 µl) was mixed with 20 µl of filtered M. pneumoniae supernatant into sterile, 96-well, polystyrene microtiter plates. All conditions were tested at least in triplicate. Plates were incubated in a TECAN reader at 37 °C with shaking and the OD600 was measured every 20 min.
The animals used in all the studies were CD1 mice (female and male, weight 18–22 g and aged 4–6 weeks), purchased from Charles River Laboratories, and specific pathogen free. Group animal size were computed with G*Power software. The number of animals used in each experiment is specified in the figure legends.
The experiments, aimed to set up the routes of administration, the M. pneumoniae doses and the CV2 strain safety, were performed either at the Institute of Agrobiotechnology facilities (registration no. ES/31-2016-000002-CR-SU-US) or at the Barcelona Biomedical Research Parc (PRBB) facilities (registration no. B9900073). All the procedures involving animals were legislated for by the European Directive 86/609/EEC and the National law (Real Decreto 53/2013), in accordance with the FELASA and ARRIVE guidelines and the agreement of the Universidad Pública de Navarra (UPNa), the PRBB Animal Experimentation Committee (Comité de Ética, Experimentación Animal y Bioseguridad) and the local government authorization. The experiments aimed at studying the efficacy in vivo were performed in the UK under the Home Office Licence PA67E0BAA with local ethical committee clearance (Animal Welfare and Ethical Review Body). All the experiments were performed in dedicated Biohazard 2 facilities (this site holds a Certificate of Designation). On receipt at the facility, animals were housed in sterilized, individually ventilated cages connected to HEPA (high-efficiency particulate absorbing)-filtered sterile air and allowed to acclimatize for at least 7 d. Mice always had free access to food and water (sterile) and aspen chip bedding. The room temperature was 22 °C ± 1 °C, with a relative humidity of 60% and maximum background noise of 56 dB. Mice were exposed to 12:12 h light:dark cycles. Mice were monitored at least once daily for their clinical condition and assessed for their clinical score. The clinical score was given as follows: 1 = no deterioration in clinical condition, may include slight piloerection, normal activity; 2 = slight piloerection, slightly hunched, dehydrated, weight loss <20%; 3 = piloerection, moderate intermittent hunching, dehydrated, weight loss <20%, orbital tightening/eye discharge, irregular breathing, slightly reduced mobility, slightly reduced activity, sides pinched in, slight drop in temperature: animal can continue on study but should be monitored closely; 4 = piloerection, moderate persistent hunching for up to 1 h, dehydrated, weight loss >20%, orbital tightening/eye discharge, reduced breathing rate, increased breathing depth, subdued, reduced activity, cold to touch, pale in color: animal has reached moderate endpoint and should be euthanized.
To prepare cell suspension for the inoculations, M. pneumoniae strains were grown in a T75 culture flask (Sarstedt) with Hayflick-ampicillin 100 µg ml−1 (H-Amp100) broth (37 °C, 3–4 d, 5% CO2). After washing, cells were scraped with PBS and passed through a syringe (25G). Appropriate suspensions (c.f.u. µl−1 indicated in each experiment) were prepared and an aliquot was plated on H-Amp100 agar to assess bacterial counts. P. aeruginosa PAO1 was grown overnight in TSB broth at 37 °C on shaking and diluted with PBS to an optimal concentration. For the efficacy studies, mice were rendered neutropenic with two subcutaneous injections of cyclophosphamide: 150 mg kg–1 at 4 d before PAO1 infection and 100 mg kg–1 at 1 d before PAO1 infection. Before inoculation with M. pneumoniae or PAO1, mice were anesthetized with isoflurane 2% (ISOFLO, Covegan). Intratracheal inoculation was performed by introducing 100 µl of cell suspension through a sterile 20G (1.1-mm diameter) Vialon intravenous catheter (Becton-Dickinson) inserted into the trachea. Intranasal inoculation was performed by pipetting 20 µl of cell suspension into both nostrils (total volume was 40 µl). Mice were then released into their cages and monitored until they regained consciousness.
Mice were necropsied at 2, 14 and 45 d.p.i. Lungs were collected and processed for histological studies according to Morton and Snider65. Briefly, lungs were insufflated with 10% formalin through the trachea in situ and then removed and fixed in formalin for 24 h for histological analysis.
For RNA extraction, lungs were sectioned and immediately frozen in liquid nitrogen and stored at –80 °C until use. When required, BALF samples were obtained by intratracheal perfusion and harvesting of 0.7 ml of PBS pe rmouse, with a sterile 20G Vialon catheter.
For bacteriological analysis, lung and BALF samples were serially tenfold diluted in sterile PBS and plated by triplicate to determine the number of viable bacteria on Hayflick-ampicillin agar (for M. pneumoniae) or Pseudomonas agar (Oxoid, for P. aeruginosa). Plates were incubated at 37 °C for 14 d (for M. pneumoniae) or 16–24 h (for P. aeruginosa), and then colonies were counted using a Leica Zoom 2000 plate microscope at ×10 magnification.
Lung RNA extraction and RT–qPCR analysis
Lungs previously stored at –80 °C were homogenized using Ultra-Turrax (IKA) and total RNA was isolated using RNeasy Mini Kit (QIAGEN), following the manufacturer’s instructions. RNA concentrations were measured spectrophotometrically using Nanodrop One (Thermo Fisher Scientific), and sample RNA integrity was confirmed by 1% agarose gel electrophoresis. RNA samples with the ratio of absorbance at 260 nm:280 nm of 1.8–2.1 were used. Complementary DNA from whole lung cells was synthesized from total RNA (1 μg) using SuperScript II Reverse Transcriptase reagents (Invitrogen). PCR amplification was performed using SYBR Premix Ex Taq II (Tli RNaseH Plus; Takara) and fluorescence was analyzed with AriaMx Real-Time PCR System (Agilent Technologies). The comparative threshold cycle (Ct) method70 was used to obtain relative quantities of messenger RNAs that were normalized using gapdh as an endogenous control. Primer sequences for the genes tnf, il1b, il6, il12a, il23a, ifng, ccl2, ccl3, cxcl1 and gapdh are shown in Supplementary Table 7.
Histopathological analysis of lung samples
After necropsy, lung samples were insufflated with formalin, fixed for at least 24 h, trimmed and then automatically processed in ethanol series and xylene substitute (Citadel 2000 Tissue Processor, Thermo Fisher Scientific). Thereafter, tissues were embedded in paraffin (HistoStar Embedding Workstation, Thermo Fisher Scientific), sectioned at 4 μm (Finesse ME + Microtome, Thermo Fisher Scientific), stained with haematoxylin and eosin (H&E) (Gemini AS Automated Slide Stainer, Thermo Fisher Scientific) and mounted on glass slides (CTM6 Coverslipper Thermo Fisher Scientific). For light microscopy analysis, histological images were obtained using a digital camera (MC170 HD, Leica) connected to an optical microscope (DM2000, Leica) using a commercial software (Leica Application Suite, v.4.6.0). Sections were examined blind as sets by a trained veterinary pathologist and lesions were scored based on five parameters: (A) peribronchial/peribronchiolar inflammatory infiltrate affectation (0, none; 1, <25%; 2, 25–75%, 3, >75%); (B) peribronchial/peribronchiolar inflammatory infiltrate intensity (0, none; 1, incomplete infiltration; 2, complete infiltration, <5 cells thick; 3, complete infiltration, ≥5 cells thick); (C) bronchial/bronchiolar luminal exudate intensity (0, none; 1, <25% of lumen occlusion; 2, >25% of lumen occlusion); (D) perivascular inflammatory infiltrate affectation (0, none; 1, <10%; 2, 10–50%; 3, >50%); and (E) interstitial pneumonia intensity (0, none; 3, multifocal foci of interstitial pneumonia; 5, multifocal-coalescing foci to diffuse interstitial pneumonia). According to previous studies62,63, a final score (0–26) was obtained with the formula A + (3 × (B + C)) + D + E.
Dispersal of ETT biofilms from patients
ETTs from patients receiving MV were collected from September 2015 to December 2017. They were selected from patients with a positive respiratory culture for P. aeruginosa during intubation, ventilated over 11 (6.00–16.50) d and in the confirmed presence of P. aeruginosa in ETTs (2.57 (2.20–4.81) log10(c.f.u. ml–1)) at extubation of the patient. ETTs were frozen until analysis, in a collection carried out in compliance with the Declaration of Helsinki (current version, Fortaleza, Brazil, October 2013). The collection was approved by the institution’s internal review board (Ethical Committee for Research in Medicines, Hospital Clinic of Barcelona, Spain), with the registry no. R190311-203;HCB/2019/026. Afterwards, ETTs were slowly unfrozen to room temperature and sliced into the following sections with different treatments: control (Hayflick medium alone without treatment); CV2_HA_PL1 (~1 × 108 log(c.f.u. ml–1)), C/T (Zerbaxa 1 g per 0.5 g powder, 5 µg ml–1) and CV2_HA_P1 + C/T. The CV2_HA_P1 inoculum contained 7.32 (8.26–9.20) log(c.f.u. ml–1) (Fig. 4a)71.
Each ETT section and treatment condition were adjusted to a final volume of 1,600 µl with Hayflick medium and incubated at 37 °C for 24 h. Before diluting (–1 to –5(log10)) and culturing on MacConkey and blood agar (Becton-Dickinson GmbH), samples were sonicated for 5 min at 40 kHz in ultrasound-cleaning equipment (Branson 3510 E-MT; Bransonic) as previously published71. P. aeruginosa counts in each treatment were reported in log10(c.f.u. ml–1). A complete antibiogram (amikacin, colistin, piperacillin/tazobactam, aztreonam, tobramycin, ceftazidime, meropenem or imipenem) was performed for each P. aeruginosa strain using the Kirby–Bauer method, with the P. aeruginosa American Type Culture Collection 27853 strain as a control. The interpretation of results was carried out according to the European Committee on Antimicrobial Susceptibility Testing. P. aeruginosa was considered to be multidrug resistant when nonsusceptible to three or more families of antipseudomonal antimicrobials72. In addition, molecular epidemiology was analyzed by multilocus sequence typing (https://pubmlst.org/paeruginosa). Phylogenetic analysis was carried out using the eBURST algorithm (http://www.phyloviz.net/goeburst).
Categorical variables were reported as number (%), whereas continuous variables were reported as mean ± s.d. or median (interquartile range (IQR)), if the distribution was normal or non-normal, respectively. Continuous variables between groups were compared using the one-way analysis of variance (ANOVA) followed by a post-hoc, pairwise Tukey’s honestly significant difference (HSD) or a Kruskal–Wallis test, as appropriate. Paired samples were compared using the paired Student’s t-test or nonparametric Wilcoxon’s signed-rank test when appropriate. Spearman’s correlation analyses were performed to determine associations between continuous variables. In all the cases, P ≤ 0.05 was considered to be statistically significant and the exact P value is specified in figure legends when possible. Data were analyzed using StatsDirect software (v.3.1.8) or GraphPad Prism (v.8.0.1).
Further information on research design is available in the Nature Portfolio Reporting Summary linked to this article.
The MS dataset has been submitted to the public data repository PRIDE (PRoteomics IDEntifications database) with the following accession no.: PXD037233.
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This work was supported by the European Research Council under the European Union’s Horizon 2020 research and innovation program, under grant agreement no. 670216 (MYCOCHASSIS). We thank the Spanish Ministry of Economy, Industry and Competitiveness to the EMBL partnership, the Centro de Excelencia Severo Ochoa and the CERCA Program from the Generalitat de Catalunya, the European Union’s Horizon 2020 Research and Innovation Programme, grant no. 634942 (MycoSynVac), La Caixa Health (HR18-00058), CB 06/06/0028/CIBER de enfermedades respiratorias-Ciberes and ICREA Academy/Institució Catalana de Recerca i Estudis Avançats, 2.603/IDIBAPS, SGR/Generalitat de Catalunya for their support. M.L.-S. thanks the funder Instituto de Salud Carlos III (ISCIII, Acción Estratégica en Salud 2016, FEDER project, reference CP16/00094) for support of the research of this work. We also thank the staff of the CRG/UPF Proteomics Unit, which is part of the Spanish Infrastructure for Omics Technologies unit and a member of the ProteoRed PRB3 consortium, supported by grant no. PT17/0019 of the PE I+D+i 2013–2016 from the ISCIII and European Regional Development Fund.
The results published in this article are covered by patents US10745450B2, EP3262061A1 and PCT/EP2021/057122 (licensed to Pulmobiotics S.L) and PCT/EP2021/059142. L.S. and M.L. are shareholders of Pulmobiotics S.L.. R.M., C.P. and M.L. are employees and have stock options of Pulmobiotics S.L. The remaining authors declare no competing interests.
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Extended Data Fig. 1 Delivery route and lung infection dynamic of M. pneumoniae WT and mutant strains generated in this study.
a, CFUs per lung (left) or BALF (right) in CD1 mice infected using the same dose (~1× 107 CFU/mice), by intranasal (IN, 20 µl. Five animals) or intratracheal (IT, 100 µl. Six animals) administration. Mice were euthanized at 2 days post-infection (dpi) to determine bacterial load in lungs (left panel, log10 CFU/lung) and in BALF (right panel, log10 CFU/lung or BALF). Data are expressed as mean ± standard deviation (SD). Statistical comparison was performed using two-sided t-test. *P = 0.032. b, The WTΔmpn453 mutant strain is eliminated faster than the WT strain. Two-sided t-test was used (*P = 0.04 and P = 0.02). Data are expressed as mean ± standard deviation (SD). c, Lung infection dynamics of M. pneumoniae WT and CV2 chassis strains. Bacterial counts were obtained at 2 dpi (n = 15), 4 dpi (n = 15) or 14 dpi (n = 3) for both strains. Data are shown as means values ± SD of log10 CFU/lung. Statistical comparisons were performed using two-sided t-test. *P < 0.05. Red line, experimental detection limit (log10 CFU/lung = 0.7–0.9). Infections were performed in all cases in groups of at least five mice per strain and/or time point (n ≥ 5).
Extended Data Fig. 2 Analysis of the lungs of the animals inoculated with WT or CV2.
a, CFUs of the strains WT or CV2, at 2 or 14 days post-inoculation (dpi), found in three major lung lobes (RCr,right cranial; RM, right medium; and L, left. N = 3 animals per group). LOD = limit of detection. Data are expressed as mean ± SD. b, Scoring of the individual parameters analyzed in the histopathologic study of lung sections from mice inoculated with PBS, WT or CV2, analysed at 2, 14 or 45 dpi. See Methods for a detailed description of the histopathological scoring system used. Data are presented as mean values ± SD. Statistical comparisons were performed with One-way ANOVA + Tukey’s multiple comparison test; *P < 0.05. c, Pulmonary inflammatory response to M pneumoniae is independent of il1b, il6, il-12a or il23a. Gene expression was analysed by RT-qPCR at 2-, 4- and 45 dpi from lungs inoculated with PBS or with WT or CV2 M. pneumoniae strains. Data are presented as mean values ± SD. Each animal is represented as an individual plot (At 2 dpi: PBS n = 4; CV2 n = 5; CV2_HA_P1 n = 4; at 14 dpi, PBS n = 5; CV2 n = 4; CV2_HA_P1 n = 4 M; at 45 dpi: PBS n = 2; CV2 n = 4; CV2_HA_P1 n = 4).
Extended Data Fig. 3 Effect of CV2_HA on P. aeruginosa PAO1 biofilm and growth.
a, Dispersal activity of CV2_HA on PAO1 biofilm, quantified after staining with crystal violet or Alcian blue. Pseudomonas biofilms were generated by seeding in 96-well plates and incubating at 37 °C for 24 h. Biofilms were then treated at 37 °C for 4 h with M. pneumoniae CV2_HA supernatants, to allow the activity of the dispersal enzymes. The remaining biofilm was stained with crystal violet or Alcian blue and quantified with a plate reader at the indicated absorbances (OD 595 or OD 620). Three independent experiments performed. Data are presented as mean values ± SD. **P = 0.009 and P = 0.007, two-sided t-test. b. Activity of CV2_HA_P1 on PAO1 biofilm, quantified as CFUs/ml. Pseudomonas biofilms were generated by seeding in 96-well plates and incubating at 37 °C for 24 h. Biofilms were then treated at 37 °C for 4 h with the indicated supernatants, and then the remaining biofilm was resuspended in PBS and seeded on Pseudomonas agar plates. Three independent experiments performed. Data are presented as mean values ± SD. ***P < 0.001, two-sided t-test. c, Growth curves of P. aeruginosa strain PAO1 in presence of supernatant from CV2, CV2_HA or CV2_HA_P1. Results from triplicate samples are shown. Data are presented as mean values ± SD. Details of the assay are given in the Methods.
Extended Data Fig. 4 Study of effect of antibiotics on growth curves and biofilms formation.
a, Effect of treatment with the WT M. pneumoniae strain expressing pyocin L1 or pyocin S5 on the growth of the P. aeruginosa Boston 41501 strain. b, Growth curves of CV2 and different P. aeruginosa strains (SAT290, PAO1 or C117) in the presence of different doses of the antibiotic combination piperacillin/tazobactam. Growth was measured by absorbance determination at OD 430/560 or OD 600. c, Crystal violet assay measuring P. aeruginosa SAT290 biofilm degradation using different antibiotics at different concentrations. Two independent experiments performed. Data are presented as mean values ± SD. **P = 0.004, two-sided t-test. No significant effects on biofilm degradation were observed as compared to the untreated control. Details of the assays are given in the Methods.
Extended Data Fig. 5 Tissue lesions and inflammatory response of lungs infected with M. pneumoniae WT and CV2_HA_P1 strain at 108 CFUs.
CD1 mice were inoculated intratracheally with M. pneumoniae CV2_HA_P1, WT or PBS (as control), and lungs were analysed at 2-, 14- and 45 dpi. a, CFUs of the strains WT or CV2_HA_P1, at 2, 14 or 45 days post-inoculation (dpi) recovered in lungs (n = 3, 2 and 2, respectively). b, Lung lesions evaluation, expressed as the total final score of the histological analysis performed on three major lobes, with five animals per group (each data point is the average of the total score of the Right Cranial, Right Middle and Left of each animal). Data are presented as mean values of each group ± SD. *P < 0.05; One-way ANOVA + Tukey’s multiple comparison test. For detailed description of the scoring system used in the histopathological analysis, see Methods. c, Representative H&E-stained lung sections (100⋅, scale bar 100 µm) from the left lobe, obtained using a digital camera (MC170 HD, Leica) connected to an optical microscope (DM2000, Leica) using a commercial software (Leica Application Suite, version 4.6.0). d, Gene expression of inflammatory markers, assessed by RT-qPCR. Data are shown as mean ± SD of 2-ΔΔCt. Each animal is indicated as an individual plot. Each animal is represented as an individual plot (PBS, n = 4; CV2, n = 3; CV2_HA_P1, n = 3). *P < 0.05, One-way ANOVA + Tukey’s multiple comparison test.
Extended Data Fig. 6 Set up of acute model of P. aeruginosa infection.
CD1 mice were IT infected with different amounts of P. aeruginosa PAO1 (1.0× 103, 5.3× 103, 1.1× 104, 2.0× 105 or 1.5× 106 CFU/mouse). a, Evaluation of body weight of mice infected with different doses of P. aeruginosa PAO1. b, Endpoints at which mice were euthanized by pentobarbitone overdose. c, Clinical score (see Methods) of the mice infected with different doses of P. aeruginosa PAO1 (Five animals per groups. Data are presented as mean values ± SD.). d, Number of CFUs recovered from the lung of mice after inoculation with different doses of PAO1 at different time points post-inoculation (2, 8 or 18 hpi. N = two or four animals per group, as indicated by the data points). LOD = Limit of detection.
Extended Data Fig. 7 M. pneumoniae CFUs detected in lungs of animals of the efficacy assays.
Number of CFUs of M. pneumoniae strains CV2 and CV2_HA_P1 strains (inoculated at 1× 107 or 1× 108 CFU/mouse) recovered from the lung at 24 hpi. Animals (n = 3 for CV2 controls, and n = 5 for CV2_HA_P1 group) were sacrificed and the lungs were homogenized and serial diluted on Hayflick-agar plates. Data are presented as mean values ± SD.
Extended Data Fig. 8 Preventive effect of CV2_HA_P1 on pneumonia induced by PAO1.
a, Schematic representation of the experimental design. Two amounts (1× 105 or 1× 107 CFU) of different M. pneumoniae strains, alone or in combination with P. aeruginosa PAO1 cells, were inoculated intratracheally in the animals (five animals per group). After 8 h, mice were sacrificed, and lungs were homogenized and seeded on Hayflick agar plates to quantify the CFU of M. pneumoniae strains (in b) or seeded on Pseudomonas agar to quantify PAO1 (in c). *P < 0.05, ***P < 0.001; P values of Kruskal–Wallis H test compared to the control at 8 h are indicated.
Supplementary Tables 1–7
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Mazzolini, R., Rodríguez-Arce, I., Fernández-Barat, L. et al. Engineered live bacteria suppress Pseudomonas aeruginosa infection in mouse lung and dissolve endotracheal-tube biofilms. Nat Biotechnol (2023). https://doi.org/10.1038/s41587-022-01584-9
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