Priming with intranasal lactobacilli prevents Pseudomonas aeruginosa acute pneumonia in mice
Abstract Background Increasing resistance to antibiotics of Pseudomonas aeruginosa leads to therapeutic deadlock and alternative therapies are needed. We aimed to evaluate the effects of Lactobacillus clinical isolates in vivo, through intranasal administration on a murine model of Pseudomonas aerug...
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doaj-dd6379fad72d406abfae54d4de98078d2021-07-04T11:08:24ZengBMCBMC Microbiology1471-21802021-06-0121111110.1186/s12866-021-02254-7Priming with intranasal lactobacilli prevents Pseudomonas aeruginosa acute pneumonia in miceMarie-Sarah Fangous0Philippe Gosset1Nicolas Galakhoff2Stéphanie Gouriou3Charles-Antoine Guilloux4Christopher Payan5Sophie Vallet6Geneviève Héry-Arnaud7Rozenn Le Berre8Laboratoire de biologie médicale, Centre Hospitalier de CornouailleUniversity of Lille, CNRS UMR9017, Inserm U1019, CHRU Lille, Institut Pasteur de Lille, CIIL - Center for Infection and Immunity of Lille- OpInfIELDUniv Brest, Inserm, EFS, UMR 1078, GGBUniv Brest, Inserm, EFS, UMR 1078, GGBUniv Brest, Inserm, EFS, UMR 1078, GGBUniv Brest, Inserm, EFS, UMR 1078, GGBUniv Brest, Inserm, EFS, UMR 1078, GGBUniv Brest, Inserm, EFS, UMR 1078, GGBUniv Brest, Inserm, EFS, UMR 1078, GGBAbstract Background Increasing resistance to antibiotics of Pseudomonas aeruginosa leads to therapeutic deadlock and alternative therapies are needed. We aimed to evaluate the effects of Lactobacillus clinical isolates in vivo, through intranasal administration on a murine model of Pseudomonas aeruginosa pneumonia. Results We screened in vitro 50 pulmonary clinical isolates of Lactobacillus for their ability to decrease the synthesis of two QS dependent-virulence factors (elastase and pyocyanin) produced by Pseudomonas aeruginosa strain PAO1. Two blends of three Lactobacillus isolates were then tested in vivo: one with highly effective anti-PAO1 virulence factors properties (blend named L.rff for L. rhamnosus, two L. fermentum strains), and the second with no properties (blend named L.psb, for L. paracasei, L. salivarius and L. brevis). Each blend was administered intranasally to mice 18 h prior to PAO1 pulmonary infection. Animal survival, bacterial loads, cytological analysis, and cytokines secretion in the lungs were evaluated at 6 or 24 h post infection with PAO1. Intranasal priming with both lactobacilli blends significantly improved 7-day mice survival from 12% for the control PAO1 group to 71 and 100% for the two groups receiving L.rff and L.psb respectively. No mortality was observed for both control groups receiving either L.rff or L.psb. Additionally, the PAO1 lung clearance was significantly enhanced at 24 h. A 2-log and 4-log reduction was observed in the L.rff + PAO1 and L.psb + PAO1 groups respectively, compared to the control PAO1 group. Significant reductions in neutrophil recruitment and proinflammatory cytokine and chemokine secretion were observed after lactobacilli administration compared to saline solution, whereas IL-10 production was increased. Conclusions These results demonstrate that intranasal priming with lactobacilli acts as a prophylaxis, and avoids fatal complications caused by Pseudomonas aeruginosa pneumonia in mice. These results were independent of in vitro anti-Pseudomonas aeruginosa activity on QS-dependent virulence factors. Further experiments are required to identify the immune mechanism before initiating clinical trials.https://doi.org/10.1186/s12866-021-02254-7LactobacillusProbioticsIntranasal administrationPseudomonas aeruginosaRespiratory tract infectionMice |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marie-Sarah Fangous Philippe Gosset Nicolas Galakhoff Stéphanie Gouriou Charles-Antoine Guilloux Christopher Payan Sophie Vallet Geneviève Héry-Arnaud Rozenn Le Berre |
spellingShingle |
Marie-Sarah Fangous Philippe Gosset Nicolas Galakhoff Stéphanie Gouriou Charles-Antoine Guilloux Christopher Payan Sophie Vallet Geneviève Héry-Arnaud Rozenn Le Berre Priming with intranasal lactobacilli prevents Pseudomonas aeruginosa acute pneumonia in mice BMC Microbiology Lactobacillus Probiotics Intranasal administration Pseudomonas aeruginosa Respiratory tract infection Mice |
author_facet |
Marie-Sarah Fangous Philippe Gosset Nicolas Galakhoff Stéphanie Gouriou Charles-Antoine Guilloux Christopher Payan Sophie Vallet Geneviève Héry-Arnaud Rozenn Le Berre |
author_sort |
Marie-Sarah Fangous |
title |
Priming with intranasal lactobacilli prevents Pseudomonas aeruginosa acute pneumonia in mice |
title_short |
Priming with intranasal lactobacilli prevents Pseudomonas aeruginosa acute pneumonia in mice |
title_full |
Priming with intranasal lactobacilli prevents Pseudomonas aeruginosa acute pneumonia in mice |
title_fullStr |
Priming with intranasal lactobacilli prevents Pseudomonas aeruginosa acute pneumonia in mice |
title_full_unstemmed |
Priming with intranasal lactobacilli prevents Pseudomonas aeruginosa acute pneumonia in mice |
title_sort |
priming with intranasal lactobacilli prevents pseudomonas aeruginosa acute pneumonia in mice |
publisher |
BMC |
series |
BMC Microbiology |
issn |
1471-2180 |
publishDate |
2021-06-01 |
description |
Abstract Background Increasing resistance to antibiotics of Pseudomonas aeruginosa leads to therapeutic deadlock and alternative therapies are needed. We aimed to evaluate the effects of Lactobacillus clinical isolates in vivo, through intranasal administration on a murine model of Pseudomonas aeruginosa pneumonia. Results We screened in vitro 50 pulmonary clinical isolates of Lactobacillus for their ability to decrease the synthesis of two QS dependent-virulence factors (elastase and pyocyanin) produced by Pseudomonas aeruginosa strain PAO1. Two blends of three Lactobacillus isolates were then tested in vivo: one with highly effective anti-PAO1 virulence factors properties (blend named L.rff for L. rhamnosus, two L. fermentum strains), and the second with no properties (blend named L.psb, for L. paracasei, L. salivarius and L. brevis). Each blend was administered intranasally to mice 18 h prior to PAO1 pulmonary infection. Animal survival, bacterial loads, cytological analysis, and cytokines secretion in the lungs were evaluated at 6 or 24 h post infection with PAO1. Intranasal priming with both lactobacilli blends significantly improved 7-day mice survival from 12% for the control PAO1 group to 71 and 100% for the two groups receiving L.rff and L.psb respectively. No mortality was observed for both control groups receiving either L.rff or L.psb. Additionally, the PAO1 lung clearance was significantly enhanced at 24 h. A 2-log and 4-log reduction was observed in the L.rff + PAO1 and L.psb + PAO1 groups respectively, compared to the control PAO1 group. Significant reductions in neutrophil recruitment and proinflammatory cytokine and chemokine secretion were observed after lactobacilli administration compared to saline solution, whereas IL-10 production was increased. Conclusions These results demonstrate that intranasal priming with lactobacilli acts as a prophylaxis, and avoids fatal complications caused by Pseudomonas aeruginosa pneumonia in mice. These results were independent of in vitro anti-Pseudomonas aeruginosa activity on QS-dependent virulence factors. Further experiments are required to identify the immune mechanism before initiating clinical trials. |
topic |
Lactobacillus Probiotics Intranasal administration Pseudomonas aeruginosa Respiratory tract infection Mice |
url |
https://doi.org/10.1186/s12866-021-02254-7 |
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