Application of Lactobacillus gasseri 63 AM supernatant to Pseudomonas aeruginosa- infected wounds prevents sepsis in murine models of thermal injury and dorsal excision
. Severely burned patients are susceptible to bacterial infection within their burn wounds, which frequently leads to sepsis, multiple organ failure and death. The opportunistic pathogen , an organism inherently resistant to multiple antibiotics, is a common cause of sepsis in these patients. . Deve...
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Veröffentlicht in: | Journal of medical microbiology 2019-10, Vol.68 (10), p.1560-1572 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | . Severely burned patients are susceptible to bacterial infection within their burn wounds, which frequently leads to sepsis, multiple organ failure and death. The opportunistic pathogen
, an organism inherently resistant to multiple antibiotics, is a common cause of sepsis in these patients.
. Development of a topical treatment unrelated to conventional antibiotics is essential for prevention of
infection and sepsis, leading to a role for the direct application of probiotics or their by-products.
. We examined the effectiveness of 20× concentrated supernatant from
strain 63 AM (LgCS) grown in de Man, Rogosa and Sharpe broth in inhibiting
biofilms
, as well as in reducing wound bioburden and
sepsis
.
. LgCS inhibited the growth of
strain PAO1, prevented its biofilm development and eliminated partially developed PAO1 biofilms. In the murine model of thermal injury, a single injection of LgCS following injury and PAO1 infection reduced mortality to 0 % and prevented systemic spread (sepsis). Furthermore, a second injection of LgCS 24 h after the first eliminated PAO1 from the wound. In the murine dorsal excision infection model, either LgCS or ceftazidime treatment of the PAO1-infected wound significantly reduced the mortality rate among infected mice, while combining LgCS with ceftazidime eliminated mortality.
. These results suggest the potential of LgCS in preventing sepsis from
infection in severely burned and other immunocompromised patients. |
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ISSN: | 0022-2615 1473-5644 |
DOI: | 10.1099/jmm.0.001066 |