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Effect of Lactobacillus acidophilus & epidermal growth factor on experimentally induced Clostridium difficile infection

BACKGROUND & OBJECTIVES: Clostridium difficile-associated disease (CDAD) remains an important nosocomial ailment. Antimicrobial therapy used for CDAD gives inconsistent results. This experimental study was planned to investigate the beneficial effects of Lactobacillus acidophilus and epidermal g...

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Autores principales: Kaur, Sukhminderjit, Vaishnavi, Chetana, Prasad, Kaushal Kishor, Ray, Pallab, Kochhar, Rakesh
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103179/
https://www.ncbi.nlm.nih.gov/pubmed/21537099
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author Kaur, Sukhminderjit
Vaishnavi, Chetana
Prasad, Kaushal Kishor
Ray, Pallab
Kochhar, Rakesh
author_facet Kaur, Sukhminderjit
Vaishnavi, Chetana
Prasad, Kaushal Kishor
Ray, Pallab
Kochhar, Rakesh
author_sort Kaur, Sukhminderjit
collection PubMed
description BACKGROUND & OBJECTIVES: Clostridium difficile-associated disease (CDAD) remains an important nosocomial ailment. Antimicrobial therapy used for CDAD gives inconsistent results. This experimental study was planned to investigate the beneficial effects of Lactobacillus acidophilus and epidermal growth factor (EGF) for CDAD management. METHODS: Among 10 groups of BALB/c mice (6 in each), group 1 served as controls receiving no inoculum. Animals in groups 2-10 received C. difficile, those in groups 3, 6 and 9 received L. acidophilus and those in groups 4, 7 and 10 received EGF after C. difficile inoculation. Animals in groups 5-7 were pre-treated with ampicillin and those in groups 8-10 with lansoprazole prior to C. difficile. The animals were killed and investigated for colonisation by C. difficile and toxin production, myeloperoxidase (MPO) activity and histopathology. RESULTS: Colonisation by C. difficile was found to be significantly different (P<0.001) in the various groups. C. difficile toxin titres and MPO activity were significantly lower in animals given L. acidophilus and EGF after ampicillin (groups 6 and 7) and lansoprazole (groups 9 and 10). The severity of acute inflammation was also significantly less (P<0.05) in caecal and colonic segments of animals in groups 6 and 7 compared to those in group 5. Although the severity of acute inflammation was less in the caecal and colonic segment of animals in groups 9 and 10, the reduction was not significant compared to group 8. INTERPRETATION & CONCLUSIONS: Our findings showed that the administration of L. acidophilus and EGF reduced the severity of C. difficile infection in the experimental animals.
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spelling pubmed-31031792011-06-08 Effect of Lactobacillus acidophilus & epidermal growth factor on experimentally induced Clostridium difficile infection Kaur, Sukhminderjit Vaishnavi, Chetana Prasad, Kaushal Kishor Ray, Pallab Kochhar, Rakesh Indian J Med Res Original Article BACKGROUND & OBJECTIVES: Clostridium difficile-associated disease (CDAD) remains an important nosocomial ailment. Antimicrobial therapy used for CDAD gives inconsistent results. This experimental study was planned to investigate the beneficial effects of Lactobacillus acidophilus and epidermal growth factor (EGF) for CDAD management. METHODS: Among 10 groups of BALB/c mice (6 in each), group 1 served as controls receiving no inoculum. Animals in groups 2-10 received C. difficile, those in groups 3, 6 and 9 received L. acidophilus and those in groups 4, 7 and 10 received EGF after C. difficile inoculation. Animals in groups 5-7 were pre-treated with ampicillin and those in groups 8-10 with lansoprazole prior to C. difficile. The animals were killed and investigated for colonisation by C. difficile and toxin production, myeloperoxidase (MPO) activity and histopathology. RESULTS: Colonisation by C. difficile was found to be significantly different (P<0.001) in the various groups. C. difficile toxin titres and MPO activity were significantly lower in animals given L. acidophilus and EGF after ampicillin (groups 6 and 7) and lansoprazole (groups 9 and 10). The severity of acute inflammation was also significantly less (P<0.05) in caecal and colonic segments of animals in groups 6 and 7 compared to those in group 5. Although the severity of acute inflammation was less in the caecal and colonic segment of animals in groups 9 and 10, the reduction was not significant compared to group 8. INTERPRETATION & CONCLUSIONS: Our findings showed that the administration of L. acidophilus and EGF reduced the severity of C. difficile infection in the experimental animals. Medknow Publications 2011-04 /pmc/articles/PMC3103179/ /pubmed/21537099 Text en © The Indian Journal of Medical Research http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kaur, Sukhminderjit
Vaishnavi, Chetana
Prasad, Kaushal Kishor
Ray, Pallab
Kochhar, Rakesh
Effect of Lactobacillus acidophilus & epidermal growth factor on experimentally induced Clostridium difficile infection
title Effect of Lactobacillus acidophilus & epidermal growth factor on experimentally induced Clostridium difficile infection
title_full Effect of Lactobacillus acidophilus & epidermal growth factor on experimentally induced Clostridium difficile infection
title_fullStr Effect of Lactobacillus acidophilus & epidermal growth factor on experimentally induced Clostridium difficile infection
title_full_unstemmed Effect of Lactobacillus acidophilus & epidermal growth factor on experimentally induced Clostridium difficile infection
title_short Effect of Lactobacillus acidophilus & epidermal growth factor on experimentally induced Clostridium difficile infection
title_sort effect of lactobacillus acidophilus & epidermal growth factor on experimentally induced clostridium difficile infection
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103179/
https://www.ncbi.nlm.nih.gov/pubmed/21537099
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