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Pathological Changes in Experimental Intramammary Infection with Different Staphylococcus Species in Mice
INTRODUCTION: Mastitis is caused by different Staphylococcus species, produce great economic loss to farmers. Present study was conducted to know pathological changes in mice inoculated with Staphylococcus epidermidis, S. chromogenes, S. haemolyticus and S. aureus isolated from bovine milk. MATERIAL...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130252/ https://www.ncbi.nlm.nih.gov/pubmed/30221133 http://dx.doi.org/10.4103/JMAU.JMAU_21_18 |
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author | Krishnamoorthy, P. Satyanarayana, M. L. Shome, B. R. Rahman, H. |
author_facet | Krishnamoorthy, P. Satyanarayana, M. L. Shome, B. R. Rahman, H. |
author_sort | Krishnamoorthy, P. |
collection | PubMed |
description | INTRODUCTION: Mastitis is caused by different Staphylococcus species, produce great economic loss to farmers. Present study was conducted to know pathological changes in mice inoculated with Staphylococcus epidermidis, S. chromogenes, S. haemolyticus and S. aureus isolated from bovine milk. MATERIALS AND METHODS: Mice were inoculated with 50 μl (2x104 cfu organisms) per mammary gland and euthanized at 6, 12, 24, 48, 72 and 96 h. Mammary gland weight, gross and histopathological changes of mammary gland, liver, kidney, spleen, heart, lung and inguinal lymph node were studied. RESULTS: Mammary gland weight and percentage of body weight increased at 6 and 96 h in S. aureus and S. haemolyticus infected mice. Gross changes were observed in mammary gland but not in other organs. Mammary gland revealed gross changes from 24 to 72 h in three Coagulase negative staphylococcal (CNS) species and persisted up to 96 h in S. aureus infected mice. Histopathological changes in mammary glands was severe in S. aureus and moderate in CNS species. S. aureus infected mice revealed severe damage to alveoli and loss of alveolar architecture at 96 h but three CNS species infection was overcome by host factors which was evident by proliferation of alveolar epithelial cells. No histological changes were observed in kidney, spleen, lung, heart and inguinal lymph nodes. CONCLUSIONS: S. aureus caused severe mastitis in mice when compared to CNS species. Further, it is first report of mice to study CNS mastitis, and in future it can be used as model for CNS mastitis. |
format | Online Article Text |
id | pubmed-6130252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61302522018-09-14 Pathological Changes in Experimental Intramammary Infection with Different Staphylococcus Species in Mice Krishnamoorthy, P. Satyanarayana, M. L. Shome, B. R. Rahman, H. J Microsc Ultrastruct Original Article INTRODUCTION: Mastitis is caused by different Staphylococcus species, produce great economic loss to farmers. Present study was conducted to know pathological changes in mice inoculated with Staphylococcus epidermidis, S. chromogenes, S. haemolyticus and S. aureus isolated from bovine milk. MATERIALS AND METHODS: Mice were inoculated with 50 μl (2x104 cfu organisms) per mammary gland and euthanized at 6, 12, 24, 48, 72 and 96 h. Mammary gland weight, gross and histopathological changes of mammary gland, liver, kidney, spleen, heart, lung and inguinal lymph node were studied. RESULTS: Mammary gland weight and percentage of body weight increased at 6 and 96 h in S. aureus and S. haemolyticus infected mice. Gross changes were observed in mammary gland but not in other organs. Mammary gland revealed gross changes from 24 to 72 h in three Coagulase negative staphylococcal (CNS) species and persisted up to 96 h in S. aureus infected mice. Histopathological changes in mammary glands was severe in S. aureus and moderate in CNS species. S. aureus infected mice revealed severe damage to alveoli and loss of alveolar architecture at 96 h but three CNS species infection was overcome by host factors which was evident by proliferation of alveolar epithelial cells. No histological changes were observed in kidney, spleen, lung, heart and inguinal lymph nodes. CONCLUSIONS: S. aureus caused severe mastitis in mice when compared to CNS species. Further, it is first report of mice to study CNS mastitis, and in future it can be used as model for CNS mastitis. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6130252/ /pubmed/30221133 http://dx.doi.org/10.4103/JMAU.JMAU_21_18 Text en Copyright: © 2018 Journal of Microscopy and Ultrastructure http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Krishnamoorthy, P. Satyanarayana, M. L. Shome, B. R. Rahman, H. Pathological Changes in Experimental Intramammary Infection with Different Staphylococcus Species in Mice |
title | Pathological Changes in Experimental Intramammary Infection with Different Staphylococcus Species in Mice |
title_full | Pathological Changes in Experimental Intramammary Infection with Different Staphylococcus Species in Mice |
title_fullStr | Pathological Changes in Experimental Intramammary Infection with Different Staphylococcus Species in Mice |
title_full_unstemmed | Pathological Changes in Experimental Intramammary Infection with Different Staphylococcus Species in Mice |
title_short | Pathological Changes in Experimental Intramammary Infection with Different Staphylococcus Species in Mice |
title_sort | pathological changes in experimental intramammary infection with different staphylococcus species in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130252/ https://www.ncbi.nlm.nih.gov/pubmed/30221133 http://dx.doi.org/10.4103/JMAU.JMAU_21_18 |
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