Mammary Gland Pathology Subsequent to Acute Infection with Strong versus Weak Biofilm Forming Staphylococcus aureus Bovine Mastitis Isolates: A Pilot Study Using Non-Invasive Mouse Mastitis Model

BACKGROUND: Biofilm formation by Staphylococcus aureus is an important virulence attribute because of its potential to induce persistent antibiotic resistance, retard phagocytosis and either attenuate or promote inflammation, depending upon the disease syndrome, in vivo. This study was undertaken to...

Full description

Bibliographic Details
Main Authors: Gogoi Tiwari, Jully, Williams, Vincent, Waryah, Charlene, Costantino, Paul, Al-Salami, Hani, Mathavan, Sangeetha, Wells, Kelsi, Tiwari, H., Hegde, N., Isloor, S., Al-Sallami, H., Mukkur, Trilochan
Format: Journal Article
Published: Public Library of Science 2017
Online Access:http://hdl.handle.net/20.500.11937/58338
_version_ 1848760234775937024
author Gogoi Tiwari, Jully
Williams, Vincent
Waryah, Charlene
Costantino, Paul
Al-Salami, Hani
Mathavan, Sangeetha
Wells, Kelsi
Tiwari, H.
Hegde, N.
Isloor, S.
Al-Sallami, H.
Mukkur, Trilochan
author_facet Gogoi Tiwari, Jully
Williams, Vincent
Waryah, Charlene
Costantino, Paul
Al-Salami, Hani
Mathavan, Sangeetha
Wells, Kelsi
Tiwari, H.
Hegde, N.
Isloor, S.
Al-Sallami, H.
Mukkur, Trilochan
author_sort Gogoi Tiwari, Jully
building Curtin Institutional Repository
collection Online Access
description BACKGROUND: Biofilm formation by Staphylococcus aureus is an important virulence attribute because of its potential to induce persistent antibiotic resistance, retard phagocytosis and either attenuate or promote inflammation, depending upon the disease syndrome, in vivo. This study was undertaken to evaluate the potential significance of strength of biofilm formation by clinical bovine mastitis-associated S. aureus in mammary tissue damage by using a mouse mastitis model. METHODS: Two S. aureus strains of the same capsular phenotype with different biofilm forming strengths were used to non-invasively infect mammary glands of lactating mice. Biofilm forming potential of these strains were determined by tissue culture plate method, ica typing and virulence gene profile per detection by PCR. Delivery of the infectious dose of S. aureus was directly through the teat lactiferous duct without invasive scraping of the teat surface. Both bacteriological and histological methods were used for analysis of mammary gland pathology of mice post-infection. RESULTS: Histopathological analysis of the infected mammary glands revealed that mice inoculated with the strong biofilm forming S. aureus strain produced marked acute mastitic lesions, showing profuse infiltration predominantly with neutrophils, with evidence of necrosis in the affected mammary glands. In contrast, the damage was significantly less severe in mammary glands of mice infected with the weak biofilm-forming S. aureus strain. Although both IL-1ß and TNF-a inflammatory biomarkers were produced in infected mice, level of TNF-a produced was significantly higher (p<0.05) in mice inoculated with strong biofilm forming S. aureus than the weak biofilm forming strain. CONCLUSION: This finding suggests an important role of TNF-a in mammary gland pathology post-infection with strong biofilm-forming S. aureus in the acute mouse mastitis model, and offers an opportunity for the development of novel strategies for reduction of mammary tissue damage, with or without use of antimicrobials and/or anti-inflammatory compounds for the treatment of bovine mastitis.
first_indexed 2025-11-14T10:12:33Z
format Journal Article
id curtin-20.500.11937-58338
institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T10:12:33Z
publishDate 2017
publisher Public Library of Science
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-583382018-01-12T01:13:56Z Mammary Gland Pathology Subsequent to Acute Infection with Strong versus Weak Biofilm Forming Staphylococcus aureus Bovine Mastitis Isolates: A Pilot Study Using Non-Invasive Mouse Mastitis Model Gogoi Tiwari, Jully Williams, Vincent Waryah, Charlene Costantino, Paul Al-Salami, Hani Mathavan, Sangeetha Wells, Kelsi Tiwari, H. Hegde, N. Isloor, S. Al-Sallami, H. Mukkur, Trilochan BACKGROUND: Biofilm formation by Staphylococcus aureus is an important virulence attribute because of its potential to induce persistent antibiotic resistance, retard phagocytosis and either attenuate or promote inflammation, depending upon the disease syndrome, in vivo. This study was undertaken to evaluate the potential significance of strength of biofilm formation by clinical bovine mastitis-associated S. aureus in mammary tissue damage by using a mouse mastitis model. METHODS: Two S. aureus strains of the same capsular phenotype with different biofilm forming strengths were used to non-invasively infect mammary glands of lactating mice. Biofilm forming potential of these strains were determined by tissue culture plate method, ica typing and virulence gene profile per detection by PCR. Delivery of the infectious dose of S. aureus was directly through the teat lactiferous duct without invasive scraping of the teat surface. Both bacteriological and histological methods were used for analysis of mammary gland pathology of mice post-infection. RESULTS: Histopathological analysis of the infected mammary glands revealed that mice inoculated with the strong biofilm forming S. aureus strain produced marked acute mastitic lesions, showing profuse infiltration predominantly with neutrophils, with evidence of necrosis in the affected mammary glands. In contrast, the damage was significantly less severe in mammary glands of mice infected with the weak biofilm-forming S. aureus strain. Although both IL-1ß and TNF-a inflammatory biomarkers were produced in infected mice, level of TNF-a produced was significantly higher (p<0.05) in mice inoculated with strong biofilm forming S. aureus than the weak biofilm forming strain. CONCLUSION: This finding suggests an important role of TNF-a in mammary gland pathology post-infection with strong biofilm-forming S. aureus in the acute mouse mastitis model, and offers an opportunity for the development of novel strategies for reduction of mammary tissue damage, with or without use of antimicrobials and/or anti-inflammatory compounds for the treatment of bovine mastitis. 2017 Journal Article http://hdl.handle.net/20.500.11937/58338 10.1371/journal.pone.0170668 http://creativecommons.org/licenses/by/4.0/ Public Library of Science fulltext
spellingShingle Gogoi Tiwari, Jully
Williams, Vincent
Waryah, Charlene
Costantino, Paul
Al-Salami, Hani
Mathavan, Sangeetha
Wells, Kelsi
Tiwari, H.
Hegde, N.
Isloor, S.
Al-Sallami, H.
Mukkur, Trilochan
Mammary Gland Pathology Subsequent to Acute Infection with Strong versus Weak Biofilm Forming Staphylococcus aureus Bovine Mastitis Isolates: A Pilot Study Using Non-Invasive Mouse Mastitis Model
title Mammary Gland Pathology Subsequent to Acute Infection with Strong versus Weak Biofilm Forming Staphylococcus aureus Bovine Mastitis Isolates: A Pilot Study Using Non-Invasive Mouse Mastitis Model
title_full Mammary Gland Pathology Subsequent to Acute Infection with Strong versus Weak Biofilm Forming Staphylococcus aureus Bovine Mastitis Isolates: A Pilot Study Using Non-Invasive Mouse Mastitis Model
title_fullStr Mammary Gland Pathology Subsequent to Acute Infection with Strong versus Weak Biofilm Forming Staphylococcus aureus Bovine Mastitis Isolates: A Pilot Study Using Non-Invasive Mouse Mastitis Model
title_full_unstemmed Mammary Gland Pathology Subsequent to Acute Infection with Strong versus Weak Biofilm Forming Staphylococcus aureus Bovine Mastitis Isolates: A Pilot Study Using Non-Invasive Mouse Mastitis Model
title_short Mammary Gland Pathology Subsequent to Acute Infection with Strong versus Weak Biofilm Forming Staphylococcus aureus Bovine Mastitis Isolates: A Pilot Study Using Non-Invasive Mouse Mastitis Model
title_sort mammary gland pathology subsequent to acute infection with strong versus weak biofilm forming staphylococcus aureus bovine mastitis isolates: a pilot study using non-invasive mouse mastitis model
url http://hdl.handle.net/20.500.11937/58338