Evidence map›Paper›PMID 28129375›Full record

ArticlePloS one2017

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.

Jully Gogoi-Tiwari, Vincent Williams, Charlene Babra Waryah, Paul Costantino, Hani Al-Salami, Sangeetha Mathavan, Kelsi Wells, Harish Kumar Tiwari, Nagendra Hegde, Shrikrishna Isloor and 2 more

Abstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Article
  2. Evaluation ofApplied and environmental microbiology · 2025
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  12. Phenotypic PIA-Dependent Biofilm Production by Clinical Non-TypeableAnimals : an open access journal from MDPI · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Jully Gogoi-TiwariSchool of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia.
Vincent WilliamsSchool of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia.
Charlene Babra WaryahSchool of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia.
Paul CostantinoSchool of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia.
Hani Al-SalamiSchool of Pharmacy, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia.
Sangeetha MathavanSchool of Pharmacy, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia.
Kelsi WellsSchool of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia.
Harish Kumar TiwariSchool of Veterinary and Life Sciences, Murdoch University, Perth, Western Australia, Australia.
Nagendra HegdeElla Foundation, Genome Valley, Hyderabad, India.
Shrikrishna IsloorVeterinary College, Karnataka Veterinary, Animal and Fisheries Sciences University, Bangalore, India.
Hesham Al-SallamiSchool of Pharmacy, University of Otago, Dunedin, New Zealand.
Trilochan MukkurSchool of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBiofilm 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.

methodsTwo 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.

resultsHistopathological 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-1β and TNF-α inflammatory biomarkers were produced in infected mice, level of TNF-α produced was significantly higher (p<0.05) in mice inoculated with strong biofilm forming S. aureus than the weak biofilm forming strain.

conclusionThis finding suggests an important role of TNF-α 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.

Indexed as

AnimalsBiofilmsCattleDisease Models, AnimalFemaleInterleukin-1betaMammary Glands, AnimalMastitis, BovineMicePilot ProjectsStaphylococcal InfectionsStaphylococcus aureusTumor Necrosis Factor-alphaInterleukin-1betaTumor Necrosis Factor-alpha

Identifiers

PMID28129375
PMCPMC5271311

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.