Evidence map›Paper›PMID 41724895›Full record

ArticleBrazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]2026

Host-pathogen interactions during early stages of bovine mastitis: divergent macrophage responses to distinct bovine-associated Staphylococci species and strains.

Sarah Antonieta de Oliveira Veríssimo, Ygor Fagundes Ruas, Filipe Aguera Pinheiro, Luiza Campos Reis, Bernardina Amorim Uscata, Hiro Goto, Soraia Araújo Diniz, Adriana Cortez, Sarne De Vliegher, Marcos Bryan Heinemann and 3 more

Abstract read
In one paragraph

Article in Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology], 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Sarah Antonieta de Oliveira VeríssimoDepartamento de Tecnologia e Inspeção de Produtos de Origem Animal, Escola de Veterinária, Universidade Federal de Minas Gerais, Belo Horizonte, 31270-901, Brazil.
Ygor Fagundes RuasCentro Nacional de Pesquisa em Energia e Materiais (CNPEM), Ilum Escola de Ciência, Rua Lauro Vannucci, São Paulo, Campinas, 1020, 13087-548, Brazil.
Filipe Aguera PinheiroDepartamento de Medicina Veterinária Preventiva e Saúde Animal, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, São Paulo, 05508-270, Brazil.
Luiza Campos ReisEscuela Profesional de Medicina Humana, Facultad de Medicina, Universidad Nacional Toribio Rodríguez de Mendoza de Amazonas, Chachapoyas, 01000, Peru.
Bernardina Amorim UscataLaboratório de Sorologia e Imunobiologia, Faculdade de Medicina, Instituto de Medicina Tropical, Universidade de São Paulo, São Paulo, 05403-000, Brazil.
Hiro GotoLaboratório de Sorologia e Imunobiologia, Faculdade de Medicina, Instituto de Medicina Tropical, Universidade de São Paulo, São Paulo, 05403-000, Brazil.
Soraia Araújo DinizUniversidade Federal do Vale do Jequitinhonha e Mucuri - Campus Unaí, Unaí, 38610-000, Brazil.
Adriana CortezUniversidade Santo Amaro, UNISA, São Paulo, São Paulo, 04743-030, Brazil.
Sarne De VliegherM-team and Mastitis and Milk Quality Research Unit, Department of Internal Medicine, Reproduction and Population Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, Merelbeke, 9820, Belgium.
Marcos Bryan HeinemannDepartamento de Medicina Veterinária Preventiva e Saúde Animal, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, São Paulo, 05508-270, Brazil.
Eduardo Milton Ramos-SanchezEscuela Profesional de Medicina Humana, Facultad de Medicina, Universidad Nacional Toribio Rodríguez de Mendoza de Amazonas, Chachapoyas, 01000, Peru.
Fernando Nogueira de SouzaLaboratório de Soroepidemiologia e Imunobiologia, Faculdade de Medicina, Instituto de Medicina Tropical, Universidade de São Paulo, Av. Dr. Enéas de Carvalho de Aguiar 470, São Paulo, 05403-000, Brazil. nogueirasouza@usp.br.ORCID http://orcid.org/0000-0002-5380-0939
Mônica Maria Oliveira Pinho CerqueiraDepartamento de Tecnologia e Inspeção de Produtos de Origem Animal, Escola de Veterinária, Universidade Federal de Minas Gerais, Belo Horizonte, 31270-901, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBovine mastitis is the most economically significantdisease in dairy farming, with Staphylococcus aureus and Staphylococcus chromogenes asprominent agents, the former posing a major threat. As principal immune sentinels in themammary gland, macrophages orchestrate early pathogen recognition and immune activation,critically influencing the trajectory and outcome of infection. Thus, this study aimed tocharacterize the early macrophage responses to distinct bovine-associated S. aureus and S.chromogenes strains.

methodsHere, RAW 264.7 cells were challenged with four differentstrains: S. aureus [isolated from nose (SN), and intramammary infection (IMI)] and S.chromogenes [IMI, and teat apex (TA)] were evaluated after 90- and 180-min. Nitric oxide (NO)production was analyzed in the supernatants, and mRNA levels of IL-1β, IL-18, NLRP3, NOS2,Arg1, Bax, and Bcl2 were assessed in the cells.

resultsMacrophages challenged with S. aureusIMI strains showed elevated Nos2 expression but negligible NO production, indicating a potentialimmune evasion mechanism. The commensal S. aureus SN strain uniquely maintained arginaseexpression, suggesting M2-like polarization that may promote immune tolerance and bacterialcolonization. Both S. aureus strains significantly upregulated the anti-apoptotic Bcl2 gene, atranscriptional response that may be associated with host cell survival, which may facilitatebacterial intracellular persistence. In contrast, S. chromogenes strains induced strong NOS2expression, robust NLRP3 inflammasome activation, and increased IL-1β production, indicatingM1 polarization and a pro-inflammatory response. The pro-apoptotic Bax gene showed an earlydecrease followed by a later increase exclusively in S. aureus-infected macrophages, indicating atime-dependent transcriptional modulation of apoptosis-related genes.

conclusionsThesegenotype-dependent macrophage responses reveal complex immune modulation shaping mastitis pathogenesis. However, our findings are based solely on transcriptional data on the murine cells and require further validation.

Indexed as

Host-Pathogen InteractionsMacrophagesMastitis, BovineStaphylococcal InfectionsStaphylococcusStaphylococcus aureusAnimalsCattleCytokinesFemaleInterleukin-1betaMiceNitric OxideRAW 264.7 CellsCytokinesInterleukin-1betaNitric OxideDairy cowImmune responseMastitisNon-aureus staphylococciStaphylococcus aureus

Identifiers

PMID41724895
PMCPMC12926279

What Socratic holds

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Registered trials

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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 Socratic graph.