Resumo Staphylococcus coagulase-negativos (SCN) são os principais micro-organismos responsáveis pela mastite ovina e o tratamento ao final da lactação pode ser usado como método de controle contra a doença. Porém, o longo período seco apresentado pelas ovelhas em alguns sistemas de criação pode prejudicar os efeitos positivos do tratamento antimicrobiano. Os objetivos deste trabalho foram identificar as principais espécies de SCN na etiologia da mastite ovina antes e após o tratamento ao final da lactação das ovelhas, bem como investigar a persistência das espécies mais prevalentes na glândula mamária na lactação seguinte. Sessenta ovelhas foram divididas em dois grupos experimentais, um deles formado por animais sem tratamento antimicrobiano, enquanto o outro era composto por ovelhas cujas metades mamárias foram tratadas com cloxacilina-benzatina por via intramamária. As amostras de leite foram obtidas antes da secagem e aos 15 e 30 dias após o parto da lactação seguinte. As espécies prevalentes foram S. warneri, S. simulans e S. epidermidis. Clones das três espécies de maior ocorrência foram identificados antes e depois do tratamento, ou seja, mesmo com o extenso período seco entre as duas lactações consecutivas, os micro-organismos ainda foram identificados no interior da glândula mamária.

Abstract Coagulase-negative Staphylococci (CNS) are the main microorganisms responsible for mastitis in sheep and the treatment in the end of lactation can be used as a control method against disease. However, the long dry period presented by ewes in some breeding systems may impair the positive effects of antimicrobial treatment. The aims of this study were to identify the main CNS species in the etiology of ovine mastitis before and after treatment at dry-off of the ewes, as well as investigate the persistence of the most prevalent species in the mammary gland at the next lactation. Sixty sheep were divided into two experimental groups, one consisting of animals without antimicrobial treatment, while the other was composed by sheep whose mammary halves were treated with cloxacillin-benzathine intramammary. The milk samples were obtained before drying-off and at 15 and 30 days after calving the next lactation. The prevalent species were S. warneri, S. simulans and S. epidermidis. Clones of the three species more prevalent were identified before and after treatment, i.e., even with the extensive dry period between the two consecutive lactations, the microorganisms were still identified in the mammary gland.

The objective of this study was to characterize the clonal profile, virulence factors and antimicrobial resistance, particularly oxacillin resistance, of Staphylococcus aureus isolated from sheep milk. Milk samples were collected from all teats for the California Mastitis Test (CMT), somatic cell count, identification of S. aureus, investigation in these strains of genes encoding toxins (sea, seb, sec, sed, tst), biofilm (icaA, icaC, icaD, bap), leukocidin (luk-PV) oxacillin resistance by mecA gene detection and susceptibility testing (12 antibiotics). Messenger RNA expression was evaluated by RT-PCR in isolates carrying toxin and biofilm genes. Biofilm formation was also evaluated phenotypically by adherence to polystyrene plates. The clonal profile of S. aureus was investigated by pulsed-field gel electrophoresis. A total of 473 milk samples were collected from 242 animals on three farms and 20 S. aureus strains were isolated and none carried the mecA gene. The two sec gene-positive isolates and the isolates carrying the tst and luk-PV genes were positive by RT-PCR. Staphylococcus aureus isolated from the three flocks studied showed high susceptibility to the drugs tested and none was biofilm producer, indicating that biofilm formation was not a virulence factor causing infection by these strains. The typing of 17 S. aureus isolates revealed the presence of a common clone on the three farms studied, and the presence and expression of the sec and tst genes in one strain of this clone suggest the possible acquisition of virulence genes by this clone, a fact that is important for animal health and food hygiene.

The aim of this study was to perform SCCmec typing in Staphylococcus aureus isolates and to characterize the clonal profile of these isolates. Forty-six mecA gene-positive strains isolated between 2002 and 2006 were submitted to antimicrobial resistance testing by the E-test, SCCmec typing by multiplex PCR, and clonal profile analysis by pulsed-field gel electrophoresis. Forty-one (89.1%) isolates were typed as SCCmec III and five (10.9%) as SCCmec IV. Four circulating clones were detected, one of them comprising isolates related to the Brazilian epidemic clone. This clone was detected throughout the study period. The SCCmec III isolates were associated with a high rate of multidrug resistance and clonal dissemination of methicillin-resistant S. aureus in the wards of the University Hospital of the Botucatu School of Medicine, Universidade Estadual Paulista.