Jóse Antonio Ruiz Santa Quiteria

Enterotoxin and toxic shock syndrome toxin-one production by staphylococci isolated from mastitis in sheep.

From 160 staphylococci isolated from ovine mastitis, 125 were identified as coagulase‐positive staphylococci (CPS) and 35 as coagulase‐negative staphylococci (CNS). Of these, 108 (87.8%) S. aureus produced at least one of the staphylococcal enterotoxins (SE) described. However, no CNS was found to be enterotoxigenic. Enterotoxin C (SEC) was the type most frequently produced. TSST‐1 was shown to be produced by 91 (74.0%) of S. aureus, almost invariably in combination with SEC. Three CNS strains were also found to produce TSST‐1 (two strains of S. xylosus and one strain of S. epidermidis).;

Seroprevalence of Besnoitia besnoiti infection and associated risk factors in cattle from an endemic region in Europe.

Bovine besnoitiosis, caused by the parasite Besnoitia besnoiti, is a chronic, debilitating disease with both cutaneous and systemic clinical signs that has re-emerged in Europe. This is the first random cross-sectional prevalence study of B. besnoiti infection in cattle carried out in an endemic area in Europe (Navarra, Spain). Dairy (n = 372) and beef (n = 340) cattle >1 year of age were randomly blood sampled. Serum was evaluated using a validated ELISA. True animal prevalence data were restricted to beef cattle (16.0%). The prevalence significantly increased with age and seropositive animals were mostly located in mountainous areas where the disease is endemic. Breed and sex were not found to be risk factors.

Polyclonal antibodies against Staphylococcus aureus ATCC 12 600 catalase do not recognize any protein in cellular extracts from S. aureus subsp. anaerobius

Rabbits were immunized with electrophoretically pure catalase from Staphylococcus aureus ATCC 12 600. The antiserum was used to study whether S. aureus subsp. anaerobius was able to synthesize the apoprotein of catalase. Proteins were separated on polyacrylamide gels (SDS-PAGE) and transferred to nitrocellulose membranes and were detected by immunoblotting. No protein reacting with the purified immunoglobulins against S. aureus ATCC 12,600 catalase could be detected in crude and partially purified cellular extracts from S. aureus subsp. anaerobius or its aerotolerant mutants.

Investigation of risk factors associated with infections caused by small ruminant lentiviruses

Abstract An epidemiological study was conducted to identify risk factors related to small ruminant lentivirus (SRLV) infection in the central region of Spain. Between October 1998 and October 2000, a total of 194 sheep from 10 flocks and 163 goats from three flocks were tested for SRLV antibodies, resulting in 65.5% and 8.0% of seroprevalence, respectively. The relationship between differences in prevalence of SRLV, geographical location of the flock, and possible factors related to the flock that could enhance transmission were studied. Results of multivariable analysis showed an association between SRLV infection and geographical location of the flock and the rearing system. In addition, the differences in the productivity between infected and non-infected animals were explored. The productivity parameters were measured in 62 sheep and 28 goats. All productivity parameters studied (milk production, number of milking days, and lambing rate) appeared to be reduced in the SRLV-seropositive group in both goats and sheep. Even though, these differences were not statistically significant, it seems that animals infected are less productive than these non-infected. Statistical analyses comparing infected and non-infected sheep showed no statistical relationship between SRLV infection and milk quality.