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1.
Ir Vet J ; 67(1): 11, 2014.
Article in English | MEDLINE | ID: mdl-24959346

ABSTRACT

BACKGROUND: Schmallenberg virus (SBV) was first detected in Germany in November 2011. Confirmation of infection in Ireland was reported on October 30(th) 2012. The results of a national serological survey carried out in early 2013 suggested that the first introduction of SBV into Ireland probably occurred in the south or southeast of Ireland in the spring or summer of 2012, with subsequent spread eastwards and northwards. It was unclear at that stage whether the virus had survived the winter period and would continue to spread in 2013. The purpose of this study was to monitor the spread of the virus in the mid-west region through the summer and autumn of 2013 using bulk tank milk from selected dairy herds. FINDINGS: Seventy two dairy farmers were recruited to participate in the bulk milk tank study. Each farmer agreed to collect a bulk tank milk sample on a weekly basis from early June. A total of 988 samples were received between June 5(th) and December 3(rd) 2013 and these were analysed using an indirect ELISA test. Of the initial set of 72 samples received between June 5(th) and July 16(th), nine were positive, one was inconclusive and 62 were negative. By the end of the study in early December 2013 only one new farm turned positive. This was the farm that had initially tested inconclusive. CONCLUSION: The study results suggest that the anticipated spread of SBV across Ireland from the south and south-east did not occur during 2013.

2.
Anal Chim Acta ; 651(1): 98-104, 2009 Sep 28.
Article in English | MEDLINE | ID: mdl-19733742

ABSTRACT

Caseous lymphadenitis (CLA), a disease affecting sheep and goats, is caused by Corynebacterium pseudotuberculosis and is difficult to detect, especially at early stages in its development. A surface plasmon resonance-based biosensor assay for the detection of antibodies to the phospholipase D (PLD) exotoxin of C. pseudotuberculosis in sheep serum was successfully generated. It employed a recombinant form of PLD, which was immobilised, and all aspects of the assay including minimisation of non-specific binding, and the regeneration of the chip, were optimised. The applicability of the assay was initially demonstrated using sera collected from experimentally infected sheep and from sheep with no prior history of infection. The assay was then evaluated on a panel of clinical samples and the results obtained compared very favourably to those obtained by a double sandwich ELISA (over 90% similarity) and clearly verified its analytical value.


Subject(s)
Antibodies, Bacterial/blood , Biosensing Techniques/methods , Corynebacterium Infections/veterinary , Corynebacterium pseudotuberculosis/immunology , Sheep Diseases/diagnosis , Surface Plasmon Resonance/methods , Animals , Corynebacterium Infections/diagnosis , Enzyme-Linked Immunosorbent Assay , Goats , Phospholipase D/immunology , Phospholipase D/metabolism , Reagent Kits, Diagnostic , Recombinant Proteins/immunology , Recombinant Proteins/metabolism , Sheep
3.
Appl Environ Microbiol ; 73(6): 1858-63, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17261517

ABSTRACT

Salmonella spp. infection is a major cause of gastroenteritis, with many thousands of cases reported in the European Union every year. The use of probiotics offers the potential to improve this situation. Here, we investigate the effects of oral treatment of pigs with a defined lactic acid bacteria culture mixture on both clinical and microbiological signs of Salmonella enterica serovar Typhimurium infection. Fifteen weaned pigs blocked by sex and weight were administered control milk or a mixture of five probiotic strains as either a milk fermentate or milk suspension for a total of 30 days. The mixture consisted of two strains of Lactobacillus murinus and one strain each of Lactobacillus salivarius subsp. salivarius, Lactobacillus pentosus, and Pediococcus pentosaceous. Following probiotic administration for 6 days, animals were challenged orally with serovar Typhimurium; the health of the animals and the microbiological composition of their feces were monitored for 23 days postinfection. Animals treated with probiotic showed reduced incidence, severity, and duration of diarrhea. These animals also gained weight at a greater rate than control pigs administered skim milk. Mean fecal numbers of Salmonella were significantly reduced in probiotic-treated animals at 15 days postinfection (P = 0.01). The administered probiotic bacteria improved both the clinical and microbiological outcome of Salmonella infection. These strains offer significant benefit for use in the food industry and may have potential in human applications.


Subject(s)
Feces/microbiology , Probiotics , Salmonella Infections, Animal/microbiology , Salmonella Infections, Animal/physiopathology , Salmonella typhimurium/growth & development , Swine Diseases/microbiology , Swine Diseases/physiopathology , Administration, Oral , Animals , Body Weight , Colony Count, Microbial , Diarrhea/physiopathology , Diarrhea/veterinary , Disease Models, Animal , Lactobacillus , Pediococcus , Probiotics/administration & dosage , Swine , Time Factors
4.
Appl Environ Microbiol ; 71(12): 8236-40, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16332808

ABSTRACT

Salmonella enterica serovar Typhimurium is frequently isolated from humans and animals. Phage typing is historically the first-line reference typing technique in Europe. It is rapid and convenient for laboratories with appropriate training and experience, and costs of consumables are low. Phage typing and pulsed-field gel electrophoresis (PFGE) were performed on 503 isolates of serovar Typhimurium. Twenty-nine phage types and 53 PFGE patterns were observed. Most isolates of phage types DT104, DT104b, and U310 are not distinguishable from other members of their phage type by PFGE. By contrast, PFGE of isolates of phage types DT193 and U302 shows great heterogeneity. Analysis of experience with PFGE and phage typing can facilitate the selective application of PFGE to maximize the yield of epidemiologically relevant additional information while controlling costs.


Subject(s)
Electrophoresis, Gel, Pulsed-Field/methods , Salmonella Phages/classification , Salmonella typhimurium/classification , Animals , Bacterial Typing Techniques , Humans , Salmonella Phages/isolation & purification , Salmonella typhimurium/isolation & purification , Salmonella typhimurium/virology
5.
Foodborne Pathog Dis ; 2(3): 274-81, 2005.
Article in English | MEDLINE | ID: mdl-16156708

ABSTRACT

One hundred and seven Salmonella isolates of various serotypes were investigated for resistance to a panel of nine antimicrobial agents by standardized methods. Thirty four isolates were susceptible to the selected antimicrobial agents. Thirty-six (of 107) were resistant to three or more antimicrobial agents and defined as multidrug resistant (MDR). Salmonella Typhimurium was the most resistant serotype. All resistant isolates were examined for the presence of class 1 integrons. Thirty-two integron-associated gene cassettes (of varying sizes) were identified. A 1,000-bp amplicon similar to that flanking the distal region of the Salmonella Genomic Island (SGI)-1 in Salmonella Typhimurium was detected in a majority of the S. Typhimurium isolates in this study. In contrast, a 1,800-bp amplicon was identified in all Salmonella Infantis isolates. This amplicon was completely characterized in one isolate. The presence of class 1 integrons in Salmonella spp. in pigs may be important if these zoonotic pathogens were to enter the food chain.


Subject(s)
Anti-Bacterial Agents/pharmacology , DNA, Bacterial/chemistry , Drug Resistance, Bacterial/genetics , Salmonella Infections, Animal/drug therapy , Salmonella/drug effects , Swine Diseases/drug therapy , Abattoirs , Animals , Base Sequence , Colony Count, Microbial/veterinary , DNA, Bacterial/analysis , Drug Resistance, Multiple, Bacterial , Gene Amplification , Ireland/epidemiology , Microbial Sensitivity Tests/veterinary , Molecular Sequence Data , Polymerase Chain Reaction/veterinary , Salmonella/genetics , Salmonella Infections, Animal/epidemiology , Salmonella Infections, Animal/microbiology , Swine , Swine Diseases/epidemiology , Swine Diseases/microbiology
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