Biological control of sheep parasites using Duddingtonia flagrans: trials on commercial farms in Sweden.

Trials were conducted on 3 commercial sheep farms in Sweden to assess the effect of administering spores of the nematode trapping fungus, Duddingtonia flagrans, together with supplementary feed to lactating ewes for the first 6 weeks from turn-out on pastures in spring. Also control groups of ewes, receiving only feed supplement, were established on all 3 farms. Groups were monitored by intensive parasitological investigation. The ewes and their lambs were moved in late June to saved pastures for summer grazing, the lambs receiving an anthelmintic treatment at this time. After approximately 6 weeks on summer pasture the lambs were weaned, treated a second time with anthelmintic, and returned to their original lambing pastures for finishing. Decisions as to when lambs were to be marketed were entirely at the discretion of the farmer co-operators. No difference in lamb performance was found between the two treatments on all three farms. This was attributed to the high levels of nutrition initially of the ewes limiting their post-partum rise in nematode faecal egg counts in spring, which in turn resulted in low levels of nematode infection on pastures throughout the autumn period. Additionally, pastures were of good quality for the lambs during the finishing period, so they grew at optimal rates as far as the farmers were concerned.

Evaluation of biological control of sheep parasites using Duddingtonia flagrans under commercial farming conditions on the island of Gotland, Sweden.

Field trials, conducted over 3 consecutive years, were aimed at assessing farmer opinions of the practicality and effectiveness of using Duddingtonia flagrans to control nematode parasites in their flocks on the Swedish island of Gotland. These trials were also monitored by intensive parasitological investigation. On Gotland, lambing occurs in spring, and around mid-summer (late June), ewes and lambs are moved to saved pastures due to pasture deterioration caused by dry conditions. Weaned lambs are then returned to original lambing pastures in early autumn for finishing. One farm (B) was used for 2001-2003 and a second farm (N) was also used in 2002 and 2003. On each farm, two flocks (each of 20 ewes + twin lambs) were managed separately, namely: fungus group which received a daily supplement + fungal spores from lambing until the summer move (6 weeks) and: control group which received supplement only. For Farm B, the numbers of lambs that were marketed prior to the end of the grazing season, were 13, 18, 19 for the fungus treatment whereas corresponding numbers for the control treatment were 8, 16 and 11 for years 2001, 2002 and 2003, respectively. Final weights of the remaining lambs at the end of each year were also consistently heavier, and the numbers of lambs retained for finishing during winter were less, on the fungus treatment compared with the control treatment. On Farm N, similar results were recorded, with more lambs marketed earlier in the fungus group (25 and 19) compared with the control (19 and 15) in 2002 and 2003, respectively. The weights of the remaining lambs at the end of the trial in 2003 showed a 4.5 kg weight gain advantage of the fungus group compared to the controls. Tracer tests during autumn 2001 on Farm B, showed that Teladorsagia circumcincta plus Trichostrongylus spp. levels were significantly less on the fungus treatment (P=0.018). The summer/autumn of 2002 was one of the driest on record for Gotland. This resulted in very low levels of infective larval availability. But on both farms, T. circumcincta numbers were less on the fungus than on the control paddocks (P=0.048 on Farm B). In 2003 very low numbers of infective larvae were recorded in the autumn tracers for both treatments on both farms. Both farmer co-operators were encouraged with these results and consider that biological control of nematode parasites in their flocks, using D. flagrans, is of practical value.

Penicillium verrucosum in feed of ochratoxin A positive swine herds.

Ochratoxin A contamination of cereal feed grain was monitored during October 1989-September 1990 by analysis of blood samples from slaughter swine in Sweden. The detection of ochratoxin A in swine blood was used as a method to identify swine herds fed ochratoxin A contaminated feed. The contamination level of ochratoxin A in the blood of the positive herds was in the range 2-45 ng/ml with the mean concentration 5.2 ng/ml. Feed samples for mycological analysis were collected from both ochratoxin A positive herds (greater than or equal to ng/ml blood) and ochratoxin A negative herds (less than 2 ng/ml blood). From the ochratoxin A positive herds and the ochratoxin A negative herds 22 and 21 feed samples were collected, respectively. No quantitative differences in mould content, as determined by colony forming units, were observed between the two groups. However, there were differences in the mycoflora. The incidence of storage fungi (Penicillium and Aspergillus spp.) was significantly higher (p less than 0.05) in feed from ochratoxin A positive herds. Particularly, Penicillium verrucosum was found to be significantly more common (p less than 0.001). Altogether 274 isolates were screened for their ability to produce ochratoxin A. Ochratoxin A producers were found only within P. verrucosum; 38% of the 63 isolates produced detectable amounts of ochratoxin A. Ochratoxin A producing isolates of P. verrucosum were found in 60% of the feed samples collected from ochratoxin A positive swine herds and in one sample (5%) of the feed samples collected from the ochratoxin A negative herds.

Isolation of Coxiella burnetii in Sweden.

Coxiella burnetii was isolated from sheep placentas, which had been collected from farms harbouring humans seropositive to the organism. The isolation of these bacteria is the final evidence that Q fever is a domestic disease in Sweden.

Biochemical characterization of unidentified microaerophilic cocci isolated from heifer and dry-cow mastitis.

Thirty-nine strains of gram-positive microaerophilic cocci isolated from cases of heifer and dry-cow mastitis were biochemically characterized with the API 50E and API-ZYM test kit systems, gas-liquid chromatography for analysis of end products of glucose metabolism, and anaerobic biochemical tests (L. V. Holdeman, E. P. Cato, and W. E. C. Moore, Anaerobe Laboratory Manual, Virginia Polytechnic Institute, Blacksburg, 1977). Strains were screened for production of a variety of extracellular enzymes on substrate-containing agar plates and for hemolysin and coagulase production. Antibiotic susceptibility and sensitivity tests were also performed. The microaerophilic cocci displayed homogeneity with respect to the majority of the biochemical tests used; i.e., greater than or equal to 90% of the strains were consistently positive or negative in any one test and probably represent one species. All produced deoxyribonuclease, ribonuclease, and hyaluronidase, and 92% were positive for chondroitin sulfatase. Catalase and coagulase tests were negative. Greening was observed on bovine blood agar. Acetic and succinic acids were produced by all strains as the only detectable products of glucose metabolism. The strains were susceptible to penicillin G, cefoxitin, doxycycline, and chloramphenicol and were resistant to clindamycin, novobiocin, and metronidazole. Their taxonomic position remains unclear.

Biochemical, enzymatic, and serological differentiation of Peptococcus indolicus (Christiansen) Sørensen from Peptococcus asaccharolyticus (Distaso) Douglas.

Peptococcus indolicus (formerly Micrococcus indolicus) is an asaccharolytic anaerobic coccus that is frequently isolated from udder secretions from cases of heifer and dry-cow mastitis (summer mastitis). To facilitate better identification and its differentiation from Peptococcus asaccharolyticus, a variety of biochemical, enzymatic, and serological properties were studied. Seventy-nine strains of P. indolicus of bovine origin and 10 strains of P. asaccharolyticus of human origin were examined using the API 20A and API-ZYM test kit systems. In addition, production of extracellular enzymes by using sensitive substrate-containing agar plate tests, production of peptocoagulase (a plasma-clotting factor), hemolytic properties, metabolic end products by gas chromatography, and serological characteristics with a set of P. indolicus typing antisera were investigated. P. indolicus and P. asaccharolyticus were not satisfactorily differentiated solely by the API 20A system. P. indolicus differed from P. asaccharolyticus in producing H(2)S, reducing nitrate to nitrite, producing peptocoagulase, possessing alkaline phosphatase, and producing large amounts of propionate from lactate. Moreover, none of the strains of P. asaccharolyticus was typable with the P. indolicus typing antisera. The majority (88%) of P. indolicus strains also gave weak hydrolysis of ribonucleic acid, and 6 out of 79 produced deoxyribonuclease. All strains in this study were sensitive to metronidazole (5 mug) by disk diffusion tests.