Evaluation of mono- and polyclonal antibody-based antigen detection immunoassays for diagnosis of Trypanosoma evansi infection in the dromedary camel.

Two enzyme-linked immunosorbent assays (ELISA), one based on a mouse anti-Trypanosoma brucei group-specific monoclonal antibody and the other on rabbit anti-Trypanosoma evansi polyclonal antibodies, have been evaluated for their ability to detect circulating trypanosome antigens in camel sera as a means for the diagnosis of T. evansi infections. All 91 sera from a negative control camel herd from Kenya gave negative antigen-ELISA results in the monoclonal antibody-based ELISA and only 2 of them (2.2%) gave false positive results in the polyclonal antibody-based ELISA. In subsequent analyses of sera from infected camels (as determined by mouse inoculation), the monoclonal antibody-based ELISA detected antigens in 90 (83.3%) out of the 108 sera tested. This percentage was lower for the polyclonal antibody-based ELISA which was able to detect antigens in 67 (60.9%) out of the 110 sera tested. The two tests detected probably different antigens and when the results were combined, 99 out of 107 (92.5%) sera were shown to be ELISA positive. In a survey involving 316 camels from the Gao and Nara areas, in Mali, a high proportion of animals tested were antigen positive (43.5 and 42.9%, respectively for the mono- and polyclonal antibody-based ELISA) compared to only 22 (7.0%) diagnosed by the parasite detection techniques. Thus, these immunoassays were at least six times more sensitive than the haematocrit centrifugation technique. As a large proportion of cases may be antigen positive but parasite negative, these two of "surra" immunoassays should be used in routine diagnosis in addition to the parasite detection techniques in the dromedary camel.     

Actinobacillosis in an alpaca (Lama pacos)

The death of a 6-week-old alpaca being treated for acute polyarthritis is described. Post-mortem and histological findings included fibrinous mural endocarditis, lung abscessation, acute passive congestion of the liver, embolic suppurative nephritis and chronic nonsuppurative polyarthritis. Actinobacillus suis was isolated from the heart lesion and in pharyngeal swabs from four of six clinically normal alpacas in the same flock.     

The use of separate root and shoot tests in the screening of herbicides for strawberries

The tolerance of strawberries to herbicides was tested by applications to the roots of plants growing in sand and by foliage applications to plants grown in compost, and compared with tolerance in the field. Dimefuron was safe as a foliar application but much more toxic than simazine when applied in sand or in the field. Metamitron caused slight injury as a foliar spray; in sand and in the field it was intermediate in toxicity between simazine and lenacil. At normal rates propachlor was safe as a foliar spray and much safer than lenacil when applied in sand. High rates had no adverse effect in the field. Ethofumesate and pendimethalin caused some temporary stunting when applied to foliage, but were less toxic than lenacil when applied to roots in sand. Field applications of both herbicides at 1–1.5 kg/ha were safe. Foliage sprays of bentazone, oxadiazon and oxyfluorfen severely damaged the sprayed leaves, but these herbicides were less active than lenacil when applied to the roots. In the field they caused severe leaf damage, but by the end of the growing season the plants had recovered. The experiments demonstrated the value of separate root and shoot activity tests for indicating which herbicides merit further field testing.     

The use of immunochemically purified anti-brucella antibody in a direct fluorescent antibody test for Brucella abortus

Antibodies specific for Brucella abortus were purified from the serum of hyperimmunized sheep using immunochemical procedures. They were conjugated to fluorescein isothiocyanate and used in a fluorescent antibody (FA) test for B. abortus. The conjugate did not stain any heterologous bacterial or fungal species tested and background fluorescence associated with its use on smears and sections of abortion materials was particularly low. Of 239 cases of abortion examined fluorescent microscopy demonstrated B. abortus in all 12 cases in which the organism was isolated. A few areas of fluorescence typical of B. abortus were also seen in 3 cases from which the organism was not cultured. B. abortus was demonstrated in lymph nodes from 6 of 36 Brucella reactor cows by culture and 7 by the FA test. However, only very low numbers of B. abortus were isolated or seen and sampling errors would have been significant. Use of the FA test allows diagnosis of Brucellosis to be made in 2 hours, compared to 6 days by the usual cultural procedures.