Outbreaks of early-season trichostrongylosis in calves in Denmark

This paper describes clinically manifest infections occurring as early as June and early July in first-season grazing calves in Denmark during the period 1972-1987. Two severe outbreaks in 1976, included in our experiments, were studied in detail. Herbage infectivity was particularly high in grass tufts surrounding cow pats that were present in high numbers around the time of turnout. It is hypothesized that the preceding extremely dry summer followed by a hard winter had indirectly retarded degradation of dung pats and thereby favoured the overwintering of the larval populations in the dung reservoirs. In a third experiment, conducted in the same year, the epidemiological pattern was more normal; presumably due to artificial irrigation of the pasture during the drought. Early-season cases that were recorded in 1980 and 1987 could possibly be related to cold winters and/or very early turnout. The findings are discussed in the light of ecological factors responsible for the breakdown of cow pats. The clinical implications are seen in relation to current control methods.     

Impaired purine biosynthesis affects pathogenicity of <Emphasis Type="Italic">Fusarium oxysporum</Emphasis> f. sp. <Emphasis Type="Italic">melonis</Emphasis>

The vascular wilt pathogen Fusarium oxysporum f. sp. melonis causes worldwide yield losses of muskmelon. In this study, we characterized a UV-induced non-pathogenic mutant (strain 4/4) of F. oxysporum f. sp. melonis, previously identified as a potential biological control agent. During comparative analysis of vegetative growth parameters using different carbon sources, mutant strain 4/4 showed a delay in development and secretion of extracellular enzymes, compared to the wild type strain. Amendments of the growth medium with yeast extract, adenine or hypoxanthine, but not guanine, complemented the growth defect of strain 4/4, as well as secretion and partial activity of cellulases and endopolygalacturonases, indicating that the strain is an adenine auxotroph. Incubation of strain 4/4 conidia in adenine solution, prior to inoculation of muskmelon plants, partially restored pathogenicity to the mutant strain.     

Development of sequence tagged site markers to identify races of Fusarium oxysporum f. sp. lactucae

By random amplified polymorphic DNA (RAPD) analysis of the representative isolates of each race of Fusarium oxysporum f. sp. lactucae, RAPD fragments of 0.6, 1.6, and 2.9kb were obtained. The 0.6-kb RAPD fragment was common to the representative isolates of all three races. Amplification of the 1.6- and 2.9-kb fragments were unique to the isolates of races 1 and 2, respectively. Sequence tagged site (STS) marker FLA0001, FLA0101, and FLA0201 were generated from the 0.6-, 1.6-, and 2.9-kb RAPD fragments, respectively. Polymerase chain reaction (PCR) analysis showed that FLA0001 was common to all 49 isolates of F. oxysporum f. sp. lactucae. FLA0101 was specifically generated from all 23 isolates of race 1 but not from races 2 or 3. FLA0201 was specifically amplified from all 12 isolates of race 2 but not from races 1 or 3. In two isolates of F. oxysporum f. sp. lactucum, PCR amplified FLA0001 and FLA0101 but not FLA0201. On the other hand, these STS markers were not detected from isolates of five other formae speciales. Because these STS markers were not generated from isolates of other plant pathogenic fungi, bacteria, or plant materials examined in this study, PCR analysis combined with the three STS markers should be a useful means for rapid identification of races of F. oxysporum f. sp. lactucae.     

Stimulation of axillary shoot formation of cuttings of Hylocereus trigonus (Cactaceae) by pre-soaking in benzyladenine solution

Either before or after curing their cut surfaces for 5 days, 7 cm- and 15-cm-long decapitated Hylocereus trigonus cuttings were treated by soaking their apical or basal ends in benzyladenine (BA) solution. They were then planted and grown in a greenhouse.For the 7 cm-long cuttings, BA (25–100 mg l^?1) applied to the apical ends for 24 h increased the ratio of cuttings with sprouted buds to 64–100%, the number of sprouted buds to 1.9–3.1 and of shoots to 1.6–2.8, and the shoot length to 35–60 mm, compared to the water control which showed 13%, 1.0, 1.0 and 12.5 mm, respectively. Soaking the basal part had only a small effect.Naphthylacetic acid (NAA) applied to the basal ends of cuttings immediately after cutting increased the number of sprouted buds and shoots by inducing early rooting. The number and length of BA-induced axillary shoots in the longer cuttings was greater than those in the shorter ones.In the 15-cm-long cuttings, increasing the soaking time from 5 min to 24 h resulted in a greater promotive effect of BA on shoot formation. BA applied before curing showed the same effect as that given after curing but caused necrosis of the tissue just under the cut surface. Enlarging the area soaked in BA solution from 5 cm to 10 cm decreased the number of sprouting buds and shoots.