Influence of Age of Apple Flowers on Growth of Erwinia amylovora and Biological Control Agents.

The influence of flower age on growth of Erwinia amylovora, the causal pathogen of fire blight of apples and pears, was investigated under humid and arid conditions in Hamilton, New Zealand (NZ), and Logan, UT, USA, respectively. 'Royal Gala' apple flowers ranging from 1 to 8 days old were atomized with E. amylovora. Pistils were dissected and washed separately from the remaining floral parts (flowers ex pistils) for estimation of bacterial numbers. Pistils, 1 to 3 days old (USA) and 1 to 4 days old (NZ), supported exponential growth of E. amylovora, but bacterial populations did not increase when older flowers were inoculated. Scanning electron microscopy showed round and turgid papillae on stigmas of 1-day-old flowers. Papillae on 4- to 6-day-old stigmas were completely collapsed and covered in mucilage. Populations of E. amy-lovora on the flowers ex pistils were characteristically lower than pistil populations. High populations of saprophytic bacteria were found on both floral parts of all ages, but there was no difference in their numbers on 3- to 6-day-old pistils. This suggests their presence did not inhibit the growth of E. amylovora on older stigmas. The results demonstrate that stigmas on 1- to 3-day-old flowers often support rapid growth of E. amylovora, but flowers inoculated when more than 4 to 5 days old do not support growth or only limited growth. The same location and pattern of bacterial growth occurred with the biological control agents Pseudomonas fluorescens PfA506n and Pantoea agglomerans (Erwinia herbicola) Eh318nr. The distinct effect of flower age on growth of antagonistic bacteria and E. amylovora may be important in deciding when to treat with biological control organisms or bactericides.

A Study on the Phylogeny of the Dyer's Woad Rust Fungus and Other Species of Puccinia from Crucifers.

ABSTRACT The identity of a Puccinia species occurring on the introduced weed dyer's woad (Isatis tinctoria) was studied using sequences from the internal transcribed spacer of the nuclear ribosomal DNA. The relationship of this fungus to other Puccinia species occurring on the family Brassicaceae in Europe and North America was examined, and we tested the hypothesis that P. thlaspeos and P. monoica are correlated species. The data suggest that the Puccinia species from dyer's woad is closely related to the North American species P. consimilis and may be derived from an indigenous strain of P. consimilis that switched hosts. Thus, the Puccinia species from dyer's woad is probably native to North America and is unlikely to cause disease epidemics on indigenous plants if used as a biological control agent against dyer's woad. P. thlaspeos appears to be polyphyletic and, therefore, P. thlaspeos and P. monoica do not appear to be correlated species. Additional DNA sequence data will be needed to clarify further the phylogeny of Puccinia species on the family Brassicaceae.

Mutagenic activity of Fusarium moniliforme isolates in the Salmonella typhimurium assay.

A total of 33 isolates of Fusarium moniliforme from several food or feed crops were grown on sterile cracked corn, and chloroform-isopropanol extracts were assayed for mutagenic activity in the Salmonella typhimurium-microsome system by using tester strain TA98 or TA100 or both. Extracts of 21 (64%) of the isolates assayed against TA100 were mutagenic. Activities of seven of these extracts were increased markedly with incorporation of the liver homogenate (S-9) into the assay. Seven (33%) of the isolates assayed against TA98 were weakly active, with the liver homogenate having little effect on reversion rates.

Detection of mutagens produced by fungi with the Salmonella typhimurium assay.

Forty-one fungal isolates (one isolate per species) representing common plant pathogens and food crop contaminants were grown on sterile, polished rice and assayed for mutagenic activity in the Salmonella typhimurium-microsome system. Initially, single doses of aqueous and chloroform extracts of the moldy rice were assayed against the TA100 tester strain by incorporating extracts into the growth medium and by applying small quantities on disks placed on the agar surface. Suspected activity was examined further by analysis of several doses in the plate incorporation assay. Extracts of two aflatoxin-producing isolates (Aspergillus flavus and A. parasiticus) showed pronounced mutagenic activity, as did extracts of five other isolates (A. heterothallicus, A. nidulans, A. terricola, Alternaria tenuis, and Fusarium moniliforme) which did not contain detectable aflatoxins. Seven additional isolates (Botrytis cineria, Ceratocystis fimbriata, Cladosporium herbarum, Fusarium solani f. sp. pisi, Penicillium oxalicum, Thermomyces lanuginosus, and Verticilium albo-atrum) revealed activity which was possibly mutagenic; i.e., mutagenic responses were not observed in both the disk and incorporation assays, and clear dose-related activity was not observed in the incorporation assay. Extracts of the remaining fungi were not mutagenic in the bacterial assay.

Pierce's disease of grapevines: isolation of the causal bacterium.

A Gram-negative, rod-shaped bacterium has been consistently isolated from grapevines with Pierce's disease. Grapevines inoculated with the bacterium developed Pierce's disease, and the bacterium was reisolated from the plants. The bacterium was serologically and ultrastructurallv indistinguishable from the one in naturally infected plants, and also indistinguishable from a bacterium isolated from almonds with almond leaf scorch disease.