In October 2001, a wilting disorder of new aetiology was reported affecting banana ( Musa sp.) within the Mukono district of Uganda. The disorder was characterized by a rapid yellowing and wilting of the younger leaves, a discoloration of the internal vascular vessels, occasionally a dieback initiating from the male floral parts with internal rotting of banana fruits. These symptoms were notably distinct from fusarium wilt ( Fusarium oxysporum ) and 'Matooke wilt' (a wilt-like disorder of unknown aetiology), but strongly resembled Moko disease caused by Ralstonia solanacearum , although this particular pathogen had not previously been recorded on banana in Africa.A bacterium was isolated on nutrient agar that was identified by fatty acid (Microbial ID Inc. [MIDI]) and metabolic (Biolog, Inc, Hayward, CA, USA) analyses as Xanthomonas axonopodis (ID probability score < 0·4) and Xanthomonas campestris (ID probability score ∼ 0·9), respectively. The presence of the Xanthomonas specific fatty acids 11:0 ISO, 11:0 ISO 3OH and 13:0 ISO 3OH was recorded. Pathogenicity tests on disease-free tissue culture-derived banana plantlets by stem inoculation with a bacterial suspension induced wilt symptoms consistent with field observations after 3 weeks. Reisolation and identification, as outlined above, confirmed Koch's postulates. Reference to the literature suggested the bacterium was Xanthomonas campestris pv. musacearum (Yirgou & Bradbury, 1968). However, this bacterium is relatively poorly described and not contained within either the MIDI or Biolog databases. To support the identification, rep-PCR (Louws et al ., 1994) using ERIC and BOX primers was performed on the Ugandan banana isolate, cultures of X. campestris pv. musacearum from Ensete and Musa in Ethiopia (IMI 349461, IMI 349986, IMI350025) and other cultures of Xanthomonas spp. from Africa. These analyses revealed an identical DNA fingerprint for all isolates from Musa and Ensete , but distinct fingerprints for the isolates from other hosts. This is the first report of X. campestris pv. musacearum outside of Ethiopia, where it is recorded as a pathogen of ensete and, to a lesser extent, banana. Accordingly, this pathogen has been given the common name of ensete bacterial wilt, although the aptness of this now looks questionable. The risk posed by this new disease record to the contiguous banana plantation of Uganda is undetermined, but significant spread is already being observed. The causative organism for this new disease record has been deposited within the CABI Genetic Resource Collection as IMI 386970. References

Wild mushrooms are a vital source of income and nutrition for many poor communities and of value to recreational foragers. Literature relating to the edibility of mushroom species continues to expand, driven by an increasing demand for wild mushrooms, a wider interest in foraging, and the study of traditional foods. Although numerous case reports have been published on edible mushrooms, doubt and confusion persist regarding which species are safe and suitable to consume. Case reports often differ, and the evidence supporting the stated properties of mushrooms can be incomplete or ambiguous. The need for greater clarity on edible species is further underlined by increases in mushroom‐related poisonings. We propose a system for categorizing mushroom species and assigning a final edibility status. Using this system, we reviewed 2,786 mushroom species from 99 countries, accessing 9,783 case reports, from over 1,100 sources. We identified 2,189 edible species, of which 2,006 can be consumed safely, and a further 183 species which required some form of pretreatment prior to safe consumption or were associated with allergic reactions by some. We identified 471 species of uncertain edibility because of missing or incomplete evidence of consumption, and 76 unconfirmed species because of unresolved, differing opinions on edibility and toxicity. This is the most comprehensive list of edible mushrooms available to date, demonstrating the huge number of mushrooms species consumed. Our review highlights the need for further information on uncertain and clash species, and the need to present evidence in a clear, unambiguous, and consistent manner.

Polymerase chain reaction (PCR) assays were used to detect phytoplasmas in foliage samples from Chinaberry ( Melia azedarach ) trees displaying symptoms of yellowing, little leaf and dieback in Bolivia. A ribosomal coding nuclear DNA (rDNA) product (1·8 kb) was amplified from one or more samples from seven of 17 affected trees by PCR employing phytoplasma-universal rRNA primer pair P1/P7. When P1/ P7 products were reamplified using nested rRNA primer pair R16F2n/R16R2, phytoplasmas were detected in at least one sample from 13 of 17 trees with symptoms. Restriction fragment length polymorphism (RFLP) analysis of P1/ P7 products indicated that trees CbY1 and CbY17 harboured Mexican periwinkle virescence (16SrXIII )-group and X-disease (16SrIII)-group phytoplasmas, respectively. Identification of two different phytoplasma types was supported by reamplification of P1/ P7 products by nested PCR employing X-diseasegroup-specific rRNA primer pair R16mF2 / WXint or stolbur-group-related primer pair fSTOL/rSTOL. These assays selectively amplified rDNA products of 1656 and 579 bp from nine and five trees with symptoms, respectively, of which two trees were coinfected with both phytoplasma types. Phylogenetic analysis of 16S rDNA sequences revealed Chinaberry yellows phytoplasma strain CbY17 to be most similar to the chayote witches'-broom (ChWBIII-Ch10) agent, a previously classified 16SrIII-J subgroup phytoplasma. Strain CbY1 resembled the Mexican periwinkle virescence phytoplasma, a 16SrXIII-group member. The latter strain varied from all known phytoplasmas composing group 16SrXIII. On this basis, strain CbY1 was assigned to a new subgroup, 16SrXIII-C.

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Two independent surveys were performed in Peru during February and November 2007 to detect the presence of phytoplasmas within any crops showing symptoms resembling those caused by phytoplasmas. Molecular identifications and characterisations were based on phytoplasma 16S and 23S rRNA genes using nested PCR and terminal restriction fragment length polymorphism (T-RFLP). The surveys indicated that phytoplasmas were present in most of the locations sampled in Peru in both cultivated crops, including carrots, maize, native potatoes, improved potato, tomato, oats, papaya and coconut, and in other plants such as dandelion and the ornamental Madagascar periwinkle (Catharanthus roseus). Phylogenetic analysis of the sequences confirmed that while most of the isolates belong to the 16SrI aster yellows group, which is ubiquitous throughout other parts of South America, one isolate from potato belongs to the 16SrII peanut witches' broom group, and one isolate from tomato and one from dandelion belong to the 16SrIII X-disease group. The use of T-RFLP was validated for the evaluation of phytoplasma-affected field samples and provided no evidence for mixed infection of individual plants with more than one phytoplasma isolate. These data represent the first molecular confirmation of the presence of phytoplasmas in a broad range of crops in Peru.

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Plant health clinics, Bolivia, National plant healthcare systems, Research/extension links, Global plant clinic,