Summary A new disease of unknown bacterial aetiology has been observed in eucalyptus stands since 2009. It is characterized by die‐back, wilting and lesions on the branches, petiole and midrib in association with macroscopic and microscopic bacterial ooze. To date, this disease has been observed in stands of clonal Eucalyptus saligna, E. grandis and E. urophylla x E. grandis hybrids and in E. dunnii seedling plantations in the states of São Paulo, Rio Grande do Sul and Mato Grosso do Sul. Considering the economic importance of eucalyptus plantations and the potential losses caused by this disease, this study aimed to identify and characterize the causal agent. Thirty‐four strains were obtained from infected plants, which were collected in the field from four locations. The inoculation of detached leaves and intact rooted cuttings supported pathogenicity in eucalyptus. The phylogenetic analysis of four housekeeping genes (16S rDNA, gapA, recA and rpoB) as well as biochemical tests confirmed the identity of strains belonging to the species Erwinia psidii. This is the first report of E. psidii as the cause of wilt and die‐back in Eucalyptus spp. in Brazil.

The dieback and wilting caused by Erwinia psidii are emerging eucalypt diseases that have been observed since 2014 in the south and central-south regions of Brazil. Field observations have shown variability in disease severity resistance among Eucalyptus spp. clones and species. It is hypothesized that this variability is due to genetic resistance. To confirm this hypothesis, inoculations in genetically distinct eucalypt plants are necessary. However, lack of an inoculation method and disease assessment makes difficult to select resistant genotypes for use in commercial plantations or genetic breeding programmes. Three inoculation methods were tested on eight clones of Eucalyptus spp. Among them, inoculum deposition with bacteria-impregnated toothpick on the axillary buds was the simplest and most effective, capable to reproduce the disease symptoms observed under conditions of natural infection. We also developed a rating scale for disease assessment. Among eight clones tested, only Clone 1 (Eucalyptus saligna) and Clone 2 (Eucalyptus urophylla) were resistant.

Ceratocystis wilt, caused by Ceratocystis fimbriata is one of the most serious limiting factors for mango production in Brazil. Despite efforts in the selection and the identification of mango cultivars resistant to Ceratocystis wilt, the genetic basis of the resistance remains unknown. Therefore, the objective of this study was to understand the inheritance of resistance to C. fimbriata by artificial inoculations of the pathogen in progenies of six commercial varieties of mango using "Tommy Atkins" as the male parent. The cultivars "Keitt", "Palmer", "Tommy Atkins" and "Van Dyke" were confirmed as moderately resistant, whereas "Coquinho", "Espada" and "Haden" were susceptible. The results of the inoculation on the progenies of these cultivars revealed that the resistance in mango is polygenic with a prevalence of genes expressing the effects of dominance and epistasis. The genetic gain with the selection of the 10 more resistant plants was 46%, which indicated a 46% reduction in disease severity. In general, a low frequency of the alleles favorable to disease resistance was observed in the population studied, which suggests the need for the introduction of new sources of genetic materials carrying the genes responsible for resistance.

O objetivo do estudo foi avaliar os atributos químicos e físicos do solo e o desenvolvimento inicial de teca em sistema agroflorestal. O experimento foi instalado em 2010 no município de Figueirópolis D’Oeste, Mato Grosso. O delineamento experimental utilizado foi blocos casualizados, com 12 tratamentos e quatro blocos, no esquema de parcelas subdivididas. O primeiro fator foi o preparo do solo em três tipos (covas, escarificação e convencional). O segundo fator, o tipo de propagação de muda (seminal e clonal). O terceiro fator, o milho nas entrelinhas da teca, em duas situações (presença e ausência). Foi realizado a análise de componentes principais (ACP) com todas as variáveis do solo coletadas aos 12 meses de idade para verificar quais variáveis apresentavam mais influência na análise multivariada. A análise discriminante (AD) foi realizada com todas as variáveis do solo e dendrométricas (ht e d5cm) dos tratamentos, com o intuito de se obter uma separação dos grupos, entre os tratamentos que apresentaram desenvolvimentos superiores e inferiores. Em seguida foi realizada a análise multivariada da variância (MANOVA) e o teste Tukey para verificar as diferenças. A análise foi executada com recursos do software SAS versão 9.4. Para a teca em sua fase inicial de desenvolvimento, as variáveis Ca, Ca+Mg, SB, CTC, Areia, H, pH CaCl2, Mg e MO foram as mais influentes demonstrado pela análise de componentes principais (ACP). Teca clonal implantados em preparo de solo convencional, covas e escarificação apresenta maior crescimento em relação aos demais sistemas de cultivo aos 36 meses de idade. A cultura agrícola influencia no crescimento de teca aos 12 meses de idade. A análise multivariada dos atributos do solo foi adequada para identificar os nutrientes que apresentam maior influência sobre o crescimento da teca em sistemas agroflorestais.

In the summer of 2011, in a nursery located in Viçosa City, Minas Gerais State, brownish, necrotic, irregular spots were observed on leaves of Mabea fistulifera Mart. (Euphorbiaceae), an indigenous forest species commonly found in Brazil. Around 6,300 seedlings were evaluated and as many as 60% of them showed disease symptoms, including severe defoliation and plant death. Leaves with coalescing lesions turned papery in texture and had a blighted appearance. Bacterial colonies were isolated from these symptomatic leaves on King B's medium and identified based on biochemical and molecular analysis, as a member of the Enterobacteriaceae family. Like other members of the Enterobacteriaceae family, the bacteria were facultative anaerobic, gram-negative, cream-colored on YDC medium, urease and oxidase negative, as well as catalase and asparagine positive. Bacterial DNA was extracted from pure culture grown overnight in liquid 523 medium at 28°C using the Wizard Genomic DNA Purification kit (Promega) and conserved sequences in 16S rDNA (3) and rpoB (1) were amplified by PCR. The sequence of the 1,300-bp 16S rDNA fragment and the 750-bp rpoB gene were analyzed by NCBI BLAST. Related sequences were aligned and analyzed by ClustalW in MEGA 5 software. Phylogenetic analysis by maximum likelihood, using PAUP version 4.0 and TBR algorithm with 1,000 bootstrap replications, grouped the isolate in a clade with Enterobacter cowanii and the result showed 99% and 98% identity to the 16s rDNA and rpoB, respectively. The isolate clustered closely with the type strain of E. cowanii in both phylogenetic trees constructed. Pathogenicity tests were carried out by inoculating leaves of healthy seedlings either by spraying or cutting with a scissor previously dipped into a 108 CFU/ml bacterial suspension. The experiment was in a completely randomized design, with six replications. A pot with one plant was considered one experimental unit. Control seedlings were sprayed or cut with a scissor treated with saline solution. Prior to and after inoculation, plants were kept in a humid chamber for 24 h at 26°C in the dark and at room temperature. Subsequently, plants were transferred to growth chamber at 26°C, under a 12-h photoperiod (40 μmol/s/m2). Consistent with the symptoms observed originally, 7 days after inoculation, all seedlings developed leaf spots. No characteristic symptoms could be observed in the negative control. Furthermore, Koch's postulates were confirmed by reisolation of the bacterium from symptomatic tissues. In summary, the phenotypic, biochemical, and molecular tests identified the pathogen as E. cowanii. Recently, E. cowanii was isolated from Eucalyptus trees with symptoms of bacterial blight, although its pathogenicity was not demonstrated (2). To the best of our knowledge, this is the first report of a member of the Enterobacteriaceae family causing disease in M. fistulifera. The result has a great importance to better understand the role of E. cowanii as a pathogen-causing disease on a forest species. References: (1) C. L. Brady et al. Syst. Appl. Microbiol. 31:447, 2008. (2) C. L. Brady et al. Lett. Appl. Microbiol. 49:461, 2009. (3) W. G. Weisburg et al. J. Bacteriol. 173:697, 1991.