Disease screening to determine the threat Puccinia psidii poses to plantation and native eucalypts in Australia was undertaken in half-sib families of two contrasting eucalypt species, Eucalyptus cloeziana and E. argophloia. Artificial inoculation with a single-lesion isolate of P. psidii was used to screen these species for resistance to the biotype of P. psidii established in Australia. The objective was to characterize resistance to P. psidii within these two distinct species: E. argophloia, a vulnerable species with a narrow distribution, and E. cloeziana, a species with a broad and extensive distribution in Queensland. Results for E. cloeziana indicate that inland provenances are more resistant to P. psidii infection than provenances from coastal regions. Heritability estimates for the two assessment systems used (resistance on a 1-to-5 ordinal scale verses resistance on a 0-to-1 binomial scale) were low to high (0.24 to 0.63) for E. argophloia and moderate to high (0.4 to 0.91) for E. cloeziana, indicating a significant level of additive genetic variance for rust resistance within the populations. This study demonstrates the potential to select resistant families within the tested populations and indicates that P. psidii could detrimentally affect these species in native forests, nurseries, and plantations.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1094/PDIS-04-14-0353-RE | DOI Listing |
3 Biotech
December 2024
Morphogenesis and Reproductive Biology of Plants Laboratory, Department of Biological Sciences, University Campus, "Luiz de Queiroz" College of Agriculture, University of São Paulo (ESALQ/USP), 11, Pádua Dias Ave., POB 9, Piracicaba, SP 13418-900 Brazil.
Micropropagation is an important tool for the propagation for recalcitrant species, like This is a first reported about a complete study of the , it includes the vegetative rescue protocol of mature trees, its micropropagation up to the implementation of a mini-garden and clonal micro-garden and evaluation of adventitious rooting of their propagules. The in vitro rejuvenation of genotypes (03, 05, 06, 13 and 15), over 21 successive subcultures, was evaluated by comparing minicutting and microcutting techniques and the efficiency of this biotechnological tool for cloning of the mature trees. The results provide evidence of the in vitro rejuvenation occurring in the mature trees during micropropagation, leading to increases in the multiplication ratios of the microstumps of three genotypes (03, 05 and 15).
View Article and Find Full Text PDFBraz J Biol
March 2024
Universidade Federal de Minas Gerais - UFMG, Instituto de Ciências Agrárias, Montes Claros, MG, Brasil.
J Nematol
February 2023
Department of Entomology and Plant Pathology, Universidade Estadual do Norte Fluminense Darcy Ribeiro. Av. Alberto Lamego, 2000, Campos dos Goytacazes, Brazil, 28013-600.
Eucalypts are cultivated worldwide, but little is known about their status as hosts of root-knot nematodes (RKN) ( spp.). Moreover, information is scarce regarding the nature of the damage caused by RKN to eucalypt seedlings and trees.
View Article and Find Full Text PDFPlant Dis
November 2023
Chongqing Three Gorges University, 372323, College of Biological and Food Engineering, tianxing street, Wanzhou, Wanzhou, Chongqing, China, 404120.
J Nat Prod
September 2023
School of Environment and Science, Griffith University, Gold Coast, Queensland 4222, Australia.
Amyloid protein aggregates are linked to the progression of neurodegenerative conditions and may play a role in life stages of , the parasite responsible for malaria. We hypothesize that amyloid protein aggregation inhibitors may show antiplasmodial activity and vice versa. To test this hypothesis, we screened antiplasmodial active extracts from 25 Australian eucalypt flowers using a binding affinity mass spectrometry assay to identify molecules that bind to the Parkinson's disease-implicated protein α-syn.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!