Background: Single-and low-copy genes are less likely subject to concerted evolution, thus making themselves ideal tools for studying the origin and evolution of polyploid taxa. Leymus is a polyploid genus with a diverse array of morphology, ecology and distribution in Triticeae. The genomic constitution of Leymus was assigned as NsXm, where Ns was presumed to be originated from Psathyrostachys, while Xm represented a genome of unknown origin. In addition, little is known about the evolutionary history of Leymus. Here, we investigate the phylogenetic relationship, genome donor, and evolutionary history of Leymus based on a single-copy nuclear Acc1 gene.
Significant progress has been made in the biochemical and genetic characterization of the host-pathogen interaction mediated by insect pathogenic fungi, with the most widely studied being the Ascomycetes (Hypocrealean) fungi, Metarhizium robertsii and Beauveria bassiana. However, few studies have examined the consequences and effects of host (insect) microbes, whether compatible or antagonistic, on the development and survival of entomopathogenic fungi. Host microbes can act on the insect cuticular surface, within the gut, in specialized insect microbe hosting structures, and within cells, and they include a wide array of facultative and/or obligate exosymbionts and endosymbionts. The insect microbiome differs across developmental stages and in response to nutrition (e.g., different plant hosts for herbivores) and environmental conditions, including exposure to chemical insecticides. Here, we review recent advances indicating that insect-pathogenic fungi have evolved a spectrum of strategies for exploiting or suppressing host microbes, including the production of antimicrobial compounds that are expressed at discrete stages of the infection process. Conversely, there is increasing evidence that some insects have acquired microbes that may be specialized in the production of antifungal compounds to combat infection by (entomopathogenic) fungi. Consideration of the insect microbiome in fungal insect pathology represents a new frontier that can help explain previously obscure ecological and pathological aspects of the biology of entomopathogenic fungi. Such information may lead to novel approaches to improving the efficacy of these organisms in pest control efforts.
Wide crosses and synthetic amphiploids have played an important role in introgressing desirable traits from related species into cultivated wheat. Hybrids between Triticum aestivum cv. ÔJ-11Õ and Psathyrostachys huashanica were treated with colchicine, to produce a new intergeneric amphiploid (PHW-SA). The morphological characteristics of PHW-SA resembled the parent ÔJ-11Õ. PHW-SA plants have purple internodes and pubescence in the basal spikelet, inherited from the P. huashanica parent. Somatic chromosome numbers varied from 2n = 51 to 2n = 56, with 70.59% of plants having 56 chromosomes. At metaphase I, PHW-SA (2n = 56) plants showed an average of 1.15 univalents, 27.34 bivalents, 0.03 trivalents and 0.02 tetravalents per cell; complete chromosome pairing occurred in 50% of the pollen mother cells. A survey of disease resistances revealed that the stripe rust resistance from P. huashanica was expressed, but powdery mildew resistance was suppressed. The fertility of PHW-SA was 60%.
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