Structural studies of the development of infection structures of cowpea rust, Uromyces phaseoli var. vignae. I. Nucleoli and nuclei

1978 ◽  
Vol 56 (6) ◽  
pp. 648-661 ◽  
Author(s):  
Michèle C. Heath ◽  
I. Brent Heath

Light microscopical observations of living germ tubes and infection structures of cowpea rust were combined with an ultrastructural study to show that a nucleolus was present in the interphase nucleus at all stages of development from uredospore germination through to new uredospore formation. Vacuolate nucleoli were common in germ tubes but only nonvacuolate nucleoli were observed at other stages of fungal development. When grown on oil-containing collodion membranes, germinating uredospores, germ tubes, appressoria, and infection hyphae without haustorial mother cells all contained nucleoli composed primarily of nongranular material. Predominantly granular nucleoli were observed in developing uredospores and all parasitic stages in the leaf after the formation of the first haustorial mother cell. However, the fact that granular nucleoli were also seen in a membrane-grown infection hypha after haustorial mother cell formation suggested that the host was not required to stimulate the resumption of nucleolar activity. Electron-opaque patches, presumed to be condensed chromatin, were most prominent in the nucleoplasm of haustorial mother cells and virtually absent in germinating uredospores and germ tubes. The significance of this observation is discussed. A reduction in nuclear volume was observed in living material prior to cytokinesis in the appressorium and the substomatal vesicle. Evidence suggested that this reduction was produced by the expulsion of part of the nucleoplasm, plus the nucleolus, during mitosis rather than before as suggested for other rusts. Nuclei of haustorial mother cells and haustoria were also smaller than those in intercellular hyphae but the mechanism by which this was achieved could not be determined.

1967 ◽  
Vol 45 (4) ◽  
pp. 447-450 ◽  
Author(s):  
Ramesh Maheshwari ◽  
A. C. Hildebrandt ◽  
P. J. Allen

Urediospores of Uromyces phaseoli var. typica (Pers.) Wint. race 32 Arth. germinated on mineral oil – nitrocellulose membranes and sequentially developed appressoria, vesicles, and infection hyphae. The nuclear behavior during in vitro differentiation of infection structures was studied by use of the Feulgen technique. The two urediospore nuclei divided in the germ tube before the formation of appressorium. This was followed by a second division of the four daughter nuclei in the appressorium, and occasionally by a third division of the eight nuclei in the vesicle and infection hypha. Haustorial mother cells were formed in infection hyphae in vitro and contained from two to five nuclei. In contrast, nuclear division did not occur in germ tubes where growth continued linearly. Infection structures that developed in vitro resembled those produced during infection of the host by urediospores of other species of rust fungi.


1979 ◽  
Vol 57 (17) ◽  
pp. 1830-1837 ◽  
Author(s):  
I. Brent Heath ◽  
Michèle C. Heath

During development of infection structures of cowpea rust, Uromyces phaseoli var. vignae, migration of cytoplasm from one structure to the next is accompanied by production of vacuoles. The developmental pathway of these vacuoles appears to differ in different sites of production. In germinating uredospores, appressoria, and substomatal vesicles, their development includes the formation and enlargement of electron-opaque globule-containing vesicles, termed vacuole precursor vesicles (VPVs). In contrast, in the elongating germ tubes and vacuolating haustorial mother cells, VPVs do not appear during vacuolation. During development of VPVs into vacuoles there seems to be a control system which selectively activates only a portion of the VPV population.


1988 ◽  
Vol 66 (4) ◽  
pp. 736-741 ◽  
Author(s):  
Michèle C. Heath ◽  
C. J. Perumalla

The development of infection structures by the rust fungus Uromyces vignae was observed on oil-containing collodion membranes. About 40% of infection hyphae formed a haustorial mother cell, but this structure commonly senesced and died more rapidly than the infection hypha to which it was attached. These data suggest that the continued development of the haustorial mother cell requires some component normally provided by the host plant. Before they died, many haustorial mother cells apparently formed the thickened region of the wall which normally is traversed by the penetration peg during haustorium formation. Such a peg was observed in the centre of up to 40% of these thickened regions. However, no pegs protruded beyond the haustorial mother cell far enough to be called a haustorial neck. The thickened region of the haustorial mother cell wall could be differentiated from the rest of the wall by its lack of fluorescence under ultraviolet irradiation when mounted in Calcofluor or SITS (4-acetomido-4′-iso-thiocyanatostilbene-2,2′-disulphonic acid). Treatment with alkali, acid, chloroform–methanol, protease, and laminarinase did not affect this differential fluorescence, and the haustorial mother cell wall stained uniformly for proteins, carbohydrates, and chitin. Since Calcofluor normally binds to chitin, these data suggest that the thickened region of the haustorial mother cell wall may physically exclude the dye or may contain potential binding sites that are masked by other wall components.


1989 ◽  
Vol 67 (12) ◽  
pp. 3570-3579 ◽  
Author(s):  
C. W. Mims ◽  
J. Taylor ◽  
E. A. Richardson

Peanut rust disease proved to be an excellent system for ultrastructural study of development of infection structures by the fungus Puccinia arachidis. Fungal structures were clearly visible by light microscopy in fixed and embedded samples and could be located either on leaf surfaces or within the large substomatal chambers of peanut leaves. Samples could easily be oriented for thin sectioning. The infection process was a highly orchestrated process involving precisely timed events and highly specialized structures. Infection pegs developed from appressoria over stomata and entered the leaf by growing into the openings between guard cells. Once past the rim formed by the guard cell walls, the infection peg expanded to form a substomatal vesicle in which a synchronous mitotic division of the four nuclei occurred. A primary infection hypha then developed from the vesicle and grew into the mesophyll of the leaf until its tip or side contacted a host cell. A septum then delimited a binucleate or trinucleate terminal haustorial mother cell from the remainder of the infection hypha. The wall of the haustorial mother cell became closely appressed to that of the host cell. Following differentiation of the haustorial mother cell, a penetration peg arose from it and penetrated the host cell wall. The peg invaginated the host cell plasma membrane as it elongated and then expanded at its tip to form the haustorium body into which most of the contents of the haustorial mother cell moved. Meanwhile, the primary infection hypha formed secondary hyphae that gave rise to additional haustorial mother cells and haustoria. Key words: Puccinia arachidis, peanut rust, infection process, ultrastructure.


1993 ◽  
Vol 71 (9) ◽  
pp. 1236-1242 ◽  
Author(s):  
M. Stark-Urnau ◽  
K. Mendgen

Aecidiospores and uredospores are the two dikaryotic spore forms of the cowpea rust fungus Uromyces vignae. After germination they can be induced to develop a series of infection structures including appressoria, infection hyphae, and haustorial mother cells. Haustoria are then formed within host cells. The differentiation of infection structures was compared on polystyrene membranes with defined topographies, on scratched polyethylene membranes, and in planta. On polystyrene membranes with defined topographies both sporelings showed highest rates of differentiation on ridges 0.3 μm high but aecidiosporelings responded less efficiently to this stimulus than uredosporelings. On scratched polyethylene membranes, almost 90% of both sporelings differentiated appressoria, but only 10% formed haustorial mother cells; haustoria were not observed. On the host plant, by contrast, only 50% of the sporelings differentiated appressoria, but most of these formed haustorial mother cells and haustoria. In planta haustorial mother cell development occurred approximately 6 h earlier than on inductive membranes. Infection structures formed on artificial membranes and on host plants were similar in morphology and nuclear condition. Key words: cowpea rust fungus, nucleus, appressorium.


Forests ◽  
2021 ◽  
Vol 12 (11) ◽  
pp. 1598
Author(s):  
Wenju Lu ◽  
Enbo Wang ◽  
Weijuan Zhou ◽  
Yifan Li ◽  
Zhaoji Li ◽  
...  

Dacrydium pectinatum de Laubenfels is a perennial gymnosperm species dominant in tropical montane rain forests. Due to severe damages by excessive deforestation, typhoons, and other external forces, the population of the species has been significantly reduced. Furthermore, its natural regeneration is poor. To better understand the male cone development in D. pectinatum, we examined the morphological and anatomical changes, analyzed the endogenous hormone dynamics, and profiled gene expression. The morpho-histological observations suggest that the development of D. pectinatum male cone can be largely divided into four stages: microspore primordium formation (April to May), microspore sac and pollen mother cell formation (July to November), pollen mother cell division (January), and pollen grain formation (February). The levels of gibberellins (GA), auxin (IAA), abscisic Acid (ABA), cytokinin (CTK), and jasmonic acid (JA) fluctuated during the process of male cone development. The first transcriptome database for a Dacrydium species was generated, revealing >70,000 unigene sequences. Differential expression analyses revealed several floral and hormone biosynthesis and signal transduction genes that could be critical for male cone development. Our study provides new insights on the cone development in D. pectinatum and the foundation for male cone induction with hormones and studies of factors contributing to the species’ low rate of seed germination.


2008 ◽  
Vol 133 (1) ◽  
pp. 107-116 ◽  
Author(s):  
Pablo Bolaños-Villegas ◽  
Shih-Wen Chin ◽  
Fure-Chyi Chen

The development of new cultivars in Doritaenopsis Guillaum. & Lami orchids is often hindered by factors such as low seed count in hybrids. Cytological study may offer the ability to develop new hybrids by revealing cultivars with good chromosome pairing and high pollen viability, which are somewhat difficult to obtain under current breeding programs. Cross pollination, pollen viability, and chromosomal behavior during meiosis were analyzed to reveal the relation between seed fertility and capsule set in Doritaenopsis hybrids. The number of mature capsules harvested and their relative seed content were used as indices of crossing availability. The results of meiosis were evaluated according to pollen viability detected by fluorescein diacetate and quantification of sporad types by acid fuchsin staining. Chromosome number and pairing at meiosis were observed in root tips or in samples of pollen mother cells. A positive relation was found among high seed set, high frequency of viable tetrads, high degree of chromosome pairing, and low frequency of chromosomal aberrations such as inversions and translocations. On the basis of these factors, three types of hybrids could be distinguished. In type one hybrids, chromosomes paired as bivalents, pollen mother cells divided into tetrads, and capsule setting occurred after pollination of pollen acceptors. In type two hybrids, chromosomes remained mainly as univalents that developed into micromeiocytes, pollen mother cell division was disrupted, and seed recovery was low after pollination. Type three hybrids showed chromosomes paired mostly as multivalents, chromosome bridges, pollen mother cell division with massive failure, and little fertility. In Doritaenopsis orchids, high pollen viability and high fertility depends on a high frequency of normal tetrads, and low seed set in cross-pollination is predicted with micronuclei in the end products of meiosis. The occurrence of chromosomal aberrations may suggest a process of genome differentiation that could compromise breeding efforts if not taken into consideration.


2013 ◽  
Vol 24 (23) ◽  
pp. 3697-3709 ◽  
Author(s):  
Lihong Li ◽  
Shawna Miles ◽  
Zephan Melville ◽  
Amalthiya Prasad ◽  
Graham Bradley ◽  
...  

Yeast that naturally exhaust the glucose from their environment differentiate into three distinct cell types distinguishable by flow cytometry. Among these is a quiescent (Q) population, which is so named because of its uniform but readily reversed G1 arrest, its fortified cell walls, heat tolerance, and longevity. Daughter cells predominate in Q-cell populations and are the longest lived. The events that differentiate Q cells from nonquiescent (nonQ) cells are initiated within hours of the diauxic shift, when cells have scavenged all the glucose from the media. These include highly asymmetric cell divisions, which give rise to very small daughter cells. These daughters modify their cell walls by Sed1- and Ecm33-dependent and dithiothreitol-sensitive mechanisms that enhance Q-cell thermotolerance. Ssd1 speeds Q-cell wall assembly and enables mother cells to enter this state. Ssd1 and the related mRNA-binding protein Mpt5 play critical overlapping roles in Q-cell formation and longevity. These proteins deliver mRNAs to P-bodies, and at least one P-body component, Lsm1, also plays a unique role in Q-cell longevity. Cells lacking Lsm1 and Ssd1 or Mpt5 lose viability under these conditions and fail to enter the quiescent state. We conclude that posttranscriptional regulation of mRNAs plays a crucial role in the transition in and out of quiescence.


2019 ◽  
Vol 20 (12) ◽  
pp. 3051 ◽  
Author(s):  
Vasily V. Ashapkin ◽  
Lyudmila I. Kutueva ◽  
Nadezhda I. Aleksandrushkina ◽  
Boris F. Vanyushin

Unlike in animals, the reproductive lineage cells in plants differentiate from within somatic tissues late in development to produce a specific haploid generation of the life cycle—male and female gametophytes. In flowering plants, the male gametophyte develops within the anthers and the female gametophyte—within the ovule. Both gametophytes consist of only a few cells. There are two major stages of gametophyte development—meiotic and post-meiotic. In the first stage, sporocyte mother cells differentiate within the anther (pollen mother cell) and the ovule (megaspore mother cell). These sporocyte mother cells undergo two meiotic divisions to produce four haploid daughter cells—male spores (microspores) and female spores (megaspores). In the second stage, the haploid spore cells undergo few asymmetric haploid mitotic divisions to produce the 3-cell male or 7-cell female gametophyte. Both stages of gametophyte development involve extensive epigenetic reprogramming, including siRNA dependent changes in DNA methylation and chromatin restructuring. This intricate mosaic of epigenetic changes determines, to a great extent, embryo and endosperm development in the future sporophyte generation.


1985 ◽  
Vol 33 (8) ◽  
pp. 809-812 ◽  
Author(s):  
M E Rey ◽  
H M Garnett

Digitaria eriantha pentzii was fed 3H-glucose prior to inoculation with uredospores of Puccinia digitariae Pole Evans. Twenty-one hours after inoculation, uptake of label from 3H-glucose by the primary infection structures of P. digitariae was demonstrated employing autoradiography. These results indicate that an exchange of nutrients between host and pathogen occurs very early on in the infection process, during the formation of the primary infection structures. Despite contrary reports that obligate parasites receive no nutrition before establishment of haustoria, this study supports the work of Andrews (Can J Bot 53:1103, 1975), who demonstrated uptake of 3H-glucose label from lettuce cotyledons into the primary and secondary infection vesicles, appressoria, and germ tubes of Bremia lactucae.


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