A spectrophotometric approach for determining sporangium and zoospore viability of Plasmopara viticola

A spectrophotometric method for determining the viability of sporangia and zoospores of the oomycete Plasmopara viticola (causal agent of grapevine downy mildew) is described and evaluated to overcome the limitations of currently available methods for assessing propagule viability. Sporangia produced on leaf discs in the laboratory were harvested at different days after the initiation of sporulation (DAS) to yield differences in sporangium viability. Sporangia were suspended in sterile water, the suspensions were placed in a cuvette, and sporangium germination was monitored in a spectrophotometer (λ = 600 nm) at 2- to 3-min intervals for 5 hr. Absorbance started to increase after sporangia were suspended in water for ~30–60 min followed by major peak(s) for younger sporangia (1–3 DAS), whereas low to no increase in absorbance was observed for senescent sporangia (>7 DAS). Microscopic observation confirmed that the increase in absorbance corresponded to the release and active swimming of zoospores, whereas absorbance decreased when zoospores encysted and settled. A positive correlation (r = .839, p = .0365) was observed when the time to the initial increase in absorbance was plotted against the age of sporangia. The time to the absorbance peak (marking the time of maximum zoospore movement) was shortest for immature sporangia (0 DAS), longest for young sporangia (2 DAS) and decreased for mature and senescent sporangia. A similar pattern was observed for the standardized area under the absorbance curve (indicating the overall quantity of zoospores released), for which values were lowest for immature and senescent sporangia, highest for young sporangia and intermediate for mature sporangia. Consistent patterns obtained across two independent experiments suggest that the method is reproducible and may be further developed for other zoospore-releasing pathogens.     

The attenuated phenotype of a Salmonella typhimurium flgM mutant is related to expression of FliC flagellin.

The flgM gene of Salmonella typhimurium encodes a negative regulator of flagellin synthesis that acts by inhibiting the flagellum-specific sigma factor FliA (sigma 28), but only when a mutation in a flagellar basal body, hook, or switch gene is present. We previously showed that FlgM is also necessary for the virulence of S. typhimurium in the mouse model of typhoid fever and proposed that FlgM is required to modulate the activity of the FliA sigma factor, which, in turn, regulates a gene involved in virulence. In this investigation, we observed that (i) the in vitro generation times of flgM mutant and wild-type strains of S. typhimurium were indistinguishable, as were the amounts of flagellin produced by the strains; (ii) the 50% lethal doses of fliA mutant and wild-type strains of S. typhimurium were similar in orally infected mice; and (iii) inactivation of the FliA-regulated flagellin gene fliC in an flgM S. typhimurium mutant resulted in a virulent phenotype. Therefore, we now conclude that expression of the FliC flagellin subunit in an flgM strain is responsible for the attenuated phenotype of an flgM mutant and that FliA does not appear to positively regulate virulence genes in S. typhimurium. Our results suggest that the normal regulation of flagellum synthesis appears to be necessary for virulence and that there may be an advantage conferred in vivo by expression of a particular flagellar phenotype of S. typhimurium.     

Spore emission,sporangium proliferation and spore germination In situ in monosporangia of Acrochaetium virgatulum

Monospore release is effected mainly by an apical tear accompanied by momentary spore distortion, and sometimes with a distinct ‘blow-out’ of the sporangium apex; orientation of the paths of spore release is seen with serially arranged sporangia. Sporangium proliferation is common in cultures, but spore germination in situ is rare. Attempts at experimental induction of the process resulted in some sporangia with early developmental stages coming to resemble tetrasporangia.     

Synaptonemal complex formation and meiosis in the resting sporangium ofBlastocladiella emersonii

Summary Blastocladiella emersonii Cantino etHyatt (Phycomycetes, Blastocladiales) has aBrachyallomyces type of life cycle (sensu Emerson 1941) or aBlastocladiella type of life cycle (sensu Karling 1973), with a regular formation of zoosporangia and resting sporangia and no sexual stages.Synaptonemal complex formation (a characteristic stage in meiotic prophase—pachytene) occurs during development of the resting sporangium inB. emersonii.During resting sporangium germination, two meiotic nuclear divisions give rise to nuclei which have approximately one-fourth of the nuclear volume of the diplotene nucleus. The life cycle ofBlastocladiella emersonii resembles that ofCatenaria anguillulae. The time of diploidization (n2 n) has not been determined.     

SULLITHECA DACTYLIFERA GEN. ET SP. N.: A NEW MEDULLOSAN POLLEN ORGAN AND ITS EVOLUTIONARY SIGNIFICANCE

The pteridosperm (Medullosaceae) pollen organ Sullitheca dactylifera gen. et sp. n. is described from middle Pennsylvanian coal balls. The proximally fused units of the obpyriform compound synangium separate and extend distally as finger-like projections. Each projection contains 4–6 vertically oriented cylindrical sporangia arranged in pairs along the radius of the unit; each unit extends from the outer cover wall toward the center. The distal portion of the compound synangium is hollow as a result of the lateral separation of the centripetally and distally directed synangial units. About 40 tubular sporangia are present in all and dehiscence occurs along a lateral slit in each sporangium. Vascular strands are disposed around the periphery of the organ in addition to a single strand paralleling each sporangium. Two- or three-cell trichomes and stomata are present on the organ surface. Pollen of the Monoletes type is present. A paired row of sporangia in Sullitheca composing a synangial unit is considered the homologue of a paired row of sporangia in the more compact and highly evolved genus, Dolerotheca.     

中华水韭孢子囊发育研究

采用半薄切片法,连续观察了极度濒危级(CR)植物中华水韭大小孢子囊的发育过程,以期从无性生殖的角度,为探讨其濒危原因提供直观可靠的理论根据。结果显示:(1)中华水韭的大小孢子叶相间排列,无混生孢子囊。(2)隔丝为孢子供给营养,其体积直接影响孢子的大小、产量和育性。(3)大小孢子囊都近半数败育,小孢子囊为整齐发育,大孢子囊为不整齐发育。(4)大小孢子囊均无柄,且都不存在开裂结构,只有孢子囊壁腐烂后才能散播孢子。研究认为,中华水韭的濒危与孢子囊的发育特征密切相关,孢子囊的高频率败育、没有开裂结构以及对环境的依赖,是造成中华水韭濒危的重要因素之一;通过与近缘类群孢子囊的比较,发现仅水韭孢子的散播借助外力,对生境要求较高,即验证了水韭古老的系统学地位,同时说明水韭更具有监测生境地区环境指标的能力。     

A Phytophthora infestans G-protein beta subunit is involved in sporangium formation

The heterotrimeric G-protein pathway regulates cellular responses to a wide range of extracellular signals in virtually all eukaryotes. It also controls various developmental processes in the oomycete plant pathogen Phytophthora infestans, as was concluded from previous studies on the role of the G-protein α-subunit PiGPA1 in this organism. The expression of the P. infestans G-protein β-subunit gene Pigpb1 was induced in nutrient-starved mycelium before the onset of sporangium formation. The gene was hardly expressed in mycelium incubated in rich growth medium. The introduction of additional copies of Pigpb1 into the genome led to silencing of the gene and resulted in transformants deficient in PiGPB1. These Pigpb1-silenced mutants formed very few asexual spores (sporangia) when cultured in rye sucrose medium and produced a denser mat of aerial mycelium than the wild type. Partially Pigpb1-silenced mutants showed intermediate phenotypes with regard to sporulation, and a relatively large number of their sporangia were malformed. The results show that PiGPB1 is important for vegetative growth and sporulation and, therefore, for the pathogenicity of this organism.