EFFECT OF NITROGEN,SULFUR AND OTHER FACTORS ON ZOOSPORE PRODUCTION BY PROTOSIPHON BOTRYOIDES

O'Kelley , J. C., and T. R. Deason . (U. Alabama, University.) Effect of nitrogen, sulfur and other factors on zoospore production by Protosiphon botryoides. Amer. Jour. Bot. 49(7): 771–777. Illus. 1962.—Nutrient-medium pH, osmotic pressure, staling products, and mineral depletion were studied in relation to zoospore production by Protosiphon botryoides in liquid media. In an intermediate range (pH 5.1–7.7), pH has little or no influence specifically on zoospore production. Although distilled water is an unsuitable medium for zoospore production, if a balanced nutrient medium is supplied, osmotic pressure is without pronounced influence over a wide range. Staling products in old cultures exert a minor inhibitory effect. Deficiencies of nitrate, sulfate, or calcium in liquid media can decrease drastically zoospore production or release, and nitrate or calcium depletion appears to be mainly responsible for loss of the capacity of Protosiphon to produce and release zoospores in aged liquid cultures.     

In vitro production of zoospores by the mosquito pathogen Lagenidium giganteum (Oomycetes: Lagenidiales) on solid media

Reliable, large-scale production of Lagenidium giganteum zoospores was obtained on solid media. The fungus was grown for 7 days in a liquid medium of wheat germ, hemp seed, yeast extract, and glucose, then placed onto hemp-seed agar. Zoosporogenesis was induced on agar by immersing the fungal cultures into water. Zoospore production began 10 hr postimmersion, peaked at 18 hr, and ceased by 36 hr. A single, 10-cm Petri dish of fungus on hemp-seed agar produced 1.7?3.8 × 10⁷ zoospores during the 26 hr of zoosporogenesis. Optimal zoospore production occurred with 4- to 7-day-old cultures; cultures older than 10 days produced few zoospores. The temperature range for zoosporogenesis was 15–35°C. The extent of zoosporogenesis was directly related to the volume of water used to induce zoospore formation and inversely proportional to agar thickness. Bioassay of zoospores against second instar Culex quinquefasciatus larvae yielded an LD₅₀ of 400 zoospores/ml.     

EFFECTS OF CA AND SR ON ZEA MAYS SEEDLING PRIMARY ROOT GROWTH

Either Ca or Sr in a mineral nutrient medium prevented toxic effects of other nutrient ions on aerated primary roots of maize; other monovalent or divalent, cations substituted for Ca did not. Calcium in the complete nutrient solution, or as CaCl₂ alone, stimulated the division of apical meristem cells in these roots, as compared to division in water alone, but Sr did not. However, the replacement of Ca in the nutrient medium by Sr resulted in the development of additional secondary roots, probably in part by decreasing the rate of cell division in the apical meristem of the primary root and thereby diminishing apical dominance.     

Reduction of Phytophthora Stem Rot Disease on Soybeans by the Application of CaCl2 and Ca(NO3)2

This study investigated the effect of CaCl₂ and Ca(NO₃)₂ on fungal growth of Phytophthora sojae isolates, disease reduction on two cultivars of Glycine max (L.) Merr. cv. Chusei‐Hikarikuro (black soybean) and cv. Sachiyutaka (white soybean) and zoospore release. A concentration of 20–30 mm CaCl₂ or 30 mm Ca(NO₃)₂ led to a slight decrease of the growth rate of two isolates on PDA; however, 0.4 and 4 mm of CaCl₂ and Ca(NO₃)₂ increased growth. The application of 4 mm CaCl₂ or more than 4 mm Ca(NO₃)₂ before inoculation greatly inhibited infection in the two soybean cultivars. Disease suppression recorded in laboratory experiments using pathogen mycelium was because of the response of plant tissues rather than a direct inhibition of pathogen hyphal growth by the application of calcium. Furthermore, Ca(NO₃)₂ was more effective than CaCl₂. The calcium contents in plants increased at the time of inoculation. The extent of disease reduction was related to an increased calcium uptake by plants of the two cultivars, except for some cases involving cv. Chusei‐Hikarikuro. Results showed that the effective element in reducing Phytophthora stem rot was calcium and that differences existed between the two cultivars in terms of the mechanisms of calcium uptake and the effect on disease suppression. The presence of 4–30 mm CaCl₂ and Ca(NO₃)₂ decreased the release of zoospores from isolates on lima bean agar, although 0.4 mm CaCl₂ and Ca(NO₃)₂ significantly induced zoospore release. These results suggest the possibility of applying a solution containing more than 4 mm of calcium to decrease the incidence of disease in agricultural fields by the inhibition of zoospore release.     

The Effects of Inorganic Elements on the Reduction of Phytophthora Stem Rot Disease of Soybean, the Growth Rate and Zoospore Release of Phytophthora sojae

The effects of several inorganic elements contained in B5 medium on Phytophthora stem rot disease reduction of Glycine max (L.) Merr. cv. Chusei‐Hikarikuro, fungal growth of Phytophthora sojae isolate and zoospore release were investigated. Application of B5 solution and macro inorganic nutrients in the B5 medium prior to inoculation significantly inhibited infection, compared with controls. Various concentrations of KNO₃, (NH₄)₂SO₄, MgSO₄, CaCl₂ and NaH₂PO₄ in the presence of macro inorganic nutrients were investigated in an effort to determine the elements most effective in suppressing the incidence of disease. A concentration of 2.47–24.7 mm KNO₃ and 0.1–10.2 mm CaCl₂ greatly inhibited infection. Although mycelium growth of the isolate was affected by the potassium and calcium concentration, no significant relationship was observed between inhibition of the growth rate and disease reduction at 2.47 mm KNO₃ and 0.1–5.1 mm CaCl₂ application. Disease suppression recorded in laboratory experiments using pathogen mycelium was due to the response of plant tissues rather than a direct inhibition of pathogen fungal growth by the application of potassium or calcium. The extent of disease reduction was related to an increased potassium and calcium uptake by plants, suggesting that the effective elements in reducing Phytophthora stem rot were potassium and calcium. The presence of 2.47–247 mm KNO₃ and 5.1–10.2 mm CaCl₂ decreased the release of zoospores, although 0.1–2.5 mm CaCl₂ significantly induced zoospore release. These results suggest that applying a solution containing more than 2.47 mm of potassium and 5.1 mm of calcium can decrease the incidence of disease in agricultural fields by the inhibition of zoospore release.     

PERIODIC ZOOSPORE PRODUCTION BY PROTOSIPHON BOTRYOIDES UNDER ALTERNATING LIGHT-DARK PERIODS

The effect of light-dark periods, of 24 hr or longer complete cycle, on time of zoospore production by Protosiphon botryoides Klebs was investigated in unstirred flask cultures and in stirred cultures supplied 1% CO₂ in air. Synchronized zoospore production was observed in both types of cultures. In stirred cultures supplied 1% CO₂ a light-dark cycle of 36–12 hr gave better synchrony than did a cycle of 12–12 or 60–12 hr. Illumination by cool-white fluorescent bulbs inhibited zoospore formation strongly, possibly by inhibiting cytoplasmic cleavage in parent cells. Darkness, in comparison to illumination, promoted the formation of zoospores, and their synchronous production under alternating light-dark cycles occurred as a consequence.     

A CLASSROOM DEMONSTRATION OF ZOOSPORE PRODUCTION IN THE GREEN ALGA SCHIZOMERIS LEIBLEINII KUETZ.12

Using the parenchymatous ulotrichalean green alga Schizomeris leibleinii, a dependable technique for the classroom demonstration of zoospore production is described. The onset of zoospore release can be predicted accurately by controlling light, temperature, and medium. Large numbers of zoospores are released.     

Survival and death of Chara internodal cells in electrolyte solutions and calcium release from the cell wall

Abstract. Survival and death of Chara internodal cells were investigated in one of the alkali metal salts KCl, some of the alkali earth metal salts CaCl₂, Ca(NO₃)₂, MgCl₂, Mg(NO₃)₂, SrCl₂, Sr(NO₃)₂, BaCl₂ and Ba(NO₃)₂, potassium phosphate pH buffer solution (pH 7.0), Tris-maleate pH buffer solution (pH 7.0), HEPES (N-2-hydroxyethylpiperazine-N′-2-ethanesulphonic acid)-KOH (pH 7.0) pH buffer solution, calcium buffer solutions, and deionized water. Most of the internodal cells died within a day or a few days in KCl, MgCl₂, Mg(NO₃)₂, BaCl₂ and Ba(NO₃)₂ solutions of higher concentrations, calcium buffer solutions of pCa 6.0, 10.0 mol m^-3 potassium phosphate pH buffer solution and 10.0 mol m^-3 Trismaleate pH buffer solution. However, all of the internodal cells survived more than 10 d in deionized water, 80.0 mol m^-3 CaCl₂, 80.0 mol m^-3 Ca(NO₃)₂, 80.0 mol m^-3 SrCl₂, 80.0 mol m^-3 Sr(NO₃)₂ calcium buffer solutions of pCa 4.0 and pCa 5.0, and 10.0 mol m^-3 HEPES-KOH (pH 7.0) pH buffer solution. Addition of Ca²⁺ or Sr²⁺ to K⁺, Mg²⁺ and Ba²⁺ salt solutions increased the survival rates of the internodal cells. Calcium release from the internodal cell wall was measured in deionized water, KCl, NaCl, MgCl₂, CaCl₂, SrCl₂ and BaCl₂ solutions. Except in deionized water and CaCl₂ solution, most of the calcium binding to the cell wall was released within one or a few hours in respective electrolyte solutions. Thus, survival and death of the internodal cells in the electrolyte solutions tested were interpreted in terms of the calcium release from the cell wall and the cell membrane, and intrinsic ability of Sr²⁺ to maintain the cell membrane normal.     

Solute effects on Lagenidium giganteum: zoospore motility and bioassay reproducibility

The zoospores of Lagenidium giganteum rapidly lose motility when dispersed in deionized water. Several organic solutes were tested for the ability to prolong zoospore activity. Peptone at 0.2 and 0.05 g/liter was more effective than methionine and glucose, individually or in combination. The use of 0.2 g/liter of peptone as a medium for bioassays of L. giganteum against 3-day-old Aedes aegypti reduced the mean LD₅₀ to 12.9 zoospores/ml as compared to 133 with field water and 124 with deionized water. The use of peptone also dramatically improved the reproducibility of the assays and the goodness of fit of the resultant probit regression lines. The mean χ² values were 7.4 for 0.2 g/liter of peptone, 26.8 for field water, and 47.8 for deionized water. It is suggested that the erratic results obtained from use of deionized water are due to variation in the osmotic stress to which the zoospores were exposed, depending on the amount of debris that is introduced into the assays along with the mosquito larvae.     

Influence des pretraitements par KCl et des rapports Ca/Na du milieu sur la croissance de vitroplants de tomate en milieu NaCl

The 18-day-old tomato vitroplants were obtained in axenic conditions by culture of expiants (including the terminal bud and the last internode of the stem) on agar-agar nutritive medium with 0 or 75 mM NaCl. The growth and the mineral content of the vitroplants were compared when the expiants were grown on media either with low or high K/Na and Ca/Na ratios, or with low K/Na and Ca/Na ratios after pretreatments of expiants by KC1, NaCl or CaCl₂ (from 0 to – 4.5 bar). The KCl pretreatment (-1.1 bar) during one day brings about an increase in vitroplant growth greater than that produced by a high Ca/Na ratio medium. The Cl accumulation was similar in expiants pretreated by KCl or NaCl. Ion content per gram of fresh matter was similar in 18-day-old vitroplants pretreated by KCl, NaCl or CaCl₂; the Na accumulation by KC1 pretreated vitroplants was not lower than that of 18-day-old vitroplants grown on a high Ca/Na ratio medium. These results show the relation between Na content of expiants and the growth of vitroplants in a NaCl medium.     

Phytophthora nicotianae transformants lacking dynein light chain 1 produce non-flagellate zoospores

Biflagellate zoospores of the highly destructive plant pathogens in the genus Phytophthora are responsible for the initiation of infection of host plants. Zoospore motility is a critical component of the infection process because it allows zoospores to actively target suitable infection sites on potential hosts. Flagellar assembly and function in eukaryotes depends on a number of dynein-based molecular motors that facilitate retrograde intraflagellar transport and sliding of adjacent microtubule doublets in the flagellar axonemes. Dynein light chain 1 (DLC1) is one of a number of proteins in the dynein outer arm multiprotein complex. It is a 22 kDa leucine-rich repeat protein that binds to the catalytic motor domain of the dynein γ heavy chain. We report the cloning and characterization of DLC1 homologues in Phytophthora cinnamomi and Phytophthora nicotianae (PcDLC1 and PnDLC1). PcDLC1 and PnDLC1 are single copy genes that are more highly expressed in sporulating hyphae than in vegetative hyphae, zoospores or germinated cysts. Polyclonal antibodies raised against PnDLC1 locallized PnDLC1 along the length of the flagella of P. nicotianae zoospores. RNAi-mediated silencing of PnDLC1 expression yielded transformants that released non-flagellate, non-motile zoospores from their sporangia. Our observations indicate that zoospore motility is not required for zoospore release from P. nicotianae sporangia or for breakage of the evanescent vesicle into which zoospores are initially discharged.     

Characteristics of Serially Produced Zoospore Suspensions of Polymyxa betae for Transmission of Beet Necrotic Yellow Vein Virus

Zoospore suspensions of Polymyxa betae were analysed for their potential as inocula to infect sugar beet plants with beet necrotic yellow vein furovirus. The infectivity could be maintained when zoospore suspensions were serially transferred. When zoospore-producing seedlings were individually transferred some of these seedlings lost their infectivity after several passages. Infectivity was first detected in suspensions within I day after inoculation of the plant by zoospores. The suspensions remained infectious for at least 10 h after removal of the plants producing viruliferous zoospores. Both the number of test plants infected and the concentration of virus that developed were greater at 25 C than at 20 C.     

THE EFFECTS OF REPLACEMENT OF CALCIUM BY STRONTIUM ON THE REPRODUCTION OF CHLOROCOCCUM ECHINOZYGOTUM

In liquid inorganic axenic cultures of Chlorococcum echinozygotum containing 20 ppm CaCl₂, which was optimal for growth, motile cells were released in abundance; gametic fusion occurred commonly and the resulting zygospores reached a maximum of 31% of the total cell population. In a Sr-replaeement medium, less growth, not quite equivalent to that with 5 ppm CaCl₂, occurred, and more than 99% of the cells were non-motile vegetative cells. Old Sr-replacement cultures contained much-enlarged vegetative cells which, upon transfer to fresh Sr-medium, produced entrapped motile cells equivalent in number to those produced and released upon transfer to fresh Ca-medium. Release of these entrapped cells, after their production in Sr, was induced in 4 hr by transferring them to Ca (25 ppm CaCl₂).     

Flow cytometric determination of zoospore DNA content and population DNA distribution in cultured Pfiesteria spp. (Pyrrhophyta)

The relative cellular DNA content from 23 different clonal cultures of Pfiesteria spp. zoospores was determined using a DNA fluorochrome and flow cytometry. Significant differences between Pfiesteria piscicida and P. shumwayae were detected, both in mean zoospore DNA content and population cell cycle DNA distribution. Intraspecific differences in DNA content were found between clonal zoospore cultures established from different geographical regions. Long-term cultures (years) of P. piscicida were available for testing, and a negative correlation was observed between zoospore DNA content and time in culture. Zoospore cell cycle-related DNA distributions were also markedly different between the two species in these clonal cultures. In most cultures tested, P. piscicida zoospores exhibited bimodal DNA flow histograms with G1-S-G2+M distributions, typical of eukaryotic asynchronously cycling cells. In contrast, cultures of P. shumwayae zoospores exhibited one DNA peak distribution, indicative of synchronized cells. The data are consistent with the hypothesis that P. shumwayae zoospores are interphasic cells, and mitosis in zoospore cultures of this species predominantly occurs as benthic or adherent non-motile division cysts. Light microscopy observations of the nuclear condition of electrostatically sorted zoospores of each Pfiesteria species also support this hypothesis. If highly conserved, this disparity in modes of vegetative reproduction would ramify the population dynamics of the two Pfiesteria species.     

Activation of pig oocytes by intracytoplasmic injection of strontium and barium

Ovulated mouse oocytes are activated by exposure to culture medium containing Sr2+ or Ba2+ or by intracytoplasmic injection of the divalent cations. It is known that in vitro matured pig oocytes are activated by the intracytoplasmic injection of Ca2+. In this study, we examined the effect of exposure and of intracytoplasmic injection of Sr2+ or Ba2+ on in vitro matured pig oocytes (MII-oocytes). When MII-oocytes were exposed to the medium containing divalent cations, no oocytes were activated. However, in the case of oocytes that were injected with Sr2+, Ba2+ and Ca2+, at 6 h after injection, 64%, 71% and 86% of the oocytes had been released from MII-arrest, and 51%, 67% and 84% formed female pronuclei, respectively. The initial transient in intracellular Ca2+ concentration ([Ca2+]i) was measured by the Ca2+ indicator dye fluo-4 dextran. Microinjection of Sr2+, Ba2+ or Ca2+ induced a rapid elevation of [Ca2+]i. The exocytosis of cortical granules was examined by staining with fluorescein isothiocyanate (FITC)-labelled peanut agglutinin. After an injection of divalent cations, a release of cortical granules was observed in the oocytes. Maturation promoting factor (MPF) activity declined to a low level after 6 h in all the oocytes injected with divalent cations. To test their developmental ability, injected oocytes were treated with cytochalasin B and then cultured for 168 h in NCSU23 medium. After 168 h, 29% (Sr2+), 29% (Ba2+) and 51% (Ca2+) of the oocytes had developed to the blastocyst stage. These results indicate that intracytoplasmic injection of Sr2+ and Ba2+, like that of Ca2+, induces in vitro matured pig oocytes to be released from MII-arrest and leads them into a series of events related to oocyte activation.     

A STUDY OF LIGHT INTENSITY,PERIODICITY, AND WAVELENGTH ON ZOOSPORE PRODUCTION BY PROTOSIPHON BOTRYOIDES KLEBS12

When mature Protosiphon cells were placed in darkness, zoospore production was more extensive and was completed in a shorter time at a temperature of 27 C than at 22 or 15 C. Cool-white fluorescent (Sylvania) light inhibited the process measurably at a radiation intensity of 0.6±10³ ergsjcm²-sec; inhibition was 96% complete at 14±10³ ergs/cm²-sec. For mature cells previously grown under repeated 12-12 hr light-dark cycles, a dark period of approximately 2 hr at 22 C allowed cell division to proceed to a stage such that reillumination did not inhibit continued development of zoospores. Monochromatic light from 402 to approximately -494 nm, as compared to darkness, inhibited zoospore formation; maximal inhibition was at 432-461 nm. In contrast, monochromatic light from 522 to 726 nm stimulated zoospore formation relative to darkness. Synchronous zoospore production was obtained using the following regimes: (A) 12 hr cool-white alternated with 12 hr yellow, (B) 12 hr cool-white alternated with 12 hr blue. Under regime A synchronous zoospore release (following synchronous production) occurred near the end of the yellow irradiation period, while under regime B it occurred near the end of the cool-white irradiation period. The significance of this in terms of photoprocesses and possible photoreceptors is discussed.     

Calcium and action potentials of bullfrog sympathetic ganglion cells

Bullfrog sympathetic ganglion cells were capable of producing action potentials (Ca spikes) in an isotonic (84 mM) CaCl2 solution. The peak level of Ca spikes showed an approximately 30 mv increase with a 10-fold increase in the Ca concentration. Na as well as Ca ions were capable of acting as charge carriers during the production of action potentials in a solution containing relatively high Ca and relatively low Na ions. A decrease in the external Ca concentration depressed the maximum rate of rise at a fixed resting potential level, and increased the maximum rate of rise of the Na spikes at a high resting potential level at which Na inactivation was completely depressed. Compared to Na spikes, Ca spikes were less sensitive to TTX and procaine. Ganglion cells were also capable of producing action potentials (Sr spikes) in an isotonic SrCl₂ solution and prolonged action potentials in an isotonic BaCl₂ solution, but these cells were rendered inexcitable in an isotonic MgCl₂ solution. The peak level of the Sr spikes was dependent on the external Sr concentration and was insensitive to both TTX and procaine. Sr ions, like Ca ions, reduced Na inactivation during the resting state, and depressed the maximum rate of rise of the Na spikes at a high resting potential level. It was concluded that Ca (and Sr) ions exert dual actions on the membrane; namely, regulating the Na permeability and acting as charge carriers during the active state of the membrane.     

Zoospore development in the oomycetes

Oomycetes cause destructive diseases on both animals and plants. The epidemic spread of oomycete diseases is primarily based on rapid dispersal from host to host by free swimming zoospores. These single-nucleated spores are formed in sporangia and are only released in aqueous environments. Oomycetes are classified in the Kingdom of the Stramenopiles or Chromista, which is comprised of several organisms, including the golden brown algae. The unique shared attribute found in most Stramenopiles is the morphology of the zoospores and especially the structure of their two flagella. They have one tinsel flagellum, and one whiplash flagellum. Only the tinsel flagellum has distinctive flagellar hairs. Zoospore formation can occur within minutes and it is considered one of the fastest developmental processes in any biological system. Once released from the sporangium they are able to exhibit chemotactic responses, electrotaxis, and autotaxis or autoaggregation to target new hosts for infection. Here we discuss the latest discoveries in the development and biology of the oomycete zoospore.     

Na+-dependent alkaline earth metal uptake in cardiac sarcolemmal vesicles

The ability of alkaline earth metals (M2+) to substitute for Ca2+ in Na+-Ca2+ exchange was examined in sarcolemmal vesicles isolated from the canine heart. 85Sr2+ and 133Ba2+, in addition to 45Ca2+, were used to determine the characteristics of Na+-M2+ exchange. The Na+i-dependent M2+ uptake was measured as a function of time, with t ranging from 0.5 to 360 s, [Na+]i = 140 mM and [M2+]o = 40 microM. This function was linear for Ca2+ and Sr2+ uptake for approx. 6 s and for Ba2+ for about 60 s. Plateau levels were achieved within 120 s for Ca2+ and Sr2+ but Ba2+ took considerably longer. The Km values for Na+-M2+ exchange, derived from Eadie-Hofstee plots, were 30, 58, and 73 microM for Ca2+, Sr2+ and Ba2+, respectively. The Na+i-dependent uptake of all three ions was stimulated in the presence of 0.36 microM valinomycin. Na+-Ca2+ exchange was also measured in the presence of either 20 microM Sr2+ or 100 microM Ba2+. Both of these ions behaved (at these concentrations) as competitive inhibitors of Na+-Ca2+ exchange with the KI being 32 microM for Sr2+ and 92 microM for Ba2+. Passive efflux was determined by first allowing Na+-M2+ exchange to continue to plateau values and then diluting the loaded vesicles in the presence of EGTA. The rate constants for the passive efflux were 8.4, 6.3 and 4.4 min-1 for Ca2+, Sr2+ and Ba2+, respectively.