Spore Germination and Germ Tube Growth of a Vesicular-Arbuscular Mycorrhizal Fungus in vitro

Mycologia ◽  
1982 ◽  
Vol 74 (6) ◽  
pp. 952 ◽  
Author(s):  
J. O. Siqueira ◽  
D. H. Hubbell ◽  
N. C. Schenck
Keyword(s):  
Spore Germination ◽  
Germ Tube ◽  
Arbuscular Mycorrhizal Fungus ◽  
Mycorrhizal Fungus ◽  
Arbuscular Mycorrhizal ◽  
Tube Growth ◽  
Vesicular Arbuscular ◽  
Germ Tube Growth

In vitro culture of arbuscular mycorrhizal fungus and Frankia for inoculation of micropropagated Casuarina equisetifolia L.

1999 ◽  
Vol 77 (9) ◽  
pp. 1391-1397
Author(s):  
Genevieve Louise Mark ◽  
John E Hooker ◽  
Alexander Hahn ◽  
Chris T Wheeler
Keyword(s):  
Spore Germination ◽  
Mycorrhizal Fungi ◽  
Arbuscular Mycorrhizal Fungus ◽  
Mycorrhizal Fungus ◽  
Arbuscular Mycorrhizal ◽  
Dichlorophenoxyacetic Acid ◽  
Casuarina Equisetifolia ◽  
Half Strength ◽  
2,4 Dichlorophenoxyacetic Acid

Micropropagated, rooted, and calli explants of Casuarina equisetifolia L. were inoculated with Frankia UGL 020605S and the arbuscular mycorrhizal fungus (AMF) Glomus mosseae, in single and dual co-culture, in vitro. Different micropropagation media formulations were evaluated for their capacity to stimulate germination of G. mosseae spores and growth of Frankia. Murashige and Skoog basal nutrient (half strength) medium, supplemented with 6-benzylaminopurine (BAP), 2,4-dichlorophenoxyacetic acid (2,4-D), and pyruvate was selected for the in vitro co-culture of C. equisetifolia callus explants, G. mosseae, and Frankia. This medium (M4) supported 70% AMF spore germination with 44 and 34% of the germinating spores producing single and branched hyphal strands, respectively. Hoaglands (quarter strength, modified by Hoaglands and Arnon (1950)) nutrient medium (M5) with no supplements was selected for the in vitro co-culture of rooted C. equisetifolia explants, G. mosseae, and Frankia and supported 57% AMF spore germination with 29 and 40% of the germinating spores producing single and branched hyphal strands, respectively. Both media supported significant growth of Frankia. In both cases agar was substituted with Terragreen(r). AMF appressoria and intercellular hyphae were observed in rooted C. equisetifolia at 28 days; arbuscule formation occurred at 56 days postinoculation. Frankia infection was evident after 28 days. This was observed in both dual and single in vitro co-cultures. No specific immunofluorescent or immunogold reactions to monoclonal antibodies (mABs) anti-Frankia < 8C5 > and anti-G. mosseae < F5G5 > were evident in C. equisetifolia callus explants.Key words: arbuscular mycorrhizal fungi (AMF), Frankia, Casuarina, micropropagation, immunofluorescent labelling.

scholarly journals In vitro effect of substrate, temperature and photoperiod on Phakopsora pachyrhizi urediniospore germination and germ tube growth

2015 ◽  
Vol 41 (2) ◽  
pp. 101-106
Author(s):  
Marta Maria Casa Blum ◽  
Erlei Melo Reis ◽  
Francieli Tavares Vieira ◽  
Rita Carlini
Keyword(s):  
Substrate Temperature ◽  
Spore Germination ◽  
Leaf Extract ◽  
Germ Tube ◽  
Tube Growth ◽  
Tube Length ◽  
Germ Tube Length ◽  
Soybean Leaf ◽  
Germ Tube Growth

In vitro experiments were conducted to assess the effects of substrate, temperature and time of exposure to temperature and photoperiod on P. pachyrhizi uredospore germination and germ tube growth. The following substrates were tested: water-agar and soybean leaf extract-agar at different leaf concentrations (0.5, 1.0, 2.0 and 4.0 g of leaves and 15g agar/L water), temperatures (10, 15, 20, 25, 30, and 35oC) and times of exposure (1, 2, 3, 4, 5, 6, 7, and 8 hours) to temperature and 12 different photoperiods. The highest germination and germ tube length was found for the soybean leaf extract agar. Maximum P. pachyrhizi uredospore germination was obtained at 21.8 and 22.3°C, and maximum germ tube growth at 21.4 and 22.1°C. The maximum uredospore germination was found at 6.4 hours exposure, while the maximum germ tube length was obtained at 7.7 h exposure. Regarding photoperiod, the maximum spore germination and the maximum uredospore germ tube length were found in the dark. Neither spore germination nor uredospore germ tube growth was completely inhibited by the exposure to continuous light.

Suppression of vesicular–arbuscular mycorrhizal fungus spore germination by nonsterile soil

1989 ◽  
Vol 67 (1) ◽  
pp. 18-23 ◽  
Author(s):  
G. W. T. Wilson ◽  
B. A. Daniels Hetrick ◽  
D. Gerschefske Kitt
Keyword(s):  
Spore Germination ◽  
Arbuscular Mycorrhizal Fungus ◽  
Mycorrhizal Fungus ◽  
Arbuscular Mycorrhizal ◽  
Dry Weight ◽  
Available Phosphorus ◽  
Nonsterile Soil ◽  
Surface Sterilization ◽  
Vesicular Arbuscular ◽  
Fungus Spore

When the effect of nonsterile soil on vesicular–arbuscular mycorrhizal fungus spore germination was examined, significantly fewer Glomus etunicatum (22 vs. 63 and 64%) or Glomus mosseae (23 vs. 80 and 79%) spores germinated in nonsterile soil than in autoclaved or pasteurized soil, respectively. In some cases, addition of nonsterile soil sievings to autoclaved or pasteurized soil also reduced germination, as compared with germination in unamended pasteurized or autoclaved soil. Germination was reduced by as much as 45% in autoclaved or pasteurized soil if spores were surface sterilized. However, surface sterilization of G. etunicatum spores did not affect dry weight of inoculated big bluestem plants, but mycorrhizal root colonization was reduced when spore-associated microbes were removed from spores by surface sterilization. The detrimental effect of soil microbes on spore germination and mycorrhizal growth response may reflect microbial competition for nutrients since germination of G. etunicatum and G. mosseae was reduced when pasteurized soil was amended with 15, 30, or 60 ppm phosphorus and 60 ppm phosphorus, respectively. An optimum range of available phosphorus may exist, above or below which germination is suppressed.

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