zoospore formation
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Science ◽  
2010 ◽  
Vol 330 (6010) ◽  
pp. 1549-1551 ◽  
Author(s):  
Laura Baxter ◽  
Sucheta Tripathy ◽  
Naveed Ishaque ◽  
Nico Boot ◽  
Adriana Cabral ◽  
...  

Many oomycete and fungal plant pathogens are obligate biotrophs, which extract nutrients only from living plant tissue and cannot grow apart from their hosts. Although these pathogens cause substantial crop losses, little is known about the molecular basis or evolution of obligate biotrophy. Here, we report the genome sequence of the oomycete Hyaloperonospora arabidopsidis (Hpa), an obligate biotroph and natural pathogen of Arabidopsis thaliana. In comparison with genomes of related, hemibiotrophic Phytophthora species, the Hpa genome exhibits dramatic reductions in genes encoding (i) RXLR effectors and other secreted pathogenicity proteins, (ii) enzymes for assimilation of inorganic nitrogen and sulfur, and (iii) proteins associated with zoospore formation and motility. These attributes comprise a genomic signature of evolution toward obligate biotrophy.


2010 ◽  
Vol 100 (5) ◽  
pp. 522-527 ◽  
Author(s):  
Hancheng Wang ◽  
Haiyan Sun ◽  
Gerd Stammler ◽  
Jianxia Ma ◽  
Mingguo Zhou

Four isolates of Peronophythora litchii with resistance to carboxylic acid amide (CAA) fungicides were selected on fungicide-amended agar. These isolates had various levels of resistance, as evidenced by their resistance factor (RF), which is the 50% effective concentration (EC50) value of a particular isolate divided by that of the wild-type parent. RF values to dimethomorph for the four isolates were 15, 24, 141, and >1,500. Resistance was stable for two isolates, while the EC50 values decreased for the other two after repeated subculturing on fungicide-free medium. Cross-resistance occurred with all CAAs tested here (dimethomorph, mandipropamid, flumorph, and pyrimorph), but not with strobilurins (azoxystrobin and famoxadone) or other fungicides (metalaxyl, cymoxanil, and mancozeb). Studies on fitness parameters (mycelial growth, sporulation, spore germination, zoospore formation, aggressiveness, and temperature tolerance) in the parent wild-type and resistant isolates demonstrated that penalties in different parameters may be associated with CAA resistance, depending on the isolate. These studies show that Peronophythora litchii is able to express CAA resistance under laboratory conditions but it is not known if resistant strains could become established in the field and sensitivity monitoring studies are recommended.


Plant Disease ◽  
2009 ◽  
Vol 93 (1) ◽  
pp. 30-35 ◽  
Author(s):  
T. L. Widmer

Phytophthora species produce sporangia that either germinate directly or release zoospores, depending upon environmental conditions. Previous Phytophthora spp. inoculation trials have used both sporangia and zoospores as the inoculum type. However, it is unknown what impact propagule type has on disease. Rhododendron leaf disks were inoculated with P. ramorum zoospores (75, 500, or 2,400 per disk), sporangia (75 per disk), or sporangia plus trifluoperazine hydrochloride (TFP) (75 per disk), a chemical that inhibits zoospore formation. Combining results from two different isolates, the highest concentration of zoospores (2,400 per disk) induced a significantly higher percentage of necrotic leaf disk area (96.6%) than sporangia (87.6%) and 500 zoospores per disk (88.7%). The sporangia plus TFP treatment had the lowest necrosis at 47.5%. Rooted rhododendron cuttings had a higher percentage of necrotic leaves per plant when inoculated with zoospores (3,000 or 50,000 per ml) or cysts (50,000 per ml) than with sporangia (3,000 per ml) with or without TFP. The percentage of necrotic leaf area was significantly higher when cysts or zoospores were inoculated at 50,000 per ml than sporangia without TFP and zoospores at 3,000 per ml. All treatments were significantly higher in the percentage of necrotic leaf area than the leaves treated with sporangia plus TFP. This demonstrates that the full inoculum potential may not be achieved when sporangia are used as the inoculum propagule.


Plant Disease ◽  
2005 ◽  
Vol 89 (2) ◽  
pp. 146-152 ◽  
Author(s):  
L. D. Porter ◽  
N. Dasgupta ◽  
D. A. Johnson

The effects of tuber depth, soil type, and soil moisture on potato tuber infection due to Phytophthora infestans were assessed under greenhouse conditions in soil contained in large pots. Healthy tubers were used to assess infection and were either hand buried in soil at specific depths or naturally formed from potato plants growing in the soil. A spore suspension of P. infestans was chilled to induce zoospore formation and a suspension of resulting zoospores and sporangia were applied to the soil. Soil depth at which tubers became infected was used to determine the extent of spore movement in the soils. Tuber infection significantly decreased with increasing soil depth. Most infected tubers were found at the surface of soil; infection was rare on tubers at 5 cm or deeper in the soil. Amount of tuber infection varied among soil types. Significantly less tuber infection occurred in a Shano silt loam than in medium and fine sands. Only tubers on the soil surface were infected in the Shano silt loam. Depth in soil at which tubers became infected did not differ significantly among Quincy fine sand, Quincy loamy fine sand, and Quincy medium sand. Increased soil moisture did not significantly increase the soil depth at which tuber infection occurred, regardless of the soil type.


Plant Disease ◽  
2005 ◽  
Vol 89 (2) ◽  
pp. 207-207 ◽  
Author(s):  
R. Zapata ◽  
A. M. Romero ◽  
P. H. Maseda

Production of arugula (Eruca sativa) has increased greatly in Argentina. Since 2002, particularly during the fall, a foliar disease has affected commercial crops in Capilla del Señor (northeast of Buenos Aires Province, Argentina). The disease appeared in foci, spreading throughout the whole production field or greenhouse. Severely affected crops were plowed under. Diseased leaves were chlorotic and had white sori that emerged through the abaxial epidermis. Sori corresponded to the white rust agent, Albugo candida (Pers.) Kunze (1). Sporangiophores were hyaline and clavate, and sporangia were globose and hyaline with a mean diameter of 16.2 μm (14.2 to 19.2 μm). Pathogenicity tests were performed by spraying a suspension of 106 zoospores/ml or 5 × 104 sporangia/ml on four healthy 30-day-old arugula plants. Inoculum was prepared by scrapping sporangia from infected leaves. Sporangia were used directly or incubated in sterile distilled water (SDW) for 14 h at 5°C to induce zoospore formation (2). Four additional healthy plants were sprayed with SDW to serve as controls. Plants were kept in plastic bags for 48 h and maintained in the greenhouse thereafter. White rust symptoms, similar to those observed on the original plants from the field, were observed on inoculated plants 10 days after inoculation. To our knowledge, this is the fist report of A. candida on arugula in Argentina. References: (1) K. Mukerji. No. 458 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, Surrey, UK, 1975. (2) H. Scheck and S. Koike. Plant Dis. 83:877, 1999.


Plant Disease ◽  
2004 ◽  
Vol 88 (2) ◽  
pp. 205-209 ◽  
Author(s):  
S. Sanogo

The response of chile pepper to salinity and infection by Phytophthora capsici was assessed under greenhouse conditions in plants susceptible or resistant to P. capsici. Additionally, the effect of salinity on mycelial growth and production of sporangia and zoospores by P. capsici was evaluated in the laboratory. Salinity treatments consisted of varying levels of electrical conductivity (from 1.8 to 14.4 dS/m) achieved by amending irrigation water or growth media with a mixture of sodium chloride and calcium chloride. In plants susceptible to P. capsici, disease severity increased by approximately 1.3 to 2.7-fold with increasing salinity level, whereas no such effect was observed in plants resistant to P. capsici. Mycelial dry weight increased by 8 to 16%, and radial growth of mycelium was augmented by 5 to 30% with increase in salinity level. Production of sporangia and zoospore formation were reduced by approximately 3 to 85 and 1 to 93%, respectively, under saline conditions. These results indicate that salinity may predispose susceptible chile pepper plants to infection by P. capsici.


Mycoscience ◽  
2002 ◽  
Vol 43 (2) ◽  
pp. 119-125 ◽  
Author(s):  
Masateru Hakariya ◽  
Natsuki Masuyama ◽  
Masatoshi Saikawa
Keyword(s):  

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