scholarly journals First Report from Morocco of Phytophthora infestans Isolates with Metalaxyl Resistance

Plant Disease ◽  
1997 ◽  
Vol 81 (7) ◽  
pp. 831-831 ◽  
Author(s):  
M. Sedegui ◽  
R. B. Carroll ◽  
A. L. Morehart ◽  
A. Arifi ◽  
R. Lakhdar

Late blight of potato (Solanum tuberosum L.) caused by Phytophthora infestans (Mont.) de Bary first appeared in Africa in 1941. It has been observed sporadically in Morocco for decades but only recently became a major problem. Significant losses have been recorded in the last two growing seasons in spite of the use of various disease control programs that included combinations of systemic and protectant fungicides. Phytophthora infestans was cultured from diseased foliage collected from commercial potato fields near Larache, Morocco. Isolates were analyzed to determine pathogenicity on several potato and tomato cultivars, mating type, genotype at two allozyme loci (2), and relative sensitivity to metalaxyl. Responses of the isolates to metalaxyl were assayed by mycelial radial growth on metalaxyl-amended agar, by floating leaves inoculated with P. infestans on metalaxyl solutions, and via potato tuber disks placed on filter paper saturated with metalaxyl solutions (1). Koch's postulates were completed; all isolates were pathogenic to potato and tomato cultivars tested, are consistent with the A1 mating type, and have the same allozyme pattern (Gpi 100/100, Pep 92/100) as US-6 genotype. All tests indicated resistance to metalaxyl up to 250 ppm. References: (1) K. L. Deahl et al. Am. Potato J. 70:779, 1993. (2) S. B. Goodwin et al. Plant Dis. 79:1181, 1995.

Plant Disease ◽  
1997 ◽  
Vol 81 (9) ◽  
pp. 1093-1093 ◽  
Author(s):  
M. Sedegui ◽  
R. B. Carroll ◽  
A. L. Morehart ◽  
R. P. Mulroony ◽  
J. M. Whalen

Prior to 1995, late blight of potatoes (Solanum tuberosum L.) caused by Phytophthora infestans (Mont.) de Bary had not been reported from Delaware for decades. In that year, the fungus was isolated from potato foliage collected from fields in the Dover area that sustained severe foliage loss due to the disease. To establish pathogenicity, potato and tomato plants grown in the greenhouse were inoculated with the isolates obtained and Koch's postulates were completed. Analyses to determine mating type, genotype at two allozyme loci (2), Gpi and Pep, and sensitivity to metalaxyl were also completed. Measurements were made every 5 days and EC50 values were calculated for radial mycelial growth on metalaxyl-amended agar, for leaflets inoculated with P. infestans floated in metalaxyl solutions, and for inoculated potato tuber disks deposited on filter paper saturated with metalaxyl (1). Isolates were pathogenic to potatoes and tomatoes, were A2 mating type with Gpi 100/111/122 and Pep 100/100 (same as US-8), and displayed resistance to metalaxyl up to 140 mg/l. References: (1) K. L. Deahl et al. Am. Potato J. 70:779, 1993. (2) S. B. Goodwin et al. Plant Dis. 79:1181, 1995.


Plant Disease ◽  
2007 ◽  
Vol 91 (5) ◽  
pp. 634-634 ◽  
Author(s):  
L. M. Winton ◽  
R. H. Leiner ◽  
A. L. Krohn ◽  
K. L. Deahl

Phytophthora infestans, causal agent of late blight, was included in a list of plant pathogens found in Alaska in 1934 (1). No notes of symptoms, extent of disease, or dates were recorded. The only reference to the location was given as Wrangell, a town in southeast Alaska with subsistence gardening. Neither P. infestans nor late blight was noted again in the state for another 59 years. Late blight first appeared in Alaska's major potato-growing region in south-central Alaska's Matanuska Valley in 1995. Subsequent outbreaks have been sporadic, occurring only in 1998, 2005, and 2006. Each of these outbreaks was identified from rapidly enlarging brown foliar lesions with branched sporangiophores and lemon-shaped sporangia (~25 × 30 μm). The 1995 and 1998 potato late blight outbreaks in Alaska were not sampled extensively nor have they previously been formally reported. We recovered single isolates of P. infestans from symptomatic potato foliage in the 1995 and 1998 outbreaks. In 2005, symptomatic foliage was collected from individual potato plants in 10 commercial fields and from tomato plants in greenhouses at two locations. Sporulating stem and leaf tissue were used to inoculate semiselective rye medium and 147 isolates from potato and six from tomato were recovered. The isolates from the 1995, 1998, and 2005 outbreaks were analyzed to determine genotype at the allozyme loci GPI and PEP (3), mitochondrial haplotype (4), mating type, and metalaxyl sensitivity (2). The 1998 and 2005 outbreaks were similar because both were caused by the relatively aggressive US-11 allozyme genotype and had significant economic impact for commercial potato growers. All 153 isolates from potato and tomato in 2005 displayed the same allozyme pattern as the US-11 genotype, possessed the IIB mitochondrial haplotype, and were mating type A1. Of the 16 isolates tested, all were determined to be metalaxyl resistant because isolates grown on 5 and 100 μg/ml metalaxyl exhibited growth greater than 40% of the unamended control. The 1995 outbreak was caused by the relatively rare US-7 genotype and started so late during the season that economic impact was minimal. Similarly, the 2006 outbreak was noted from only one commercial potato field at the time of harvest in September 2006. However, the genotype of the 2006 isolate has not been determined because the patch was destroyed before adequate samples could be collected. Because the disease occurs so sporadically in Alaska, fungicides are not routinely in use, but it is unlikely that the pathogen has persisted locally between outbreaks. The source of P. infestans is unknown for each of the occurrences in Alaska. However, possible routes include seed potatoes for home gardens or commercial farms, tomato transplants, and retail vegetables shipped to Alaska from out of state. While potato is Alaska's main vegetable crop, there are less than 405 ha (1,000 acres) of potatoes planted in the state, with the majority planted in the Matanuska Valley. To our knowledge, this is the first formal report of P. infestans on both tomato and commercial potato in Alaska. References: (1) E. K. Cash. Plant Dis. Rep. 20:121, 1936. (2) D. E. L. Cooke et al. Plant Pathol. 52:181, 2003. (3) S. B. Goodwin et al. Plant Dis. 79:1181, 1995. (4) G. W. Griffith and D. S. Shaw. Appl. Environ. Microbiol. 64:4007, 1998.


2003 ◽  
Vol 83 (4) ◽  
pp. 425-429 ◽  
Author(s):  
B. J. Zebarth ◽  
Y. Leclerc ◽  
G. Moreau ◽  
R. Gareau ◽  
P. H. Milburn

Information on inorganic N content in commercial potato fields in Atlantic Canada is limited. Soil inorganic N measurements were collected from 228 commercial potato fields from 1999 to 2001. Soil NO3 content to 30 cm depth at planting ranged from 2 to 124 kg N ha-1, and was generally higher for preceding potato, red clover, or hay crops compared to preceding cereal or other crops. Soil NH4 content to 30 cm depth measured at planting ranged from 3 to 64 kg N ha-1, indicating that both soil NO3 and NH4 need to be measured to assess plant-available soil N content in spring. Soil NO3 content to 30-cm depth at tuber harvest ranged from 3 to 250 kg N ha-1, generally increased with increasing fertilizer N application rate, and differed among different potato cultivars. Soil NO3 content measured to 30-cm depth in spring ranged from 3 to 100% of soil NO3 at harvest in the preceding fall, indicating that highly variable losses of soil NO3 from the root zone occur between growing seasons. Key words: Nitrate, ammonium, Solanum tuberosum L.


1998 ◽  
Vol 88 (3) ◽  
pp. 265-271 ◽  
Author(s):  
P. J. Oyarzun ◽  
A. Pozo ◽  
M. E. Ordoñez ◽  
K. Doucett ◽  
G. A. Forbes

Sixty Ecuadorian isolates of Phytophthora infestans from potato and 60 isolates from tomato were compared for dilocus allozyme genotype, mitochondrial DNA haplotype, mating type, and specific virulence on 11 potato R-gene differential plants and four tomato cultivars, two of which contained different Ph genes. Restriction fragment length polymorphism (RFLP) fingerprints of subsamples of isolates from each host were compared by using RG57 as the probe. All potato isolates had the allozyme genotype, haplotype, and mating type of the clonal lineage EC-1, which had been previously described in Ecuador. With the same markers, only one isolate from tomato was classified as EC-1; all others belonged to the globally distributed US-1 clonal lineage. RFLP fingerprints of isolate subsets corroborated this clonal lineage classification. Specific virulence on potato differentials was broadest among potato isolates, while specific virulence on tomato cultivars was broadest among tomato isolates. Some tomato isolates infected all tomato differentials but no potato differentials, indicating that specific virulence for the two hosts is probably controlled by different avirulence genes in P. infestans. In two separate experiments, the diameters of lesions caused by nine isolates from potato and 10 from tomato were compared on three tomato and three potato cultivars. All isolates produced larger lesions on the host from which they were isolated. No isolates were found that were highly aggressive on both tomato and potato. We conclude that there are two different populations of P. infestans in Ecuador and that they are separated by host.


2012 ◽  
Vol 119 (2) ◽  
pp. 45-52 ◽  
Author(s):  
Eve Runno-Paurson ◽  
Asko Hannukkala ◽  
Stanislav Trdan ◽  
Ingrid Williams ◽  
Mati Koppel ◽  
...  

2001 ◽  
Vol 20 (5) ◽  
pp. 379-388 ◽  
Author(s):  
J. Mukalazi ◽  
E. Adipala ◽  
T. Sengooba ◽  
J.J. Hakiza ◽  
M. Olanya ◽  
...  

Plant Disease ◽  
2013 ◽  
Vol 97 (8) ◽  
pp. 1112-1112 ◽  
Author(s):  
C. A. López Orona ◽  
A. R. Martínez ◽  
T. T. Arteaga ◽  
H. G. García ◽  
D. Palmero ◽  
...  

Phytophthora infestans causes severe symptoms of wilt disease on potato crops (Solanum tuberosum) in the Toluca Valley (Mexico) despite the use of fungicides. P. infestans oospores produced by sexual reproduction can survive in the soil for many years, resisting harsh environments. In many agroecosystems, oospores germinate in the beginning of a season, which represents the initial inoculum for epidemics. The sexual cycle of the pathogen allows the generation of recombinant genotypes that can be more pathogenic or even resistant to chemicals. This paper presents a study of 20 isolates of P. infestans collected from potato crops in the Toluca Valley within the municipality of Zinacantepec (Mexico State). Isolates were obtained from potato foliar infected tissues. The pathogen was confirmed as P. infestans on the basis of morphological characters (1). Sporangia were caducous, ovoid, limoniform, semipapillate, and were 28.4 ± 1.3 × 17.6 ± 1.2 μm (height × width). Mycelium was coenocytic with hyphal diameter of 5 to 8 μm. Five isolates were collected in 2011, and 15 in 2012. Isolates were transferred by hyphal tip to culture medium plates with V8 juice agar and incubated at 19°C. All the isolates were mated to determine the mating type with the reference isolates J104 (A1) and J204 (A2), which were provided by the Michoacana University of San Nicolás de Hidalgo (Mx). Isolates that produced oospores with both A1 and A2 testers (J104 and J204) and in a single culture were designated homothallic. Results show that two out of the five isolates collected in 2011 were homothallic and the other three were type A1. Regarding the 15 isolates collected in 2012, six were typed as A1, five as A2, and four were homothallic. The heterothallic isolates only produce oospores when mated with the opposite mating type. The homothallic isolates possessed the ability to act as A1 and A2 during heterothallic mating and were found capable of producing sexual structures (oogonia and amphigynous antheridia) in a single culture, a phenomenon not observed in isolates that are strictly A1 or A2. Oospores formed were aplerotic and measured 32.2 ± 3.3 μm in diameter. Single-sporangium progeny were produced from the six homothallic isolates to be analyzed to confirm the occurrence of the self-fertility. Assessment of 48 single-sporangium progeny from the homothallic isolates resulted in 22 homothallic, 12 A1, 10 A2, and four sterile. These results differ from those found by Grünwald et al. (3), who conducted a study with isolates collected from the Toluca Valley region in 1997 and 1998, finding a 1:1 frequency between compatibility types A1 and A2. Fernandez et al. (2) studied a broad population of 27 isolates from potato crops in the state of Michoacán (Mx), and found two homothallic isolates among heterothallic isolates; the ratio was 1:1. Also, homothallic isolates have been found in Spain and China (4). To our knowledge, this is the first report of the occurrence of homothallic P. infestans isolates in commercial potato crops (S. tuberosum) in the Toluca Valley, Mexico. References: (1) D. C. Erwin and O. K. Ribeiro, Page 346 in: Phytophthora Diseases Worldwide. The American Phytopathological Society. St. Paul, MN, 1996. (2) S. P. Fernández et al. Rev. Mexicana Fitopatol. 23:191, 2005. (3) N. J. Grünwald et al. Phytopathology 91:883, 2001. (4) M. Han et al. J. Eukaryotic Microbiol. 60:79, 2013.


Author(s):  
Eric R. Larson ◽  
Lukas E. Migliano ◽  
Yu Chen ◽  
Amanda J. Gevens

The contemporary dominant clonal lineage of heterothallic Phytophthora infestans in Wisconsin, US-23, is classified as sensitive to the systemic fungicide mefenoxam and is of the A1 mating type. With the sporadic appearance of clonal lineage US-8, classified as resistant to mefenoxam and of the A2 mating type, there is a need for ongoing monitoring and characterization. Isolates of P. infestans collected from Wisconsin during the 2017 and 2018 growing seasons were tested for sensitivity to mefenoxam with discriminatory dose of 100 ppm. In 2017, both US-23 and US-8 were isolated. On average, isolates of US-23 were significantly more sensitive to mefenoxam than were US-8 isolates (P = 8e-04). There were significant differences in the sensitivity levels among the US-8 isolates (P = 2.02e-06), with a single isolate testing sensitive at 100 ppm of mefenoxam based on the one-way ANOVA. There were significant differences in the sensitivity levels among US-23 isolates (P = 3.75e-09), with two isolates showing resistance. In 2018 only US-23 was found, and isolates were tested for mefenoxam response at 0, 0.1, 1, 10, and 100 ppm. At 0.1 ppm, isolates showed significantly different levels of sensitivity (P = 2.1e-09), and a single isolate showed complete resistance. Isolates from both clonal lineages and years that exhibited moderate levels of resistance had greater variability among replicates. The phenotype of this multigenic trait comes through in the variability seen in isolates that are showing more resistance. Continued screening of P. infestans for mefenoxam sensitivity will help track the development and mechanism of resistance, as well as aid in development of best management approaches.


Plant Disease ◽  
2003 ◽  
Vol 87 (8) ◽  
pp. 896-900 ◽  
Author(s):  
Ailton Reis ◽  
Christine D. Smart ◽  
William E. Fry ◽  
Luiz A. Maffia ◽  
Eduardo S. G. Mizubuti

The population of Phytophthora infestans in Brazil was first characterized 12 years ago. In this research, isolates of P. infestans from potato (n = 184) and tomato (n = 267) collected in southern and southeastern Brazil were characterized to provide more detailed analysis of the current structure of the population. All 451 isolates were analyzed for mating type, and subsets of the isolates were analyzed for allozymes, restriction fragment length polymorphism fingerprint, mtDNA haplotypes, and metalaxyl resistance. Tomato isolates were all of A1 mating type, mtDNA Ib, and US-1 genotype or some variant within this clonal lineage. Of the potato isolates, 82% were A2 mating type, mtDNA IIa, BR-1 genotype, which is a new lineage of P. infestans. All A2 isolates were found on potato, whereas 91% of the A1 isolates were from tomato. A1 and A2 isolates were never found in the same field. The frequency of resistance to metalaxyl was higher in isolates from tomato (55%) than in isolates from potato (38%). After more than a decade of coexistence of isolates of the A1 and A2 mating types, the population was highly clonal, dominated by the BR-1 and US-1 clonal lineages.


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