scholarly journals Phytophthora heterospora sp. nov., a New Pseudoconidia-Producing Sister Species of P. palmivora

2021 ◽  
Vol 7 (10) ◽  
pp. 870
Author(s):  
Bruno Scanu ◽  
Thomas Jung ◽  
Hossein Masigol ◽  
Benedetto Teodoro Linaldeddu ◽  
Marília Horta Jung ◽  
...  

Since 1999, an unusual Phytophthora species has repeatedly been found associated with stem lesions and root and collar rot on young olive trees in Southern Italy. In all cases, this species was obtained from recently established commercial plantations or from nursery plants. Morphologically, the Phytophthora isolates were characterized by the abundant production of caducous non-papillate conidia-like sporangia (pseudoconidia) and caducous papillate sporangia with a short pedicel, resembling P. palmivora var. heterocystica. Additional isolates with similar features were obtained from nursery plants of Ziziphus spina-christi in Iran, Juniperus oxycedrus and Capparis spinosa in Italy, and mature trees in commercial farms of Durio zibethinus in Vietnam. In this study, morphology, breeding system and growth characteristics of these Phytophthora isolates with peculiar features were examined, and combined mitochondrial and nuclear multigene phylogenetic analyses were performed. The proportion between pseudoconidia and sporangia varied amongst isolates and depended on the availability of free water. Oogonia with amphigynous antheridia and aplerotic oospores were produced in dual cultures with an A2 mating type strain of P. palmivora, indicating all isolates were A1 mating type. Phylogenetically, these isolates grouped in a distinct well-supported clade sister to P. palmivora; thus, they constitute a separate taxon. The new species, described here as Phytophthora heterospora sp. nov., proved to be highly pathogenic to both olive and durian plants in stem inoculation tests.

Plant Disease ◽  
2002 ◽  
Vol 86 (9) ◽  
pp. 1052-1052 ◽  
Author(s):  
E. Moralejo ◽  
S. Werres

Phytophthora ramorum has been recently described (4) from isolates collected since approximately 1993, from Rhododendron and Viburnum in the Netherlands and Germany. Since 2001 and 2002, respectively, there have been unconfirmed reports from Poland and Great Britain (1). There are growing concerns about this oomycete since it has been recognized as the causal agent of sudden oak death in California, where thousands of oaks and tanoaks (Quercus agrifolia, Q. kelloggii, Q. parvula var. shrevei, and Lithocarpus densiflorus) have died. Since the first outbreak in Marin County, California in 1995, (3) the epidemic has remained concentrated mainly along the Pacific Coast near San Francisco but has been reported in Oregon (2). There have been no reports of oaks or other trees affected in Europe. During February 2002, E. Moralejo surveyed several nurseries in Mallorca, (Balearic Islands, Spain) to verify the presence of P. ramorum on rhododendron. Two shipments of rhododendrons, from the towns of Palma and Santa Maria del Camí, showed twig blight and necrotic spots at leaf tips and margins. Less than 0.5% of the aerial parts of the potted plants of both sets were affected. Isolations from symptomatic tissue consistently yielded cultures of Phytophthora using selective media (corn meal agar supplemented with nystatin, rifampicin, and ampicillin). Pure cultures were obtained from three isolates by hyphal-tip transfers on carrot piece agar (CPA) and identified as P. ramorum on the basis of morphological and cultural characters (4). Colonies grown on CPA at 17°C were appressed with sparse aerial mycelium and formed typical concentric growth rings under 16 h fluorescent light. Cardinal temperatures for vegetative growth were 2°C (minimum), 20°C (optimum), and 28°C (maximum). Daily radial growth was 3 to 3.2 mm at 20°C. Sporangia formed singly or in clusters on aerial sporangiophores in the absence of free water, and were mainly semipapillate, caducous, with a very short or no pedicel, ellipsoidal to elongated-ovoid, with a length/breath ratio of 1.9 to 2.1. Large spherical, terminal, and intercalary chlamydospores, 32 to 72 μm in diameter, were readily formed in agar. The mating type of these isolates from Mallorca was A1 based on dual cultures on CPA with four different heterothallic Phytophthora species. Crossing was successful with P. cryptogea BBA 63651 mating type A2. Oogonia were subglobose and measured 24 to 32 μm in diameter. Oospores were plerotic. Antheridia were always amphigynous, and mainly barrel-shaped to spherical, 14 to 22 μm in diameter One of the three isolates also produced a very small number of gametangia with the A2 tester strain P. cinnamomi BBA 62660, but the oospores appeared degenerate. Only A1 mating type strains of P. ramorum have been found in Europe. The Mallorca isolates have been deposited in the culture collection of the Federal Biological Research Centre for Agriculture and Forestry (BBA), Germany. To our knowledge, this is the first report of P. ramorum in Spain. Further research is urgently needed to assess whether the Mediterranean evergreen oak ecosystem is in danger. References: (1) EPPO Reporting Service. Published on-line, http://www.eppo.org/PUBLICATIONS/EPPO_RS/reporting_service.html Publication no. 2002/040 and 2002/077. (2) E. M. Goheen et al. Plant Dis. 86:441, 2002. (3) D. M. Rizzo et al. Plant Dis. 86:205, 2002. (4) S. Werres et al. Mycol. Res. 105:1155, 2001.


2003 ◽  
Vol 93 (6) ◽  
pp. 650-656 ◽  
Author(s):  
G. W. Douhan ◽  
T. D. Murray ◽  
P. S. Dyer

Eyespot of wheat is caused by Tapesia yallundae and T. acuformis. Historically, T. yallundae has been considered the more important causal agent of the disease in Washington state and consists of a large homogeneous population with a genetic structure consistent with both sexual and asexual reproduction. T. acuformis has increased significantly in Washington in the past 10 years and apothecia were found recently under natural field conditions, indicating that T. acuformis may have a more important role in eyespot of wheat than previously was thought. To determine the genetic structure of T. acuformis in Washington, 141 single conidial isolates were sampled from four subpopulations in the eastern wheat-growing region of the state. Isolates were scored for mating type and six amplified fragment length polymorphism markers. All markers segregated in a 1:1 ratio and were determined to be unlinked based on genetic analysis of 24 progeny from an in vitro cross. No significant differences in allele frequencies (0.127 < P < 0.809) were found among individual loci across the four subpopulations and over all loci based on contingency table analysis of the log-likelihood ratio statistic G2. Likewise, no overall differences between subpopulations were detected using the population differentiation statistic θ (θ = -0.004, P = 0.537). Random mating could not be rejected within each subpopulation or for the combined data using clone-corrected data sets based on (i) 1:1 ratio of mating-type, (ii) multilocus gametic disequilibrium analyses (index of association), (iii) phylogenetic analyses (parsimony tree length permutation test), and (iv) genotypic diversity analyses. T. acuformis has a genetic structure similar to that of sympatric populations of T. yallundae in Washington, with both sexual and asexual reproduction contributing to the structuring of this species.


IMA Fungus ◽  
2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Gang Wang ◽  
Yuanyuan Wang ◽  
Lianfu Chen ◽  
Hongbo Wang ◽  
Lin Guo ◽  
...  

AbstractThe mating compatibility in fungi is generally governed by genes located within a single or two unlinked mating type (MAT) loci. Hypsizygus marmoreus is an edible mushroom in the order Agaricales with a tetrapolar system, which contains two unlinked MAT loci-homeodomain (HD) transcription factor genes and pheromone/pheromone receptor genes (P/R). In this study, we analyzed the genetic structure and diversity of MAT loci in tetrapolar system of H. marmoreus through sequencing of 54 heterokaryon and 8 homokaryon strains. Although within the HD loci, the gene order was conserved, the gene contents were variable, and the HD loci haplotypes were further classified into four types. By analyzing the structure, phylogeny, and the HD transmissibility based on the progeny of these four HD mating-type loci types, we found that they were heritable and tightly linked at the HD loci. The P/R loci genes were found to comprise three pheromone receptors, three pheromones, and two pheromone receptor-like genes. Intra- and inter-specific phylogenetic analyses of pheromone receptors revealed that the STE3 genes were divided into three groups, and we thus theorize that they diverged before speciation. Comparative analysis of the MAT regions among 73 Basidiomycete species indicated that the diversity of HD and P/R loci in Agaricales and Boletales may contribute to mating compatibility. The number of HD genes were not correlated with the tetrapolar or bipolar systems. In H. marmoreus, the expression levels of these genes at HD and P/R loci of compatible strains were found higher than in those of homonuclear/homokaryotic strains, indicating that these mating genes acted as switches for mating processes. Further collinear analysis of HD loci in interspecific species found that HD loci contains conserved recombination hotspots showing major rearrangements in Coprinopsis cinerea and Schizophyllum commune, suggesting different mechanisms for evolution of physically linked MAT loci in these groups. It seems likely that gene rearrangements are common in Agaricales fungi around HD loci. Together, our study provides insights into the genomic basis of mating compatibility in H. marmoreus.


1986 ◽  
Vol 37 (3) ◽  
pp. 277 ◽  
Author(s):  
T Wicks ◽  
TC Lee

Phytophthora cambivora, P. citrophthora, P. cryptogea, and P. megasperma were isolated from either crown cankers or the soil around the crown of declining almond trees in South Australia. Severe root rot and crown cankers developed on Chellaston almond seedlings grown in soil artificially infested with the A1 but not the A2 mating type of P. cambivora. Cankers on inoculated plants were similar to those on naturally infected plants. Cankers did not develop on almond seedlings grown in soil infested with either P. citrophthora, P. cryptogea or P. megasperma. Neither extensive root rotting nor crown cankers developed in apricot and peach seedlings grown in soil artificially infested with the A1 mating type of P. cambivora. Phytophthora spp. were detected in 44% of the soil samples collected near the crown of dead and declining trees from 26 commercial almond orchards. In a severely affected orchard up to 17% of mature trees were either dead, missing or in a serious state of decline. Naturally infected trees were frequently found in poorly drained soils and were often associated with dripper irrigation outlets placed close to the trunk.


2016 ◽  
Vol 106 (11) ◽  
pp. 1376-1385 ◽  
Author(s):  
S. Albu ◽  
R. W. Schneider ◽  
P. P. Price ◽  
V. P. Doyle

Cercospora kikuchii has long been considered the causal agent of Cercospora leaf blight (CLB) and purple seed stain (PSS) on soybean, but a recent study found C. cf. flagellaris associated with CLB and PSS in Arkansas (United States) and Argentina. Here, we provide a broader perspective on the distribution of C. cf. flagellaris on soybean and alternate hosts within the United States (Arkansas, Louisiana, Mississippi, Missouri, and Kansas). We used a multilocus phylogenetic approach with data from actin, calmodulin, translation elongation factor 1-α, histone 3, the internal transcribed spacer region of rDNA and the mating-type locus to determine that two species, C. cf. flagellaris (200 of 205 isolates) and C. cf. sigesbeckiae (five of 205 isolates), are associated with CLB and PSS in the United States. In our phylogenetic analyses, species-level lineages were generally well-supported, though deeper-level evolutionary relationships remained unresolved, indicating that these genes do not possess sufficient phylogenetic signal to resolve the evolutionary history of Cercospora. We also investigated the potential for sexual reproduction in C. cf. flagellaris in Louisiana by determining the frequency of MAT1-1/MAT1-2 mating-type idiomorphs within the Louisiana population of C. cf. flagellaris. Though the MAT 1-2 idiomorph was significantly more common in our collection, the presence of both mating types suggests the potential for sexual reproduction exists.


Plant Disease ◽  
2009 ◽  
Vol 93 (7) ◽  
pp. 765-765 ◽  
Author(s):  
A. M. Vettraino ◽  
G. Lucero ◽  
P. Pizzuolo ◽  
S. Franceschini ◽  
A. Vannini

In Argentina, olives (Olea europaea) are planted on approximately 90,000 ha located primarily in the northwest continental regions. During a 2005 survey, root rot was recorded at several olive plantations in Catamarca, La Rioja, and San Juan provinces (3). Aboveground symptoms associated with root rot were twigs wilting with or without chlorosis, defoliation, and death. Symptoms were initiated on lateral branches and sometimes affected the entire crown. Even if young (5-year-old) trees displayed root rot, aerial symptoms may or may not be seen until years later. Disease incidence varied from 3 to 30%. Rotted rootlets were associated mainly with the infection of Phytophthora palmivora Butler and less frequently with another Phytophthora species. Isolates of this species were heterothallic, had a fluffy growth on carrot agar, and arachnoid growth on potato dextrose agar. Chlamydospores approximately 36 μm in diameter were also produced. The species developed prominent, papillate, noncaducous sporangia of different shapes ranging from ellipsoid to spherical when submerged in saline solution. Sporangia were 35 to 57 × 25 to 45 μm (average 44 × 33 μm), L:B ratio from 1.1 to 1.7. Isolates formed oogonia and amphyginous antheridia following mating type assays. On the basis of morphological features, these isolates were identified as P. nicotianae Breda de Haan. Identity was confirmed by sequencing the rDNA internal transcribed spacer (GenBank Accession No. FJ746693) (1). One-year-old O. europea seedlings were challenged with P. nicotianae (A1 isolates 306G and 339) through soil infestation assay in a growth chamber at 25°C. Infested and uninfested autoclaved millet grains moistened with V8 juice were used to inoculate 15 olive seedlings per isolate and controls, respectively. Fifty days after inoculation, seedlings showed foliar symptoms similar to those observed in the field and had an average of 50% reduction in the root system. Control plants remained healthy. P. nicotianae was always reisolated from symptomatic roots. P. nicotianae was reported on Citrus aurantium in Argentina in 1947 and is currently associated with several hosts (2). In 2002, the same species was reported associated with olive root rot in southern Italy (4). It is possible that P. nicotianae was recently introduced into Argentina through importation of Mediterranean olive varieties. The demonstrated pathogenicity of P. nicotianae on olive together with the recently reported detection of P. palmivora (3) presents a serious threat to olive cultivation in Argentina. References: (1) D. E. L. Cooke et al. Fungal Genet. Biol. 30:17, 2000. (2) M. J. Frezzi. Rev. Investig. Agric. 4:47, 1950. (3) G. Lucero et al. Plant Pathol. 56:728, 2007. (4) F. Nigro and A. Ippolito. Acta Hortic. 586:777, 2002.


Plant Disease ◽  
2010 ◽  
Vol 94 (11) ◽  
pp. 1374-1374 ◽  
Author(s):  
A. Pane ◽  
R. Faedda ◽  
S. O. Cacciola ◽  
C. Rizza ◽  
S. Scibetta ◽  
...  

Approximately 150,000 potted mandevillas (Apocynaceae) are produced each year in the Etna District of eastern Sicily. Since 2004, leaf chlorosis, wilt, and sudden collapse of the entire plant associated with root and basal stem rot of 6- to 12-month-old potted mandevillas, including Mandevilla × amabilis ‘Alice du Pont’, M. splendens, and M. sanderi ‘Alba’, ‘My Fair Lady’, and ‘Scarlet Pimpernel’, have been observed in six nurseries. Incidence of affected plants varied from 5 to 40%. Four Phytophthora species were consistently isolated from rotted roots and stems on a selective medium (2). Pure cultures of the first species produced colonies with a camellia pattern on potato dextrose agar and grew between 10 and 37°C with an optimum of 27°C. On V8 juice agar they produced ellipsoid to obpyriform (length/breadth [l/b] 1.45:1), nonpapillate sporangia with internal proliferation, coralloid, spherical hyphal swellings and both terminal and intercalary chlamydospores. In dual cultures with A1 and A2 isolates of P. nicotianae, all isolates produced oogonia with amphyginous antheridia only with A2 isolates. Isolates of the second species formed petaloid colonies, had an optimum growth temperature of 25°C, and produced mono- and bipapillate, ovoid to limoniform sporangia (l/b 1.40:1); they did not produce gametangia. Isolates of the third species formed colonies with a slight petaloid pattern and grew between 2 and 30°C with an optimum of 25°C. Sporangia were obpyriform (l/b 1.48:1), nonpapillate, and proliferous. All isolates were A2 mating type. The isolates of the fourth species formed arachnoid colonies, grew between 8 and 38°C with an optimum of 30°C, and produced mono- and bipapillate, ellipsoid, and obpyriform (l/b 1.3:1) sporangia and apical chlamydospores. All isolates were A2 mating type. DNA was extracted from mycelium and amplified by PCR using the ITS 4/ITS 6 primers (1). Blast search of the rDNA-ITS sequence of isolate IMI 397618 (GenBank Accession No. GQ388261) of the first species showed 100% identity with the ITS sequence of an isolate of P. cinnamomi var. parvispora (EU748548). The sequences (GQ463703 and GQ463704) of isolates IMI 397471 and IMI 397472 of the second species showed 99% similarity with the sequences of a P. citrophthora isolate (EU0000631). The sequence of isolate IMI 397473 (GQ463702) of the third species showed 99% similarity with the sequence of a P. cryptogea isolate (AY659443.1), while the sequence of isolate IMI 397474 (GU723474) of the fourth species showed 99% similarity with the sequence of a P. nicotianae isolate (EU331089). The pathogenicity of individual isolates IMI 397618, IMI 397471, IMI 397472, IMI 397473, and IMI 397474 was tested on 3-month-old potted plants (10 plants per isolate) of mandevilla ‘Alice du Pont’ by applying 10 ml of a suspension (2 × 104 zoospores/ml) to the root crown. Plants were maintained at 25°C and 95 to 100% relative humidity. All inoculated plants wilted after 4 weeks, while noninoculated control plants remained healthy. The four Phytophthora spp. were subsequently reisolated only from symptomatic plants. To our knowledge, this is the first report of P. cinnamomi var. parvispora in Italy and on mandevilla worldwide. In recent years, Phytophthora root and stem rot has become the most serious disease of potted mandevillas in Sicily. References: (1) D. E. L. Cooke et al. Fungal Genet. Biol. 30:17, 2000. (2) H. Masago et al. Phytopathology 67:425, 1977.


Plant Disease ◽  
2007 ◽  
Vol 91 (5) ◽  
pp. 633-633 ◽  
Author(s):  
B. W. Schwingle ◽  
J. Juzwik ◽  
J. Eggers ◽  
B. Moltzan

Periodic episodes of oak decline have occurred in the Missouri Ozark forests since the early 1900s and the disease is currently severe (2). Several Phytophthora spp. contribute to oak decline in Europe (1), but the role of Phytophthora spp. in oak decline in the eastern United States is not known. Mineral soils collected around the bases of declining and nondeclining oaks in paired sites in central Missouri forests were assayed for the presence of these taxa by baiting flooded soil with Quercus robur leaves. Q. rubra and Q. velutina were the oak species on three sites and Q. alba was on the fourth. Isolates from symptomatic baits plated on PARPNH selective medium were identified tentatively on classical taxonomic characteristics. Five isolates of P. cambivora, two of P. quercina, and eight of P. cinnamomi were obtained from soils around one, one, and three trees, respectively, on decline sites. The internal transcribed spacer sequences for each isolate were compared to those in GenBank; BLAST searches for all isolates had nucleotide identities of 99% and E values of 0, which confirmed the identifications. Greenhouse pot trials were conducted to assess pathogenicity of isolates on stems of 2-year-old Q. alba and Q. rubra. A mycelial agar plug was inserted into a 1-cm long slit cut into the cambium 5 cm above the root collar and covered with sterile, moist cotton and wrapped with laboratory film. The treatments included two isolates of P. cambivora, one of P. quercina, three of P. cinnamomi, and a sterile agar plug. Each host × isolate combination was replicated four times, and the experiment was conducted twice in the greenhouse (natural lighting; temperature ≤32°C in summer and ≥7°C in winter). Stem lesions were produced commonly by P. cambivora (28 of 32 seedlings) and P. cinnamomi (46 of 48 seedlings) within 3 months; none was found on control seedlings or those inoculated with P. quercina. Mean lengths (cm) of lesions caused by P. cinnamomi were greater for Q. rubra (5.6) than for Q. alba (4.3) and lesion lengths for P. cambivora were greater for Q. alba (5.2) than for Q. rubra (4.4). Seven Q. alba seedlings inoculated with P. cambivora and one Q. alba inoculated with P. cinnamomi died before 3 months. All Phytophthora species were recovered from inoculated stems at 3 months except that P. quercina was not recovered in one trial. To our knowledge, this is the first report of Phytophthora species in soils of Missouri oak forests, of P. quercina in the United States, and of the ability of P. cambivora to cause stem lesions on Q. alba. P. cinnamomi and P. cambivora should be investigated in situ as possible contributing factors of oak decline in Missouri. References: (1) T. Jung et al. Plant Pathol. 49:706, 2000. (2) R. Lawrence et al. MO. Conserv. 63:11, 2002.


Plant Disease ◽  
2010 ◽  
Vol 94 (3) ◽  
pp. 378-378 ◽  
Author(s):  
Q. H. Tang ◽  
F. Gao ◽  
G. Y. Li ◽  
H. Wang ◽  
X. B. Zheng ◽  
...  

Phytophthora sansomeana E.M. Hansen & Reeser is a newly described species and infects Douglas-fir, alfalfa, and soybean (1). Soybean production is an important part of the local economy in Yili State in Xinjiang Uygur Autonomous Region, northwest China. Unfortunately since 2005, root and stem rot disease has emerged on a number of farms. To identify the causal agent, plant samples with symptoms, including whole plant wilting or yellowing and stunting, were collected from fields during 2005 and 2008. Tissue from the edges of stem lesions was placed on selective lima bean agar (LBA) at 20°C for 3 to 4 days (2,3). Four single zoospore isolates of Phytophthora were obtained and maintained on LBA or 10% V8 juice liquid medium for examination of morphological and physiological characteristics. The colonies on LBA were aerial and rosaceous. The isolates were homothallic, and oogonia and oospores were readily produced in culture after 7 days on LBA plates. Oogonia averaged 38 μm and oospore width ranged from 23 to 48 μm and averaged 31 μm. Antheridia were approximately 15 × 12 μm and predominantly amphigynous in V8 juice. Sporangia were terminal or paragynous on persistent sporangiophores, nonpapillate, ovoid to obpyriform, and measured 52 × 35 μm with an average length/breadth ratio of 1.5. Hyphal swellings were produced in V8 juice 2 days after inoculation. The optimum temperature for growth was approximately 25°C and none occurred at 0 or 35°C. The internal transcribed spacer (ITS) sequence of this Phytophthora species (GenBank FJ966880) agreed 100% with sequences of P. sansomeana isolates deposited in GenBank (GQ853880 and EU925375). Pathogenicity tests were performed by hypocotyl inoculation method (2) using isolate Yili71 and potted soybean cv. Williams. Plants were grown in a growth chamber for 10 days before inoculation in 16-cm-diameter pots (2). Plants were inoculated with 2- × 2-mm plugs of mycelium grown for 4 days on LBA at 25°C, the plugs were adhered to the sides of wounded lower hypocotyls. As controls, plants were inoculated with LBA agar plugs without mycelium (2). Inoculated plants were maintained in a growth chamber at approximately 25°C with a 10-h dark/14-h light cycle and 50% relative humidity and symptom development was monitored daily for 1 week. Wounded stems inoculated with mycelium developed water-soaked lesions, which were similar to those seen on naturally infected plants. A Phytophthora sp. was reisolated from the margins of expanding lesions on wounded stems. To our knowledge, this is the first report of P. sansomeana infection of soybean in China and the threat it may pose to soybean production is unclear. References: (1) E. M. Hansen et al. Mycologia 101:129. 2009. (2) Z. Y. Wang et al. Fungal Genet. Biol. 43:826, 2006. (3) X. B. Zheng. Methods in Phytophthora. Chinese Agriculture Press. Beijing, China, 1995.


Plant Disease ◽  
2016 ◽  
Vol 100 (2) ◽  
pp. 500-509 ◽  
Author(s):  
Jaimin S. Patel ◽  
Anne Vitoreli ◽  
Aaron J. Palmateer ◽  
Ashraf El-Sayed ◽  
David J. Norman ◽  
...  

This report investigates population structure and genetic variability of Phytophthora spp. isolated from botanically diverse plants in Florida. Internal transcribed spacer-based molecular phylogenetic analyses indicate that Phytophthora isolates recovered from ornamental plants in Florida represent a genetically diverse population and that a majority of the isolates belong to Phytophthora nicotianae (73.2%), P. palmivora (18.7%), P. tropicalis (4.9%), P. katsurae (2.4%), and P. cinnamomi (0.8%). Mating type analyses revealed that most isolates were heterothallic, consisting of both mating type A1 (25.2%) and mating type A2 (39.0%), and suggesting that they could outcross. Fungicide sensitivity assays determined that several isolates were moderate to completely insensitive to mefenoxam. In addition, several isolates were also moderately insensitive to additional fungicides with different modes of action. However, correlation analyses did not reveal occurrence of fungicide cross-resistance. These studies suggest that a genetically diverse Phytophthora population infects ornamental crops and the occurrence of mefenoxam-insensitive Phytophthora populations raises concerns about disease management in ornamentals. Mitigating fungicide resistance will require prudent management strategies, including tank mixes and rotation of chemicals with different modes of actions.


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