scholarly journals Hypocrea/Trichoderma viridescens ITV43 with potential for biocontrol of Moniliophthora roreri Cif Par, Phytophthora megasperma and Phytophthora capsici

2014 ◽  
Vol 8 (16) ◽  
pp. 1704-1712 ◽  
Author(s):  
A. Cuervo-Parra J. ◽  
Snchez-Lpez V. ◽  
Romero-Cortes T. ◽  
Ramrez-Lepe M.
Keyword(s):  
Phytophthora Capsici ◽  
Phytophthora Megasperma ◽  
Moniliophthora Roreri

Cytology of somatic and gametangial nuclei in Phytophthora capsici and Phytophthora megasperma var. sojae

1974 ◽  
Vol 52 (9) ◽  
pp. 2055-2060 ◽  
Author(s):  
L. W. Stephenson ◽  
D. C. Erwin ◽  
J. V. Leary
Keyword(s):  
Chromosome Number ◽  
Chromosome Numbers ◽  
Phytophthora Capsici ◽  
Relative Size ◽  
Pollen Tubes ◽  
Reduction Division ◽  
Phytophthora Megasperma ◽  
Linear Alignment ◽  
Size Of Nuclei

Nuclear divisions in the hyphae and gametangia of Phytophthora capsici and in hyphae of Phytophthora megasperma var. sojae resembled those of typical mitosis. The chromosomal configurations in prophase are similar to classical angiosperm prophase configurations. However, in metaphase the linear alignment of chromosomes resembled the pattern reported in pollen tubes of Lilium and Tradescantia. The relative size of nuclei and numbers of chromosomes per nucleus remained constant during gametangial development. Somatic and gametangial nuclei were about equal in size and chromosome number. Chromosome numbers in somatic and gametangial nuclei of P. capsici and P. megasperma var. sojae were about six and eight, respectively. There was no evidence of reduction division in gametangia.

scholarly journals Facile Synthesis of Carboxymethyl Cellulose Coated Core/Shell SiO2@Cu Nanoparticles and Their Antifungal Activity against Phytophthora capsici

Polymers ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 888
Author(s):  
Nguyen Thi Thanh Hai ◽  
Nguyen Duc Cuong ◽  
Nguyen Tran Quyen ◽  
Nguyen Quoc Hien ◽  
Tran Thi Dieu Hien ◽  
...  
Keyword(s):  
Antifungal Activity ◽  
Carboxymethyl Cellulose ◽  
Chemical Reduction ◽  
Low Cost ◽  
Phytophthora Capsici ◽  
Reduction Process ◽  
Spherical Shape ◽  
Core Shell ◽  
Cu Nanoparticles ◽  
Average Size

Cu nanoparticles are a potential material for creating novel alternative antimicrobial products due to their unique antibacterial/antifungal properties, stability, dispersion, low cost and abundance as well as being economical and ecofriendly. In this work, carboxymethyl cellulose coated core/shell SiO2@Cu nanoparticles (NPs) were synthesized by a simple and effective chemical reduction process. The initial SiO2 NPs, which were prepared from rice husk ash, were coated by a copper ultrathin film using hydrazine and carboxymethyl cellulose (CMC) as reducing agent and stable agent, respectively. The core/shell SiO2@Cu nanoparticles with an average size of ~19 nm were surrounded by CMC. The results indicated that the SiO2@Cu@CMC suspension was a homogenous morphology with a spherical shape, regular dispersion and good stability. Furthermore, the multicomponent SiO2@Cu@CMC NPs showed good antifungal activity against Phytophthora capsici (P. capsici). The novel Cu NPs-based multicomponent suspension is a key compound in the development of new fungicides for the control of the Phytophthora disease.

Estimation of genetic parameters associated with frosty pod rot (Moniliophthora roreri) and cacao production in Mexico

2021 ◽  
Vol 17 (3) ◽  
Author(s):  
José Luis Solís Bonilla ◽  
Uilson Vanderlei Lopes ◽  
Alfredo Zamarripa Colmenero ◽  
Biaani Beeu Martínez Valencia ◽  
Carlos Hugo Avendaño Arrazate ◽  
...  
Keyword(s):  
Genetic Parameters ◽  
Moniliophthora Roreri ◽  
Frosty Pod Rot ◽  
Estimation Of Genetic Parameters

scholarly journals A Genome-Wide Analysis of Pathogenesis-Related Protein-1 (PR-1) Genes from Piper nigrum Reveals Its Critical Role during Phytophthora capsici Infection

Genes ◽  
2021 ◽  
Vol 12 (7) ◽  
pp. 1007
Author(s):  
Divya Kattupalli ◽  
Asha Sreenivasan ◽  
Eppurathu Vasudevan Soniya
Keyword(s):  
Phytophthora Capsici ◽  
Regulatory Elements ◽  
Piper Nigrum ◽  
Binding Motif ◽  
Altered Expression ◽  
Genome Wide ◽  
A Genome ◽  
Pathogenesis Related Protein ◽  
Pathogenesis Related

Black pepper (Piper nigrum L.) is a prominent spice that is an indispensable ingredient in cuisine and traditional medicine. Phytophthora capsici, the causative agent of footrot disease, causes a drastic constraint in P. nigrum cultivation and productivity. To counterattack various biotic and abiotic stresses, plants employ a broad array of mechanisms that includes the accumulation of pathogenesis-related (PR) proteins. Through a genome-wide survey, eleven PR-1 genes that belong to a CAP superfamily protein with a caveolin-binding motif (CBM) and a CAP-derived peptide (CAPE) were identified from P. nigrum. Despite the critical functional domains, PnPR-1 homologs differ in their signal peptide motifs and core amino acid composition in the functional protein domains. The conserved motifs of PnPR-1 proteins were identified using MEME. Most of the PnPR-1 proteins were basic in nature. Secondary and 3D structure analyses of the PnPR-1 proteins were also predicted, which may be linked to a functional role in P. nigrum. The GO and KEGG functional annotations predicted their function in the defense responses of plant-pathogen interactions. Furthermore, a transcriptome-assisted FPKM analysis revealed PnPR-1 genes mapped to the P. nigrum-P. capsici interaction pathway. An altered expression pattern was detected for PnPR-1 transcripts among which a significant upregulation was noted for basic PnPR-1 genes such as CL10113.C1 and Unigene17664. The drastic variation in the transcript levels of CL10113.C1 was further validated through qRT-PCR and it showed a significant upregulation in infected leaf samples compared with the control. A subsequent analysis revealed the structural details, phylogenetic relationships, conserved sequence motifs and critical cis-regulatory elements of PnPR-1 genes. This is the first genome-wide study that identified the role of PR-1 genes during P. nigrum-P. capsici interactions. The detailed in silico experimental analysis revealed the vital role of PnPR-1 genes in regulating the first layer of defense towards a P. capsici infection in Panniyur-1 plants.

scholarly journals Characteristic of the Pepper CaRGA2 Gene in Defense Responses against Phytophthora capsici Leonian

2013 ◽  
Vol 14 (5) ◽  
pp. 8985-9004 ◽  
Author(s):  
Ying-Li Zhang ◽  
Qing-Li Jia ◽  
Da-Wei Li ◽  
Jun-E Wang ◽  
Yan-Xu Yin ◽  
...  
Keyword(s):  
Phytophthora Capsici ◽  
Defense Responses

scholarly journals First Report of Phytophthora megasperma and Pythium irregulare As Olive Tree Root Pathogens

Plant Disease ◽  
1997 ◽  
Vol 81 (10) ◽  
pp. 1216-1216 ◽  
Author(s):  
M. E. Sánchez-Hernández ◽  
A. Ruiz-Dávila ◽  
A. Trapero-Casas
Keyword(s):  
Root Rot ◽  
Olive Tree ◽  
The United States ◽  
Damping Off ◽  
Phytophthora Megasperma ◽  
Root Rots ◽  
Foliar Symptoms ◽  
Root Pathogens ◽  
Root Necrosis ◽  
Olive Trees

Several species of the genus Phytophthora are associated with root rot and trunk cankers in olive trees (Olea europaea L.). Among them, Phytophthora megasperma has been cited as being associated with olive root rots in Greece (1). Unidentified species of Pythium and Phytophthora have also been associated with olive tree root rots in the United States. However, the status of P. megasperma and Pythium spp. as olive tree root pathogens has remained unclear. Following a 5-year period of severe drought in southern Spain, autumn-winter rainfall rates in 1996 to 1997 steadily increased in both quantity and frequency. Under these unusually wet conditions, olive trees remained waterlogged for several months. During this period, we observed foliar wilting, dieback, and death of young trees, and later found extensive root necrosis. In 46 of 49 affected plantations surveyed, P. megasperma was consistently isolated from the rotted rootlets, particularly in young (<1- to 10-year-old trees) plantations. This fungus was not detected on plant material affected by damping-off from several Spanish olive tree nurseries. The opposite situation occurred with P. irregulare. This species was not associated with rotted rootlets in the field. In contrast, it was consistently isolated from necrotic rootlets from young olive plants affected by damping-off. These plants were grown in a sand-lime-peat soil mixture under greenhouse conditions and showed foliar wilting and extensive necrosis of the root systems. Pathogenicity tests were conducted with several isolates of P. megasperma and P. irregulare on 6-month-old rooted cuttings of olive, under both weekly watering and waterlogged conditions. Under waterlogged conditions, both fungal species produced extensive root necrosis 2 weeks after inoculation that resulted in wilting of the aerial parts and rapid plant death. Waterlogged control plants remained without foliar symptoms but a low degree of root necrosis was recorded. In addition, under weekly watering conditions, plants inoculated with either species showed some degree of root rot but foliar symptoms were not evident. No differences in pathogenicity were observed within the Phytophthora or Pythium isolates. Reference: (1) H. Kouyeas and A. Chitzanidis. Ann. Inst. Phytopathol. Benaki 8:175, 1968.

scholarly journals A PCR-based Assay for Distinguishing between A1 and A2 Mating Types of Phytophthora capsici

2017 ◽  
Vol 142 (4) ◽  
pp. 260-264
Author(s):  
Ping Li ◽  
Dong Liu ◽  
Min Guo ◽  
Yuemin Pan ◽  
Fangxin Chen ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Mating Type ◽  
Phytophthora Capsici ◽  
Mating Types ◽  
Sequence Repeat ◽  
Chain Reaction ◽  
Plant Parasite ◽  
Dna Fragment ◽  
Polymerase Chain ◽  
Microsatellite Diversity

Sexual reproduction in the plant parasite Phytophthora capsici Leonian requires the interaction of two distinct mating types, A1 and A2. Co-occurrence of these mating types can enhance the genetic diversity of P. capsici and alter its virulence or resistance characteristics. Using an intersimple sequence repeat (ISSR) screen of microsatellite diversity, we identified, cloned, and sequenced a novel 1121-base pair (bp) fragment specific to the A1 mating type of P. capsici. Primers Pcap-1 and Pcap-2 were designed from this DNA fragment to specifically detect the A1 mating type. Polymerase chain reaction (PCR) using these primers amplified an expected 997-bp fragment from known A1 mating types, but yielded a 508-bp fragment from known A2 mating types. This PCR-based assay could be adapted to accurately and rapidly detect the co-occurrence of A1 and A2 P. capsici mating types from field material.

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