scholarly journals Resistance to Multiple Tuber Diseases Expressed in Somaclonal Variants of the Potato Cultivar Russet Burbank

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Tamilarasan Thangavel ◽  
Robert Steven Tegg ◽  
Calum Rae Wilson

Multiple disease resistance is an aim of many plant breeding programs. Previously, novel somatic cell selection was used to generate potato variants of “Russet Burbank” with resistance to common scab caused by infection with an actinomycete pathogen. Coexpression of resistance to powdery scab caused by a protozoan pathogen was subsequently shown. This study sought to define whether this resistance was effective against additional potato tuber diseases, black scurf, and tuber soft rot induced by fungal and bacterial pathogens. Pot trials andin vitroassays with multiple pathogenic strains identified significant resistance to both tuber diseases across the potato variants examined; the best clone A380 showed 51% and 65% reductions in disease severity to tuber soft rot and black scurf, respectively, when compared with the parent line. The resistance appeared to be tuber specific as no enhanced resistance was recorded in stolons or stem material when challengedRhizoctonia solanithat induces stolon pruning and stem canker. The work presented here suggests that morphological characteristics associated with tuber resistance may be the predominant change that has resulted from the somaclonal cell selection process, potentially underpinning the demonstrated broad spectrum of resistance to tuber invading pathogens.

Plant Disease ◽  
2004 ◽  
Vol 88 (1) ◽  
pp. 83-83 ◽  
Author(s):  
M. Truter ◽  
F. C. Wehner

Rhizoctonia disease (black scurf of tubers and stem canker) of potato (Solanum tuberosum L.) caused by Rhizoctonia solani Kühn was first recorded in South Africa in 1918 (3). Although the sclerotial form on tubers is one of the most common potato diseases in the country, it is not known which anastomosis groups (AGs) of R. solani are involved. Between 1999 and 2001, R. solani was isolated from 28 plant and 56 soil samples collected in 7 (Eastern Free State, Gauteng, KwaZulu-Natal, Limpopo, Mpumalanga, Northern Cape, and Sandveld) of the 14 potato-production regions of South Africa and screened for hyphal anastomosis with tester strains of R. solani AG-1 to AG-10 according to Carling et al. (1). Of the 411 isolates from tubers with black scurf symptoms, 408 were AG-3 and three were AG-5. Symptomless tubers yielded two AG-3 isolates and three AG-5 isolates. Of 39 isolates from symptomatic stems and roots, 32 were AG-3, five were AG-4, and two were AG-5. Of the 127 isolates obtained from soil, 86, 28, 7, 3, and 3 were AG-3, AG-4, AG-5, AG-7, and AG-8, respectively. More than one AG was isolated from five of the seven regions. Virulence of 40 isolates representative of the above AGs was determined in triplicate on sprouts growing from seed tubers of potato cultivar Up-to-Date in a sand/soil mixture as described by Carling and Leiner (2) but using cultures grown in cornmeal/sand instead of colonized agar disks as inoculum. Damage to sprouts (lesions, girdling, and death) was assessed after 28 days at 16 to 28°C according to the 0 to 4 rating scale (2). Chi-square analysis of the data indicated that AG-3 was the most virulent, with isolates from sclerotia on tubers and lesions on stems more aggressive than those from symptomless tubers or soil. AG-4 and AG-5 caused significantly less disease than AG-3, but none of the AG-7 and AG-8 isolates showed any virulence to potato sprouts. References: (1) D. E. Carling et al. Phytopathology 77:1609, 1987. (2) D. E. Carling and R. H. Leiner. Phytopathology 80:930, 1990. (3) E. M. Doidge. S. Afr. Fruit Growers 5:6, 1918.


1970 ◽  
Vol 39 (1) ◽  
pp. 107-110
Author(s):  
Md Maniruzzaman Khandaker ◽  
Md Khurshed Alam Bhuiyan ◽  
Abul Khair

Two pathogenic isolates of Rhizoctonia solani Kuhn causing stem canker/black scurf disease of potato plants and four antagonist isolates, two of binucleate Rhizoctonia and two of Trichoderma harzianum Rifai were isolated from crop fields and evaluated in vitro for their fungicidal responses against eight fungicides. Vitavax was effective in inhibiting the growth of R. solani and binucleate Rhizoctonia but it did not inhibit the growth of T. harzianum at 100 ppm concentration. Terraclor Super X, Dithane M 45 and Boric acid are the fungicides which at 100 ppm concentration did not inhibit the growth of antagonist isolates of T. harzianum and binucleate Rhizoctonia but inhibited the growth of isolates of R. solani to some extent. The in vitro findings suggest that any one of these three fungicides along with antagonist isolates of binucleate Rhizoctonia and T. harzianum can be used as biocontrol agents to reduce soil borne inocula of R. solani. Key words: Rhizoctonia solani; Binucleate; Trichoderma harzianum; Fungicide DOI: 10.3329/bjb.v39i1.5534Bangladesh J. Bot. 39(1): 107-110, 2010 (June)


2020 ◽  
Author(s):  
Renata Lebecka ◽  
Iwona Wasilewicz-Flis ◽  
Dariusz Mańkowski

AbstractPotato growers suffer losses due to potato soft rot and blackleg caused by pectinolytic bacteria of different species. These bacteria cause yield loss during cultivation and storage, and can be transmitted to the next generations through seed tubers. The prevalence of Pectobacterium atrosepticum has decreased over the last 20 years in Europe in favour of Dickeya solani and P. carotovorum subsp. brasiliense. Twenty-six diploid interspecific Solanum hybrids, previously selected for tuber resistance to P. atrosepticum, were screened for resistance to a highly aggressive D. solani strain in terms of tuber and blackleg reaction. The bacterial strain used for inoculation was characterised by a relatively high optimal growth temperature in vitro, ranging from 33 to 35 °C. Twenty-four diploid clones did not differ in terms of tuber reaction to inoculation with this strain of bacteria in comparison with the clone USA 249, which is the somatic hybrid of S. brevidens (+) S. tuberosum with proven resistance to Pectobacterium. Seventeen clones performed significantly better in terms of blackleg resistance than the resistant potato cultivar Glada. Eleven of the selected diploids produced unreduced gametes, which allows their use in improving the resistance of tetraploid potatoes to diseases caused by bacteria of both Pectobacterium and Dickeya.


Forests ◽  
2019 ◽  
Vol 11 (1) ◽  
pp. 34
Author(s):  
Xingqi Li ◽  
Xinyue Lu ◽  
Yiheng He ◽  
Mengting Deng ◽  
Yanrong Lv

Rot disease is a serious disease in pomegranate (Punica granatum L.) plantations in China. This disease usually weakens tree vigor, and seriously reduces the ornamental value, fruit yield, and quality. A better understanding of the pathogen that causes a disease is important for its control. Thus, the aims of this study were to isolate and identify the pathogen causing rot disease and to explore substances for its biological control. In this study, the morphology of the hyphae and spores of the pathogens was observed, and the pathogens were identified by morphological characteristics and the internal transcribed spacer (ITS) regions of their rDNA. Furthermore, the activity of an aqueous garlic extract as antifungal treatment for the identified pathogens was assessed. The results showed that the pathogens causing soft rot and dry rot in ‘Xinjiang Big Seed’ pomegranate were most probably Aspergillus niger and Botryosphaeria dothidea, respectively. In addition, the pathogenicity of A. niger was stronger than that of B. dothidea. The aqueous garlic extract had a strong antifungal effect on both pathogens by inhibiting mycelium growth in vitro, and the minimum inhibitory concentrations against A. niger and B. dothidea were 7.5 mg/mL and 10 mg/mL, respectively.


2016 ◽  
pp. 166-170
Author(s):  
Y.V. Masliy ◽  
◽  
I.O. Sudoma ◽  
P.S. Mazur ◽  
D.A. Mykytenko ◽  
...  

The objective: to study the possibility of using frozen blastocysts for biopsy and genetic testing and performance measurement transfer euploeded 5–7-day-old embryos after thawing, biopsies, refreezing and thawing in patients with unsuccessful implantation. Patients and methods. The object of the study was the group of patients with repeated failure of implantation (4) in programs of auxiliary reproductive technologies (ART), subject to transfer to the uterus in total (i.e. in all the programs) for at least 6 good quality embryos based on morphological characteristics). All women had sufficient ovarian reserve. The patient was treated for infertility within the ART programs of the clinic of reproductive medicine "Nadiya" in the period from 2006 to 2016. The sample included couples who were not carriers of chromosomal rearrangements, without anomalies of the uterus (congenital and acquired: a doubling of the uterus, one-horned uterus, intrauterine membrane, synechia, submucous myoma of the uterus). All women had a positive ovarian response to controlled stimulation with gonadotropins (at least 7 oocytes) and a sufficient number of cryopreserved embryos. The first group (G1) included 64 women who trophectodermal a biopsy was performed on fresh blastocysts (in a loop controlled ovarian hyperstimulation). The second group (G2) were included 31 women who underwent thawing previously cryopreserved blastocysts trophectodermal re-biopsy and vitrification of blastocysts. Results. It was found that the performance of transfers euploid embryos that were vitrified, bioptrone and revitriphted, a little lower than those that were bioptrone fresh and vitrified only once. At the same time computationa genetic diagnosis previously vitrified blastocysts using comparative genome hybridization in patients with recurrent failed implantation allows to obtain a reasonable pregnancy rate (58%), implantation rate (33.3 %) and the birth of living children (45.1 %). Conclusion. Reprising biopropane embryos does not cause significant destructive impact and allows you to achieve pregnancy and birth of the alive child. Key words: in vitro fertilization, reusable unsuccessful implantation, a method of comparative genome hybridization, refreezing.


Author(s):  
Sudhakar Sekar ◽  
Shee Sim May

The aim of the study is to formulate a modified release chitosan nanoparticles for the oral delivery of atorvastatin and to study the in vitro release of atorvastatin from chitosan nanoparticles. Atorvastatin-loaded chitosan nanoparticles were prepared with different concentration of cross-linking agent (glutaraldehyde) by emulsion interfacial reaction method. The formed nanoparticles were characterized in terms of size and morphological characteristics by scanning electron microscopy (SEM) and transmission electron microscope (TEM). Spherical and regular nanoparticles with the size range of 100-250nm were formed. Atorvastatin encapsulation efficiency of nanoparticles was found to be highest in ANP3, followed by ANP2 and ANP1. The in vitro release of atorvastatin was studied by membrane diffusion technique. The resulted cumulative percentage of drug released for ANP1, ANP2 and ANP3 were 60.08%, 34.81% and 20.39% respectively. Through this study, the nanoparticles preparation technique has shown to be a promising approach for enhancing the dissolution of hydrophobic drugs like atorvastatin calcium. The application of this novel delivery system offers good therapeutic potential in the management of hypercholesterolemia and dyslipidemia.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Maria-Argyro Karageorgou ◽  
Dimosthenis Stamopoulos

AbstractRadiolabeled magnetic nanoparticles are promising candidates as dual-modality-contrast-agents (DMCA) for diagnostic applications. The immunocompatibility of a new DMCA is a prerequisite for subsequent in vivo applications. Here, a new DMCA, namely Fe3O4 nanoparticles radiolabeled with 68Ga, is subjected to immunocompatibility tests both in vitro and in vivo. The in vitro immunocompatibility of the DMCA relied on incubation with donated human WBCs and PLTs (five healthy individuals). Optical microscopy (OM) and atomic force microscopy (AFM) were employed for the investigation of the morphological characteristics of WBCs and PLTs. A standard hematology analyzer (HA) provided information on complete blood count. The in vivo immunocompatibility of the DMCA was assessed through its biodistribution among the basic organs of the mononuclear phagocyte system in normal and immunodeficient mice (nine in each group). In addition, Magnetic Resonance Imaging (MRI) data were acquired in normal mice (three). The combined OM, AFM and HA in vitro data showed that although the DMCA promoted noticeable activation of WBCs and PLTs, neither degradation nor clustering were observed. The in vivo data showed no difference of the DMCA biodistribution between the normal and immunodeficient mice, while the MRI data prove the efficacy of the particular DMCA when compared to the non-radiolabeled, parent CA. The combined in vitro and in vivo data prove that the particular DMCA is a promising candidate for future in vivo applications.


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