In vitro Cultivation of Dipetalonema viteae Third-Stage Larvae: Evaluation of Culture Media, Serum, and Other Supplements

1984 ◽  
Vol 70 (5) ◽  
pp. 618 ◽  
Author(s):  
Eileen D. Franke ◽  
Paul P. Weinstein
PLoS ONE ◽  
2013 ◽  
Vol 8 (8) ◽  
pp. e72084 ◽  
Author(s):  
Rong-Jyh Lin ◽  
Jie-Wen He ◽  
Li-Yu Chung ◽  
June-Der Lee ◽  
Jiun-Jye Wang ◽  
...  

1977 ◽  
Vol 7 (2) ◽  
pp. 109-111 ◽  
Author(s):  
P. Viens ◽  
M.C. Lajeunesse ◽  
R. Richards ◽  
G.A.T. Targett

2022 ◽  
Vol 82 ◽  
Author(s):  
R. de-Souza ◽  
C. R. Adams ◽  
R. C. de-Melo ◽  
A. F. Guidolin ◽  
A. Michel ◽  
...  

Abstract Hops is a new culture in Brazil. Tissue culture can be an important technique for rapid hop propagation. This paper aims to characterize responses from different genotypes under different growth regulators through the interrelationship of response variables important to hop in vitro growth. Three genotypes were cultivated in six culture media with different combinations of growth regulators, BAP (6-benzylaminopurine), IAA (3-indolacetic acid) and GA3 (gibberellic acid). The means were compared by orthogonal contrasts and the interrelationship of the response variables was performed by path analysis. American genotypes showed favorable root development under the BAP + IAA combination, while the use of IAA improved shoot development. The origin of genotypes was important for defining the best protocol for in vitro cultivation. The path coefficient showed that the variable number of shoots has stronger direct effect on the number of nodal segments. Additionally, in tissue culture assays, the use of a covariable and proper error distribution significantly increased experimental accuracy.


2020 ◽  
Vol 12 (20) ◽  
pp. 8389
Author(s):  
Hassan-Sibroe A. Daanaa ◽  
Mennatullah Abdou ◽  
Hanan A. Goda ◽  
Mohamed T. Abbas ◽  
Mervat A. Hamza ◽  
...  

Although plant-based culture media enhances in vitro cultivation of rhizobacteria, studies assessing their biomass potential for large-scale applications are lacking. Here, we advance plant pellets (PPs) as a novel technology to unlock the potential of such vegan culture media for biomass production of Rhizobium leguminosarum. PP formulations were based on mixtures of Egyptian clover powder and the agro-byproducts glycerol and molasses. These mixtures were either contained or not contained in teabags during culture media preparation. Metrics of biomass included colony forming units, optical density (OD600nm), and cell dry weight (DW). Biomass comparisons between culture media based on PPs and standard yeast extract mannitol (YEM) revealed that the following PPs composition, contained in teabags, cultivated rhizobia at levels comparable to YEM: 16 g clover powder, 5% molasses, and 0.8% glycerol. This PPs composition enabled shorter generation times of rhizobia (PP: 3.83 h, YEM: 4.28 h). Strikingly, PPs mixtures supplemented with 10% molasses and not contained in teabags promoted rhizobia without apparent lag phases and produced 25% greater DW than YEM. PPs potentiate the use of dehydrated vegan feedstocks for both plant microbiota cultivation and biomass production and appear as cost- and labor-effective tools, easy to handle and store for plant-based culture media preparation.


1946 ◽  
Vol 84 (2) ◽  
pp. 181-190 ◽  
Author(s):  
Hilary Koprowski ◽  
Edwin H. Lennette

The West Nile virus was cultivated in suspended cell culture media employing several different tissue components, and it has been observed to survive in culture for at least 32 days. Continued propagation of the virus in vitro resulted in a change in its pathogenicity. The change lay in a marked reduction or a complete loss of the ability of the virus to produce fatal infections in mice and in hamsters on peripheral inoculation, although there was no obvious simultaneous alteration in the lethal effect of the virus by the cerebral route. In mice, the extent to which invasiveness was lost depended upon the passage level of the virus and the age of the test animals. The younger (and more susceptible) the mice, the greater the number of passages which was required to diminish the virulence of the virus by peripheral routes; after 68 passages, the virus still retained its full capacity to kill 3-day-old mice, while its ability to kill 8-day-old mice was reduced and its ability to kill mice 14 or more days of age was essentially abolished. How soon the loss of pathogenicity occurs in hamsters has not been determined. Prolonged cultivation rendered the virus avirulent for hamsters by the intraperitoneal route.


2021 ◽  
pp. 1-16
Author(s):  
Felipe Górski ◽  
Geysiane Moreira Gerotti ◽  
Hélida Mara Magalhães

The in vitro development of a plant is controlled by factors that promote a series of plant responses, which interfere with tissue organogenesis and morphology. For plants of the family Lamiaceae, these factors remain unknown or poorly understood, hindering in vitro cultivation of these plants. The basil cultivar ‘Grecco a palla’ has attractive chemical properties for medicinal, pharmaceutical, and cosmetic industries; however, its production is limited due to the lack of appropriate cultivation conditions. Two types of explants of this species (nodal segments and stem apexes) were grown in culture media with auxin and cytokinin, and their development was followed for 60 days. During in vitro cultivation, both explants were subjected to higher concentrations of plant growth regulators (PGRs) produced only calluses, without induction of shoots. Small amounts of regulators favored hyperhydricity as nodal segments or stem apexes in the absence of PGRs produced plants with disturbances, including brittle, light green, and thick leaves. In this case, there was an increase in the cell layers of palisade parenchyma, which had large cell spaces and larger cells. This tissue also advanced to spongy parenchyma and compressed it. The stomatal density was low; however, the stomata were larger with additions mainly in the guard cells and the stomatic opening. Therefore, stem apexes in the absence of PGRs produced more vigorous plants, whereas nodal segments with low amounts of cytokinins and auxins developed a well-branched and abundant root system.


2002 ◽  
Vol 15 (3) ◽  
pp. 401-413 ◽  
Author(s):  
Govinda S. Visvesvara

SUMMARY Although attempts to develop methods for the in vitro cultivation of microsporidia began as early as 1937, the interest in the culture of these organisms was confined mostly to microsporidia that infect insects. The successful cultivation in 1969 of Encephalitozoon cuniculi, a microsporidium of mammalian origin, and the subsequent identification of these organisms as agents of human disease heightened interest in the cultivation of microsporidia. I describe the methodology as well as the cell lines, the culture media, and culture conditions used in the in vitro culture of microsporidia such as Brachiola (Nosema) algerae, Encephalitozoon cuniculi, E. hellem, E. intestinalis, Enterocytozoon bieneusi, Trachipleistophora hominis, and Vittaforma corneae that cause human disease.


2017 ◽  
Vol 2 (2) ◽  
pp. 62
Author(s):  
Rodrigo Thibes Hoshino ◽  
Ronan Carlos Colombo ◽  
Ana Paula Zandoná ◽  
Guilherme Augusto Cito Alves ◽  
Ricardo Tadeu de Faria

Propagation of in vitro plants through other culture media rather than the traditional ones has been widely researched, with satisfactory results. However, to increase the effectiveness of these media, the addition of organic products has been presented satisfactory results. Therefore, the objective of this work was to evaluate the influence of the FishFértil® organic fertilizer on the in vitro cultivation of the Brazilian orchid Cattleya labiata. Treatments included FishFértil® fertilizer concentrations of 0; 1; 2; 3; 4; 5 and 6 mL L-1 in a simplified culture medium. At 180 days, shoot height, number of leaves, leaf area, number of roots, root average length, shoot and root dry mass and the shoot: root ratio were evaluated. The experimental design was entirely randomized, with 10 replications, each one containing 10 plantules. Data were submitted to an analysis of variance and regression analysis, at 5% of significance. The FishFértil® organic fertilizer at the concentration of 6 mL L-1 promoted better plantule growth of Cattleya labiata, subcultivated in vitro, in a simplified culture medium.


Author(s):  
Suzel Rios-Ramirez, Rodriguez-Ortiz ◽  
Judith Ruiz- Luna ◽  
Vicente Arturo Velasco- Velasco

To micropropagate agave plants, somatic tissue is obtained from selected plants that are conditioned for 2 to 6 months to improve their physiological condition and health before in vitro cultivation. The objective of this study was to evaluate the physiological condition of Agave angustifolia plants in terms of its effect on organogenic response in somatic tissue taken from these plants when they are established in similar culture media. In a nursery, growth of four groups of plants was evaluated when they were subjected to different types of irrigation for seven months: 1) water; 2) NS-50% (fertigation with nutrient solution at 50% strength); 3) NS-75%; and 4) NS-100%. At the end of the period, it was found that supplying nutrients is important for plants to achieve better physiological condition. The unfertilized plants and those that received NS-75% had increases of 3.8 and 7.8 leaves, 6.5 and 12.5 cm in length of the largest leaf, and 1610.3 and 4401.4 cm2 in leaf area. Stem tissue was obtained from these stock plants and cultured for 90 days in in vitro culture, and formation of adventitious shoots was assessed. The results showed that the magnitude of organogenesis in stem tissue for formation of adventitious shoots was positively related to the physiological condition of the stock plant. Explants taken from unfertilized stock plants formed 14.6 total shoots and 3.8 shoots on each explant, while those fertigated at 100% concentration of nutrients formed 32.7 total shoots and 8 shoots on each explant.


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