Interaction of epimastigote and trypomastigote forms of Trypanosoma cruzi with chicken macrophages in vitro

Parasitology ◽  
1980 ◽  
Vol 81 (2) ◽  
pp. 373-381 ◽  
Author(s):  
M. N. L. de Meirelles ◽  
T. C. de Araujo Jorge ◽  
W. de Souza
Keyword(s):  
Life Cycle ◽  
Trypanosoma Cruzi ◽  
Developmental Stages ◽  
Cell Contact ◽  
Blood Monocytes ◽  
Parasite Cell ◽  
Infected Cells ◽  
The Mean ◽  
Almost All

SUMMARYChicken macrophages, obtained by cultivation of blood monocytes, were infected with epimastigote and bloodstream trypomastigotes of the Y and the CL strains of Trypanosoma cruzi. The percentage of infected cells and the mean number of parasites per cell were determined after 2, 6, 12 and 24 h of parasite–cell contact. After 6 h of contact about 80% and 40% of the macrophages were infected by trypomastigotes of the Y and CL strains respectively. After longer periods of contact almost all macrophages were infected by Y trypomastigotes while only about 60% were infected by those of the CL strain. After 2 h of contact almost all macrophages were infected by CL epimastigotes while only about 50% were infected by Y epimastigotes. After 6 h of contact almost all macrophages were infected by epimastigotes of both strains. These results are discussed taking into consideration differences between parasites of the two strains and between the two developmental stages of the T. cruzi life-cycle.

scholarly journals Survey of Phenolic Acids, Flavonoids and In Vitro Antioxidant Potency Between Fig Peels and Pulps: Chemical and Chemometric Approach

Molecules ◽  
2021 ◽  
Vol 26 (9) ◽  
pp. 2574
Author(s):  
Lahcen Hssaini ◽  
Francisca Hernandez ◽  
Manuel Viuda-Martos ◽  
Jamal Charafi ◽  
Rachid Razouk ◽  
...  
Keyword(s):  
Phenolic Acids ◽  
Radical Scavenging ◽  
Fruit Peel ◽  
Mean Values ◽  
Local Cultivar ◽  
Ic50 Values ◽  
The Mean ◽  
Lipid Peroxidation Inhibition ◽  
Almost All

In the present study, chromatic coordinates, phenolic acids, flavonoids and antioxidant capacity assessed by 1,1-diphenyl-2-picrylhydrazyl (DPPH), 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonate (ABTS) and lipid peroxidation inhibition capacity (LPIC) essays and their relative IC50 were investigated in 25 fig cultivars growing in Morocco. The aims of this study were to determine (i) the variation in these compounds among light and dark-colored cultivars, (ii) their partitioning between fruit peel and pulp and (iii) to display network connections among these variables. Twelve phenolic compounds (PCs) were isolated in peel extract versus eight in pulp samples. Anthocyanins, mainly cyanidin-3,5-diglucoside and cyanidin-3-O-rutinoside, were the predominant compounds in peels, where the mean concentrations were 75.90 ± 18.76 and 77.97 ± 18.95 µg/g dw, respectively. On the other hand, (−)-epicatechin and cyanidin-3-O-rutinoside were the major compounds in the pulp extracts, where the mean values were 5.23 ± 4.03 and 9.01 ± 5.67 µg/g dw, respectively. A two-dimensional hierarchically clustered heatmap was applied to the dataset to explore correlations in the dataset and similarities between cultivars, without dimensionality reduction. Results showed that anthocyanins, particularly pelargonidin-3-O-rutinoside, cyanidin-3,5-diglucoside and cyanidin-3-O-rutinoside, were the main contributors to the peels’ free radical scavenging capacity. This capacity was particularly higher in the peel of dark-colored figs compared to the fruit pulp. The local cultivar “INRA 1301” showed the most promising phenolic profile due to its very high levels of almost all detected PCs, especially (−)-epicatechin, quercetin-3-O-rutinoside, quercetin-3-O-glucoside, cyanidine-3,5-diglucoside, cyanidine-3-O-rutinoside and pelargonidin-3-O-rutinoside (54.66, 141.08, 35.48, 494.08, 478.66, 12.56 µg/g dw, respectively). Having the darkest figs in the collection (L* = 25.72, c* = 22.09 and h° = 20.99), this cultivar has also combined promising IC50 values, which were of 19.85, 40.58 and 124.78 µg/mL for DPPH, ABTS and LPIC essays, respectively.

scholarly journals Tetraspanins CD9 and CD81 function to prevent the fusion of mononuclear phagocytes

2003 ◽  
Vol 161 (5) ◽  
pp. 945-956 ◽  
Author(s):  
Yoshito Takeda ◽  
Isao Tachibana ◽  
Kenji Miyado ◽  
Masatoshi Kobayashi ◽  
Toru Miyazaki ◽  
...  
Keyword(s):  
Complex Formation ◽  
Alveolar Macrophages ◽  
Bone Marrow Cells ◽  
Giant Cells ◽  
Mononuclear Phagocytes ◽  
Blood Monocytes ◽  
Multinucleated Cells ◽  
Infected Cells

Tetraspanins CD9 and CD81 facilitate the fusion between gametes, myoblasts, or virus-infected cells. Here, we investigated the role of these tetraspanins in the fusion of mononuclear phagocytes. Expression of CD9 and CD81 and their complex formation with integrins were up-regulated when blood monocytes were cultured under normal conditions. Under fusogenic conditions in the presence of Con A, CD9 and CD81 up-regulation was inhibited, and their complex formation with integrins was down-regulated. Anti-CD9 and -CD81 antibodies, which were previously shown to inhibit the fusion of gametes, myoblasts, and virus-infected cells, unexpectedly promoted the fusion of monocytes and alveolar macrophages. However, these effects were not due to altered cell adhesion, aggregation, or cytokine production. When stimulated in vitro or in vivo, alveolar macrophages and bone marrow cells of CD9- and CD81-null mice formed larger numbers of multinucleated cells than those of wild-type mice. Finally, CD9/CD81 double-null mice spontaneously developed multinucleated giant cells in the lung and showed enhanced osteoclastogenesis in the bone. These results suggest that CD9 and CD81 coordinately prevent the fusion of mononuclear phagocytes.

scholarly journals Fungicidal activity of rabbit alveolar and peritoneal macrophages against Candida albicans

1980 ◽  
Vol 28 (3) ◽  
pp. 1001-1008
Author(s):  
R I Lehrer ◽  
L G Ferrari ◽  
J Patterson-Delafield ◽  
T Sorrell
Keyword(s):  
Candida Albicans ◽  
Alveolar Macrophages ◽  
Fungicidal Activity ◽  
Peritoneal Macrophages ◽  
Human Monocytes ◽  
Blood Monocytes ◽  
Human Granulocytes ◽  
The Mean ◽  
Macrophage Populations

We tested the ability of rabbit macrophages to kill Candida albicans in vitro. Resident (unstimulated) alveolar macrophages killed 28.1 +/- 1.9% of ingested organisms in 4 h, whereas resident peritoneal macrophages killed only 15.2 +/- 1.3% (mean +/- standard error of the mean, P < 0.01). Peritoneal macrophages obtained from rabbits treated 3 weeks earlier with complete Freund adjuvant showed enhanced candidacidal activity relative to normally resident peritoneal cells (28.2 +/- 3.1%, P < 0.01). Candidacidal activity by alveolar macrophages recovered from such treated animals was slightly enhanced relative to untreated alveolar macrophages (32.9 +/- 2.3%). Candidacidal activity by peritoneal and alveolar macrophages was not decreased by several agents (cyanide, azide, sulfadiazine, and phenylbutazone) that inhibit the ability of human blood monocytes to kill C. albicans. In contrast, candidacidal activity by alveolar macrophages was greatly diminished by iodoacetate, an ineffective inhibitor of this function in human monocytes. We conclude that rabbit macrophages kill C. albicans by a fungicidal mechanism distinct from the peroxidase-H2O2 mechanism of human granulocytes and monocytes, and that the fungicidal properties of peritoneal and alveolar macrophage populations are enhanced after nonspecific stimulation with complete Freund adjuvant.

scholarly journals Study on the biology of groundnut bruchid, Caryedon serratus Olivier [Coleoptera: Bruchidae] on stored groundnut in Ganye area, Adamawa State, Nigeria

2020 ◽  
Vol 12 (3) ◽  
pp. 272-276
Author(s):  
C.S. Oaya
Keyword(s):  
Life Cycle ◽  
Larval Stage ◽  
Developmental Stages ◽  
Adult Stage ◽  
Pupal Stage ◽  
Male And Female ◽  
Incubation Stage ◽  
Caryedon Serratus ◽  
The Mean ◽  
Total Life

Abstract. Study on the biology of groundnut bruchid, Caryedon serratus Olivier was carried out in the Laboratory of the Department of Agricultural Technology, Adamawa State College of Agriculture, Ganye, Adamawa State from June to September, 2015. The sex of the bruchid (male and female) was assigned the sub-treatment while the period of development was the main treatment and was replicated three times. The work considered the pre-oviposition stage, incubation stage, larval stage, pupal stage, adult stage and the total life cycle of the bruchid (male and female). The experiment was carried out under Laboratory conditions at 30-35°C temperature and 70-90% relative humidity. After the experiment was established, weekly counting of the total number of eggs laid was carried out at intervals. The results showed that, the mean developmental stages in both female and male bruchids were: 6.50 and 6.00 days; 17.00 and 18.00 days; 13.50 and 13.50 days; 12.00 and 13.50 days; 48.00 and 50.00 days for incubation stage, larval stage, pupal stage, adult stage and total life cycle of the bruchids, respectively. Moreover, the mean pre-oviposition and oviposition stages in female adult bruchid were 1.50 and 5.50 days, respectively.

scholarly journals Ivermectin the Promising Drug to Stave off the COVID-19 Crisis: A Review

2021 ◽  
Vol 7 (2) ◽  
pp. 95-98
Author(s):  
Zakia Jahan ◽  
Masudul Hassan
Keyword(s):  
Infectious Diseases ◽  
Specific Treatment ◽  
In Vitro Study ◽  
Antiviral Effect ◽  
Viral Particles ◽  
The World ◽  
Infected Cells ◽  
Almost All ◽  
First Time

The Coronavirus disease 2019 (COVID-19) outbreak, forcing us to face unprecedented moments in the world. The huge devastating impact of the world due to the covid-19 attack causes the brink of no return. However, there is no proven and specific treatment for Covid -19. Very few medications have received Emergency Use of Authorization. A recent in vitro study was the first time to find out and to assess the antiviral effect of Ivermectin on COVID-19. The study showed that Ivermectin was active against COVID- 19-infected cells, was able to kill effectively almost all viral particles within 48 h. In these moments of crisis, FDA-approved ivermectin is a ray of hope. Bangladesh Journal of Infectious Diseases 2020;7(2):95-98

Studies on the life-cycle of Asymphylodora tincae Modeer, 1790) Trematoda: Monorchiidae) in a small lake near Amsterdam: Part 2: The relations between Asymphylodora tincae and its definitive host, Tinca tinca

1981 ◽  
Vol 55 (4) ◽  
pp. 239-246 ◽  
Author(s):  
M. A. Zietse ◽  
Elisabeth Van Den Broek ◽  
Elze E. A. Erwteman-Ooms
Keyword(s):  
Life Cycle ◽  
Definitive Host ◽  
Natural Infection ◽  
Early Spring ◽  
Summer Season ◽  
Tinca Tinca ◽  
Mean Intensity ◽  
The Mean ◽  
Infection Experiments

ABSTRACTThe natural infection of tench by Asymphylodora tincae in a lake was studied during one summer season. The incidence of infection was 57%, the mean intensity about 50. The distribution of the digencans along the host's intestine showed a maximum in the second half; this could be modified by the presence of other helminth species. Tench caught in early spring and kept in the laboratory retained their natural infection throughout the summer. Starvation of hosts during two months caused disappearance of the infection. Experiments showed that metaecrcariae, introduced into the intestine of tench, can excyst within one hour. In vitro, cysts in contact with tench bile opened within 15 seconds. Bile of several other cyprinid fisli species caused excystment within 60 seconds. Asymphylodora eggs appeared in tench faeces 7 to 10 days after infection. Progenetic specimens of A. tincae probably disintegrate in the intestine of the tench and their eggs arc passed out with the faeces.

Trypanosoma cruzi: Differential expression and distribution of an 85-kDa polypeptide epitope by in vitro developmental stages

1990 ◽  
Vol 71 (2) ◽  
pp. 207-217 ◽  
Author(s):  
M.Ali Ouaissi ◽  
J.F. Dubremetz ◽  
J.P. Kusnierz ◽  
J. Cornette ◽  
M. Loyens ◽  
...  
Keyword(s):  
Trypanosoma Cruzi ◽  
Differential Expression ◽  
Developmental Stages

scholarly journals The Transcriptome of Schistosoma mansoni Developing Eggs Reveals Key Mediators in Pathogenesis and Life Cycle Propagation

2021 ◽  
Vol 2 ◽  
Author(s):  
Zhigang Lu ◽  
Geetha Sankaranarayanan ◽  
Kate A. Rawlinson ◽  
Victoria Offord ◽  
Paul J. Brindley ◽  
...  
Keyword(s):  
Life Cycle ◽  
Schistosoma Mansoni ◽  
Developmental Stages ◽  
Developmental Time ◽  
Rna Seq ◽  
Cycle Progression ◽  
Cytoskeleton Organization ◽  
Late Embryogenesis ◽  
Venom Allergen

Schistosomiasis, the most important helminthic disease of humanity, is caused by infection with parasitic flatworms of the genus Schistosoma. The disease is driven by parasite eggs becoming trapped in host tissues, followed by inflammation and granuloma formation. Despite abundant transcriptome data for most developmental stages of the three main human-infective schistosome species—Schistosoma mansoni, S. japonicum and S. haematobium—the transcriptomic profiles of developing eggs remain under unexplored. In this study, we performed RNAseq of S. mansoni eggs laid in vitro during early and late embryogenesis, days 1-3 and 3-6 post-oviposition, respectively. Analysis of the transcriptomes identified hundreds of up-regulated genes during the later stage, including venom allergen-like (VAL) proteins, well-established host immunomodulators, and genes involved in organogenesis of the miracidium larva. In addition, the transcriptomes of the in vitro laid eggs were compared with existing publicly available RNA-seq datasets from S. mansoni eggs collected from the livers of rodent hosts. Analysis of enriched GO terms and pathway annotations revealed cell division and protein synthesis processes associated with early embryogenesis, whereas cellular metabolic processes, microtubule-based movement, and microtubule cytoskeleton organization were enriched in the later developmental time point. This is the first transcriptomic analysis of S. mansoni embryonic development, and will facilitate our understanding of infection pathogenesis, miracidial development and life cycle progression of schistosomes.

scholarly journals Concentration of hydrogen ions in several calcium hydroxide pastes over different periods of time

2009 ◽  
Vol 20 (5) ◽  
pp. 382-388 ◽  
Author(s):  
Morgana Eli Vianna ◽  
Danila M. Zilio ◽  
Caio Cezar Randi Ferraz ◽  
Alexandre Augusto Zaia ◽  
Francisco José de Souza-Filho ◽  
...  
Keyword(s):  
Calcium Hydroxide ◽  
Local Anesthetics ◽  
Glass Plate ◽  
In Vitro Study ◽  
Hydrogen Ions ◽  
Sterile Water ◽  
The Mean ◽  
Almost All ◽  
Chlorhexidine Gel

The purpose of this in vitro study was to measure the concentration of hydrogen ions (pH) of calcium hydroxide [(Ca(OH)2] pastes combined with different vehicles over 7 periods of time. The Ca(OH)2 was manipulated with the following vehicles: i: sterile water; ii: iodoform plus sterile water; iii: local anesthetics (Lydocaine 2% with 1: 100,000 epinephrine); iv: polyethyleneglycol; v: glycerin; vi: 2.0% chlorhexidine gel; vii: camphorated paramonochlorophenol (CMCP); viii: (CMCP) + glycerin; and ix: polyethyleneglycol plus CMCP. The pastes were made on a glass plate to toothpaste consistency and the pH was measured at the following times: 5 min, 1, 24, 48 h; 7, 14 and 28 days. The data were statistically analyzed (Kruskal-Wallis at p<0.05). At 5 min, 1 and 24 h, the pH of all tested pastes ranged from 13.05 to 11.16. At 48 h and 7 days the pH of all tested pastes ranged from 11.66 to 8.92. At 14 and 28 days almost all pastes had pH means lower than 10. In conclusion, the mean pH of all tested calcium hydroxide pastes decreased with the time. Pastes made with aqueous vehicles (especially with sterile water), followed by oily vehicles (especially with CMCP + glycerin), held the highest pH means over the periods of time tested.

scholarly journals Improved Method for In Vitro Secondary Amastigogenesis ofTrypanosoma cruzi: Morphometrical and Molecular Analysis of Intermediate Developmental Forms

2010 ◽  
Vol 2010 ◽  
pp. 1-10 ◽  
Author(s):  
L. A. Hernández-Osorio ◽  
C. Márquez-Dueñas ◽  
L. E. Florencio-Martínez ◽  
G. Ballesteros-Rodea ◽  
S. Martínez-Calvillo ◽  
...  
Keyword(s):  
Life Cycle ◽  
Molecular Mechanisms ◽  
Developmental Stages ◽  
Transformation Kinetics ◽  
Improved Method ◽  
Gradual Reduction ◽  
Molecular Analyses ◽  
Biphasic Life Cycle ◽  
Molecular Studies

Trypanosoma cruziundergoes a biphasic life cycle that consists of four alternate developmental stages. In vitro conditions to obtain a synchronic transformation and efficient rates of pure intermediate forms (IFs), which are indispensable for further biochemical, biological, and molecular studies, have not been reported. In the present study, we established an improved method to obtain IFs from secondary amastigogenesis. During the transformation kinetics, we observed progressive decreases in the size of the parasite body, undulating membrane and flagellum that were concomitant with nucleus remodeling and kinetoplast displacement. In addition, a gradual reduction in parasite movement and acquisition of the amastigote-specific Ssp4 antigen were observed. Therefore, our results showed that the in vitro conditions used obtained large quantities of highly synchronous and pure IFs that were clearly distinguished by morphometrical and molecular analyses. Obtaining these IFs represents the first step towards an understanding of the molecular mechanisms involved in amastigogenesis.

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