A new isolate of Nosema fumiferanae (Microsporidia: Nosematidae) from the date moth Apomyelois (Ectomyelois) ceratoniae, Zeller, 1839 (Lepidoptera: Pyralidae)

Parasitology ◽  
2020 ◽  
Vol 147 (13) ◽  
pp. 1461-1468
Author(s):  
Onur Tosun
Keyword(s):  
Direct Contact ◽  
Sequence Similarity ◽  
Polar Filament ◽  
Cell Cytoplasm ◽  
Development Stages ◽  
Molecular Features ◽  
Host Cell Cytoplasm ◽  
Lepidoptera Pyralidae ◽  
Ultrastructural Characteristics ◽  
Carob Moth

AbstractIn this study, a microsporidian pathogen of the date moth (Apomyelois (Ectomyelois) ceratoniae, Zeller, 1839) also known as the carob moth, is described based on light microscopy, ultrastructural characteristics and comparative molecular analysis. The pathogen infects the gut and hemolymph of A. ceratoniae. All development stages are in direct contact with the host cell cytoplasm. Fresh spores with nuclei arranged in a diplokaryon are oval and measured 3.29 ± 0.23 μm (4.18–3.03 μm, n = 200) in length and 1.91 ± 0.23 μm (2.98–1.66 μm, n = 200) in width. Spores stained with Giemsa's stain measured 3.11 ± 0.31 μm (3.72–2.41 μm, n = 150) in length and 1.76 ± 0.23 μm (2.16–1.25 μm, n = 150) in width. Spores have an isofilar polar filament with 10-12 coils. An 1110 bp long alignment of the current microsporidium showed an SSU rRNA gene difference of only 0.0009, corresponding to >99.91% sequence similarity with Nosema fumiferanae, while RPB1 gene sequences were 98.03% similar within an alignment of 969 bp. All morphological, ultrastructural and molecular features indicate that the microsporidian pathogen of A. ceratoniae is the new isolate of the N. fumiferanae and is named here as Nosema fumiferanae TY61.

A new microsporidian parasite, Potaspora morhaphis n. gen., n. sp. (Microsporidia) infecting the Teleostean fish, Potamorhaphis guianensis from the River Amazon. Morphological, ultrastructural and molecular characterization

Parasitology ◽  
2008 ◽  
Vol 135 (9) ◽  
pp. 1053-1064 ◽  
Author(s):  
G. CASAL ◽  
E. MATOS ◽  
M. L. TELES-GRILO ◽  
C. AZEVEDO
Keyword(s):  
Developmental Stages ◽  
Polar Filament ◽  
Large Subunit ◽  
Small Subunit ◽  
Maximum Parsimony Analysis ◽  
Rrna Gene ◽  
Microsporidian Parasite ◽  
Host Cell Cytoplasm ◽  
Ultrastructural Characteristics ◽  
Large Subunit Rrna

SUMMARYA fish-infecting Microsporidia Potaspora morhaphis n. gen., n. sp. found adherent to the wall of the coelomic cavity of the freshwater fish, Potamorhaphis guianensis, from lower Amazon River is described, based on light microscope and ultrastructural characteristics. This microsporidian forms whitish xenomas distinguished by the numerous filiform and anastomosed microvilli. The xenoma was completely filled by several developmental stages. In all of these stages, the nuclei are monokaryotic and develop in direct contact with host cell cytoplasm. The merogonial plasmodium divides by binary fission and the disporoblastic pyriform spores of sporont origin measure 2·8±0·3×1·5±0·2 μm. In mature spores the polar filament was arranged into 9–10 coils in 2 layers. The polaroplast had 2 distinct regions around the manubrium and an electron-dense globule was observed. The small subunit, intergenic space and partial large subunit rRNA gene were sequenced and maximum parsimony analysis placed the microsporidian described here in the clade that includes the genera Kabatana, Microgemma, Spraguea and Tetramicra. The ultrastructural morphology of the xenoma, and the developmental stages including the spores of this microsporidian parasite, as well as the phylogenetic analysis, suggest the erection of a new genus and species.

Unikaryon slaptonleyi sp.nov. (Microspora: Unikaryonidae) isolated from echinostome and strigeid larvae from Lymnaea peregra: observations on its morphology, transmission and pathogenicity

Parasitology ◽  
1983 ◽  
Vol 87 (2) ◽  
pp. 175-184 ◽  
Author(s):  
Elizabeth U. Canning ◽  
Rosalind J. Barker ◽  
Jill C. Hammond ◽  
J. P. Nicholas
Keyword(s):  
Host Cell ◽  
Fasciola Hepatica ◽  
Polar Filament ◽  
Pieris Brassicae ◽  
Cell Cytoplasm ◽  
Terrestrial Arthropods ◽  
Host Cell Cytoplasm ◽  
Lymnaea Peregra ◽  
High Doses ◽  
Germinal Tissue

SUMMARYA microsporidium, isolated from echinostome and strigeid larval trematodes in Lymnaea peregra, is described as a new species Unikaryon slaptonleyi sp.nov. The nuclei isolated at all stages of development, the disporoblastic sporogony and development in contact with host cell cytoplasm are used to assign the species to the genus Unikaryon. The absence of a vacuolar membrane to isolate the meronts and stages of sporulation from the host cell cytoplasm differentiates this genus from Encephalitozoon. Spores are uninucleate, have 17–21 turns of the polar filament coil and measure 5·0 × 2·8/μm fresh. U. slaptonleyi was isolated from rediae and metacercariae of Echinoparyphium recurvatum and sporo-cysts and cercariae of an unidentified strigeid trematode in L. peregra. It was transmitted in the laboratory to unidentified echinostomes in L. peregra and to unidentified strigeids in Planorbis planorbis by feeding the spores to field-collected snails from which cercariae were already emerging. In these natural and experimental hyperinfections the snail tissues were lightly infected but, in the helminths, much of the parenchyma and germinal tissue was destroyed, so that few cercariae were released and most of those were distorted. Similar heavy infections were produced in Fasciola hepatica in Lymnaea truncatula, when spores were fed to the snails 14 days after miracidial penetration, but even high doses (106 spores/snail) produced only light infections in Schistosoma mansoni in Biomphalaria glabrata, in only 2 out of 9 snails. No infections were obtained in larvae producing xiphidiocercariae in P. planorbis although echinostomes became infected under the same conditions. Of a number of aquatic and terrestrial arthropods tested for susceptibility by feeding or by inoculation of spores into the haemocoele, only Pieris brassicae became infected. In a small proportion of pupae surviving from larvae which had been inoculated with spores at 3rd or 4th instar, there was clear evidence of spore replication.

scholarly journals Molecular Forces Governing the Biological Function of Per-Arnt-Sim-B (PAS-B) Domains: A Comparative Computational Study

Biophysica ◽  
2021 ◽  
Vol 1 (1) ◽  
pp. 1-14
Author(s):  
João Victor de Souza ◽  
Piotr Zaborniak ◽  
Sylvia Reznikov ◽  
Matthew Kondal ◽  
Ruidi Zhu ◽  
...  
Keyword(s):  
Juvenile Hormone ◽  
Hormone Receptor ◽  
Redox Regulation ◽  
Biological Function ◽  
Computational Study ◽  
Sequence Similarity ◽  
Molecular Characteristics ◽  
Drosophila Suzukii ◽  
Xenobiotic Stress ◽  
Molecular Features

Per-Arnt-Sim (PAS) domains are evolutionarily-conserved regions found in proteins in all living systems, involved in transcriptional regulation and the response to hypoxic and xenobiotic stress. Despite having low primary sequence similarity, they show an impressively high structural conservation. Nonetheless, understanding the underlying mechanisms that drive the biological function of the PAS domains remains elusive. In this work, we used molecular dynamics simulations and bioinformatics tools in order the investigate the molecular characteristics that govern the intrinsic dynamics of five PAS-B domains (human AhR receptor, NCOA1, HIF1α, and HIF2α transcription factors, and Drosophila Suzukii (D. Suzukii) juvenile hormone receptor JHR). First, we investigated the effects of different length of N and C terminal regions of the AhR PAS-B domain, showing that truncation of those segments directly affects structural stability and aggregation propensity of the domain. Secondly, using the recently annotated PAS-B located in the methoprene-tolerant protein/juvenile hormone receptor (JHR) from D. Suzukii, we have shown that the mutation of the highly conserved “gatekeeper” tyrosine to phenylalanine (Y322F) does not affect the stability of the domain. Finally, we investigated possible redox-regulation of the AhR PAS-B domain by focusing on the cysteinome residues within PAS-B domains. The cysteines in AhR PAS-B are directly regulating the dynamics of the small molecule ligand-gating loop (residues 305 to 326). In conclusion, we comprehensibly described several molecular features governing the behaviour of PAS-B domains in solution, which may lead to a better understanding of the forces driving their biological functions.

The RhopH complex is transferred to the host cell cytoplasm following red blood cell invasion by Plasmodium falciparum

2008 ◽  
Vol 160 (2) ◽  
pp. 81-89 ◽  
Author(s):  
Laetitia Vincensini ◽  
Gamou Fall ◽  
Laurence Berry ◽  
Thierry Blisnick ◽  
Catherine Braun Breton
Keyword(s):  
Plasmodium Falciparum ◽  
Blood Cell ◽  
Host Cell ◽  
Cell Invasion ◽  
Red Blood Cell ◽  
Cell Cytoplasm ◽  
Host Cell Cytoplasm

EFFECT OF BIOCHEMICAL METABOLITES OF DATES ON NUTRITIONAL PERFORMANCES OF CAROB MOTH, (ECTOMYELOIS CERATONIAE ZELLER (LEPIDOPTERA: PYRALIDAE))

2021 ◽  
Vol 77 (2) ◽  
Author(s):  
Ayoub Hadjeb ◽  
Mehaoua M. Seghir ◽  
Adjami Yasmine ◽  
Lebbouz Ismahane ◽  
Ouakid M. Laid
Keyword(s):  
Ectomyelois Ceratoniae ◽  
Lepidoptera Pyralidae ◽  
Carob Moth

scholarly journals Brefeldin A inhibits transport of the glycophorin-binding protein from Plasmodium falciparum into the host erythrocyte

1994 ◽  
Vol 300 (3) ◽  
pp. 821-826 ◽  
Author(s):  
J Benting ◽  
D Mattei ◽  
K Lingelbach
Keyword(s):  
Plasmodium Falciparum ◽  
Golgi Apparatus ◽  
Host Cell ◽  
Protein Secretion ◽  
Secretory Pathway ◽  
Binding Protein ◽  
Brefeldin A ◽  
Cell Cytoplasm ◽  
Parasite Cell ◽  
Host Cell Cytoplasm

Plasmodium falciparum, a protozoan parasite of the human erythrocyte, causes the most severe form of malaria. During its intraerythrocytic development, the parasite synthesizes proteins which are exported into the host cell. The compartments involved in the secretory pathway of P. falciparum are still poorly characterized. A Golgi apparatus has not been identified, owing to the lack of specific protein markers and Golgi-specific post-translational modifications in the parasite. The fungal metabolite brefeldin A (BFA) is known to inhibit protein secretion in higher eukaryotes by disrupting the integrity of the Golgi apparatus. We have used the parasite-encoded glycophorin-binding protein (GBP), a soluble protein found in the host cell cytoplasm, as a marker to investigate the effects of BFA on protein secretion in the intracellular parasite. In the presence of BFA, GBP was not transported into the erythrocyte, but remained inside the parasite cell. The effect caused by BFA was reversible, and the protein could be chased into the host cell cytoplasm within 30 min. Transport of GBP from the BFA-sensitive site into the host cell did not require protein synthesis. Similar observations were made when infected erythrocytes were incubated at 15 degrees C. Incubation at 20 degrees C resulted in a reduction rather than a complete block of protein export. The relevance of our findings to the identification of compartments involved in protein secretion from the parasite cell is discussed.

A new microsporidian parasite, Heterosporis saurida n. sp. (Microsporidia) infecting the lizardfish, Saurida undosquamis from the Arabian Gulf, Saudi Arabia: ultrastructure and phylogeny

Parasitology ◽  
2012 ◽  
Vol 139 (4) ◽  
pp. 454-462 ◽  
Author(s):  
S. AL-QURAISHY ◽  
A. S. ABDEL-BAKI ◽  
H. AL-QAHTANI ◽  
M. DKHIL ◽  
G. CASAL ◽  
...  
Keyword(s):  
Saudi Arabia ◽  
Polar Filament ◽  
Phylogenetic Analyses ◽  
Abdominal Cavity ◽  
Arabian Gulf ◽  
Its Region ◽  
Rrna Genes ◽  
Microsporidian Parasite ◽  
Ultrastructural Characteristics ◽  
A New Species

SUMMARYA new microsporidian that infects the lizardfish Saurida undosquamis (Richardson, 1848) that are caught in the Arabian Gulf in Saudi Arabia is described here. This parasite invades the skeletal muscle of the abdominal cavity forming white, cyst-like structures containing numerous spores. The prevalence of the infection was 32·1% (135/420). The spores were oval to pyriform in shape and measured approximately 3·3 μm×2·0 μm. The developing spores were found within parasitophorous vacuoles. In mature spores, the polar filament was arranged into 5 coils in a row. Molecular analysis of the rRNA genes, including the ITS region, and phylogenetic analyses using maximum parsimony, maximum likelihood, and Bayesian inference were performed. The ultrastructural characteristics and phylogenetic analyses support the recognition of a new species, herein named Heterosporis saurida n. sp.

scholarly journals Inhibition of the master regulator of Listeria monocytogenes virulence enables bacterial clearance from spacious replication vacuoles in infected macrophages

2022 ◽  
Vol 18 (1) ◽  
pp. e1010166
Author(s):  
Thao Thanh Tran ◽  
Carmen D. Mathmann ◽  
Marcela Gatica-Andrades ◽  
Rachel F. Rollo ◽  
Melanie Oelker ◽  
...  
Keyword(s):  
Transcriptional Activity ◽  
Host Cells ◽  
Intracellular Bacteria ◽  
Bacterial Clearance ◽  
Lysosomal Degradation ◽  
Cell Cytoplasm ◽  
Host Cell Cytoplasm ◽  
Molecule Inhibitor ◽  
Bacterial Replication ◽  
Cell Spread

A hallmark of Listeria (L.) monocytogenes pathogenesis is bacterial escape from maturing entry vacuoles, which is required for rapid bacterial replication in the host cell cytoplasm and cell-to-cell spread. The bacterial transcriptional activator PrfA controls expression of key virulence factors that enable exploitation of this intracellular niche. The transcriptional activity of PrfA within infected host cells is controlled by allosteric coactivation. Inhibitory occupation of the coactivator site has been shown to impair PrfA functions, but consequences of PrfA inhibition for L. monocytogenes infection and pathogenesis are unknown. Here we report the crystal structure of PrfA with a small molecule inhibitor occupying the coactivator site at 2.0 Å resolution. Using molecular imaging and infection studies in macrophages, we demonstrate that PrfA inhibition prevents the vacuolar escape of L. monocytogenes and enables extensive bacterial replication inside spacious vacuoles. In contrast to previously described spacious Listeria-containing vacuoles, which have been implicated in supporting chronic infection, PrfA inhibition facilitated progressive clearance of intracellular L. monocytogenes from spacious vacuoles through lysosomal degradation. Thus, inhibitory occupation of the PrfA coactivator site facilitates formation of a transient intravacuolar L. monocytogenes replication niche that licenses macrophages to effectively eliminate intracellular bacteria. Our findings encourage further exploration of PrfA as a potential target for antimicrobials and highlight that intra-vacuolar residence of L. monocytogenes in macrophages is not inevitably tied to bacterial persistence.

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