Publications by authors named "Camila S Goncalves"

All insect trypanosomatids of the subfamily Strigomonadinae harbor a proteobacterial symbiont in their cytoplasm and unique ultrastructural cell organization. Here, we report an unexpected finding within the Strigomonadinae subfamily: the identification of a new species lacking bacterial symbiont, represented by two isolates obtained from Calliphoridae flies in Brazil and Uganda. This species is hereby designated as Kentomonas inusitatus n.

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Article Synopsis
  • Trypanosomes exhibit a unique genomic organization with polycistronic transcription and lack of dedicated promoters for individual genes, which complicates gene expression regulation.
  • The study focused on Trypanosoma cruzi, revealing that chromatin changes during differentiation significantly influence gene expression, associated with developmental chromatin regulation.
  • The findings indicate a strong link between active chromatin states and steady-state transcription levels, highlighting how chromatin dynamics contribute to the parasite's unusual regulatory mechanisms across its life stages.
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Angomonas deanei coevolves in a mutualistic relationship with a symbiotic bacterium that divides in synchronicity with other host cell structures. Trypanosomatid mitochondrial DNA is contained in the kinetoplast and is composed of thousands of interlocked DNA circles (kDNA). The arrangement of kDNA is related to the presence of histone-like proteins, known as KAPs (kinetoplast-associated proteins), that neutralize the negatively charged kDNA, thereby affecting the activity of mitochondrial enzymes involved in replication, transcription and repair.

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Trypanosomatids have a cytoskeleton arrangement that is simpler than what is found in most eukaryotic cells. However, it is precisely organized and constituted by stable microtubules. Such microtubules compose the mitotic spindle during mitosis, the basal body, the flagellar axoneme and the subpellicular microtubules, which are connected to each other and also to the plasma membrane forming a helical arrangement along the central axis of the parasite cell body.

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Article Synopsis
  • * Recent studies show that glycosomes are multifunctional, engaging in both catabolic (breaking down molecules) and anabolic (building up molecules) processes, and they interact with other cellular compartments for coordinated metabolism.
  • * Research suggests that protein transport systems are vital for metabolite movement across glycosomal membranes, which could lead to potential new treatments for Chagas disease, a condition caused by these parasites that lacks effective current therapies.
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Kinetoplastid parasites, included Trypanosoma cruzi, the causal agent of Chagas disease, present a unique genome organization and gene expression. Although they control gene expression mainly post-transcriptionally, chromatin accessibility plays a fundamental role in transcription initiation control. We have previously shown that High Mobility Group B protein from Trypanosoma cruzi (TcHMGB) can bind DNA in vitro.

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Background: Trypanosoma cruzi uses several strategies to survive in different hosts. A key step in the life-cycle of this parasite is metacyclogenesis, which involves various morphological, biochemical, and genetic changes that induce the differentiation of non-pathogenic epimastigotes into pathogenic metacyclic trypomastigotes. During metacyclogenesis, T.

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Background: Dental implants, indicated for re-establishing both mastigatory and aesthetic functions, can be placed in the sockets immediately after tooth extraction. Most studies investigate the anterior and upper regions of the dental arch, whereas few examine longitudinal appraisal of immediate implant installation in the mandibular molar region.

Objective: The aim of this retrospective study was to evaluate the success rate of immediate dental implants placement in mandibular molars within a follow-up period as long as 8 years.

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