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Current Methods in Trypanosomatids Research

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Marcelo S. da Silva

Marcelo S. da Silva

São Paulo State University

Dr. Marcelo S. da Silva received his bachelor’s degree in Biological Sciences from the São Paulo State University in 2009 and he obtained his PhD in Genetics and Molecular Biology from the University of Campinas in 2014, where he elucidated the consequences of oxidative stress in Leishmania and found that this parasite has two distinct modes of nucleus and kinetoplast segregation. During his PhD, he also studied telomere homeostasis at Centre National de la Recherche Scientifique (CNRS), Paris, France. Dr. da Silva began his work in DNA metabolism of trypanosomatids parasites during his postdoc at Butantan Institute and throughout his brief postdoc at the University of Glasgow, UK. Next, he received a grant from São Paulo Research Foundation for a position as an independent researcher at São Paulo State University. Currently, he heads a team of 4 students. His lab performs studies on DNA metabolism in trypanosomatids, focusing on DNA repair, DNA replication, and cell cycle. It is also worth pointing that Dr. da Silva makes an international effort to bring students from low-income countries to be trained as future independent researchers, which will help develop scientific knowledge worldwide.

Collection Overview

Trypanosomatids (family Trypanosomadidae) are single-celled eukaryotes, most of them obligate parasites. Some of these organisms can cause human diseases, such as Trypanosoma brucei (the causative agent of sleeping sickness), Trypanosoma cruzi (etiological agent of Chagas disease), and Leishmania spp. (the causative agents of the different spectra of leishmaniases). These diseases infect millions of individuals globally, mainly in low-income regions, causing a significant public health issue. Despite efforts, so far, there are no effective vaccines, and most treatment options rely on drugs developed several decades ago, where the risk of significant side effects are higher than the benefits of treatment. These pathogens present a dixenous life cycle, which means that to survive and replicate inside their two hosts, they must overcome several barriers, including host defense mechanisms and unfavorable environmental conditions. Researches worldwide have been exploring these and other global features in the search to develop and adapt methods and approaches to understand better the molecular mechanisms involved in the pathways and stages of the complex life cycle of these organisms.

The main goal of this Methods Collection is to provide detailed state-of-the-art procedures in basic and applied science involving parasitic trypanosomatids and other close-related organisms, such as kinetoplastids. I believe that this in-depth sharing of knowledge and techniques will improve the outcome and the development of trypanosomatids research. Also, this compilation of knowledge will contribute to expanding the array of technologies currently available to the entire scientific community, which includes students, young and senior researchers.

Articles

<em>In Vitro</em> Drug Screening Against All Life Cycle Stages of <em>Trypanosoma cruzi</em> Using Parasites Expressing &#946;-galactosidase
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In Vitro Drug Screening Against All Life Cycle Stages of Trypanosoma cruzi Using Parasites Expressing β-galactosidase

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Cited by 7

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2021

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Abstracts

Effect of Butionina-Sulfaximina (BSO) and Fluphenazine as specific drugs against axenic amastigotes and promastigotes of Leishmania peruviana and Leishmania braziliensis

Jesús Rojas-Jaimes *1

1Facultad de Ciencias de la Salud, Universidad Privada del Norte, Lima-Perú; Escuela de Medicina Humana, Universidad Científica del Sur, Lima-Perú

Obtaining Axenic Amastigotes of Leishmania peruviana

Jesús Rojas Jaimes*1

11.- Facultad de Ciencias de la Salud, Universidad Privada del Norte, Lima-Perú 2.-Escuela de Medicina Humana, Universidad Científica del Sur, Lima-Perú

Electronic von Frey associated with the Mouse Grimace Scale to Assess Allodynia and Pain in Trypanosoma evansi-infected Mice

Amanda Leite Bastos Pereira*1

1Federal University of Santa Catarina: Universidade Federal de Santa Catarina Araranguá, Santa Catarina BRAZIL

Optimisation of Chromatin Preparation Variables for ChIP-seq of TY1-Epitope-Tagged Proteins in T. brucei

Rifat Ara Reza1,

Tim Nicolai Siegel*1

1LMU-Munich/ BMC