Canadian Sciences Speakers Network

Réseau Canadien de Panélistes Scientifiques


Maritza Jaramillo: CSSN Speaker

Maritza Jaramillo

Laval, Quebec

Position: Professor

Organization: Institut National de la Recherche Scientifique

Over the past 30 years, Dr. Jaramillo’s main research interest has been to investigate the transcriptional and post-transcriptional mechanisms involved in the dysregulation of host gene expression during protozoan parasitic infections of clinical relevance; namely toxoplasmosis, leishmaniasis, and malaria. Dr. Jaramillo obtained her B.Sc in Biology from Universidad Nacional de Colombia (Bogotá, Colombia). Subsequently, she obtained her master’s and Ph.D. degrees in Microbiology and immunology at Université Laval (Quebec, QC, Canada). During her graduate studies, Dr. Jaramillo worked on transcriptional regulation of pro-inflammatory molecules induced during protozoan parasitic infections. Subsequently, she did a postdoctoral training in the laboratory of Dr. Nahum Sonenberg at McGill University (Montreal, QC, Canada) where she worked on translational control (i.e., regulation of mRNA translation) of viral and parasitic infections. In 2012, Dr. Jaramillo joined the Institut National de la Recherche Scientifique (INRS) – Centre Armand-Frappier Santé Biotechnologie (Laval, QC, Canada) as an Assistant Professor in host-parasite interactions. In 2018, Dr. Jaramillo was promoted to the rank of Associate Professor and obtained tenure. She is a Senior Research Fellow of the Fonds de Recherche du Québec en Santé (FRQS) and her research program is currently funded by the Canadian Institutes of Health Research (CIHR) and the Natural Sciences and Engineering Research Council of Canada (NSERC). Dr. Jaramillo’s team and collaborators were the first to define the translatome of cells infected by Toxoplasma gondii and Leishmania at a global scale (Leroux et al. Infect Immun 2018; Chaparro et al. PLoS Pathogens 2020). These findings constitute the proof-of-principle that these parasites selectively reprogram the translational landscape of the host cell to promote infection. Dr. Jaramillo’s long-term goal is to uncover novel targets and regulators of mRNA translation and decay with potential applications, such as the identification of biomarkers of disease severity, and promising candidates for therapeutic treatments to combat morbidity and mortality associated with toxoplasmosis and leishmaniasis.

Areas of Expertise:

+ molecular parasitology
+ innate immunity
+ RNA biology

Language(s):

+ English
+ French
+ Spanish


My Work

What I do:

My overall objective as an independent researcher is to establish whether dysregulated translation and turnover of specific host mRNAs contributes to the pathogenesis of toxoplasmosis and leishmaniasis, two infections of major clinical relevance that are caused by the protozoan parasites Toxoplasma gondii (T. gondii) and Leishmania spp., respectively. In parallel, I utilize different stressors to elucidate the molecular mechanisms of translational control underlying macrophage functions. To achieve my research objectives, I have implemented a cutting-edge and dynamic research program that combines semi-high throughput drug screenings, cellular models of infection in primary cells, reverse and forwards genetics, in vivo models of infection using transgenic mice, multi-omics approaches, image flow cytometry, and field parasite isolates and mutant strains. Our long-term goal is to validate the use of translatome-based approaches to uncover novel targets and regulators of mRNA translation with potential applications, such as the identification of biomarkers of disease severity, and promising candidates for therapeutic treatments to combat morbidity and mortality associated with toxoplasmosis and leishmaniasis.

Ask me about:

Regulatory mechanisms of mRNA translation in innate immune cells, macrophage biology, molecular parasitology (Leishmania, Toxoplasma gondii, Plasmodium).

Why me:

My main research interest is to investigate the post-transcriptional mechanisms involved in the dysregulation of host gene expression during protozoan parasitic infections of clinical relevance; namely leishmaniasis, toxoplasmosis, and malaria. My postdoctoral work provided the first evidence that the host mRNA translation machinery can be hijacked by a protozoan parasite (i.e., Leishmania) to survive and provided in vivo evidence that translational control (i.e., regulation of protein synthesis) plays a crucial role in the outcome of a parasitic infection (Jaramillo et al. Cell Host & Microbe 2011). These discoveries opened a new area of high importance for medical research and allowed me to build my own niche as an independent investigator. To the best of our knowledge, my team is the only one in Canada that is currently investigating how dysregulated host mRNA translation contributes to the pathogenesis of protozoan parasitic infections, and more specifically leishmaniasis and toxoplasmosis.

Fun facts:

I am particularly committed to strengthen the parasitology community in Canada. Initially, I served served as a member of the organizing committee of the Annual Montreal Parasitology Symposium (2020, 2022). Even though several provincial parasitology networks existed in our country, there was not a national initiative to promote collaborations, highly qualified personnel training, and build research capacity in parasitic infections and tropical medicine. To fill in this gap, I co-led the creation of the Canadian Parasitology Network (CPN). The response of the Canadian parasitology community has been overwhelming. CPN currently gathers more than 50 research laboratories and 250 student/trainees across the country. Within this framework, I spearheaded the implementation of a monthly CPN virtual seminar series and I led the organization of the fist annual CPN meeting in Montreal (2023), which was a great success and benefited from the support of the Infection and Immunity Institute (III) – CIHR Planning and Dissemination Grants initiative.


About Me

English proficiency: Read, Write, Speak

French proficiency: Read, Write, Speak

Other Language(s): Spanish

Willing to Mentor: Yes

Available for Trainees: Yes

Title: Dr.

Pronouns: She/Her/Hers

Gender: Female

Awards: FRQS Junior 1, Junior 2, and Senior Salary Awards, March of Dimes Foundation USA Basil O’Connor Starter Scholar Research Award


Recent Publications

Title Year
Toxoplasma gondii infection inhibits invasion and migration of human extravillous trophoblasts through dysregulation of FOXO1- and FOXO3a-dependent and -independent mechanisms2025
Toxoplasma gondii infection induces the expression of the chemokine CXCL16 in macrophages to promote chemoattraction of CXCR6 + cells2024
Leukemia inhibitory factor drives transcriptional programs that promote lipid accumulation and M2 polarization in macrophages2024
Esquizofrenia y valoración del lenguaje pragmático en usuarios atendidos en centros de salud mental comunitarios2024
Hormonal regulation of miRNA during mammary gland development2024
Leishmania donovani Exploits Tunneling Nanotubes for Dissemination and Propagation of B Cell Activation2023
Toxoplasma gondii inhibits the expression of autophagy-related genes through AKT-dependent inactivation of the transcription factor FOXO3a2023
Cap-dependent translation initiation monitored in living cells2022
Revisiting Leishmania GP63 host cell targets reveals a limited spectrum of substrates2022
Transcriptional profiling of macrophages reveals distinct parasite stage-driven signatures during early infection by Leishmania donovani2022
Infection by the Protozoan Parasite Toxoplasma gondii Inhibits Host MNK1/2-eIF4E Axis to Promote Its Survival2020
Translational profiling of macrophages infected with Leishmania donovani identifies mTOR- and eIF4A-sensitive immune-related transcripts2020
4E-BP–Dependent Translational Control of Irf8 Mediates Adipose Tissue Macrophage Inflammatory Response2020
Induction of an Alternative mRNA 5′ Leader Enhances Translation of the Ciliopathy Gene Inpp5e and Resistance to Oncolytic Virus Infection2019
Translational repression of Ccl5 and Cxcl10 by 4E‐BP1 and 4E‐BP2 restrains the ability of mouse macrophages to induce migration of activated T cells2019
Leishmania donovani Lipophosphoglycan Increases Macrophage-Dependent Chemotaxis of CXCR6-Expressing Cells via CXCL16 Induction2019
Exploitation of the Leishmania exosomal pathway by Leishmania RNA virus 12019
Analysis of the Trichuris suis excretory/secretory proteins as a function of life cycle stage and their immunomodulatory properties2018
Active-site mTOR inhibitors augment HSV1-dICP0 infection in cancer cells via dysregulated eIF4E/4E-BP axis2018
The Protozoan Parasite Toxoplasma gondii Selectively Reprograms the Host Cell Translatome2018
eIF4E-Binding Proteins 1 and 2 Limit Macrophage Anti-Inflammatory Responses through Translational Repression of IL-10 and Cyclooxygenase-22018
Metformin requires 4E-BPs to induce apoptosis and repress translation of Mcl-1 in hepatocellular carcinoma cells2016
Associations between drug/alcohol use and emotional abuse: Who perpetrates emotional abuse against Latina women?2015
DAP5 associates with eIF2β and eIF4AI to promote Internal Ribosome Entry Site driven translation2015
Deficiency in Either 4E-BP1 or 4E-BP2 Augments Innate Antiviral Immune Responses2014