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In vivo Imaging of Transgenic Leishmania Parasites in a Live Host
Published on: July 27, 2010
The host micro-RNA cfa-miR-346 is induced in canine leishmaniasis
Gloria Buffi1, Aurora Diotallevi2, Marcello Ceccarelli1
1Department of Biomolecular Sciences, Section of Biotechnology, University of Urbino Carlo Bo, via Arco d'Augusto 2, 61032, Fano, PU, Italy.
Background:
Leishmaniases are a group of anthropo-zoonotic parasitic diseases caused by a protozoan of the Leishmania genus, affecting both humans and other vertebrates, including dogs. L. infantum is responsible for the visceral and occasionally cutaneous form of the disease in humans and canine leishmaniasis. Previously, we have shown that L. infantum induces a mild but significant increase in endoplasmic reticulum (ER) stress expression markers to promote parasites survival in human and murine infected macrophages. Moreover, we demonstrated that the miRNA hsa-miR-346, induced by the UPR-activated transcription factor sXBP1, was significantly upregulated in human macrophages infected with different L. infantum strains. However, the ER stress response in infected dogs, which represent an important reservoir for Leishmania parasite, was described once recently, whereas the miR-346 expression was not reported before. Therefore, this study aimed to investigate these pathways in the canine macrophage-like cell line DH82 infected by Leishmania spp. and to evaluate the presence of cfa-miR-346 in plasma of non-infected and infected dogs. The DH82 cells were infected with L. infantum and L. braziliensis parasites and the expression of cfa-mir-346 and several ER stress markers was evaluated by quantitative PCR (qPCR) at different time points. Furthermore, the cfa-miR-346 was monitored in plasma collected from non-infected dogs (n = 11) and dogs naturally infected by L. infantum (n = 18).
Results:
The results in DH82 cells showed that cfa-mir-346 was induced at both 24 h and 48 h post-infection with all Leishmania strains but not with tunicamycin, accounting for a mechanism of induction independent from sXBP1, unlike what was previously observed in human cell lines. Moreover, the cfa-miR-346 expression analysis on plasma revealed a significant increase in infected dogs compared to non-infected dogs.
Conclusions:
Here for the first time, we report the upregulation of cfa-miR-346 induced by Leishmania infection in canine macrophage-like cells and plasma samples of naturally infected dogs. According to our results, the cfa-miR-346 appears to be linked to infection, and understanding its role and identifying its target genes could contribute to elucidate the mechanisms underlying the host-pathogen interaction in leishmaniasis.
Insights
Canine leishmaniasis involves endoplasmic reticulum (ER) stress and microRNA (miRNA) changes. This study found that cfa-miR-346 is upregulated in infected dogs and canine cells, suggesting its role in Leishmania infection.
Area of Science:
- Parasitology
- Molecular Biology
- Veterinary Medicine
Background:
- Leishmaniases are parasitic diseases affecting humans and animals, with dogs serving as a significant reservoir for Leishmania parasites.
- Previous studies indicated Leishmania infantum induces endoplasmic reticulum (ER) stress in human macrophages and upregulates hsa-miR-346.
- The ER stress response and miR-346 expression in infected dogs remained largely uncharacterized.
Purpose of the Study:
- To investigate ER stress pathways and cfa-miR-346 expression in canine macrophage-like cells (DH82) infected with Leishmania spp.
- To evaluate the presence and levels of cfa-miR-346 in plasma from non-infected and naturally infected dogs.
Main Methods:
- Canine DH82 cells were infected with Leishmania infantum and Leishmania braziliensis.
- Quantitative PCR (qPCR) was used to assess cfa-mir-346 and ER stress marker expression at different time points post-infection.
- cfa-miR-346 levels were measured in plasma samples from 11 non-infected and 18 L. infantum-infected dogs.
Main Results:
- cfa-mir-346 was induced in DH82 cells 24 and 48 hours post-infection with Leishmania strains, independent of sXBP1.
- Plasma analysis revealed a significant increase in cfa-miR-346 expression in dogs naturally infected with L. infantum compared to non-infected controls.
- The induction mechanism of cfa-miR-346 differed from that observed in human cell lines.
Conclusions:
- This study reports for the first time the upregulation of cfa-miR-346 in canine macrophages and plasma during Leishmania infection.
- cfa-miR-346 appears to be associated with Leishmania infection in dogs.
- Further research into cfa-miR-346's target genes could elucidate host-pathogen interactions in canine leishmaniasis.
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