Both host and parasite non-coding RNAs co-ordinate the regulation of macrophage gene expression to reduce pro-inflammatory immune responses and promote tissue repair pathways during infection with fasciola hepatica.
- Publisher:
- TAYLOR & FRANCIS INC
- Publication Type:
- Journal Article
- Citation:
- RNA Biol, 2024, 21, (1), pp. 62-77
- Issue Date:
- 2024-01
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Full metadata record
| Field | Value | Language |
|---|---|---|
| dc.contributor.author |
Sais, D |
|
| dc.contributor.author | Chowdhury, S | |
| dc.contributor.author | Dalton, JP | |
| dc.contributor.author |
Tran, N |
|
| dc.contributor.author |
Donnelly, S |
|
| dc.date.accessioned | 2024-11-05T02:12:32Z | |
| dc.date.available | 2024-11-05T02:12:32Z | |
| dc.date.issued | 2024-01 | |
| dc.identifier.citation | RNA Biol, 2024, 21, (1), pp. 62-77 | |
| dc.identifier.issn | 1547-6286 | |
| dc.identifier.issn | 1555-8584 | |
| dc.identifier.uri | http://hdl.handle.net/10453/181742 | |
| dc.description.abstract | Parasitic worms (helminths) establish chronic infection within mammalian hosts by strategically regulating their host's immune responses. Deciphering the mechanisms by which host non-coding RNAs (ncRNA) co-ordinate the activation and regulation of immune cells is essential to understanding host immunity and immune-related pathology. It is also important to comprehend how pathogens secrete specific ncRNAs to manipulate gene expression of host immune cells and influence their response to infection. To investigate the contribution of both host and helminth derived ncRNAs to the activation and/or regulation of innate immune responses during a parasite infection, we examined ncRNA expression in the peritoneal macrophages from mice infected with Fasciola hepatica. We discovered the presence of several parasitic-derived miRNAs within host macrophages at 6 hrs and 18 hrs post infection. Target prediction analysis showed that these Fasciola miRNAs regulate host genes associated with the activation of host pro-inflammatory macrophages. Concomitantly, there was a distinct shift in host ncRNA expression, which was significant at 5 days post-infection. Prediction analysis suggested that these host ncRNAs target a different cohort of host genes compared to the parasite miRNAs, although the functional outcome was predicted to be similar i.e. reduced pro-inflammatory response and the promotion of a reparative/tolerant phenotype. Taken together, these observations uncover the interplay between host and parasitic ncRNAs and reveal a complementary regulation of the immune response that allows the parasite to evade immune detection and promote tissue repair for the host. These findings will provide a new understanding of the molecular interaction between parasites and host. | |
| dc.format | Print-Electronic | |
| dc.language | eng | |
| dc.publisher | TAYLOR & FRANCIS INC | |
| dc.relation | http://purl.org/au-research/grants/arc/DP210101337 | |
| dc.relation.ispartof | RNA Biol | |
| dc.relation.isbasedon | 10.1080/15476286.2024.2408706 | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | 0604 Genetics | |
| dc.subject.classification | Developmental Biology | |
| dc.subject.classification | 3101 Biochemistry and cell biology | |
| dc.subject.classification | 3105 Genetics | |
| dc.subject.mesh | Animals | |
| dc.subject.mesh | Fasciola hepatica | |
| dc.subject.mesh | Mice | |
| dc.subject.mesh | Fascioliasis | |
| dc.subject.mesh | Host-Parasite Interactions | |
| dc.subject.mesh | MicroRNAs | |
| dc.subject.mesh | Gene Expression Regulation | |
| dc.subject.mesh | Macrophages | |
| dc.subject.mesh | RNA, Untranslated | |
| dc.subject.mesh | Immunity, Innate | |
| dc.subject.mesh | Macrophages, Peritoneal | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Macrophages | |
| dc.subject.mesh | Macrophages, Peritoneal | |
| dc.subject.mesh | Animals | |
| dc.subject.mesh | Mice | |
| dc.subject.mesh | Fasciola hepatica | |
| dc.subject.mesh | Fascioliasis | |
| dc.subject.mesh | MicroRNAs | |
| dc.subject.mesh | RNA, Untranslated | |
| dc.subject.mesh | Gene Expression Regulation | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Host-Parasite Interactions | |
| dc.subject.mesh | Immunity, Innate | |
| dc.subject.mesh | Animals | |
| dc.subject.mesh | Fasciola hepatica | |
| dc.subject.mesh | Mice | |
| dc.subject.mesh | Fascioliasis | |
| dc.subject.mesh | Host-Parasite Interactions | |
| dc.subject.mesh | MicroRNAs | |
| dc.subject.mesh | Gene Expression Regulation | |
| dc.subject.mesh | Macrophages | |
| dc.subject.mesh | RNA, Untranslated | |
| dc.subject.mesh | Immunity, Innate | |
| dc.subject.mesh | Macrophages, Peritoneal | |
| dc.subject.mesh | Female | |
| dc.title | Both host and parasite non-coding RNAs co-ordinate the regulation of macrophage gene expression to reduce pro-inflammatory immune responses and promote tissue repair pathways during infection with fasciola hepatica. | |
| dc.type | Journal Article | |
| utslib.citation.volume | 21 | |
| utslib.location.activity | United States | |
| utslib.for | 0604 Genetics | |
| pubs.organisational-group | University of Technology Sydney | |
| pubs.organisational-group | University of Technology Sydney/Faculty of Engineering and Information Technology | |
| pubs.organisational-group | University of Technology Sydney/Faculty of Science | |
| pubs.organisational-group | University of Technology Sydney/Faculty of Science/School of Life Sciences | |
| pubs.organisational-group | University of Technology Sydney/Faculty of Engineering and Information Technology/School of Biomedical Engineering | |
| pubs.organisational-group | University of Technology Sydney/UTS Groups | |
| pubs.organisational-group | University of Technology Sydney/UTS Groups/Centre for Health Technologies (CHT) | |
| pubs.organisational-group | University of Technology Sydney/UTS Groups/Australian Institute for Microbiology & Infection (AIMI) | |
| pubs.organisational-group | University of Technology Sydney/UTS Groups/Australian Institute for Microbiology & Infection (AIMI)/Australian Institute for Microbiology & Infection (AIMI) Associate Member | |
| utslib.copyright.status | open_access | * |
| dc.rights.license | This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/ | |
| dc.date.updated | 2024-11-05T02:11:33Z | |
| pubs.issue | 1 | |
| pubs.publication-status | Published | |
| pubs.volume | 21 | |
| utslib.citation.issue | 1 |
Abstract:
Parasitic worms (helminths) establish chronic infection within mammalian hosts by strategically regulating their host's immune responses. Deciphering the mechanisms by which host non-coding RNAs (ncRNA) co-ordinate the activation and regulation of immune cells is essential to understanding host immunity and immune-related pathology. It is also important to comprehend how pathogens secrete specific ncRNAs to manipulate gene expression of host immune cells and influence their response to infection. To investigate the contribution of both host and helminth derived ncRNAs to the activation and/or regulation of innate immune responses during a parasite infection, we examined ncRNA expression in the peritoneal macrophages from mice infected with Fasciola hepatica. We discovered the presence of several parasitic-derived miRNAs within host macrophages at 6 hrs and 18 hrs post infection. Target prediction analysis showed that these Fasciola miRNAs regulate host genes associated with the activation of host pro-inflammatory macrophages. Concomitantly, there was a distinct shift in host ncRNA expression, which was significant at 5 days post-infection. Prediction analysis suggested that these host ncRNAs target a different cohort of host genes compared to the parasite miRNAs, although the functional outcome was predicted to be similar i.e. reduced pro-inflammatory response and the promotion of a reparative/tolerant phenotype. Taken together, these observations uncover the interplay between host and parasitic ncRNAs and reveal a complementary regulation of the immune response that allows the parasite to evade immune detection and promote tissue repair for the host. These findings will provide a new understanding of the molecular interaction between parasites and host.
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