Polyunsaturated fatty acid and oxylipin profiles of Angiostrongylus cantonensis during cerebral-to-pulmonary migration illuminate parasite and host microenvironmental lipid signatures.
Overview
Abstract
Background: Metabolic streamlining as a consequence of parasitism has resulted in the loss of lipid biosynthetic genes in nematodes. Angiostrongylus cantonensis, a zoonotic neurotropic parasite that causes eosinophilic meningitis in mammals, completes a complex migration through the rat brain before maturing in the pulmonary arteries. Polyunsaturated fatty acids (PUFAs) and their bioactive metabolites (oxylipins) are known to modulate nematode survival; however, their abundance and endogenous biosynthetic capacity in A. cantonensis remain elusive.
Methods: We integrated comparative genomics, stage-specific transcriptomics, and lipidomics to reconstruct the expression patterns of the biosynthetic enzymes in A. cantonensis and characterize their dynamic PUFA and oxylipin profiles during the neuro-pulmonary transition from brain-residing fourth-stage (L4) to lung-migrating L5 larvae.
Results: Genomic and transcriptomic analyses revealed a streamlined biosynthetic repertoire in A. cantonensis. The worm lacks Δ6 desaturase and canonical cyclooxygenase (COX), lipoxygenase (LOX), and cytochrome P450 (CYP) enzymes, and expresses only residual levels of ptges2 and lta4h, which are markedly lower than those in free-living Caenorhabditis elegans across developmental stages. Using liquid chromatography-tandem mass spectrometry, L4–L5 larvae residing in the rat brain maintained stable PUFA and oxylipin profiles. In contrast, L5 larvae migrating to the lungs accumulated n-6 PUFAs and anti-inflammatory hydroxy eicosatetraenoic acids, epoxy eicosatrienoic acids and hydroxy docosahexaenoic acids, concurrent with reduced levels of pro-inflammatory prostaglandins and 5-oxo-eicosatetraenoic acid.
Conclusions: These stage- and tissue-specific lipidomic shifts correlate with distinct host microenvironments encountered during migration. These findings provide a foundation for understanding the evolutionary adaptation of lipid metabolism in parasitic nematodes.
Supplementary Information: The online version contains supplementary material available at 10.1186/
Reproduced under the paper's license (CC BY), from the paper cited above.
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Data
Datasets cited
- figshare:33194329, at figshare; found in DataCite
Availability of data and materials
The datasets analyzed during the current study are available from public databases (Wormbase, CNGBdb, and The National Center for Biotechnology Information). All relevant accession numbers of genomes and transcriptomes are listed in Additional file 1: Table S1-S3.
Reproduced under the paper's license (CC BY), from the paper cited above.
Versions
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Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 7 authors, 5 keywords, 12 MeSH terms, 4 funders, 44 references.
Cite
This paper
Tang, Z., Lai, J., Song, Y., Li, S., Xiao, L., Feng, Y., & Yuan, D. (2026). Polyunsaturated fatty acid and oxylipin profiles of Angiostrongylus cantonensis during cerebral-to-pulmonary migration illuminate parasite and host microenvironmental lipid signatures. Parasites & vectors, 19(1), 323. https://
BibTeX
@article{tang2026polyuns
author = {Tang, Zhengxu and Lai, Jiaying and Song, Yashan and Li, Song and Xiao, Lihua and Feng, Yaoyu and Yuan, Dongjuan},
title = {{Polyunsaturated fatty acid and oxylipin profiles of Angiostrongylus cantonensis during cerebral-to-pulmonary migration illuminate parasite and host microenvironmental lipid signatures}},
journal = {Parasites \& vectors},
year = {2026},
month = jun,
volume = {19},
number = {1},
pages = {323},
publisher = {BMC},
issn = {1756-3305},
doi = {10.1186/
url = {https://
pmid = {42231446},
pmcid = {PMC13455368}
}
RIS
TY - JOUR
AU - Tang, Zhengxu
AU - Lai, Jiaying
AU - Song, Yashan
AU - Li, Song
AU - Xiao, Lihua
AU - Feng, Yaoyu
AU - Yuan, Dongjuan
TI - Polyunsaturated fatty acid and oxylipin profiles of Angiostrongylus cantonensis during cerebral-to-pulmonary migration illuminate parasite and host microenvironmental lipid signatures
T2 - Parasites & vectors
J2 - Parasit Vectors
PY - 2026
DA - 2026/
VL - 19
IS - 1
SP - 323
SN - 1756-3305
PB - BMC
DO - 10.1186/
UR - https://
LA - en
ER -
CSL-JSON
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"container-title": "Parasites & vectors",
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