» Articles » PMID: 34706780

On the Role of Dauer in the Adaptation of Nematodes to a Parasitic Lifestyle

Overview
Journal Parasit Vectors
Publisher Biomed Central
Date 2021 Oct 28
PMID 34706780
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Nematodes are presumably the most abundant Metazoa on Earth, and can even be found in some of the most hostile environments of our planet. Various types of hypobiosis evolved to adapt their life cycles to such harsh environmental conditions. The five most distal major clades of the phylum Nematoda (Clades 8-12), formerly referred to as the Secernentea, contain many economically relevant parasitic nematodes. In this group, a special type of hypobiosis, dauer, has evolved. The dauer signalling pathway, which culminates in the biosynthesis of dafachronic acid (DA), is intensively studied in the free-living nematode Caenorhabditis elegans, and it has been hypothesized that the dauer stage may have been a prerequisite for the evolution of a wide range of parasitic lifestyles among other nematode species. Biosynthesis of DA is not specific for hypobiosis, but if it results in exit of the hypobiotic state, it is one of the main criteria to define certain behaviour as dauer. Within Clades 9 and 10, the involvement of DA has been validated experimentally, and dauer is therefore generally accepted to occur in those clades. However, for other clades, such as Clade 12, this has hardly been explored. In this review, we provide clarity on the nomenclature associated with hypobiosis and dauer across different nematological subfields. We discuss evidence for dauer-like stages in Clades 8 to 12 and support this with a meta-analysis of available genomic data. Furthermore, we discuss indications for a simplified dauer signalling pathway in parasitic nematodes. Finally, we zoom in on the host cues that induce exit from the hypobiotic stage and introduce two hypotheses on how these signals might feed into the dauer signalling pathway for plant-parasitic nematodes. With this work, we contribute to the deeper understanding of the molecular mechanisms underlying hypobiosis in parasitic nematodes. Based on this, novel strategies for the control of parasitic nematodes can be developed.

Citing Articles

The fourth-stage autoinfective larva of : redescription and diagnostic implications.

Zhao H, Koehler A, Truarn C, Bradford D, New D, Speare R J Clin Microbiol. 2024; 63(1):e0102124.

PMID: 39636118 PMC: 11784425. DOI: 10.1128/jcm.01021-24.


Emergence of dauer larvae in Caenorhabditis elegans disrupts continuity of host-microbiome interactions.

Bodkhe R, Trang K, Hammond S, Jung D, Shapira M FEMS Microbiol Ecol. 2024; 100(12.

PMID: 39516048 PMC: 11590253. DOI: 10.1093/femsec/fiae149.


Life history in Caenorhabditis elegans: from molecular genetics to evolutionary ecology.

Braendle C, Paaby A Genetics. 2024; 228(3).

PMID: 39422376 PMC: 11538407. DOI: 10.1093/genetics/iyae151.


Robustness and variability in gene expression.

Corchado J, Godthi A, Selvarasu K, Prahlad V bioRxiv. 2024; .

PMID: 39229130 PMC: 11370353. DOI: 10.1101/2024.08.15.608164.


A revision of the trichostrongylid nematode Ransom, 1907, from deer game: recent integrative research confirms the existence of the ancient host-specific species (Rudolphi, 1809).

Albrechtova M, Kasparova E, Langrova I, Hart V, Neuhaus B, Jankovska I Front Vet Sci. 2024; 11:1346417.

PMID: 38389582 PMC: 10881869. DOI: 10.3389/fvets.2024.1346417.


References
1.
Zheng S, Chiu H, Boudreau J, Papanicolaou T, Bendena W, Chin-Sang I . A functional study of all 40 insulin-like peptides. J Biol Chem. 2018; 293(43):16912-16922. PMC: 6204898. DOI: 10.1074/jbc.RA118.004542. View

2.
Kaplan R, Webster A, Chitrakar R, Dent J, Baugh L . Food perception without ingestion leads to metabolic changes and irreversible developmental arrest in C. elegans. BMC Biol. 2018; 16(1):112. PMC: 6176503. DOI: 10.1186/s12915-018-0579-3. View

3.
Opperman C, Bird D, Williamson V, Rokhsar D, Burke M, Cohn J . Sequence and genetic map of Meloidogyne hapla: A compact nematode genome for plant parasitism. Proc Natl Acad Sci U S A. 2008; 105(39):14802-7. PMC: 2547418. DOI: 10.1073/pnas.0805946105. View

4.
Ma G, Wang T, Korhonen P, Hofmann A, Sternberg P, Young N . Elucidating the molecular and developmental biology of parasitic nematodes: Moving to a multiomics paradigm. Adv Parasitol. 2020; 108:175-229. DOI: 10.1016/bs.apar.2019.12.005. View

5.
Di W, Liu L, Zhang T, Li F, He L, Wang C . A DAF-3 co-Smad molecule functions in Haemonchus contortus development. Parasit Vectors. 2019; 12(1):609. PMC: 6935219. DOI: 10.1186/s13071-019-3855-3. View