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microPublication / Biology / Dauer Development Modulates Olfactory Behavior...
Dauer Development Modulates Olfactory Behavior
Johnny Vertiz1, Heather Carstensen1 and Ray Hong1
1Department of Biology, California State University, Northridge, Northridge, USA
Correspondence to: Ray Hong (ray.hong@csun.edu)

Abstract

Reproductive adults and developmentally arrested larvae often occupy different ecological niches and thus are expected to respond differently to environmental stimuli. To understand the genes that coordinate dauer development and olfactory behavior, we examined adult and dauer C. elegans in wild-type and dauer constitutive mutants (Daf-c). We found all dauers showed decreased attraction to all three odorants tested compared to adults, with daf-7 dauer larva (DL) exhibiting a concentration-dependent preference shift towards isoamyl alcohol, suggesting that the TGF-ß pathway is involved in both dauer regulation and dauer-specific odortaxis.

Figure 1. Olfactory responses of C. elegans dauer larvae: Chemotaxis between adults and dauer larvae differ significantly in response to (A) 1% 2,3-butanedione, (B) 1% 2,3-pentanedione, and (C-D) 1% and 0.1% isoamyl alcohol in wild-type N2, as well as in the Daf-c mutants daf-2 and daf-7. For (A) and (C): One-way ANOVA between adults and dauer with Kruskal-Wallis test. Blue circles denote young adults and orange circles denote dauer larvae. For (B) and (D): Two-way ANOVA between adults and dauer with Sidak’s multiple comparisons test. *P<0.05, **P<0.01, ****P<0.0001, ns: not significant. Error bars indicate the standard error of the mean. The number of assays performed is indicated at the base of each bar.

Description

In C. elegans, the dauer larva (DL) is a non-feeding and stress-resistant stage that can respond to environmental cues differently from adults. For example, C. elegans adults avoid CO2 while DL are attracted to CO2 (Hallem and Sternberg 2008; Hallem et al. 2011). Similarly, adults of the nematode Pristionchus pacificus are mildly attracted to a beetle host pheromone while its dispersive DL are highly attracted to the pheromone (Carstensen et al. 2021).

To determine if genes that affect dauer development also modulate olfactory behavior in C. elegans, we compared the odor response profiles of young adults versus DL in C. elegans of two well-studied Daf-c mutants, daf-2 and daf-7 (Riddle et al. 1981; Swanson and Riddle 1981; Kimura et al. 1997) towards three odorants. In C. elegans adults, the AWA neurons detect 2,3-butanedione (diacetyl), while the AWC neurons sense isoamyl alcohol (IAA) and 2,3-pentanedione (Sengupta et al. 1996; Chalasani et al. 2007). We found that wild-type DL showed less odor attraction than corresponding adults for 2,3-butanedione, 2,3-pentanedione, and IAA, consistent with the results of a previous study that included 2,3-butanedione (Hallem et al. 2011)(Fig. 1A-C). However, this adult-DL difference was not observed in daf-2 towards IAA or daf-7 towards 2,3-butanedione and 2,3-pentanedione. Furthermore, the response to IAA changed from attractive to repulsive in the DL of two daf-7 alleles (e1372, ok3125). To evaluate if the avoidance response to IAA is due to hypersensitivity to IAA in the daf-7 DL, we also tested their response to a 10-fold lower IAA concentration (0.1%). We found that the strong avoidance response was no longer observed, and instead the dauer IAA attraction became significantly reduced in both daf-7 alleles compared to adults, resembling the wildtype DL (Fig. 1D). In C. elegans, odor concentration-dependent preference shift has been observed for IAA for adult worms and is dependent on odr-3 function (Yoshida et al. 2012). Thus, C. elegans wild-type and Daf-c DL showed decreased attraction compared to adults to all three odorants tested, with the daf-7 mutations producing an accentuated concentration-dependent response to IAA in the DL, suggesting that the TGF-ß pathway is involved in both dauer regulation and dauer-specific response to IAA.

While remodeling of the AWC dendritic ends that increase their surface area have been speculated to heighten odor sensitivity in DL (Albert and Riddle 1988), our results show that only daf-7 alleles exhibited a potentially higher sensitivity to isoamyl alcohol, while wild-type and daf-2 DL were actually less attracted than adults to several odors. Mutation of the daf-2 gene also mostly eliminated acute CO2 avoidance in adult C. elegans, while the P. pacificus Daf-c mutant Ppa-hsd-2 exhibited greatly enhanced adult attraction to a host odor (Hallem and Sternberg 2008; Carstensen et al. 2021). These results suggest that dauer development has multiple effects on olfactory behavior, such that both wild-type and Daf-c DL should be assessed when surveying species-specific responses.

Methods

Request a detailed protocol

Nematodes were cultured on OP50-seeded NGM plates and assayed at ~22°C. The chemotaxis assays for C. elegans were set up in a quadrant with worms loaded onto the center of 6 cm plates containing MOPS/Tween agar, along with two opposing pairs of odors and controls (Nuttley et al. 2002; Margie et al. 2013; Carstensen et al. 2021). 0.5 µl of 1 M sodium azide was spotted onto each odor or counter-attractant. Since C. elegans DL are hydrophilic, we collected DL primarily from the condensations present on the underside of the lids of recently starved plates by washing the lids with sterile spring water (Arrowhead, CA). For assays with Daf-c mutants, each plate was scored for either DL or YA using visual confirmation. Chemotaxis assays lasted 1-1.5 hours.

Strain Genotype
CB1370 daf-2(e1370)III
CB1372 daf-7(e1372)III
RB2302 daf-7(ok3125)III
N2 wildtype

Reagents

MOPS buffer (pH 7)

Tween 20 (Polyoxyethylene 20-Sorbitan Monolaurate) CAS 9005-64-5

2,3-butanedione, isoamyl alcohol, and 2,3-pentanedione (Sigma-Aldrich)

References

Albert PS, Riddle DL. 1988. Mutants of Caenorhabditis elegans that form dauer-like larvae. Dev Biol 126: 270-93.
PubMed
Carstensen HR, Villalon RM, Banerjee N, Hallem EA, Hong RL. 2021. Steroid hormone pathways coordinate developmental diapause and olfactory remodeling in Pristionchus pacificus. Genetics 218: iyab071.
PubMed
Chalasani SH, Chronis N, Tsunozaki M, Gray JM, Ramot D, Goodman MB, Bargmann CI. 2007. Dissecting a circuit for olfactory behaviour in Caenorhabditis elegans. Nature 450: 63-70.
PubMed
Hallem EA, Dillman AR, Hong AV, Zhang Y, Yano JM, DeMarco SF, Sternberg PW. 2011. A sensory code for host seeking in parasitic nematodes. Curr Biol 21: 377-83.
PubMed
Hallem EA, Sternberg PW. 2008. Acute carbon dioxide avoidance in Caenorhabditis elegans. Proc Natl Acad Sci U S A 105: 8038-43.
PubMed
Kimura KD, Tissenbaum HA, Liu Y, Ruvkun G. 1997. daf-2, an insulin receptor-like gene that regulates longevity and diapause in Caenorhabditis elegans. Science 277: 942-6.
PubMed
Margie O, Palmer C, Chin-Sang I. 2013. C. elegans chemotaxis assay. J Vis Exp 74: e50069.
PubMed
Nuttley WM, Atkinson-Leadbeater KP, Van Der Kooy D. 2002. Serotonin mediates food-odor associative learning in the nematode Caenorhabditis elegans. Proc Natl Acad Sci U S A 99: 12449-54.
PubMed
Riddle DL, Swanson MM, Albert PS. 1981. Interacting genes in nematode dauer larva formation. Nature 290: 668-71.
PubMed
Sengupta P, Chou JH, Bargmann CI. 1996. odr-10 encodes a seven transmembrane domain olfactory receptor required for responses to the odorant diacetyl. Cell 84: 899-909.
PubMed
Swanson MM, Riddle DL. 1981. Critical periods in the development of the Caenorhabditis elegans dauer larva. Dev Biol 84: 27-40.
PubMed
Yoshida K, Hirotsu T, Tagawa T, Oda S, Wakabayashi T, Iino Y, Ishihara T. 2012. Odour concentration-dependent olfactory preference change in C. elegans. Nat Commun 3: 739.
PubMed

Funding

NIH TL4GM118977 to JV; NIH GM105579 to RLH

Author Contributions

Johnny Vertiz: Investigation, Methodology
Heather Carstensen: Writing - review and editing, Investigation, Data curation
Ray Hong: Data curation, Methodology, Conceptualization, Funding acquisition, Supervision, Writing - original draft.

Reviewed By

Ian Chin-Sang

History

Received: September 8, 2021
Revision received: September 22, 2021
Accepted: September 22, 2021
Published: October 14, 2021

Copyright

© 2021 by the authors. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation

Vertiz, J; Carstensen, H; Hong, R (2021). Dauer Development Modulates Olfactory Behavior. microPublication Biology. 10.17912/micropub.biology.000479.
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