Cargando…
Parasitoid wasp venom manipulates host innate behavior via subtype-specific dopamine receptor activation
The subjugation strategy employed by the jewel wasp is unique in that it manipulates the behavior of its host, the American cockroach, rather than inducing outright paralysis. Upon envenomation directly into the central complex (CX), a command center in the brain for motor behavior, the stung cockro...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8996814/ https://www.ncbi.nlm.nih.gov/pubmed/35320357 http://dx.doi.org/10.1242/jeb.243674 |
_version_ | 1784684559685648384 |
---|---|
author | Nordio, Stefania Kaiser, Maayan Adams, Michael E. Libersat, Frederic |
author_facet | Nordio, Stefania Kaiser, Maayan Adams, Michael E. Libersat, Frederic |
author_sort | Nordio, Stefania |
collection | PubMed |
description | The subjugation strategy employed by the jewel wasp is unique in that it manipulates the behavior of its host, the American cockroach, rather than inducing outright paralysis. Upon envenomation directly into the central complex (CX), a command center in the brain for motor behavior, the stung cockroach initially engages in intense grooming behavior, then falls into a lethargic sleep-like state referred to as hypokinesia. Behavioral changes evoked by the sting are due at least in part to the presence of the neurotransmitter dopamine in the venom. In insects, dopamine receptors are classified as two families, the D1-like and the D2-like receptors. However, specific roles played by dopamine receptor subtypes in venom-induced behavioral manipulation by the jewel wasp remain largely unknown. In the present study, we used a pharmacological approach to investigate roles of D1-like and D2-like receptors in behaviors exhibited by stung cockroaches, focusing on grooming. Specifically, we assessed behavioral outcomes of focal CX injections of dopamine receptor agonists and antagonists. Both specific and non-specific compounds were used. Our results strongly implicate D1-like dopamine receptors in venom-induced grooming. Regarding induction of hypokinesia, our findings demonstrate that dopamine signaling is necessary for induction of long-lasting hypokinesia caused by brain envenomation. |
format | Online Article Text |
id | pubmed-8996814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-89968142022-04-25 Parasitoid wasp venom manipulates host innate behavior via subtype-specific dopamine receptor activation Nordio, Stefania Kaiser, Maayan Adams, Michael E. Libersat, Frederic J Exp Biol Research Article The subjugation strategy employed by the jewel wasp is unique in that it manipulates the behavior of its host, the American cockroach, rather than inducing outright paralysis. Upon envenomation directly into the central complex (CX), a command center in the brain for motor behavior, the stung cockroach initially engages in intense grooming behavior, then falls into a lethargic sleep-like state referred to as hypokinesia. Behavioral changes evoked by the sting are due at least in part to the presence of the neurotransmitter dopamine in the venom. In insects, dopamine receptors are classified as two families, the D1-like and the D2-like receptors. However, specific roles played by dopamine receptor subtypes in venom-induced behavioral manipulation by the jewel wasp remain largely unknown. In the present study, we used a pharmacological approach to investigate roles of D1-like and D2-like receptors in behaviors exhibited by stung cockroaches, focusing on grooming. Specifically, we assessed behavioral outcomes of focal CX injections of dopamine receptor agonists and antagonists. Both specific and non-specific compounds were used. Our results strongly implicate D1-like dopamine receptors in venom-induced grooming. Regarding induction of hypokinesia, our findings demonstrate that dopamine signaling is necessary for induction of long-lasting hypokinesia caused by brain envenomation. The Company of Biologists Ltd 2022-03-23 /pmc/articles/PMC8996814/ /pubmed/35320357 http://dx.doi.org/10.1242/jeb.243674 Text en © 2022. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Nordio, Stefania Kaiser, Maayan Adams, Michael E. Libersat, Frederic Parasitoid wasp venom manipulates host innate behavior via subtype-specific dopamine receptor activation |
title | Parasitoid wasp venom manipulates host innate behavior via subtype-specific dopamine receptor activation |
title_full | Parasitoid wasp venom manipulates host innate behavior via subtype-specific dopamine receptor activation |
title_fullStr | Parasitoid wasp venom manipulates host innate behavior via subtype-specific dopamine receptor activation |
title_full_unstemmed | Parasitoid wasp venom manipulates host innate behavior via subtype-specific dopamine receptor activation |
title_short | Parasitoid wasp venom manipulates host innate behavior via subtype-specific dopamine receptor activation |
title_sort | parasitoid wasp venom manipulates host innate behavior via subtype-specific dopamine receptor activation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8996814/ https://www.ncbi.nlm.nih.gov/pubmed/35320357 http://dx.doi.org/10.1242/jeb.243674 |
work_keys_str_mv | AT nordiostefania parasitoidwaspvenommanipulateshostinnatebehaviorviasubtypespecificdopaminereceptoractivation AT kaisermaayan parasitoidwaspvenommanipulateshostinnatebehaviorviasubtypespecificdopaminereceptoractivation AT adamsmichaele parasitoidwaspvenommanipulateshostinnatebehaviorviasubtypespecificdopaminereceptoractivation AT libersatfrederic parasitoidwaspvenommanipulateshostinnatebehaviorviasubtypespecificdopaminereceptoractivation |