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The boom and bust of the aphid’s essential amino acid metabolism across nymphal development

Within long-term symbioses, animals integrate their physiology and development with their symbiont. In a model nutritional mutualism, aphids harbor the endosymbiont, Buchnera, within specialized bacteriocyte cells. Buchnera synthesizes essential amino acids (EAAs) and vitamins for their host, which...

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Autores principales: Pers, Daniel, Hansen, Allison K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433001/
https://www.ncbi.nlm.nih.gov/pubmed/33831149
http://dx.doi.org/10.1093/g3journal/jkab115
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author Pers, Daniel
Hansen, Allison K
author_facet Pers, Daniel
Hansen, Allison K
author_sort Pers, Daniel
collection PubMed
description Within long-term symbioses, animals integrate their physiology and development with their symbiont. In a model nutritional mutualism, aphids harbor the endosymbiont, Buchnera, within specialized bacteriocyte cells. Buchnera synthesizes essential amino acids (EAAs) and vitamins for their host, which are lacking from the aphid’s plant sap diet. It is unclear if the aphid host differentially expresses aphid EAA metabolism pathways and genes that collaborate with Buchnera for the production of EAA and vitamins throughout nymphal development when feeding on plants. It is also unclear if aphid bacteriocytes are differentially methylated throughout aphid development as DNA methylation may play a role in gene regulation. By analyzing aphid gene expression, we determined that the bacteriocyte is metabolically more active in metabolizing Buchnera’s EAAs and vitamins early in nymphal development compared to intermediate or later immature and adult lifestages. The largest changes in aphid bacteriocyte gene expression, especially for aphid genes that collaborate with Buchnera, occurred during the 3rd to 4th instar transition. During this transition, there is a huge shift in the bacteriocyte from a high energy “nutrient-consuming state” to a “recovery and growth state” where patterning and signaling genes and pathways are upregulated and differentially methylated, and de novo methylation is reduced as evidenced by homogenous DNA methylation profiles after the 2nd instar. Moreover, bacteriocyte number increased and Buchnera’s titer decreased throughout aphid nymphal development. These data suggest in combination that bacteriocytes of older nymphal and adult lifestages depend less on the nutritional symbiosis compared to early nymphal lifestages.
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spelling pubmed-84330012021-09-13 The boom and bust of the aphid’s essential amino acid metabolism across nymphal development Pers, Daniel Hansen, Allison K G3 (Bethesda) Investigation Within long-term symbioses, animals integrate their physiology and development with their symbiont. In a model nutritional mutualism, aphids harbor the endosymbiont, Buchnera, within specialized bacteriocyte cells. Buchnera synthesizes essential amino acids (EAAs) and vitamins for their host, which are lacking from the aphid’s plant sap diet. It is unclear if the aphid host differentially expresses aphid EAA metabolism pathways and genes that collaborate with Buchnera for the production of EAA and vitamins throughout nymphal development when feeding on plants. It is also unclear if aphid bacteriocytes are differentially methylated throughout aphid development as DNA methylation may play a role in gene regulation. By analyzing aphid gene expression, we determined that the bacteriocyte is metabolically more active in metabolizing Buchnera’s EAAs and vitamins early in nymphal development compared to intermediate or later immature and adult lifestages. The largest changes in aphid bacteriocyte gene expression, especially for aphid genes that collaborate with Buchnera, occurred during the 3rd to 4th instar transition. During this transition, there is a huge shift in the bacteriocyte from a high energy “nutrient-consuming state” to a “recovery and growth state” where patterning and signaling genes and pathways are upregulated and differentially methylated, and de novo methylation is reduced as evidenced by homogenous DNA methylation profiles after the 2nd instar. Moreover, bacteriocyte number increased and Buchnera’s titer decreased throughout aphid nymphal development. These data suggest in combination that bacteriocytes of older nymphal and adult lifestages depend less on the nutritional symbiosis compared to early nymphal lifestages. Oxford University Press 2021-04-08 /pmc/articles/PMC8433001/ /pubmed/33831149 http://dx.doi.org/10.1093/g3journal/jkab115 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigation
Pers, Daniel
Hansen, Allison K
The boom and bust of the aphid’s essential amino acid metabolism across nymphal development
title The boom and bust of the aphid’s essential amino acid metabolism across nymphal development
title_full The boom and bust of the aphid’s essential amino acid metabolism across nymphal development
title_fullStr The boom and bust of the aphid’s essential amino acid metabolism across nymphal development
title_full_unstemmed The boom and bust of the aphid’s essential amino acid metabolism across nymphal development
title_short The boom and bust of the aphid’s essential amino acid metabolism across nymphal development
title_sort boom and bust of the aphid’s essential amino acid metabolism across nymphal development
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433001/
https://www.ncbi.nlm.nih.gov/pubmed/33831149
http://dx.doi.org/10.1093/g3journal/jkab115
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