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Metabolic disruption impacts tick fitness and microbial relationships

Arthropod-borne microbes rely on the metabolic state of a host to cycle between evolutionarily distant species. For instance, arthropod tolerance to infection may be due to redistribution of metabolic resources, often leading to microbial transmission to mammals. Conversely, metabolic alterations ai...

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Autores principales: Samaddar, Sourabh, O’Neal, Anya J., Marnin, Liron, Rolandelli, Agustin, Singh, Nisha, Wang, Xiaowei, Butler, L. Rainer, Rangghran, Parisa, Laukaitis, Hanna J., Cabrera Paz, Francy E., Fiskum, Gary M., Polster, Brian M., Pedra, Joao H. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245996/
https://www.ncbi.nlm.nih.gov/pubmed/37292783
http://dx.doi.org/10.1101/2023.05.26.542501
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author Samaddar, Sourabh
O’Neal, Anya J.
Marnin, Liron
Rolandelli, Agustin
Singh, Nisha
Wang, Xiaowei
Butler, L. Rainer
Rangghran, Parisa
Laukaitis, Hanna J.
Cabrera Paz, Francy E.
Fiskum, Gary M.
Polster, Brian M.
Pedra, Joao H. F.
author_facet Samaddar, Sourabh
O’Neal, Anya J.
Marnin, Liron
Rolandelli, Agustin
Singh, Nisha
Wang, Xiaowei
Butler, L. Rainer
Rangghran, Parisa
Laukaitis, Hanna J.
Cabrera Paz, Francy E.
Fiskum, Gary M.
Polster, Brian M.
Pedra, Joao H. F.
author_sort Samaddar, Sourabh
collection PubMed
description Arthropod-borne microbes rely on the metabolic state of a host to cycle between evolutionarily distant species. For instance, arthropod tolerance to infection may be due to redistribution of metabolic resources, often leading to microbial transmission to mammals. Conversely, metabolic alterations aids in pathogen elimination in humans, who do not ordinarily harbor arthropod-borne microbes. To ascertain the effect of metabolism on interspecies relationships, we engineered a system to evaluate glycolysis and oxidative phosphorylation in the tick Ixodes scapularis. Using a metabolic flux assay, we determined that the rickettsial bacterium Anaplasma phagocytophilum and the Lyme disease spirochete Borrelia burgdorferi, which are transstadially transmitted in nature, induced glycolysis in ticks. On the other hand, the endosymbiont Rickettsia buchneri, which is transovarially maintained, had a minimal effect on I. scapularis bioenergetics. Importantly, the metabolite β-aminoisobutyric acid (BAIBA) was elevated during A. phagocytophilum infection of tick cells following an unbiased metabolomics approach. Thus, we manipulated the expression of genes associated with the catabolism and anabolism of BAIBA in I. scapularis and detected impaired feeding on mammals, reduced bacterial acquisition, and decreased tick survival. Collectively, we reveal the importance of metabolism for tick-microbe relationships and unveil a valuable metabolite for I. scapularis fitness.
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spelling pubmed-102459962023-06-08 Metabolic disruption impacts tick fitness and microbial relationships Samaddar, Sourabh O’Neal, Anya J. Marnin, Liron Rolandelli, Agustin Singh, Nisha Wang, Xiaowei Butler, L. Rainer Rangghran, Parisa Laukaitis, Hanna J. Cabrera Paz, Francy E. Fiskum, Gary M. Polster, Brian M. Pedra, Joao H. F. bioRxiv Article Arthropod-borne microbes rely on the metabolic state of a host to cycle between evolutionarily distant species. For instance, arthropod tolerance to infection may be due to redistribution of metabolic resources, often leading to microbial transmission to mammals. Conversely, metabolic alterations aids in pathogen elimination in humans, who do not ordinarily harbor arthropod-borne microbes. To ascertain the effect of metabolism on interspecies relationships, we engineered a system to evaluate glycolysis and oxidative phosphorylation in the tick Ixodes scapularis. Using a metabolic flux assay, we determined that the rickettsial bacterium Anaplasma phagocytophilum and the Lyme disease spirochete Borrelia burgdorferi, which are transstadially transmitted in nature, induced glycolysis in ticks. On the other hand, the endosymbiont Rickettsia buchneri, which is transovarially maintained, had a minimal effect on I. scapularis bioenergetics. Importantly, the metabolite β-aminoisobutyric acid (BAIBA) was elevated during A. phagocytophilum infection of tick cells following an unbiased metabolomics approach. Thus, we manipulated the expression of genes associated with the catabolism and anabolism of BAIBA in I. scapularis and detected impaired feeding on mammals, reduced bacterial acquisition, and decreased tick survival. Collectively, we reveal the importance of metabolism for tick-microbe relationships and unveil a valuable metabolite for I. scapularis fitness. Cold Spring Harbor Laboratory 2023-05-26 /pmc/articles/PMC10245996/ /pubmed/37292783 http://dx.doi.org/10.1101/2023.05.26.542501 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Samaddar, Sourabh
O’Neal, Anya J.
Marnin, Liron
Rolandelli, Agustin
Singh, Nisha
Wang, Xiaowei
Butler, L. Rainer
Rangghran, Parisa
Laukaitis, Hanna J.
Cabrera Paz, Francy E.
Fiskum, Gary M.
Polster, Brian M.
Pedra, Joao H. F.
Metabolic disruption impacts tick fitness and microbial relationships
title Metabolic disruption impacts tick fitness and microbial relationships
title_full Metabolic disruption impacts tick fitness and microbial relationships
title_fullStr Metabolic disruption impacts tick fitness and microbial relationships
title_full_unstemmed Metabolic disruption impacts tick fitness and microbial relationships
title_short Metabolic disruption impacts tick fitness and microbial relationships
title_sort metabolic disruption impacts tick fitness and microbial relationships
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245996/
https://www.ncbi.nlm.nih.gov/pubmed/37292783
http://dx.doi.org/10.1101/2023.05.26.542501
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