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Main Authors: Wang, Yayun, Moriyama, Minoru, Koga, Ryuichi, Oguchi, Kohei, Hosokawa, Takahiro, Takai, Hiroki, Shigenobu, Shuji, Nikoh, Naruo, Fukatsu, Takema
Format: Artículo científico
Language:en
Published: Nature microbiology 2026
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/41760926/
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author Wang, Yayun
Moriyama, Minoru
Koga, Ryuichi
Oguchi, Kohei
Hosokawa, Takahiro
Takai, Hiroki
Shigenobu, Shuji
Nikoh, Naruo
Fukatsu, Takema
author_facet Wang, Yayun
Moriyama, Minoru
Koga, Ryuichi
Oguchi, Kohei
Hosokawa, Takahiro
Takai, Hiroki
Shigenobu, Shuji
Nikoh, Naruo
Fukatsu, Takema
Wang, Yayun
Moriyama, Minoru
Koga, Ryuichi
Oguchi, Kohei
Hosokawa, Takahiro
Takai, Hiroki
Shigenobu, Shuji
Nikoh, Naruo
Fukatsu, Takema
collection PubMed - marine biology
contents Tryptophanase disruption promotes insect-bacterium mutualism. Wang, Yayun Moriyama, Minoru Koga, Ryuichi Oguchi, Kohei Hosokawa, Takahiro Takai, Hiroki Shigenobu, Shuji Nikoh, Naruo Fukatsu, Takema Animals Symbiosis Pantoea Tryptophanase Escherichia coli Tryptophan Indoles Insecta Animal-microorganism symbioses are omnipresent, with both partners often gaining benefits as mutualists. A single mutation in the carbon catabolite repression system in Escherichia coli enables mutualism with the stinkbug Plautia stali. Here we find that this mutation is not present in natural symbioses. Given that the carbon catabolite repression pathway affects the expression of >500 downstream genes, we investigated their role in mutualisms. We find that disruption of a single gene, tnaA, encoding tryptophanase makes E. coli mutualistic to P. stali, resulting in the accumulation of tryptophan and the reduction of toxic indole. A survey of wild populations of P. stali and other stinkbug species revealed that their typical microbial symbionts, Pantoea, consistently lack the tnaA gene. Some Pantoea species such as Pantoea ananatis retain the tnaA gene and cannot establish symbiosis with P. stali, but tnaA-disrupted P. ananatis partially restored the symbiotic capability. When a natural Pantoea mutualist of P. stali was transformed with a functional tna operon, its symbiotic capability reduced significantly. Our finding suggests that tryptophanase disruption may have facilitated the evolution of gut bacterial mutualists in insects.
format Artículo científico
id pubmed_41760926
institution PubMed
language en
publishDate 2026
publisher Nature microbiology
record_format pubmed
spellingShingle Tryptophanase disruption promotes insect-bacterium mutualism.
Wang, Yayun
Moriyama, Minoru
Koga, Ryuichi
Oguchi, Kohei
Hosokawa, Takahiro
Takai, Hiroki
Shigenobu, Shuji
Nikoh, Naruo
Fukatsu, Takema
Animals
Symbiosis
Pantoea
Tryptophanase
Escherichia coli
Tryptophan
Indoles
Insecta
Tryptophanase disruption promotes insect-bacterium mutualism. Wang, Yayun Moriyama, Minoru Koga, Ryuichi Oguchi, Kohei Hosokawa, Takahiro Takai, Hiroki Shigenobu, Shuji Nikoh, Naruo Fukatsu, Takema Animals Symbiosis Pantoea Tryptophanase Escherichia coli Tryptophan Indoles Insecta Animal-microorganism symbioses are omnipresent, with both partners often gaining benefits as mutualists. A single mutation in the carbon catabolite repression system in Escherichia coli enables mutualism with the stinkbug Plautia stali. Here we find that this mutation is not present in natural symbioses. Given that the carbon catabolite repression pathway affects the expression of >500 downstream genes, we investigated their role in mutualisms. We find that disruption of a single gene, tnaA, encoding tryptophanase makes E. coli mutualistic to P. stali, resulting in the accumulation of tryptophan and the reduction of toxic indole. A survey of wild populations of P. stali and other stinkbug species revealed that their typical microbial symbionts, Pantoea, consistently lack the tnaA gene. Some Pantoea species such as Pantoea ananatis retain the tnaA gene and cannot establish symbiosis with P. stali, but tnaA-disrupted P. ananatis partially restored the symbiotic capability. When a natural Pantoea mutualist of P. stali was transformed with a functional tna operon, its symbiotic capability reduced significantly. Our finding suggests that tryptophanase disruption may have facilitated the evolution of gut bacterial mutualists in insects.
title Tryptophanase disruption promotes insect-bacterium mutualism.
topic Animals
Symbiosis
Pantoea
Tryptophanase
Escherichia coli
Tryptophan
Indoles
Insecta
url https://pubmed.ncbi.nlm.nih.gov/41760926/