Transposon sequencing reveals the essential gene set and genes enabling gut symbiosis in the insect symbiont Caballeronia insecticola

Author:

Jouan Romain1,Lextrait Gaëlle1,Lachat Joy1,Yokota Aya1,Cossard Raynald1,Naquin Delphine1,Timchenko Tatiana1,Kikuchi Yoshitomo2,Ohbayashi Tsubasa13,Mergaert Peter1

Affiliation:

1. Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC) , Gif-sur-Yvette 91198, France

2. Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Hokkaido Center , Sapporo 062-8517, Japan

3. Institute for Agro-Environmental Sciences, National Agriculture and Food Research Organization (NARO) , Tsukuba 305-8604, Japan

Abstract

Abstract Caballeronia insecticola is a bacterium belonging to the Burkholderia genus sensu lato, which is able to colonize multiple environments like soils and the gut of the bean bug Riptortus pedestris. We constructed a saturated Himar1 mariner transposon library and revealed by transposon-sequencing that 498 protein-coding genes constitute the essential genome of Caballeronia insecticola for growth in free-living conditions. By comparing essential gene sets of Caballeronia insecticola and seven related Burkholderia s.l. strains, only 120 common genes were identified, indicating that a large part of the essential genome is strain-specific. In order to reproduce specific nutritional conditions that are present in the gut of Riptortus pedestris, we grew the mutant library in minimal media supplemented with candidate gut nutrients and identified several condition-dependent fitness-defect genes by transposon-sequencing. To validate the robustness of the approach, insertion mutants in six fitness genes were constructed and their growth deficiency in media supplemented with the corresponding nutrient was confirmed. The mutants were further tested for their efficiency in Riptortus pedestris gut colonization, confirming that gluconeogenic carbon sources, taurine and inositol, are nutrients consumed by the symbiont in the gut. Thus, our study provides insights about specific contributions provided by the insect host to the bacterial symbiont.

Funder

JSPS Research Fellowship for Young Scientists, Japan

Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan

Ministry of Higher Education, Research, and Innovation, France

CNRS International Research Project, France

JSPS-CNRS Bilateral Open Partnership Joint Research Project, France-Japan

Agence Nationale de la Recherche, France

Saclay Plant Sciences-SPS

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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