Infection‐Dependent Modulation of the Host Adaptor Gab2 During <i>Chlamydia trachomatis</i> Intracellular Development

Chlamydia trachomatis (Ct) is an obligate intracellular bacterium that can cause severe reproductive complications, including infertility and pelvic inflammatory disease. Its pathogenicity depends on intracellular maturation, which involves differentiation between infectious elementary (EB) and replicative reticulate bodies within inclusion vacuoles. Ct is known to modulate host PI3K-AKT signaling during this process; however, the molecular basis of this regulation remains unclear. To elucidate this mechanism, we screened host factors linked to the PI3K-AKT axis using a PI3K-AKT-mTOR compound library comprising 319 inhibitors, and identified the adaptor protein Gab2 (GRB2-associated binding protein 2) as a new target molecule of Ct. Gab2 protein levels decreased during the late phase of infection, and Gab2 silencing impaired intracellular replication without affecting EB formation. These findings demonstrate that Ct infection modulates the host adaptor Gab2 during intracellular development and provide new insights into host-pathogen interactions underlying chlamydial maturation.

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Publication Details

Journal
Microbiology and Immunology
Published
2026-07-01
DOI
https://doi.org/10.1111/1348-0421.70064
Primary Topic
Reproductive tract infections research
Type
article
Field-Weighted Citation Impact
0.00
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article

Infection‐Dependent Modulation of the Host Adaptor Gab2 During Chlamydia trachomatis Intracellular Development

Hideaki Higashi, T Deguchi, Hiroyuki Yamaguchi, Sora Kuroiwa et al.
Microbiology and Immunology
Reproductive tract infections research
article

Infection‐Dependent Modulation of the Host Adaptor Gab2 During Chlamydia trachomatis Intracellular Development

Hideaki Higashi, T Deguchi, Hiroyuki Yamaguchi, Sora Kuroiwa, S Nakamura, Torahiko Okubo
article en

Abstract

Chlamydia trachomatis (Ct) is an obligate intracellular bacterium that can cause severe reproductive complications, including infertility and pelvic inflammatory disease. Its pathogenicity depends on intracellular maturation, which involves differentiation between infectious elementary (EB) and replicative reticulate bodies within inclusion vacuoles. Ct is known to modulate host PI3K-AKT signaling during this process; however, the molecular basis of this regulation remains unclear. To elucidate this mechanism, we screened host factors linked to the PI3K-AKT axis using a PI3K-AKT-mTOR compound library comprising 319 inhibitors, and identified the adaptor protein Gab2 (GRB2-associated binding protein 2) as a new target molecule of Ct. Gab2 protein levels decreased during the late phase of infection, and Gab2 silencing impaired intracellular replication without affecting EB formation. These findings demonstrate that Ct infection modulates the host adaptor Gab2 during intracellular development and provide new insights into host-pathogen interactions underlying chlamydial maturation.

Microbiology and Immunology
Sapporo Medical University (JP), Hokkaido University (JP), Juntendo University (JP), Institute of Infection and Immunity (CA)
Good health and well-being
Openalex Percentile: Top 8%
Reproductive tract infections research
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