The chlamydial transcriptional regulator Euo is a key switch in cell form developmental progression but is not involved in the committed step to the formation of the infectious form.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY mSphere Pub Date : 2024-09-25 Epub Date: 2024-08-14 DOI:10.1128/msphere.00437-24
Cody R Appa, Nicole A Grieshaber, Hong Yang, Anders Omsland, Sean McCormick, Travis J Chiarelli, Scott S Grieshaber
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Abstract

Bacteria in the genus Chlamydia are a significant health burden worldwide. They infect a wide range of vertebrate animals, including humans and domesticated animals. In humans, C. psittaci can cause zoonotic pneumonia, while C. pneumoniae causes a variety of respiratory infections. Infections with C. trachomatis cause ocular or genital infections. All chlamydial species are obligate intracellular bacteria that replicate exclusively inside of eukaryotic host cells. Chlamydial infections are dependent on a complex infection cycle that depends on transitions between specific cell forms. This cycle consists of cell forms specialized for host cell invasion, the elementary body (EB), and a form specialized for intracellular replication, the reticulate body (RB). In addition to the EB and RB, there is a transitionary cell form that mediates the transformation between the RB and the EB, the intermediate body (IB). In this study, we ectopically expressed the regulatory protein Euo and showed that high levels of expression resulted in reversible arrest of the development cycle. The arrested chlamydial cells were trapped phenotypically at an early IB stage of the cycle. These cells had exited the cell cycle but had not shifted gene expression from RB like to IB/EB like. This arrested state was dependent on continued expression of Euo. When ectopic expression was reversed, Euo levels dropped in the arrested cells which led to the repression of native Euo expression and the resumption of the developmental cycle. Our data are consistent with a model where Euo expression levels impact IB maturation to the infectious EB but not the production of the IB form.

Importance: Bacterial species in the Chlamydiales order infect a variety of vertebrate animals and are a global health concern. They cause various diseases in humans, including genital and respiratory infections. The bacteria are obligate intracellular parasites that rely on a complex infectious cycle involving multiple cell forms. All species share the same life cycle, transitioning through different states to form the infectious elementary body (EB) to spread infections to new hosts. The Euo gene, encoding a DNA-binding protein, is involved in regulating this cycle. This study showed that ectopic expression of Euo halted the cycle at an early stage. This arrest depended on continued Euo expression. When Euo expression was reversed, the developmental cycle resumed. Additionally, this study suggests that high levels of Euo expression affect the formation of the infectious EB but not the production of the cell form committed to EB formation.

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衣原体转录调节因子 Euo 是细胞形态发育过程中的一个关键开关,但并不参与形成感染形态的承诺步骤。
衣原体属细菌是全球范围内的重大健康负担。它们可感染多种脊椎动物,包括人类和驯养动物。在人类中,鹦鹉热衣原体可引起人畜共患肺炎,而肺炎衣原体可引起各种呼吸道感染。沙眼衣原体感染会导致眼部或生殖器感染。所有衣原体都是只能在真核宿主细胞内复制的细胞内细菌。衣原体感染依赖于一个复杂的感染周期,该周期取决于特定细胞形态之间的转换。这种循环包括专门入侵宿主细胞的细胞形态--基本体(EB)和专门在细胞内复制的形态--网状体(RB)。除了 EB 和 RB,还有一种过渡细胞形态介于 RB 和 EB 之间,即中间体(IB)。在这项研究中,我们异位表达了调控蛋白 Euo,结果表明高水平的表达会导致发育周期的可逆性停滞。停滞的衣原体细胞在表型上被困在细胞周期的早期 IB 阶段。这些细胞退出了细胞周期,但基因表达还没有从 RB 型转变为 IB/EB 型。这种停滞状态依赖于 Euo 的持续表达。当异位表达被逆转时,停滞细胞中的 Euo 水平下降,导致原生 Euo 表达受抑,发育周期恢复。我们的数据与 Euo 表达水平影响 IB 成熟为传染性 EB 但不影响 IB 生成的模型相一致:衣原体目细菌感染多种脊椎动物,是全球关注的健康问题。它们会引起人类的各种疾病,包括生殖器和呼吸道感染。这些细菌是强制性细胞内寄生虫,依赖于涉及多种细胞形态的复杂感染循环。所有物种都有相同的生命周期,通过不同的状态形成感染性基本体(EB),将感染传播给新的宿主。编码 DNA 结合蛋白的 Euo 基因参与调节这一周期。这项研究表明,异位表达 Euo 可使周期在早期阶段停止。这种停止依赖于 Euo 的持续表达。当 Euo 的表达逆转时,发育周期又会恢复。此外,这项研究还表明,高水平的 Euo 表达会影响传染性 EB 的形成,但不会影响致力于 EB 形成的细胞形式的产生。
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来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
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