考拉眼部疾病的等级是根据衣原体负荷变化和 Th2 免疫反应的增加来确定的。

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Frontiers in Cellular and Infection Microbiology Pub Date : 2024-11-12 eCollection Date: 2024-01-01 DOI:10.3389/fcimb.2024.1447119
Samuel Phillips, Danielle Madden, Amber Gillett, Bonnie L Quigley, Martina Jelocnik, Sankhya Bommana, Denis O'Meally, Peter Timms, Adam Polkinghorne
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引用次数: 0

摘要

简介:本研究采用大量RNA测序、PCR和ELISA检测方法,分析影响考拉眼部感染C. pecorum的病理因素。该研究调查了与考拉眼部衣原体病不同阶段相关的免疫反应和基因表达谱:方法:对来自澳大利亚昆士兰州的 114 只考拉进行了评估,其中 47% 出现了眼部疾病的临床症状。动物被分为三个群组:急性活动性疾病(G1)、慢性活动性疾病(G2)和慢性非活动性疾病(G3),以及亚临床衣原体阳性群组(H2)和健康群组(H1):对临床、微生物、体液免疫和细胞免疫生物标记物的分析表明,不同疾病等级的衣原体载量和抗衣原体 IgG 水平各不相同,眼部衣原体载量和抗衣原体 IgG 之间呈负相关。对27只考拉的眼粘膜基因表达进行分析,发现了不同疾病组群的共同表达途径,在所有疾病阶段,IFNγ表达和色氨酸代谢均显著上调:这些发现有助于阐明考拉眼衣原体病的免疫反应动态和分子通路,为疾病管理策略提供了至关重要的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Koala ocular disease grades are defined by chlamydial load changes and increases in Th2 immune responses.

Introduction: This study employs bulk RNA sequencing, PCR, and ELISA assays to analyze the pathological factors affecting the outcomes of C. pecorum ocular infections in koalas. It investigates the immune responses and gene expression profiles associated with various stages of koala ocular chlamydiosis.

Methods: A cohort of 114 koalas from Queensland, Australia were assessed, with 47% displaying clinical signs of ocular disease. Animals were classified into three cohorts: acute active disease (G1), chronic active disease (G2), and chronic inactive disease (G3), along with subclinical Chlamydia pecorum positive (H2) and healthy (H1) cohorts.

Results: Analysis of clinical, microbiological, humoral immune and cellular immune biomarkers revealed varying chlamydial loads and anti-chlamydial IgG levels across disease grades, with a negative correlation observed between ocular chlamydial load and anti-chlamydial IgG. Koala ocular mucosa gene expression analysis from 27 koalas identified shared expression pathways across disease cohorts, with a significant upregulation of IFNγ expression and tryptophan metabolism in all disease stages.

Discussion: These findings help elucidate immune response dynamics and molecular pathways underlying koala ocular chlamydiosis, providing insights crucial for disease management strategies.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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