Differential antigenicity of individual Mycoplasma hyorhinis variable lipoproteins

IF 1.4 3区 农林科学 Q4 IMMUNOLOGY Veterinary immunology and immunopathology Pub Date : 2024-04-24 DOI:10.1016/j.vetimm.2024.110768
Precy D. Magtoto , Bailey L. Arruda , Ronaldo L. Magtoto , Juan Carlos Mora-Díaz , Rina B. Opulencia , David H. Baum , Jeff J. Zimmerman , Luis G. Giménez-Lirola
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Abstract

The Mycoplasma hyorhinis (Mhr) variable lipoprotein (Vlp) family, comprising Vlps A, B, C, D, E, F, and G, are highly variable in expression, size, and cytoadhesion capabilities across Mhr strains. The ‘Vlp system’ plays a crucial role in cytoadhesion, immune evasion, and in eliciting a host immunologic response. This pilot study described the development of Vlp peptide-based ELISAs to evaluate the antigenic reactivity of individual Vlps against Mhr antisera collected throughout a longitudinal study focused on Mhr strain 38983, reproducing Mhr-associated disease under experimental conditions. Specifically, serum samples were collected at day post-inoculation 0, 7, 10, 14, 17, 21, 24, 28, 35, 42, 49, and 56 from Mhr- and mock (Friis medium)-inoculated cesarean-derived, colostrum-deprived pigs. Significant Mhr-specific IgG responses were detected at specific time points throughout the infection, with some variations for each Vlp. Overall, individual Vlp ELISAs showed consistently high accuracy rates, except for VlpD, which would likely be associated with its expression levels or the anti-Vlp humoral immune response specific to the Mhr strain used in this study. This study provides the basis and tools for a more refined understanding of these Vlp- and Mhr strain-specific variations, which is foundational in understanding the host immune response to Mhr.

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单个透明支原体可变脂蛋白的抗原性差异
解脲支原体(Mhr)可变脂蛋白(Vlp)家族包括 Vlps A、B、C、D、E、F 和 G,它们在表达、大小和细胞粘附能力方面在不同的 Mhr 菌株之间存在很大差异。Vlp系统 "在细胞粘附、免疫逃避和引起宿主免疫反应方面发挥着至关重要的作用。这项试验性研究描述了基于Vlp肽的ELISAs的开发情况,以评估在一项以Mhr菌株38983为重点的纵向研究中收集的单个Vlp对Mhr抗血清的抗原反应性,该研究在实验条件下重现了Mhr相关疾病。具体来说,在接种后第 0、7、10、14、17、21、24、28、35、42、49 和 56 天,分别从接种 Mhr 和模拟(Friis 培养基)接种剖腹产猪、初乳缺乏猪采集血清样本。在整个感染过程中的特定时间点检测到明显的 Mhr 特异性 IgG 反应,每种 Vlp 均有一些差异。总体而言,除 VlpD 外,单个 Vlp ELISA 的准确率一直很高,这可能与 VlpD 的表达水平或本研究中使用的 Mhr 株系特有的抗 Vlp 体液免疫反应有关。这项研究为更深入地了解这些 Vlp 和 Mhr 株系特异性变异提供了基础和工具,这对于了解宿主对 Mhr 的免疫反应至关重要。
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来源期刊
CiteScore
3.40
自引率
5.60%
发文量
79
审稿时长
70 days
期刊介绍: The journal reports basic, comparative and clinical immunology as they pertain to the animal species designated here: livestock, poultry, and fish species that are major food animals and companion animals such as cats, dogs, horses and camels, and wildlife species that act as reservoirs for food, companion or human infectious diseases, or as models for human disease. Rodent models of infectious diseases that are of importance in the animal species indicated above,when the disease requires a level of containment that is not readily available for larger animal experimentation (ABSL3), will be considered. Papers on rabbits, lizards, guinea pigs, badgers, armadillos, elephants, antelope, and buffalo will be reviewed if the research advances our fundamental understanding of immunology, or if they act as a reservoir of infectious disease for the primary animal species designated above, or for humans. Manuscripts employing other species will be reviewed if justified as fitting into the categories above. The following topics are appropriate: biology of cells and mechanisms of the immune system, immunochemistry, immunodeficiencies, immunodiagnosis, immunogenetics, immunopathology, immunology of infectious disease and tumors, immunoprophylaxis including vaccine development and delivery, immunological aspects of pregnancy including passive immunity, autoimmuity, neuroimmunology, and transplanatation immunology. Manuscripts that describe new genes and development of tools such as monoclonal antibodies are also of interest when part of a larger biological study. Studies employing extracts or constituents (plant extracts, feed additives or microbiome) must be sufficiently defined to be reproduced in other laboratories and also provide evidence for possible mechanisms and not simply show an effect on the immune system.
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