S. Meazzi, S. Lauzi, A. Stranieri, S. Paltrinieri, A. Giordano
{"title":"感染冠状病毒的猫的肠道微生物群和粘膜防御:一项初步研究","authors":"S. Meazzi, S. Lauzi, A. Stranieri, S. Paltrinieri, A. Giordano","doi":"10.13130/2283-3927/8410","DOIUrl":null,"url":null,"abstract":"Feline Infectious Peritonitis (FIP) develops from a mutation of enteric feline coronaviruses (FCoVs) and an imbalance of the host immune response. The wide polymorphism of FCoVs is associated with the viral replication rate (Licitra et al. 2013) . Changes in the composition of the gut microbiota may induce quali-quantitative modifications in FCoVs and/or different immune profiles (Weese et al., 2015). Few information is available on feline gut microbiome and the association between microbiota and the predisposition to pathological conditions (Ramadan et al., 2014). The aim of this study is to provide preliminary data about the composition of gut microbiota in healthy cats compared with FCoV infected cats (with and without FIP), in order to evaluate whether changes of gut microbiota may induce changes in FCoV, in its genetic polymorphism and in the mucosal immunity. Screening analyses have been performed on 22 cats: - Routine hematology and biochemistry on EDTA and serum (included electrophoresis and alpha-1-acid glycoprotein measurement for cats suspected with FIP) - Nested RT-PCR-3’UTR on frozen faeces - Effusion evaluation - FIV/FeLV serology Due to strict inclusion criteria (cats younger than 2.5 years old, indoor and not assuming antibiotics in the previous two months) and based on the results obtained from the complete set of analysis, only 15 cats, specifically 5 cats for each of the following 3 groups: FIP- affected, healthy negative and positive for FCoV, have been recruited to perform the following analyses: - microbiota analysis through NGS of 16S rRNA gene (V4 region) amplicons followed by bioinformatic analysis - evaluation of secretory IgA (ELISA kit) - phylogenetic analysis of FCoVs S gene sequences Innovative results will be provided on the feline gut microbiota composition. These will be correlated with the presence and genetic polymorphisms of FCoV and mucosal defenses to establish significant correlations between the analysed factors.","PeriodicalId":14105,"journal":{"name":"International Journal of Health, Animal science and Food safety","volume":"24 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"The gut microbiome and mucosal defenses in cats with coronaviruses: a pilot study\",\"authors\":\"S. Meazzi, S. Lauzi, A. Stranieri, S. Paltrinieri, A. Giordano\",\"doi\":\"10.13130/2283-3927/8410\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Feline Infectious Peritonitis (FIP) develops from a mutation of enteric feline coronaviruses (FCoVs) and an imbalance of the host immune response. The wide polymorphism of FCoVs is associated with the viral replication rate (Licitra et al. 2013) . Changes in the composition of the gut microbiota may induce quali-quantitative modifications in FCoVs and/or different immune profiles (Weese et al., 2015). Few information is available on feline gut microbiome and the association between microbiota and the predisposition to pathological conditions (Ramadan et al., 2014). The aim of this study is to provide preliminary data about the composition of gut microbiota in healthy cats compared with FCoV infected cats (with and without FIP), in order to evaluate whether changes of gut microbiota may induce changes in FCoV, in its genetic polymorphism and in the mucosal immunity. Screening analyses have been performed on 22 cats: - Routine hematology and biochemistry on EDTA and serum (included electrophoresis and alpha-1-acid glycoprotein measurement for cats suspected with FIP) - Nested RT-PCR-3’UTR on frozen faeces - Effusion evaluation - FIV/FeLV serology Due to strict inclusion criteria (cats younger than 2.5 years old, indoor and not assuming antibiotics in the previous two months) and based on the results obtained from the complete set of analysis, only 15 cats, specifically 5 cats for each of the following 3 groups: FIP- affected, healthy negative and positive for FCoV, have been recruited to perform the following analyses: - microbiota analysis through NGS of 16S rRNA gene (V4 region) amplicons followed by bioinformatic analysis - evaluation of secretory IgA (ELISA kit) - phylogenetic analysis of FCoVs S gene sequences Innovative results will be provided on the feline gut microbiota composition. 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引用次数: 2
摘要
猫传染性腹膜炎(FIP)是由肠道猫冠状病毒(fcov)突变和宿主免疫反应不平衡引起的。fcov的广泛多态性与病毒复制率有关(Licitra et al. 2013)。肠道微生物群组成的变化可能导致fcov和/或不同免疫谱的质-定量改变(Weese等,2015)。关于猫肠道微生物群以及微生物群与病理状况易感性之间的关系的信息很少(Ramadan et al., 2014)。本研究的目的是提供健康猫与感染FCoV的猫(有和没有FIP)肠道微生物群组成的初步数据,以评估肠道微生物群的变化是否会引起FCoV的变化,其遗传多态性和粘膜免疫。对22只猫进行了筛选分析:-常规血液学和生化检测EDTA和血清(包括对疑似FIP的猫进行电泳和α -1-酸糖蛋白检测)-冷冻粪便的嵌套RT-PCR-3'UTR -积液评估- FIV/FeLV血清学由于严格的纳入标准(小于2.5岁、室内且前两个月未使用抗生素的猫),基于完整的分析结果,只有15只猫,具体来说,我们招募了5只猫,分别用于以下3组:受FIP影响、健康、FCoV阴性和阳性的猫,进行以下分析:-通过16S rRNA基因(V4区)扩增子的NGS分析进行微生物群分析,然后进行生物信息学分析-分泌IgA (ELISA试剂盒)评估- FCoV S基因序列的系统发育分析将提供关于猫肠道微生物群组成的创新结果。这些将与FCoV和粘膜防御的存在和遗传多态性相关,以确定所分析因素之间的显著相关性。
The gut microbiome and mucosal defenses in cats with coronaviruses: a pilot study
Feline Infectious Peritonitis (FIP) develops from a mutation of enteric feline coronaviruses (FCoVs) and an imbalance of the host immune response. The wide polymorphism of FCoVs is associated with the viral replication rate (Licitra et al. 2013) . Changes in the composition of the gut microbiota may induce quali-quantitative modifications in FCoVs and/or different immune profiles (Weese et al., 2015). Few information is available on feline gut microbiome and the association between microbiota and the predisposition to pathological conditions (Ramadan et al., 2014). The aim of this study is to provide preliminary data about the composition of gut microbiota in healthy cats compared with FCoV infected cats (with and without FIP), in order to evaluate whether changes of gut microbiota may induce changes in FCoV, in its genetic polymorphism and in the mucosal immunity. Screening analyses have been performed on 22 cats: - Routine hematology and biochemistry on EDTA and serum (included electrophoresis and alpha-1-acid glycoprotein measurement for cats suspected with FIP) - Nested RT-PCR-3’UTR on frozen faeces - Effusion evaluation - FIV/FeLV serology Due to strict inclusion criteria (cats younger than 2.5 years old, indoor and not assuming antibiotics in the previous two months) and based on the results obtained from the complete set of analysis, only 15 cats, specifically 5 cats for each of the following 3 groups: FIP- affected, healthy negative and positive for FCoV, have been recruited to perform the following analyses: - microbiota analysis through NGS of 16S rRNA gene (V4 region) amplicons followed by bioinformatic analysis - evaluation of secretory IgA (ELISA kit) - phylogenetic analysis of FCoVs S gene sequences Innovative results will be provided on the feline gut microbiota composition. These will be correlated with the presence and genetic polymorphisms of FCoV and mucosal defenses to establish significant correlations between the analysed factors.