Laboratório de Bacteriologia, Departamento de Medicina Veterinária Preventiva, Universidade Federal de Santa Maria (UFSM), Av. Roraima, 1000, Camobi, Santa Maria, Rio Grande do Sul, 97105-900, Brazil.
Laboratório de Microbiologia e Imunologia Veterinária, Medicina Veterinária, Instituto Federal Farroupilha (IFFar), Linha 7 de Setembro, BR 386 - KM 40, s/n - Centro, Frederico Westphalen, RS, 98400-000, Brazil.
Microb Pathog. 2020 Feb;139:103885. doi: 10.1016/j.micpath.2019.103885. Epub 2019 Nov 29.
The ability of Rhodococcus equi to survive in macrophages and cause pneumonia in foals depends on vapA and rhbC genes, which produce the virulence-associated protein A (VapA) and the rhequichelin siderophore, respectively. Virulent R. equi acquires Fe from transferrin by unknown mechanisms. Our objectives were to determine the role of GAPDH in Fe homeostasis, to further characterize GAPDH, rhbC, and vapA expression under iron homeostasis, and to document the occurrence of rhbC gene in R. equi isolates. Therefore, vapA + R. equi was cultured under excessive, physiologic, and restricted iron concentrations, and quantitative culture and gene expression were performed. The relative expression of GAPDH, rhbC, and vapA after 48 h of culture were analyzed by qPCR. To determine the rhbC occurrence, total DNA was extracted from R. equi isolated from foals with clinical rhodococcosis (n = 22), healthy horses (feces, n = 16; nasal swab, n = 9), soil (n = 6), and 2 ATCC reference strains. Conventional PCR was performed to identify genus/species, vapA, and rhbC genes. Iron restriction proportionally decreased R. equi growth rates, and induced high expression of both GAPDH and vapA. The putative role of GAPDH in R. equi iron homeostasis should be further investigated. rhbC was significantly up-regulated under both Fe excess and critical starvation. The rhbC gene was identified in all clinical isolates and soil, but it was absent in 2 isolates from healthy horses, suggesting that rhequichelin is not required for R. equi nasal and intestinal colonization.
马肺炎支原体能够在巨噬细胞中存活并引起驹肺炎取决于 vapA 和 rhbC 基因,它们分别产生与毒力相关的蛋白 A (VapA) 和 rhequichelin 铁载体。毒力马肺炎支原体通过未知机制从转铁蛋白中获取铁。我们的目标是确定 GAPDH 在铁稳态中的作用,进一步表征铁稳态下 GAPDH、rhbC 和 vapA 的表达,并记录 rhbC 基因在马肺炎支原体分离株中的存在情况。因此,在铁过量、生理和限制铁浓度下培养 vapA+马肺炎支原体,并进行定量培养和基因表达。通过 qPCR 分析培养 48 小时后 GAPDH、rhbC 和 vapA 的相对表达。为了确定 rhbC 的发生,从临床马肺炎支原体感染驹(n=22)、健康马(粪便,n=16;鼻拭子,n=9)、土壤(n=6)和 2 个 ATCC 参考株中提取总 DNA。进行常规 PCR 以鉴定属/种、vapA 和 rhbC 基因。铁限制成比例地降低了马肺炎支原体的生长速度,并诱导了 GAPDH 和 vapA 的高表达。GAPDH 在马肺炎支原体铁稳态中的作用应进一步研究。rhbC 在铁过量和关键饥饿下均显著上调。rhbC 基因在所有临床分离株和土壤中均被鉴定,但在 2 株来自健康马的分离株中缺失,表明 rhequichelin 不是马肺炎支原体鼻腔和肠道定植所必需的。