Chopra-Dewasthaly Rohini, Dagn Andreas, Lohinger Christian, Brunthaler René, Flöck Martina, Kargl Munkhtsetseg, Hegde Shrilakshmi, Spergser Joachim, Rosengarten Renate
Institute of Microbiology, Department of Pathobiology, University of Veterinary Medicine Vienna, Veterinaerplatz 1, A-1210 Vienna, Austria.
Institute of Pathology, Department of Pathobiology, University of Veterinary Medicine Vienna, Veterinaerplatz 1, A-1210 Vienna, Austria.
Microorganisms. 2022 Apr 14;10(4):815. doi: 10.3390/microorganisms10040815.
The significance of large multigene families causing high-frequency surface variations in mycoplasmas is not well-understood. Previously, VpmaY and VpmaU clonal variants of the Vpma family of lipoproteins of were compared via experimental sheep infections using the two corresponding 'Phase-Locked Mutants'. However, nothing is known about the infectivity of the remaining four Vpma expression variants VpmaX, VpmaW, VpmaZ and VpmaV as they were never evaluated in vivo. Here, in vivo infection and disease progression of all six Vpma expressers constituting the Vpma family of type strain PG2 were compared using the corresponding -disrupted PLMs expressing single well-characterized Vpmas. Each of the six PLMs were separately evaluated using the intramammary sheep infection model along with the control phase-variable wildtype strain PG2. Thorough bacteriological, pathological and clinical examinations were performed, including assessment of milk quality, quantity and somatic cell counts. Altogether, the results indicated that the inability to vary the Vpma expression phase does not hamper the initiation of infection leading to mastitis for all six PLMs, except for PLMU, which showed a defect in host colonization and multiplication for the first 24 h p.i. and pathological/bacteriological analysis indicated a higher potential for systemic spread for PLMV and PLMX. This is the first study in which all isogenic expression variants of a large mycoplasma multigene family are tested in the natural host.
支原体中导致高频表面变异的大型多基因家族的意义尚未得到充分理解。此前,通过使用两个相应的“锁相突变体”对绵羊进行实验性感染,比较了脂蛋白Vpma家族的VpmaY和VpmaU克隆变体。然而,其余四个Vpma表达变体VpmaX、VpmaW、VpmaZ和VpmaV的感染性尚不清楚,因为它们从未在体内进行过评估。在此,使用表达单一特征明确的Vpmas的相应基因破坏锁相突变体(PLMs),比较了构成模式菌株PG2的Vpma家族的所有六种Vpma表达菌的体内感染和疾病进展情况。使用乳房内绵羊感染模型以及对照相位可变野生型菌株PG2,分别对六种PLMs进行了评估。进行了全面的细菌学、病理学和临床检查,包括对牛奶质量、产量和体细胞计数的评估。总体而言,结果表明,除了PLMU在感染后24小时内在宿主定植和繁殖方面存在缺陷外,无法改变Vpma表达阶段并不妨碍所有六种PLMs引发导致乳腺炎的感染,并且病理学/细菌学分析表明PLMV和PLMX具有更高的全身扩散潜力。这是第一项在天然宿主中测试大型支原体多基因家族所有同基因表达变体的研究。