Mycoplasmology, Bacteriology, and Antimicrobial Resistance Unit, Ploufragan-Plouzané Laboratory, French Agency for Food, Environmental, and Occupational Health and Safety (ANSES), Ploufragan, France.
Microbiol Spectr. 2018 Jul;6(4). doi: 10.1128/microbiolspec.ARBA-0030-2018.
Mycoplasmas are intrinsically resistant to antimicrobials targeting the cell wall (fosfomycin, glycopeptides, or β-lactam antibiotics) and to sulfonamides, first-generation quinolones, trimethoprim, polymixins, and rifampicin. The antibiotics most frequently used to control mycoplasmal infections in animals are macrolides and tetracyclines. Lincosamides, fluoroquinolones, pleuromutilins, phenicols, and aminoglycosides can also be active. Standardization of methods used for determination of susceptibility levels is difficult since no quality control strains are available and because of species-specific growth requirements. Reduced susceptibility levels or resistances to several families of antimicrobials have been reported in field isolates of pathogenic species of major veterinary interest: and in poultry; , , and in swine; in cattle; and in small ruminants. The highest resistances are observed for macrolides, followed by tetracyclines. Most strains remain susceptible to fluoroquinolones. Pleuromutilins are the most effective antibiotics . Resistance frequencies vary according to the species but also according to the countries or groups of animals from which the samples were taken. Point mutations in the target genes of different antimicrobials have been identified in resistant field isolates, -selected mutants, or strains reisolated after an experimental infection followed by one or several treatments: DNA-gyrase and topoisomerase IV for fluoroquinolones; 23S rRNA for macrolides, lincosamides, pleuromutilins, and amphenicols; 16S rRNAs for tetracyclines and aminoglycosides. Further work should be carried out to determine and harmonize specific breakpoints for animal mycoplasmas so that information can be used to provide advice on selection of treatments.
支原体对作用于细胞壁的抗菌药物(磷霉素、糖肽类或β-内酰胺类抗生素)和磺胺类药物、第一代喹诺酮类药物、甲氧苄啶、多黏菌素和利福平具有固有耐药性。动物支原体感染控制中最常使用的抗生素是大环内酯类和四环素类。林可酰胺类、氟喹诺酮类、截短侧耳素类、酚类和氨基糖苷类也可能有效。由于没有质量控制菌株,并且由于物种特异性生长要求,因此难以对药敏水平测定方法进行标准化。在具有主要兽医重要性的致病性物种的田间分离株中已经报道了对几种抗菌药物家族的敏感性降低或耐药性:禽源 和 ;猪源 、 、 和 ;牛源 ;小反刍动物源 。对大环内酯类和四环素类的耐药性最高。大多数菌株仍然对氟喹诺酮类敏感。截短侧耳素类是最有效的抗生素。耐药频率因物种而异,也因采样的国家或动物群而异。在耐药的田间分离株、-选择突变体或实验感染后经一次或多次治疗再分离的菌株中,已鉴定出不同抗菌药物靶基因的点突变:氟喹诺酮类的 DNA 拓扑异构酶和拓扑异构酶 IV;大环内酯类、林可酰胺类、截短侧耳素类和氯霉素的 23S rRNA;四环素类和氨基糖苷类的 16S rRNA。应进一步开展工作以确定和协调动物支原体的特定断点,以便能够利用这些信息提供有关治疗选择的建议。