Hata Eiji, Nagai Kazuya, Murakami Kenji
Dairy Hygiene Unit, Division of Pathology and Pathophysiology, Hokkaido Research Station, National Institute of Animal Health (NIAH), National Agriculture and Food Research Organization (NARO), Sapporo, Hokkaido, Japan.
Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Morioka, Iwate, Japan.
Vet Microbiol. 2019 Feb;229:81-89. doi: 10.1016/j.vetmic.2018.12.017. Epub 2018 Dec 21.
Five mutations involved in changing of susceptibility to lincosamides and/or macrolides were investigated in field isolates of Mycoplasma californicum in Japan, and reconfirmed in laboratory-derived mutants. In addition, a quick and easy detection method for these mutations was established. Guanine at position 748 (Escherichia coli numbering) of the 23S rRNA gene (rrl) was shown to be involved with decreased susceptibility to 16-membered macrolides, and adenines at positions 2059 and 2062 of rrl were involved with decreased susceptibility to both lincosamides and macrolides. Both guanine at position 2576, and change from cytosine to thymine at position 2611 of rrl were found to be involved with decreased susceptibility to lincosamides, and the latter mutation also increased the susceptibility to erythromycin. These mutations were easily induced by several to approximately 30 passages in a medium containing the respective antimicrobial, but they did not return after their initial appearance. The melting curve analysis using hybridization probes revealed the existence of these mutations by the change in the melting curve shape and/or decrease in the melting peak temperature. The detection limit in milk samples with a somatic cell count up to 716 × 10 cell/mL was 133 cfu/mL, but an excessive increase in the cell count in milk or storage of the milk sample at chilling or freezing temperature decreased the sensitivity. This method requires only a few hours, so field veterinarians can make a same-day determination of susceptibility to macrolides and lincosamides, which are first-line antibiotics for bovine mycoplasmal mastitis.
在日本加利福尼亚支原体的田间分离株中研究了与林可酰胺类和/或大环内酯类药敏性变化相关的5种突变,并在实验室衍生的突变体中得到再次确认。此外,还建立了一种快速简便的这些突变的检测方法。结果表明,23S rRNA基因(rrl)第748位(大肠杆菌编号)的鸟嘌呤与对16元大环内酯类药物敏感性降低有关,rrl第2059位和第2062位的腺嘌呤与对林可酰胺类和大环内酯类药物敏感性降低有关。发现rrl第2576位的鸟嘌呤以及第2611位从胞嘧啶到胸腺嘧啶的变化与对林可酰胺类药物敏感性降低有关,后一种突变还增加了对红霉素的敏感性。这些突变在含有相应抗菌药物的培养基中传代几次至约30代后很容易诱导产生,但首次出现后不会恢复。使用杂交探针的熔解曲线分析通过熔解曲线形状的变化和/或熔解峰温度的降低揭示了这些突变的存在。体细胞计数高达716×10细胞/mL的牛奶样品中的检测限为133 cfu/mL,但牛奶中细胞计数的过度增加或牛奶样品在冷藏或冷冻温度下储存会降低灵敏度。该方法仅需几个小时,因此现场兽医可以在同一天确定对大环内酯类和林可酰胺类药物的敏感性,这两类药物是治疗牛支原体性乳腺炎的一线抗生素。