Chang Y F, Renshaw H W, Young R
Am J Vet Res. 1987 Mar;48(3):378-84.
Plasmid DNA screening experiments were conducted to determine whether a relationship existed between the presence of plasmids and antibiotic resistance in Pasteurella haemolytica or the capability to produce hemolysin or leukotoxin (cytotoxin). Regardless of plasmid content, all P haemolytica isolates produced characteristic hemolysis on blood agar plates. Similarly, standardized suspensions of living bacteria and sterile concentrated (approx 200:1) culture supernatant from strains representing each of the 15 recognized P haemolytica serotypes and 7 field strains of P haemolytica (biotype A, serotype 1) produced leukotoxin, which was detected by their capability to cause inhibition of the luminol-dependent chemiluminescence response of bovine neutrophils. However, neither living bacterial suspensions nor concentrated culture supernatant from 4 untypable P haemolytica strains or a P multocida strain caused an inhibition of the luminol-dependent chemiluminescence response. The production of neither hemolysin nor leukotoxin by P haemolytica seemed to be plasmid mediated. Leukotoxin production is apparently a stable phenotypic characteristic of pathogenic P haemolytica strains, and the gene(s) coding for this activity is probably located on the bacterial host chromosome. Antibiotic susceptibility profiles were determined for the different bacterial strains. Studies of ampicillin and penicillin resistance in 8 P haemolytica (biotype A, serotype 1) strains provided evidence that the plasmid, with size of approximately 5,200 base pairs, may code for their resistance to these compounds.
进行了质粒DNA筛选实验,以确定溶血巴斯德氏菌中质粒的存在与抗生素抗性之间是否存在关系,或者与产生溶血素或白细胞毒素(细胞毒素)的能力之间是否存在关系。无论质粒含量如何,所有溶血巴斯德氏菌分离株在血琼脂平板上均产生特征性溶血。同样,来自代表15种公认的溶血巴斯德氏菌血清型中的每一种的菌株以及7株溶血巴斯德氏菌(生物型A,血清型1)的田间菌株的活细菌标准化悬浮液和无菌浓缩(约200:1)培养上清液均产生白细胞毒素,可通过它们抑制牛中性粒细胞的鲁米诺依赖性化学发光反应的能力来检测。然而,来自4株无法分型的溶血巴斯德氏菌菌株或一株多杀巴斯德氏菌菌株的活细菌悬浮液或浓缩培养上清液均未引起鲁米诺依赖性化学发光反应的抑制。溶血巴斯德氏菌产生溶血素和白细胞毒素似乎均不是由质粒介导的。白细胞毒素的产生显然是致病性溶血巴斯德氏菌菌株的一个稳定表型特征,编码这种活性的基因可能位于细菌宿主染色体上。测定了不同细菌菌株的抗生素敏感性谱。对8株溶血巴斯德氏菌(生物型A,血清型1)菌株的氨苄青霉素和青霉素抗性研究提供了证据,表明大小约为5200个碱基对的质粒可能编码它们对这些化合物的抗性。