Barrow P A, Lovell M A
AFRC Institute for Animal Health, Houghton Laboratory, Huntingdon, Cambridgeshire, UK.
J Gen Microbiol. 1988 Aug;134(8):2307-16. doi: 10.1099/00221287-134-8-2307.
Eight strains of Salmonella pullorum isolated from epidemiologically independent cases of pullorum disease (bacillary white diarrhoea) in young chickens possessed at least one large molecular mass plasmid in addition to smaller molecular mass plasmids. The 85 kb large plasmid, designated pBL001, of one of these strains was 'tagged' with an ampicillin resistance marker by the insertion of transposon Tn3. The plasmid was eliminated by passage in nutrient broth containing acridine orange. It was reintroduced into the strain from which it had been eliminated by mobilization using the F plasmid. Following oral inoculation of newly hatched Rhode Island Red chickens, the parent strain produced a high level of mortality (71%) with characteristic signs of pullorum disease. Following intramuscular inoculation of chickens of the same age, the bacterial LD50 was (log10 c.f.u.) 3.38 +/- 0.43 (mean +/- SEM). The derivative lacking pBL001 produced no mortality or morbidity when inoculated orally and the bacterial LD50 value increased to (log10 c.f.u.) 5.54 +/- 0.28. This increase was statistically significant (chi 2 = 13.6, P less than 0.01). Reintroduction of pBL001 restored virulence as gauged by oral inoculation of chickens (62% mortality) and by the intramuscular bacterial LD50 value (log10 c.f.u. = 3.78 +/- 0.25). These values were not significantly different to those produced by the parent strain (chi 2 = 0.59, P = 0.4 and chi 2 = 0.66, P = 0.5, respectively). Following oral inoculation, the pBL001-cured derivative was less invasive than the parent strain and following intramuscular inoculation it persisted for a shorter period than the parent strain in the liver, spleen and the leg muscle into which it had been inoculated. In addition, the parent strain, but not the pBL001-cured derivative, localized in large numbers in the myocardium where it produced lesions typical of pullorum disease. Both the parent strain and the pBL001-cured derivative were serum resistant in the presence of rabbit serum and grew equally well in chick serum and broth.
从流行病学上独立的幼鸡白痢病例(细菌性白痢)中分离出的8株鸡白痢沙门氏菌,除了具有较小分子量的质粒外,还至少拥有一个大分子量质粒。其中一株菌株的85 kb大质粒,命名为pBL001,通过转座子Tn3的插入用氨苄青霉素抗性标记进行了“标记”。该质粒在含有吖啶橙的营养肉汤传代培养后被消除。通过使用F质粒进行转移,将其重新导入已被消除该质粒的菌株中。给新孵化的罗德岛红鸡口服接种后,亲本菌株产生了高水平的死亡率(71%),并伴有白痢病的特征性症状。给同年龄的鸡进行肌肉注射接种后,细菌的半数致死剂量(log10 c.f.u.)为3.38±0.43(平均值±标准误)。缺乏pBL001的衍生菌株口服接种后未产生死亡或发病情况,细菌半数致死剂量值增加到(log10 c.f.u.)5.54±0.28。这种增加具有统计学意义(χ2 = 13.6,P<0.01)。通过给鸡口服接种(死亡率62%)以及肌肉注射细菌半数致死剂量值(log10 c.f.u. = 3.78±0.25)来衡量,重新导入pBL001恢复了毒力。这些值与亲本菌株产生的值没有显著差异(χ2分别为0.59,P = 0.4和χ2为0.66,P = 0.5)。口服接种后,缺失pBL001的衍生菌株比亲本菌株的侵袭性小,肌肉注射接种后,它在接种的肝脏、脾脏和腿部肌肉中持续存在的时间比亲本菌株短。此外,亲本菌株而非缺失pBL001的衍生菌株大量定位于心肌,在那里产生了白痢病典型的病变。亲本菌株和缺失pBL001的衍生菌株在兔血清存在下均具有血清抗性,并且在鸡血清和肉汤中生长情况相同。