Hamrick Terri S, Horton John R, Spears Patricia A, Havell Edward A, Smoak Ida W, Orndorff Paul E
College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina 27606, USA.
Infect Immun. 2003 Sep;71(9):5202-9. doi: 10.1128/IAI.71.9.5202-5209.2003.
Pregnancy increases the risk of listeriosis, a systemic disease caused by Listeria monocytogenes. However, there is incomplete agreement on the reasons for this increased risk. We examined two features of listeriosis in gravid and nongravid female mice following intragastric (gavage) inoculation, namely, (i) disease severity (measured by lethality) and (ii) listerial infectivity (measured by liver and spleen colonization levels up to 120 h postinoculation). Two listerial strains of differing serotype (1/2a and 4nonb) were initially employed. Neither strain produced a lethal infection in nonpregnant female mice (dose range, 10(6) to 10(9) CFU/mouse), and only the 4nonb strain produced lethalities in pregnant mice (dose range, 10(6) to 10(8) CFU/mouse). The 4nonb strain also produced a higher level of liver and spleen colonization than the 1/2a strain following gavage administration. (The two strains showed similar levels of colonization if parenterally administered.) Both strains were equally capable of binding to and forming plaques upon cultured mouse enterocytes. The ability of the 4nonb strain to produce a lethal infection in pregnant animals did not correlate with an increased incidence or level of liver and spleen colonization over that in nonpregnant females. However, the lethality rate did correlate well with the rate at which embryos and their surrounding decidual covering became infected, suggesting that intrauterine infection could be responsible for the increased disease severity in the gravid females.
怀孕会增加患李氏杆菌病的风险,这是一种由单核细胞增生李斯特菌引起的全身性疾病。然而,对于这种风险增加的原因,目前尚未完全达成共识。我们在妊娠和非妊娠雌性小鼠经胃内(灌胃)接种后,研究了李氏杆菌病的两个特征,即:(i)疾病严重程度(通过致死率衡量)和(ii)李斯特菌感染性(通过接种后120小时内肝脏和脾脏的定植水平衡量)。最初使用了两种不同血清型的李斯特菌菌株(1/2a和4nonb)。两种菌株在未怀孕的雌性小鼠中均未引起致死性感染(剂量范围为10⁶至10⁹CFU/小鼠),只有4nonb菌株在怀孕小鼠中引起了致死性感染(剂量范围为10⁶至10⁸CFU/小鼠)。灌胃给药后,4nonb菌株在肝脏和脾脏中的定植水平也高于1/2a菌株。(如果采用胃肠外给药,两种菌株的定植水平相似。)两种菌株在培养的小鼠肠上皮细胞上结合并形成噬菌斑的能力相同。4nonb菌株在怀孕动物中引起致死性感染的能力与未怀孕雌性动物相比,肝脏和脾脏定植的发生率或水平增加无关。然而,致死率确实与胚胎及其周围蜕膜覆盖物被感染的速率密切相关,这表明子宫内感染可能是导致妊娠雌性动物疾病严重程度增加的原因。