Powles M A, McFadden D C, Pittarelli L A, Schmatz D M
Department of Biochemical Parasitology, Merck Sharp & Dohme Research Laboratories, Rahway, New Jersey 07065.
Infect Immun. 1992 Apr;60(4):1397-400. doi: 10.1128/iai.60.4.1397-1400.1992.
Animal models for Pneumocystis carinii, for the most part, have been limited to immunosuppressed rats and ferrets, while a dependable mouse model has been more difficult to develop. A P. carinii mouse model has now been established with several strains of mice, including C3Heb/FeJ, C3HeN, BALB/c, DBA/2N, and BALB/c nu/nu (athymic). In lieu of using invasive methods for initiating P. carinii infections, mice harboring P. carinii transmitted the disease to mice without latent infection via short-term cohabitation. After the exposure period, the seed mice were sacrificed to confirm the presence of acute P. carinii pneumonia. Acute infections in recipient mice developed at approximately 7 to 8 weeks, while control unseeded littermates remained uninfected. All recipient mice and their littermates were maintained in isolation hoods to eliminate the possibility of exposure to other sources of P. carinii. This approach allows investigators to consistently transmit P. carinii to mice and to select the strain of mouse desired for use in a particular study. The results presented here suggest that more attention should be given to the potential for patient-to-patient transmission of P. carinii in immunocompromised patients such as those with AIDS.
卡氏肺孢子虫的动物模型,在很大程度上,一直局限于免疫抑制的大鼠和雪貂,而可靠的小鼠模型则更难建立。目前已利用包括C3Heb/FeJ、C3HeN、BALB/c、DBA/2N和BALB/c nu/nu(无胸腺)在内的几种小鼠品系建立了卡氏肺孢子虫小鼠模型。代替使用侵入性方法引发卡氏肺孢子虫感染,携带卡氏肺孢子虫的小鼠通过短期同居将疾病传播给没有潜伏感染的小鼠。在暴露期过后,将接种小鼠处死以确认急性卡氏肺孢子虫肺炎的存在。受体小鼠的急性感染在大约7至8周时出现,而未接种的对照同窝小鼠仍未感染。所有受体小鼠及其同窝小鼠都饲养在隔离罩中,以消除接触卡氏肺孢子虫其他来源的可能性。这种方法使研究人员能够持续地将卡氏肺孢子虫传播给小鼠,并选择特定研究中所需的小鼠品系。此处呈现的结果表明,对于卡氏肺孢子虫在免疫受损患者(如艾滋病患者)中患者间传播的可能性,应给予更多关注。