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B细胞缺陷小鼠中卡氏肺孢子虫和嗜肺巴斯德杆菌的双重感染:诊断与治疗

Dual infection with Pneumocystis carinii and Pasteurella pneumotropica in B cell-deficient mice: diagnosis and therapy.

作者信息

Macy J D, Weir E C, Compton S R, Shlomchik M J, Brownstein D G

机构信息

Yale University School of Medicine, New Haven, Connecticut, USA.

出版信息

Comp Med. 2000 Feb;50(1):49-55.

Abstract

BACKGROUND AND PURPOSE

The clinical presentation, diagnosis, histopathologic findings, and elimination of dual respiratory tract infection with Pasteurella pneumotropica and Pneumocystis carinii were studied in 100 adult barrier-reared C.B17 and MRL- lpr mice homozygous for a targeted mutation of the JH region of the immunoglobulin heavy chain.

METHODS

Necropsy, aerobic bacteriologic culture of hematogenous and pulmonary tissues, histochemical staining of pulmonary tissues, polymerase chain reaction analysis of pulmonary tissues and feces, and viral serologic testing were performed on 19 clinically affected mice and 8 clinically normal mice, then later on antibiotic-treated and caesarian re-derived mice. Therapeutic strategies included sequential administration of trimethoprim/ sulfamethoxazole and enrofloxacin or enrofloxacin administration and caesarian rederivation.

RESULTS

Clinically affected mice had diffuse, nonsuppurative, interstitial pneumonia with superimposed pyogranulomatous lobar pneumonia that was detected microscopically. Affected lung tissue yielded pure culture of P. pneumotropica. Aged-matched, clinically normal mice of both genotypes had interstitial histiocytic pneumonia without lobar pneumonia, and P. pneumotropica was not isolated. Histochemical staining of lung tissues from normal and clinically affected mice revealed scattered cysts consistent with P. carinii, principally in the interstitium. Treatment with sulfamethoxazole/trimethoprim and enrofloxacin eliminated bacteriologic detection of P. pneumotropica, decreased mortality from 50% to 6%, and improved breeding performance.

CONCLUSION

A successful antibiotic therapy and rederivation approach, incorporating enrofloxacin, cesarian section, and isolator rearing, was developed for B cell-deficient mice with opportunistic infections.

摘要

背景与目的

对100只成年屏障饲养的C.B17和MRL-lpr小鼠进行了研究,这些小鼠因免疫球蛋白重链JH区域的靶向突变而纯合,研究内容包括嗜肺巴斯德杆菌和卡氏肺孢子虫双重呼吸道感染的临床表现、诊断、组织病理学发现及清除情况。

方法

对19只临床患病小鼠和8只临床正常小鼠进行尸检、血源性和肺组织的需氧细菌培养、肺组织的组织化学染色、肺组织和粪便的聚合酶链反应分析以及病毒血清学检测,之后对经抗生素治疗和剖腹产重新繁育的小鼠进行同样检测。治疗策略包括依次给予甲氧苄啶/磺胺甲恶唑和恩诺沙星,或给予恩诺沙星并进行剖腹产重新繁育。

结果

临床患病小鼠在显微镜下可见弥漫性、非化脓性间质性肺炎,伴有叠加的脓性肉芽肿性大叶性肺炎。受影响的肺组织培养出纯的嗜肺巴斯德杆菌。两种基因型的年龄匹配临床正常小鼠有间质性组织细胞性肺炎,无大叶性肺炎,且未分离出嗜肺巴斯德杆菌。正常和临床患病小鼠肺组织的组织化学染色显示有散在的囊肿,与卡氏肺孢子虫一致,主要位于间质。用磺胺甲恶唑/甲氧苄啶和恩诺沙星治疗消除了嗜肺巴斯德杆菌的细菌学检测,死亡率从50%降至6%,并改善了繁殖性能。

结论

针对患有机会性感染的B细胞缺陷小鼠,开发了一种成功的抗生素治疗和重新繁育方法,包括使用恩诺沙星、剖腹产和隔离饲养。

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