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汉赛巴尔通体血液传播给猫后出现复发性菌血症。

Relapsing bacteremia after blood transmission of Bartonella henselae to cats.

作者信息

Kordick D L, Breitschwerdt E B

机构信息

Department of Companion Animal and Special Species Medicine, College of Veterinay Medicine, North Carolina State University, Raleigh 27606, USA.

出版信息

Am J Vet Res. 1997 May;58(5):492-7.

PMID:9140557
Abstract

OBJECTIVES

To determine persistence of bacteremia, pathogenicity, and immunoglobulin kinetics after blood transmission of Bartonella henselae in cats.

ANIMALS

18 specific-pathogen-free (SPF) cats (16 weeks old) received blood or urine from 4 adult cats (2 SPF, 2 naturally infected with B henselae).

PROCEDURE

SPF cats were inoculated with blood IV (n = 4), blood IM (n = 4), or urine sediment IM (n = 4) from 2 bacteremic cats (donors A and B). Control cats (2/route) received inoculum from culture-negative, seronegative SPF cats (donors C and D).

RESULTS

6 cats (5 blood, 1 urine) were transiently febrile during the 213-day observation period. Two bacteremic cats developed CNS abnormalities. Transient anemia was the only hematologic abnormality. Bacteremia was induced in 7 of 8 blood recipients by postinoculation day (PID) 11. Urine recipients (n = 6) did not become bacteremic or seroconvert by PID 108, but when challenge exposed IV with blood, 4 of 6 became infected. All infected cats developed relapsing bacteremia. Initially, colony counts for donor-A recipients were 10(3) greater than those for donor-B recipients; however, during relapses, counts were similar. Polymerase chain reaction-restriction fragment length polymorphism analysis of 16S rRNA gene and the intergenic spacer region revealed no differences among isolates derived from recipient cats. Bartonella henselae-specific antibodies were detected between PID 15 and 18 in donor-A, compared with PID 46 and 181 in donor-B recipients. The peak geometric mean titer of donor-A recipients was 1,448, versus 406 for donor-B recipients.

CONCLUSIONS AND CLINICAL RELEVANCE

Blood transmission of B henselae induced subtle clinical abnormalities; the biological behavior of the 2 donor strains differed; and relapsing bacteremia can persist in conjunction with variably high antibody titers.

摘要

目的

确定猫经血液传播亨氏巴尔通体后菌血症的持续时间、致病性及免疫球蛋白动力学。

动物

18只16周龄的无特定病原体(SPF)猫接受了来自4只成年猫(2只SPF猫、2只自然感染亨氏巴尔通体的猫)的血液或尿液。

步骤

将2只菌血症猫(供体A和B)的血液经静脉接种(n = 4)、肌肉接种(n = 4)或尿液沉淀物经肌肉接种(n = 4)到SPF猫体内。对照猫(每种接种途径2只)接受来自培养阴性、血清学阴性的SPF猫(供体C和D)的接种物。

结果

在213天的观察期内,6只猫(5只接种血液,1只接种尿液)出现短暂发热。2只菌血症猫出现中枢神经系统异常。短暂贫血是唯一的血液学异常。8只接受血液接种的猫中有7只在接种后第11天(PID 11)出现菌血症。接受尿液接种的猫(n = 6)在PID 108时未出现菌血症或血清转化,但当经静脉用血液进行激发暴露时,6只中有4只被感染。所有感染猫均出现复发性菌血症。最初,供体A接种猫的菌落计数比供体B接种猫高10³ ;然而,在复发期间,计数相似。对16S rRNA基因和基因间隔区进行聚合酶链反应-限制性片段长度多态性分析,结果显示来自受体猫的分离株之间无差异。供体A接种猫在PID 15至18之间检测到亨氏巴尔通体特异性抗体,而供体B接种猫则在PID 46和181时检测到。供体A接种猫的几何平均滴度峰值为1448,而供体B接种猫为406。

结论及临床意义

亨氏巴尔通体经血液传播可引发轻微临床异常;两种供体菌株的生物学行为存在差异;复发性菌血症可与不同程度的高抗体滴度同时存在。

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