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测定感染牛白血病病毒的患淋巴细胞增多症和未患淋巴细胞增多症牛的前病毒载量。

Determination of proviral load in bovine leukemia virus-infected cattle with and without lymphocytosis.

作者信息

Juliarena Marcela A, Gutierrez Silvina E, Ceriani Carolina

机构信息

Laboratorio de Virologia, Departamento de Sanidad Animal y Medicina Preventiva, Facultad de Veterinaria, Universidad Nacional del Centro de la Provincia de Buenos Aires, Pinto 399, Tandil, Argentina.

出版信息

Am J Vet Res. 2007 Nov;68(11):1220-5. doi: 10.2460/ajvr.68.11.1220.

Abstract

OBJECTIVE

To determine proviral load in bovine leukemia virus (BLV)-infected cattle with and without persistent lymphocytosis to assess the potential of transmitting the virus.

ANIMALS

Cattle in 6 dairy herds.

PROCEDURES

Blood samples from infected cows were evaluated 3 times at 6-month intervals for determination of proviral load via PCR assay, serologic results via ELISA, and hematologic status via differential cell counts.

RESULTS

Infected cattle were classified into lymphocytotic and nonlymphocytotic groups. Lymphocytotic cattle consistently had > 100,000 copies of integrated provirus/mug of DNA (ie, high proviral load) in peripheral blood leukocytes. Titers of antibodies against BLVgp51 and BLVp24 indicated a strong immune response. Nonlymphocytotic cattle comprised 2 subgroups: a group with high proviral load and strong immune response, and a group with a weaker immune response, mostly against BLVp24, and a proviral load of < 100 copies/microg of DNA (ie, low proviral load).

CONCLUSIONS AND CLINICAL RELEVANCE

Results emphasized the importance of characterizing nonlymphocytotic BLV-infected cattle during eradication programs. The risk of transmitting BLV infection from nonlymphocytotic cattle may differ depending on the proviral load. Nonlymphocytotic cattle with high proviral load could be efficient transmitters (as efficient as lymphocytotic cattle), whereas nonlymphocytotic cattle with low proviral load could be inefficient transmitters under standard husbandry conditions. Because most cattle with low proviral load do not develop anti-BLVp24 antibodies, it appears that lack of an anti-BLVp24 antibody response may be a good marker of this condition.

摘要

目的

确定感染牛白血病病毒(BLV)且伴有或不伴有持续性淋巴细胞增多症的牛的前病毒载量,以评估病毒传播的可能性。

动物

6个奶牛群中的牛。

程序

对感染奶牛的血样每隔6个月评估3次,通过聚合酶链反应(PCR)测定前病毒载量,通过酶联免疫吸附测定(ELISA)检测血清学结果,通过细胞分类计数评估血液学状态。

结果

感染牛被分为淋巴细胞增多组和非淋巴细胞增多组。淋巴细胞增多的牛外周血白细胞中整合前病毒始终>100,000拷贝/μg DNA(即高前病毒载量)。抗BLVgp51和BLVp24抗体的滴度表明有强烈的免疫反应。非淋巴细胞增多的牛包括2个亚组:一个亚组前病毒载量高且免疫反应强烈,另一个亚组免疫反应较弱,主要针对BLVp24,前病毒载量<100拷贝/μg DNA(即低前病毒载量)。

结论及临床意义

结果强调了在根除计划中对非淋巴细胞增多的BLV感染牛进行特征描述的重要性。非淋巴细胞增多的牛传播BLV感染的风险可能因前病毒载量而异。前病毒载量高的非淋巴细胞增多的牛可能是高效传播者(与淋巴细胞增多的牛一样高效),而在前病毒载量低的标准饲养条件下,非淋巴细胞增多的牛可能是低效传播者。由于大多数前病毒载量低的牛不产生抗BLVp24抗体,因此缺乏抗BLVp24抗体反应似乎可能是这种情况的一个良好标志。

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