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使用由边缘无浆体雅博蒂卡巴尔菌株制备的DNA疫苗(pcDNA3.1/MSP1b)对牛进行免疫接种。

Immunization of bovines using a DNA vaccine (pcDNA3.1/MSP1b) prepared from the Jaboticabal strain of Anaplasma marginale.

作者信息

de Andrade G M, Machado R Z, Vidotto M C, Vidotto O

机构信息

Universidade Estadual Paulista-UNESP, Jaboticabal, SP, Brazil.

出版信息

Ann N Y Acad Sci. 2004 Oct;1026:257-66. doi: 10.1196/annals.1307.040.

Abstract

Anaplasma is a tick-borne ehrlichial pathogen of cattle that causes the disease, anaplasmosis. In the present study, a total of 11 Anaplasma marginale seronegative calves were assigned into two groups: one immunized (G1, n = 6) and one nonimmunized-control (G2, n = 5). Six calves were immunized by using a DNA vaccine containing the gene of a major surface protein, MSP1b, encoded by the plasmid identified as pcDNA3.1/MSP1b. Calves received three intramuscular inoculations of 100 microg of pcDNA3.1/MSP1b at a 20-day interval. The control group received buffer phosphate at the same schedule as the experimental group. The immune response elicited by immunization with pcDNA3.1/MSP1b was evaluated in mice and calves. Twenty days following initial immunization, specific serum antibody from four BALB/c mice bound MSP1b in immunoblots. Sixty days after the last immunization, all calves were challenged with cryopreserved A. marginale at a dose of 10(4) parasites/mL/animal by intravenous injection. Results of packed cell volume (PCV) and detection of infected erythrocytes in all experimental groups revealed that the decrease of PCV and detection of infected erythrocytes occurred at 28 to 42 days after challenge. Mean temperature values did not increase over 39.85 degrees C. Antibodies developed by immunized bovines from G2 were detected 14 days after challenge. MSP1b was characterized during the immunization period and MSP2 was the most predominant polypeptide at the challenge period. DNA of A. marginale was detected in all groups just after challenge by nested PCR assay. It can be concluded that all immunized bovines were partially protected against homologous challenge.

摘要

无形体是一种通过蜱传播的牛埃立克体病原体,可引发无浆体病。在本研究中,总共11头无浆体边缘种血清阴性的小牛被分为两组:一组进行免疫(G1,n = 6),另一组为未免疫的对照组(G2,n = 5)。6头小牛通过使用一种DNA疫苗进行免疫,该疫苗包含由鉴定为pcDNA3.1/MSP1b的质粒编码的主要表面蛋白MSP1b的基因。小牛每隔20天接受三次100微克pcDNA3.1/MSP1b的肌肉注射。对照组按照与实验组相同的时间表接受磷酸盐缓冲液。用pcDNA3.1/MSP1b免疫引发的免疫反应在小鼠和小牛中进行了评估。初次免疫后20天,来自4只BALB/c小鼠的特异性血清抗体在免疫印迹中与MSP1b结合。最后一次免疫后60天,所有小牛通过静脉注射以10(4)个寄生虫/毫升/动物的剂量接受冷冻保存的边缘无浆体的攻击。所有实验组的血细胞压积(PCV)结果和感染红细胞的检测显示,PCV的下降和感染红细胞的检测在攻击后28至42天出现。平均体温值未超过39.85摄氏度。G2组免疫牛产生的抗体在攻击后14天被检测到。在免疫期间对MSP1b进行了表征,在攻击期间MSP2是最主要的多肽。攻击后立即通过巢式PCR检测在所有组中都检测到了边缘无浆体DNA。可以得出结论,所有免疫牛都受到了部分保护,免受同源攻击。

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