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Dose response of black American mink to Aleutian mink disease virus

机译:黑人貂皮貂的剂量反应到阿列丁貂病病毒

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Introduction Aleutian mink disease virus (AMDV) causes a serious health problem for mink globally. The disease has no cure nor an effective vaccine and selection for tolerance using antibody titer is adopted by many mink farmers. The objective of this study was to investigate the effects of various doses of a local AMDV isolate on the response of black American mink to infection with AMDV. Methods Eight black American mink were each inoculated intranasally with 0.5?mL of eight serial 10‐fold dilutions (100 to 10?7) of a 10% spleen homogenate containing a local AMDV isolate. Blood samples were collected on days 0, 20, 35, 56, 84, 140, and 196 postinoculation (dpi). Anti‐AMDV antibodies and viral DNA were tested by counter‐immunoelectrophoresis (CIEP) and PCR, respectively. Animals that were PCR or CIEP positive at 196 dpi (n?=?41) were killed at 218 dpi, and samples of blood and seven organs were tested by CIEP and PCR. Results Antibody production persisted in all seroconverted mink until the termination of the experiment, whereas 71.1% of the mink showed short‐lived viremia. Significant associations were observed between inoculum dose and the incidence of viremia until 84 dpi which disappeared thereafter, whereas associations between inoculum dose and the incidence of seropositive mink were significant on all sampling occasions. Antibody titer at 218 dpi significantly decreased with decreasing inoculum dose. AMDV DNA was detected in the bone marrow, lymph nodes, and spleen samples of almost all mink inoculated at every dose but was not detected in other organs of some mink. Conclusions CIEP is more accurate than PCR for detecting AMDV infection in mink. Using antibody titer in naturally infected mink may not be accurate for the identification of tolerant mink.
机译:引言Aleutian Mink疾病病毒(AMDV)在全球貂皮中造成严重的健康问题。许多貂儿农民采用该疾病没有固化,也没有有效的疫苗和有效的耐受性耐受性耐受性。本研究的目的是探讨各种剂量局部AMDV分离物对黑人美国貂蝉对AMDV感染的影响的影响。方法八种黑色美国貂皮各自接种鼻内鼻内鼻内含有0.5×ml的含有局部AMDV分离物的10%脾均匀的八个连续10倍稀释液(100至10→7)。在第0,20,35,56,84,140和196天划分(DPI)上收集血样。通过反免疫电泳(CIEP)和PCR检测抗AMDV抗体和病毒DNA。在196 dpi(n?= 41)的PCR或CIEP阳性的动物在218dPI中丧生,并通过CIEP和PCR测试血液和七个器官的样品。结果抗体产量持续存在于所有血清转化的貂皮中,直至终止实验,而71.1%的貂皮显示出短叶病毒血症。在接种剂量和病毒血症的发生率之间观察到显着的关联,直到此后消失的84 dPI,而锯齿状剂量的关联和血清阳性水貂的发生率在所有取样场合都很重要。随着接种剂量减少,218 dpi的抗体滴度显着降低。在骨髓,淋巴结和脾脏样品中检测到AMDV DNA,几乎所有貂皮的脾样品在每种剂量上接种,但在一些貂皮的其他器官中未检测到。结论CIEP比PCR更准确,用于检测貂皮中的AMDV感染。在天然感染的貂皮中使用抗体滴度可能对耐受貂皮鉴定可能不准确。

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