牛角膜结膜炎支原体和病毒感染的研究

Parham Mottaghian, Afshin Raoofi, Omid Madadgar, Arya Badiei, Iradj Ashrafi Tamai
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引用次数: 1

摘要

背景:传染性牛角膜结膜炎(IBK或“红眼”)是全世界牛中最常见的传染性眼病。除了牛莫拉菌是主要病原体外,传染性牛鼻气管炎病毒(BHV-1)和支原体物种可能是IBK的危险因素。目的:探讨支原体、牛疱疹病毒1型(BHV-1)和牛病毒性腹泻病毒(BVDV)在眼结膜囊中的检测与IBK的关系。方法:采用聚合酶链反应(PCR)检测ibk感染和健康眼标本中的支原体sp、BHV-1和BVDV。结果:根据PCR结果,支原体在ibk病眼和健康眼的检出率分别为63.6%和47.2%。感染眼和健康眼的BHV-1检出率分别为59.1%和36.1%。病眼和健康眼的BVDV检出率分别为65.9%和58.3%。BHV-1是唯一与IBK病变显著(P<0.05)相关的药物(从59.1%的受影响眼睛和36.1%的健康眼睛中分离)。结论:根据研究结果,BHV-1可能是感染性牛角膜结膜炎发病的危险因素,其致病机制可能与免疫抑制以外的机制有关。
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A Study on Mycoplasmal and Viral Infections in Bovine Keratoconjunctivitis
Background: Infectious bovine keratoconjunctivitis (IBK or “pink eye”) is the most common infectious ocular disease in cattle worldwide. In addition to Moraxella bovis as the principal causative agent, infectious bovine rhinotracheitis virus (BHV-1) and Mycoplasma species probably act as risk factors for IBK. Objectives: This study aimed to evaluate the association between the detection of Mycoplasma sp., bovine herpesvirus 1 (BHV-1), and bovine viral diarrhea virus (BVDV) in the conjunctival sac of the eye and IBK. Methods: Polymerase chain reaction (PCR) was employed to detect Mycoplasma sp., BHV-1, and BVDV in samples collected from IBK-affected and healthy eyes. Results: Based on the PCR results, Mycoplasma sp. was detected in 63.6% and 47.2% of IBK-affected and healthy eyes, respectively. BHV-1 was detected in 59.1% and 36.1% of affected and healthy eyes, respectively. BVDV was detected in 65.9% and 58.3% of affected and healthy eyes, respectively. BHV-1 was the only agent significantly (P<0.05) associated with IBK lesions (isolated from 59.1% of affected vs 36.1% of healthy eyes). Conclusion: Based on the study results, BHV-1 may be a risk factor in the pathogenesis of infectious bovine keratoconjunctivitis, and mechanisms other than immune depression might be involved in its pathogenicity.
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来源期刊
Iranian Journal of Veterinary Medicine
Iranian Journal of Veterinary Medicine Veterinary-General Veterinary
CiteScore
0.90
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0.00%
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0
审稿时长
6 weeks
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