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利用皮肤刮屑和皮肤活检对var进行分子检测与特性分析。

Molecular detection and characterization of var using skin scrapings and skin biopsies.

作者信息

Nwufoh Onyeka Chidiebele, Sadiq Nurudeen Ayinde, Fagbohun Olusegun, Adebiyi Adebowale, Adeshina Rofiat, Emmanuel Ekeanyanwu, Emikpe Benjamin Obukowho

机构信息

Department of Veterinary Parasitology, University of Ibadan, Ibadan, Nigeria.

Federal College of Animal Health and Production Technology, Ibadan, Nigeria.

出版信息

J Parasit Dis. 2021 Mar;45(1):258-262. doi: 10.1007/s12639-020-01304-7. Epub 2020 Nov 9.

Abstract

Canine sarcopticosis is a highly infectious and debilitating parasitic skin disease of dogs. Its diagnosis stands challenging as the golden standard of diagnosis; skin scraping microscopy is characterized by several diagnostic variations. Study thus employed several alternate diagnostic approaches using Polymerase Chain Reaction (PCR) on skin scrapings and skin biopsies. Whole var mites, thirty six "3 cm × 3cm" skin scrapings and 3 mm punch biopsies from six different lesioned sites per infested dog were all obtained from six severely sarcoptes ridden dogs. Samples were mechanically disrupted for DNA extraction and amplification. Positive samples were further commercially sequenced. Amongst the thirty six (36) skin biopsy and scraping samples processed, PCR detected the DNA of var in thirty two (32) skin biopsy samples with a sensitivity of 88.88%. Twenty five (25) skin scraping samples were also positive for scabies with a sensitivity of 69.44%. The Phylogenetic analysis revealed a relationship between the var mites from Nigeria and of humans, raccoon dogs and rabbits in Pakistan, Japan and Egypt.  The diagnostic errors and false negatives accompanying the skin microscopy diagnostic technique can best be limited with the use of PCR diagnosis on skin scrapings and skin biopsies most especially. This highly sensitive diagnostic tool would certainly and effectively control the menace of sarcopticosis in dogs.

摘要

犬疥螨病是一种具有高度传染性且会使犬类衰弱的寄生虫性皮肤病。其诊断颇具挑战性,因为作为诊断金标准的皮肤刮片显微镜检查存在多种诊断差异。因此,本研究采用了几种替代诊断方法,对皮肤刮片和皮肤活检样本进行聚合酶链反应(PCR)检测。从六只患有严重疥螨病的犬只身上获取了完整的疥螨、每只感染犬六个不同病变部位的三十六份“3厘米×3厘米”皮肤刮片以及3毫米打孔活检样本。对样本进行机械破碎以提取DNA并进行扩增。对阳性样本进一步进行商业测序。在处理的三十六份皮肤活检和刮片样本中,PCR在三十二份皮肤活检样本中检测到了疥螨的DNA,灵敏度为88.88%。二十五份皮肤刮片样本也呈疥螨阳性,灵敏度为69.44%。系统发育分析揭示了来自尼日利亚的疥螨与巴基斯坦、日本和埃及人类、貉和兔子身上的疥螨之间的关系。尤其是通过对皮肤刮片和皮肤活检样本进行PCR诊断,能够最大程度地减少皮肤显微镜诊断技术伴随的诊断误差和假阴性。这种高度灵敏的诊断工具肯定能有效控制犬疥螨病的威胁。

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