Dipartimento di Patologia Animale, Igiene e Sanità Pubblica Veterinaria, Università degli Studi di Milano, Via Celoria 10, Milan, Italy.
Vet Parasitol. 2010 Aug 27;172(1-2):160-3. doi: 10.1016/j.vetpar.2010.04.027. Epub 2010 Apr 28.
Dirofilaria immitis and Dirofilaria repens are the most common species of filarial nematodes described in the dogs with increasing spread into new geographical areas. The diagnosis of canine dirofilariosis is usually based upon the microscopical detection and identification of circulating microfilariae together with ELISA detection of serum circulating heartworm antigens or antibodies. The identification of the parasite species using the traditional approaches sometimes can be difficult and can lead to misdiagnosis especially on samples from areas where both Dirofilaria are present. In this paper we report a new molecular method based on single-step multiplex PCR to detect and differentiate simultaneously and unequivocally D. immitis and D. repens on DNA extracted from canine peripheral blood. The amplification was performed using a set of primers designed on a portion of the small subunit ribosomal RNA gene of the mitochondrion (12S rDNA). The single-step multiplex PCR here described ensured high (4 mf/ml) sensitivity and specificity with reduced cost and time saving. The multiplex PCR assay represents an additional tool for epidemiological studies and routine disease assessment in areas co-endemic for the two Dirofilaria species.
犬恶丝虫属的犬恶丝虫和 Repens 是在狗中描述的最常见的丝虫种类,其传播范围逐渐扩大到新的地理区域。犬恶丝虫病的诊断通常基于对循环微丝蚴的显微镜检测和鉴定,以及对血清循环心丝虫抗原或抗体的 ELISA 检测。使用传统方法鉴定寄生虫种类有时可能很困难,并可能导致误诊,特别是在同时存在两种犬恶丝虫的地区的样本中。在本文中,我们报告了一种新的分子方法,基于一步多重 PCR 检测并区分犬外周血提取的 DNA 中的犬恶丝虫和 Repens。扩增使用一组设计在线粒体(12S rDNA)小亚基核糖体 RNA 基因的一部分上的引物进行。本文描述的一步多重 PCR 确保了高(4 mf/ml)灵敏度和特异性,同时降低了成本和节省了时间。多重 PCR 检测方法代表了在两种犬恶丝虫种流行地区进行流行病学研究和常规疾病评估的另一种工具。