Gawor Jakub, Gawor Jan, Gromadka Robert, Zwijacz-Kozica Tomasz, Zięba Filip
Witold Stefański Institute of Parasitology, Polish Academy of Sciences, Twarda 51/55, 00-818, Warsaw, Poland.
Laboratory of DNA Sequencing and Oligonucleotide Synthesis, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawińskiego 5a, 02-106, Warsaw, Poland.
Parasitol Res. 2017 Dec;116(12):3447-3452. doi: 10.1007/s00436-017-5660-2. Epub 2017 Oct 27.
Baylisascaris transfuga is a roundworm that has been reported worldwide in most bear species. In mammals and possibly humans, the larvae of B. transfuga can migrate in the tissues of aberrant hosts with larva migrans syndrome. The current study was performed to identify B. transfuga in faecal samples from free-ranging brown bears in the Tatra Mountains National Park in southern Poland. A commercial kit was used to extract genomic DNA directly from faecal samples. Additionally, a Chelex resin-based technique was successfully implemented to prepare a PCR template from eggs retrieved by flotation. Based on the flotation results of 32 collected faecal samples, the prevalence of B. transfuga was 15.6%. The parasite was confirmed in samples found to be positive during the initial flotation by a molecular assay using DNA isolated directly from faeces. The retrieved eggs were confirmed as B. transfuga after their DNA was extracted using the Chelex protocol. Based on PCR amplification and sequencing of a 413-bp segment of cytochrome c oxidase 1 (COI), the obtained sequence was 100% identical to the COI segment of B. transfuga after a BLAST comparison to the GenBank™ database. The current study includes the first molecular confirmation of B. transfuga in brown bears in the western part of the Carpathians. We show that direct extraction of parasite DNA from bear faeces is efficient for molecular assays. As an alternative, we present the effectiveness of a Chelex-based technique for fast and convenient DNA isolation from the difficult-to-disrupt eggs of B. transfuga for PCR. Molecular tests of parasite DNA extracted directly from faecal material have limits of detection related to the amount of eggs in the samples. Thus, using classical flotation to obtain eggs for PCR may increase the credibility of the results, particularly in cases with a low number of excreted eggs. The Chelex resin protocol has potential for application in studies of intestinal parasites in wildlife for which conventional flotation is routinely used for microscopy.
转续贝蛔虫是一种蛔虫,在世界范围内的大多数熊种中都有报道。在哺乳动物以及可能在人类中,转续贝蛔虫的幼虫可随幼虫移行症在异常宿主的组织中移行。本研究旨在鉴定波兰南部塔特拉山国家公园自由放养棕熊粪便样本中的转续贝蛔虫。使用一种商业试剂盒直接从粪便样本中提取基因组DNA。此外,成功实施了基于螯合树脂的技术,以从浮选回收的虫卵中制备PCR模板。根据32份收集的粪便样本的浮选结果,转续贝蛔虫的感染率为15.6%。通过使用直接从粪便中分离的DNA进行分子检测,在初次浮选时发现为阳性的样本中确认了该寄生虫。使用螯合树脂方案提取DNA后,回收的虫卵被确认为转续贝蛔虫。基于细胞色素c氧化酶1(COI)413 bp片段的PCR扩增和测序,与GenBank™数据库进行BLAST比对后,获得的序列与转续贝蛔虫的COI片段100%相同。本研究首次对喀尔巴阡山脉西部棕熊体内的转续贝蛔虫进行了分子确认。我们表明,直接从熊粪便中提取寄生虫DNA对分子检测是有效的。作为一种替代方法,我们展示了基于螯合树脂的技术从转续贝蛔虫难以破坏的虫卵中快速便捷地分离DNA用于PCR的有效性。直接从粪便材料中提取的寄生虫DNA的分子检测存在与样本中虫卵数量相关的检测限。因此,使用经典浮选法获取用于PCR的虫卵可能会提高结果的可信度,特别是在排出虫卵数量较少的情况下。螯合树脂方案在野生动物肠道寄生虫研究中具有应用潜力,在这类研究中常规浮选法通常用于显微镜检查。