van de Velde Norbert, Devleesschauwer Brecht, Leopold Mardik, Begeman Lineke, IJsseldijk Lonneke, Hiemstra Sjoukje, IJzer Jooske, Brownlow Andrew, Davison Nicholas, Haelters Jan, Jauniaux Thierry, Siebert Ursula, Dorny Pierre, De Craeye Stéphane
Department of Pathology, Bacteriology and Avian Diseases, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium; Department of Public Health and Surveillance, Scientific Institute of Public Health (WIV-ISP), Brussels, Belgium.
Vet Parasitol. 2016 Oct 30;230:25-32. doi: 10.1016/j.vetpar.2016.10.021. Epub 2016 Oct 24.
The occurrence of the zoonotic protozoan parasite Toxoplasma gondii in marine mammals remains a poorly understood phenomenon. In this study, samples from 589 marine mammal species and 34 European otters (Lutra lutra), stranded on the coasts of Scotland, Belgium, France, The Netherlands and Germany, were tested for the presence of T. gondii. Brain samples were analysed by polymerase chain reaction (PCR) for detection of parasite DNA. Blood and muscle fluid samples were tested for specific antibodies using a modified agglutination test (MAT), a commercial multi-species enzyme-linked immunosorbent assay (ELISA) and an immunofluorescence assay (IFA). Out of 193 animals tested by PCR, only two harbour porpoise (Phocoena phocoena) cerebrum samples, obtained from animals stranded on the Dutch coast, tested positive. The serological results showed a wide variation depending on the test used. Using a cut-off value of 1/40 dilution in MAT, 141 out of 292 animals (41%) were positive. Using IFA, 30 out of 244 tested samples (12%) were positive at a 1/50 dilution. The commercial ELISA yielded 7% positives with a cut-off of the sample-to-positive (S/P) ratio≥50; and 12% when the cut-off was set at S/P ratio≥20. The high number of positives in MAT may be an overestimation due to the high degree of haemolysis of the samples and/or the presence of lipids. The ELISA results could be an underestimation due to the use of a multispecies conjugate. Our results confirm the presence of T. gondii in marine mammals in The Netherlands and show exposure to the parasite in both the North Sea and the Eastern Atlantic Ocean. We also highlight the limitations of the tests used to diagnose T. gondii in stranded marine mammals.
海洋哺乳动物中出现人畜共患原生动物寄生虫刚地弓形虫仍是一个了解甚少的现象。在本研究中,对搁浅在苏格兰、比利时、法国、荷兰和德国海岸的589种海洋哺乳动物以及34只欧洲水獭(水獭属)的样本进行了刚地弓形虫检测。通过聚合酶链反应(PCR)分析脑样本以检测寄生虫DNA。使用改良凝集试验(MAT)、商业多物种酶联免疫吸附测定(ELISA)和免疫荧光测定(IFA)对血液和肌肉液样本进行特异性抗体检测。在193只通过PCR检测的动物中,只有两只港湾鼠海豚(Phocoena phocoena)的大脑样本呈阳性,这些样本取自搁浅在荷兰海岸的动物。血清学结果显示,根据所使用的检测方法不同,结果差异很大。在MAT中使用1/40稀释度的临界值时,292只动物中有141只(41%)呈阳性。使用IFA时,在1/50稀释度下,244个检测样本中有30个(12%)呈阳性。商业ELISA在样本/阳性(S/P)比值≥50的临界值下阳性率为7%;当临界值设定为S/P比值≥20时,阳性率为12%。MAT中阳性数量较多可能是由于样本溶血程度高和/或存在脂质而导致的高估。ELISA结果可能因使用多物种结合物而被低估。我们的结果证实了荷兰海洋哺乳动物中存在刚地弓形虫,并表明北海和东大西洋的海洋哺乳动物均接触过该寄生虫。我们还强调了用于诊断搁浅海洋哺乳动物中刚地弓形虫的检测方法的局限性。