Department of Animal Health, Veterinary Faculty, Universidad Complutense de Madrid, Madrid, Spain.
Centro de Rescate de Primates "RAINFER", Fuente del Saz, Madrid, Spain.
Parasit Vectors. 2018 Mar 20;11(1):185. doi: 10.1186/s13071-018-2772-1.
Some wild animals have been recognized as potential reservoirs of Leishmania infantum infection (e.g. carnivores, lagomorphs, rodents, etc.). Leishmania infantum was also identified infecting humans and lagomorphs (i.e. hares and rabbits) over the period of 2009-2016, with the latter acting as the main reservoirs involved in the human leishmaniosis outbreak in Madrid.
Two cases of clinical leishmaniosis are reported in orangutans (Pongo pygmaeus pygmaeus) housed at two different centres in Madrid. The first is the case of a 36-year-old male orangutan with severe weight loss and apathy. A complete blood count and biochemical profile revealed anaemia, neutropenia, hypoalbuminaemia and elevated transaminases. Hepato-splenomegaly was also observed. Four months later, due to worsening of clinical signs (mainly bilateral epistaxis), blood and bone marrow samples were collected. Amastigotes of L. infantum were detected in macrophages from a bone marrow aspirate and by specific polymerase chain reaction. The second case was a 34-year-old female orangutan with severe weight loss and apathy and no other apparent clinical signs. A complete blood count and biochemical profile revealed anaemia, pancytopenia and hypoalbuminaemia. Splenomegaly and pericardial effusion were also observed. As leishmaniosis was included in the differential diagnosis, both blood and bone marrow samples were collected. Leishmania infantum infection was confirmed by microscopy, molecular diagnosis and serology (immunofluorescence antibody test). Both animals were treated daily with oral miltefosine for 28 days; allopurinol was also given uninterruptedly in Case 2 for at least 6 months. During follow-up, though good clinical recovery was clear, a lack of parasitological cure was confirmed molecularly in both blood and bone marrow samples from the two orangutans. In both habitats, the presence of the sand fly vector identified as Phlebotomus perniciosus was confirmed.
To our knowledge, this is the first report of L. infantum infection in great apes and in the endangered species P. p. pygmaeus. We are presently looking for L. infantum in other non-human primates living in the same peri-urban areas. If detected, we will examine the impacts of this serious disease on these critically endangered species.
一些野生动物已被确认为利什曼原虫感染的潜在宿主(例如,食肉动物、兔形目动物、啮齿动物等)。在 2009 年至 2016 年期间,还发现利什曼原虫感染人类和兔形目动物(即野兔和兔子),后者是马德里人间利什曼病爆发的主要宿主。
报告了两例马德里两家不同中心饲养的猩猩(Pongo pygmaeus pygmaeus)的临床利什曼病病例。第一例是一例 36 岁雄性猩猩,体重严重下降,无精打采。全血细胞计数和生化谱显示贫血、中性粒细胞减少、低白蛋白血症和转氨酶升高。还观察到肝脾肿大。四个月后,由于临床症状恶化(主要是双侧鼻出血),采集了血液和骨髓样本。从骨髓抽吸物和特定聚合酶链反应中检测到利什曼原虫的无鞭毛体。第二例是一例 34 岁雌性猩猩,体重严重下降,无精打采,没有其他明显的临床症状。全血细胞计数和生化谱显示贫血、全血细胞减少和低白蛋白血症。脾肿大和心包积液也被观察到。由于利什曼病被列入鉴别诊断,采集了血液和骨髓样本。通过显微镜检查、分子诊断和血清学(免疫荧光抗体试验)确认感染了利什曼原虫婴儿。两只动物均每日口服米替福新治疗 28 天;第二例动物至少连续 6 个月不间断地给予别嘌呤醇。在随访期间,尽管临床康复良好,但在两只猩猩的血液和骨髓样本中均未确认分子寄生虫清除。在两个栖息地中,均确认了作为媒介的白蛉(Phlebotomus perniciosus)的存在。
据我们所知,这是利什曼原虫感染大型猿类和濒危物种 P. p. pygmaeus 的首例报告。我们目前正在同一城市周边地区寻找其他非人类灵长类动物中的利什曼原虫。如果发现,我们将研究这种严重疾病对这些极度濒危物种的影响。