Disease surveillance in albatrosses and petrels from the Southwest Atlantic and Southern Ocean.

IF 2.4 3区 医学 Q2 PARASITOLOGY
Patricia Pereira Serafini, Annelise Zabel Sgarioni, Richard A Phillips, Alice Pereira, Tiffany Emmerich, Thamires P Pontes, Derek B Amorim, Cristiane K M Kolesnikovas, André O S Lima, Guilherme Klafke, José Reck, Afonso C D Bainy, Karim H Lüchmann, Camille Bonneaud
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引用次数: 0

Abstract

Emerging infectious diseases pose threats to wildlife, particularly in geographically isolated populations where hosts may lack prior exposure and immunity. Seabirds inhabiting remote islands in the southwest Atlantic and Southern Ocean, including threatened albatrosses and petrels, are increasingly affected by infectious pathogens. However, baseline data on vector-borne infections in these species remain scarce. This study assessed the presence of vector-borne haemosporidian parasites (Plasmodium, Haemoproteus and Leucocytozoon) and bacterial pathogens (Borrelia burgdorferi sensu lato, Anaplasma and Ehrlichia) in albatrosses and petrels, providing insights into disease prevalence and potential threats to these populations. We analysed blood and tissue samples from 269 individuals of 5 albatross and 12 petrel species, collected over an 11-year period (2013-2023) from South Georgia and multiple sites along the Brazilian coastline. Molecular assays, including nested Polymerase Chain Reaction (PCR), were used for pathogen screening. Blood smears from birds sampled in South Georgia were also examined for haemoparasites via light microscopy. We found no molecular or microscopy evidence of infection with haemosporidian parasites, Borrelia, Anaplasma or Ehrlichia in any of the samples. These findings suggest that vector-borne pathogens are either absent or at low prevalence, possibly because of limited vector presence, natural resistance or historical isolation from infection. Continuous monitoring is critical given current environmental changes and risks of pathogen introduction via climate-driven shifts in vector distribution. Our study establishes an essential baseline for future disease surveillance, prevention and mitigation in albatrosses and petrels, underscoring the importance of long-term monitoring to detect emerging pathogens in vulnerable seabird populations.

西南大西洋和南大洋信天翁和海燕的疾病监测。
新出现的传染病对野生动物构成威胁,特别是在地理上孤立的种群中,宿主可能缺乏事先接触和免疫。居住在西南大西洋和南大洋偏远岛屿上的海鸟,包括受威胁的信天翁和海燕,越来越多地受到传染性病原体的影响。然而,这些物种中媒介传播感染的基线数据仍然很少。本研究评估了信天翁和海燕中媒介传播的血孢子虫寄生虫(疟原虫、嗜血杆菌和白细胞虫)和细菌病原体(伯氏疏螺旋体、无原体和埃利希体)的存在,为这些种群的疾病流行和潜在威胁提供了见解。我们分析了5种信天翁和12种海燕的269只个体的血液和组织样本,这些样本是在11年(2013-2023年)期间从南乔治亚州和巴西海岸线沿线的多个地点收集的。分子检测,包括巢式聚合酶链反应(PCR),用于病原体筛选。在南乔治亚州取样的鸟类的血液涂片也通过光学显微镜检查了血液寄生虫。我们在所有样本中均未发现血孢子虫寄生虫、伯氏疏螺旋体、无形体或埃利希体感染的分子或显微镜证据。这些发现表明,媒介传播的病原体要么不存在,要么流行率很低,这可能是由于媒介存在有限、自然抗性或与感染的历史隔离所致。鉴于当前的环境变化和因气候驱动的病媒分布变化导致病原体传入的风险,持续监测至关重要。我们的研究为未来信天翁和海燕的疾病监测、预防和缓解建立了基本基线,强调了长期监测以发现脆弱海鸟种群中新出现的病原体的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Parasitology
Parasitology 医学-寄生虫学
CiteScore
4.80
自引率
4.20%
发文量
280
审稿时长
3-8 weeks
期刊介绍: Parasitology is an important specialist journal covering the latest advances in the subject. It publishes original research and review papers on all aspects of parasitology and host-parasite relationships, including the latest discoveries in parasite biochemistry, molecular biology and genetics, ecology and epidemiology in the context of the biological, medical and veterinary sciences. Included in the subscription price are two special issues which contain reviews of current hot topics, one of which is the proceedings of the annual Symposia of the British Society for Parasitology, while the second, covering areas of significant topical interest, is commissioned by the editors and the editorial board.
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