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      Living in the city: Angiostrongylus cantonensis is a novel threat to an urban population of Florida burrowing owls ( Athene cunicularia floridana) in south Florida

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          Abstract

          Background

          Angiostrongylus cantonensis, the rat lungworm, is a metastrongyloid parasite that uses rodents as definitive hosts, mollusks as intermediate hosts, and a wide range of invertebrate and vertebrate species as paratenic hosts. Although this parasite poses a significant public health concern in many regions of the world, it can also cause disease in numerous domestic and wildlife aberrant host species. When parasite larvae are ingested by one of these aberrant hosts, larval migration in the central nervous system causes extensive damage, resulting in spinal cord and/or brain damage and inflammation, leading to potentially fatal neurological disease. We describe A. cantonensis infection in a novel host, the Florida burrowing owl ( Athene cunicularia floridana), on Marco Island, Collier County, Florida, USA. The Florida burrowing owl is a state-listed species that has experienced steep population declines across its range, primarily due to habitat loss and fragmentation. Many populations are now restricted to urban environments, which pose novel threats to the owls, such as exposure to anticoagulant rodenticides and novel pathogens, increased risk of predation, vehicular strike, and increased disturbance at nest sites.

          Methods

          Through diagnostic evaluation of carcasses and select tissues submitted to the Southeastern Cooperative Wildlife Disease Study from 2019 to 2023, we diagnosed nine confirmed or suspected cases of angiostrongylosis on Marco Island.

          Results

          Microscopic examination and polymerase chain reaction (PCR) testing confirmed parasite identification. In addition, ancillary testing ruled out other potential causes of neurological disease, such as rodenticides, West Nile virus, and highly pathogenic avian influenza virus.

          Conclusions

          This study underscores the importance of surveillance and monitoring efforts for A. cantonensis, particularly in regions where novel hosts may serve as indicators of public health risk. In addition, as urbanization and habitat fragmentation continue encroaching upon wildlife habitats, understanding the dynamics of host–parasite interactions becomes crucial for mitigating the spread of zoonotic diseases.

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          Most cited references71

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          Moving towards an integrated approach to molecular detection and identification of Toxoplasma gondii.

          The development of simple, sensitive and rapid methods for the detection and identification of Toxoplasma gondii is important for the diagnosis and epidemiological studies of the zoonotic disease toxoplasmosis. In the past 2 decades, molecular methods based on a variety of genetic markers have been developed, each with its advantages and limitations. The application of these methods has generated invaluable information to enhance our understanding of the epidemiology, population genetics and phylogeny of T. gondii. However, since most studies focused solely on the detection but not genetic characterization of T. gondii, the information obtained was limited. In this review, we discuss some widely used molecular methods and propose an integrated approach for the detection and identification of T. gondii, in order to generate maximum information for epidemiological, population and phylogenetic studies of this key pathogen.
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            Angiostrongylus cantonensis: a review of its distribution, molecular biology and clinical significance as a human pathogen.

            Angiostrongylus cantonensis is a metastrongyloid nematode found widely in the Asia-Pacific region, and the aetiological agent of angiostrongyliasis; a disease characterized by eosinophilic meningitis. Rattus rats are definitive hosts of A. cantonensis, while intermediate hosts include terrestrial and aquatic molluscs. Humans are dead-end hosts that usually become infected upon ingestion of infected molluscs. A presumptive diagnosis is often made based on clinical features, a history of mollusc consumption, eosinophilic pleocytosis in cerebral spinal fluid, and advanced imaging such as computed tomography. Serological tests are available for angiostrongyliasis, though many tests are still under development. While there is no treatment consensus, therapy often includes a combination of anthelmintics and corticosteroids. Angiostrongyliasis is relatively rare, but is often associated with morbidity and sometimes mortality. Recent reports suggest the parasites' range is increasing, leading to fatalities in regions previously considered Angiostrongylus-free, and sometimes, delayed diagnosis in newly invaded regions. Increased awareness of angiostrongyliasis would facilitate rapid diagnosis and improved clinical outcomes. This paper summarizes knowledge on the parasites' life cycle, clinical aspects and epidemiology. The molecular biology of Angiostrongylus spp. is also discussed. Attention is paid to the significance of angiostrongyliasis in Australia, given the recent severe cases reported from the Sydney region.
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              Species of Angiostrongylus (Nematoda: Metastrongyloidea) in wildlife: A review

              Highlights • Twenty-one species of Angiostrongylus are recognised from wildlife around the world. • Details of hosts, life cycles, pathogenesis, geographical range are known for nine. • Six species are spreading into new regions locally or globally. • Two species, A. cantonensis and A. costaricensis, are zoonotic. • A. mackerrasae, A. malaysiensis and A. siamensis are potentially zoonotic. • Debilitating disease occurs in avian and mammalian wildlife and humans in Australia.
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                Author and article information

                Contributors
                myabsley@uga.edu
                Journal
                Parasit Vectors
                Parasit Vectors
                Parasites & Vectors
                BioMed Central (London )
                1756-3305
                26 February 2025
                26 February 2025
                2025
                : 18
                : 80
                Affiliations
                [1 ]Southeastern Cooperative Wildlife Disease Study, College of Veterinary Medicine, University of Georgia, ( https://ror.org/00te3t702) Athens, GA 30602 USA
                [2 ]Department of Pathology, College of Veterinary Medicine, University of Georgia, ( https://ror.org/00te3t702) Athens, GA 30602 USA
                [3 ]Audubon Western Everglades, 12250 Tamiami Trail E. Suite 309, Naples, FL 34113 USA
                [4 ]Florida Fish and Wildlife Conservation Commission, Fish and Wildlife Research Institute, ( https://ror.org/03y5msf78) St. Petersburg, FL 33701 USA
                [5 ]Florida Fish and Wildlife Conservation Commission, ( https://ror.org/03y5msf78) 1105 SW Williston Rd, Gainesville, FL 32601 USA
                [6 ]National Park Service, Biological Resources Division, Wildlife Health Branch, ( https://ror.org/044zqqy65) Fort Collins, CO USA
                [7 ]The Mosaic Company, ( https://ror.org/01xc2fv34) 414 W Main St, Wauchula, FL 33873 USA
                [8 ]Warnell School of Forestry and Natural Resources, University of Georgia, ( https://ror.org/00te3t702) Athens, GA 30602 USA
                [9 ]Conservancy of Southwest Florida, 1495 Smith Preserve Way, Naples, FL 34102 USA
                [10 ]Center for Ecology of Infectious Diseases, University of Georgia, ( https://ror.org/00te3t702) Athens, GA 30602 USA
                [11 ]Wildlife Health Building, Southeastern Cooperative Wildlife Disease Study, Department of Population Health, University of Georgia, ( https://ror.org/00te3t702) 589 D.W. Brooks Drive, Athens, GA 30602 USA
                Article
                6700
                10.1186/s13071-025-06700-7
                11866900
                40012029
                b9967887-6acd-43aa-b2a7-6b999a031b6f
                © The Author(s) 2025

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 17 December 2024
                : 29 January 2025
                Categories
                Research
                Custom metadata
                © BioMed Central Ltd., part of Springer Nature 2025

                Parasitology
                rat lungworm,angiostrongylus cantonensis,burrowing owl,neurologic,parasite,athene cunicularia,wildlife health,florida

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