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      A cryptic species of Onchocerca (Nematoda: Onchocercidae) in blackflies ( Simulium spp.) from southern California, USA

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          Abstract

          Background

          Entomological surveillance for pathogens based on molecular screening of putative arthropod vectors such as blackflies (Diptera: Simuliidae) is becoming increasingly important. Surveillance provides a means to understand host and geographical patterns of underestimated biodiversity among North American species of Onchocerca and a pathway to identify and track expanding emergence of the zoonotic Onchocerca lupi. Herein, we have screened two blackfly species, Simulium tescorum and Simulium vittatum ( s.l.), from Los Angeles County, southern California, USA for DNA of filarioid nematodes to better understand species richness and limits within the genus Onchocerca.

          Methods

          A total of 1056 and 378 female blackflies was collected using CO 2-baited mosquito traps from March to November of 2015 and 2016, respectively. All blackflies during 2015 were individually processed for DNA extraction and PCR targeting of the cytochrome c oxidase subunit 1 ( cox1) of the mitochondrial DNA (mtDNA). Specimens of S. tescorum collected in 2016 were processed individually with heads and bodies extracted separately, whereas those of S. vittatum ( s.l.) were processed in pooled samples with heads and bodies extracted separately. A subset of filarioid-positive samples from 2015 and all samples from 2016 were screened using a PCR targeting the NADH dehydrogenase subunit 5 ( nad5) gene (mtDNA).

          Results

          In 2015, 356 S. tescorum (33.7%) and 683 S. vittatum ( s.l.) (64.7%) were collected, and an additional 17 specimens were not assessed morphologically. In 2016, a total of 378 blackflies was collected. Of these, 43 (11.6%) were S. tescorum and 327 (88.4%) were S. vittatum ( s.l.), and an additional 8 specimens were not assessed morphologically. In 2015, Onchocerca sequences were detected in 4.8% ( n = 17) of S. tescorum samples, and only one S. vittatum (0.15%). In 2016, only a single S. vittatum pool was positive for the same cryptic Onchocerca species. In phylogenetic comparisons based on nad5, the Onchocerca sequences from California formed a clade with those isolates in white-tailed deer from upstate New York, suggesting these belong to a single widespread cryptic species.

          Conclusions

          An uncharacterized species of Onchocerca associated with cervid hosts was found in blackflies from southern California. Sequence data demonstrated it is likely conspecific with an unnamed species of Onchocerca previously found in white-tailed deer from upstate New York. Current data support recognition of a broad geographical distribution across North America for an apparently cryptic species of Onchocerca that is discrete from O. cervipedis, considered to be a typical filarioid among cervids. Our data suggest that this cryptic species of Onchocerca may infect subspecies of white-tailed deer ( Odocoileus virginianus), and mule and black-tailed deer ( Odocoileus hemionus) at temporal latitudes. The blackflies Simulium tescorum and S. vittatum ( s.l.) (presumably, S. tribulatum) are putative vectors. Discovery of a cryptic complex indicates that species diversity and putative associations for definitive hosts and vectors of Onchocerca species in North America must be reassessed.

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          Most cited references53

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          Evolution in action: climate change, biodiversity dynamics and emerging infectious disease.

          Climatological variation and ecological perturbation have been pervasive drivers of faunal assembly, structure and diversification for parasites and pathogens through recurrent events of geographical and host colonization at varying spatial and temporal scales of Earth history. Episodic shifts in climate and environmental settings, in conjunction with ecological mechanisms and host switching, are often critical determinants of parasite diversification, a view counter to more than a century of coevolutionary thinking about the nature of complex host-parasite assemblages. Parasites are resource specialists with restricted host ranges, yet shifts onto relatively unrelated hosts are common during phylogenetic diversification of parasite lineages and directly observable in real time. The emerging Stockholm Paradigm resolves this paradox: Ecological Fitting (EF)--phenotypic flexibility and phylogenetic conservatism in traits related to resource use, most notably host preference--provides many opportunities for rapid host switching in changing environments, without the evolution of novel host-utilization capabilities. Host shifts via EF fuel the expansion phase of the Oscillation Hypothesis of host range and speciation and, more generally, the generation of novel combinations of interacting species within the Geographic Mosaic Theory of Coevolution. In synergy, an environmental dynamic of Taxon Pulses establishes an episodic context for host and geographical colonization.
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            A phylogenetic analysis of filarial nematodes: comparison with the phylogeny of Wolbachia endosymbionts

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              How specialists can be generalists: resolving the "parasite paradox" and implications for emerging infectious disease

              The parasite paradox arises from the dual observations that parasites (broadly construed, including phytophagous insects) are resource specialists with restricted host ranges, and yet shifts onto relatively unrelated hosts are common in the phylogenetic diversification of parasite lineages and directly observable in ecological time. We synthesize the emerging solution to this paradox: phenotypic flexibility and phylogenetic conservatism in traits related to resource use, grouped under the term ecological fitting, provide substantial opportunities for rapid host switching in changing environments, in the absence of the evolution of novel host-utilization capabilities. We discuss mechanisms behind ecological fitting, its implications for defining specialists and generalists, and briefly review empirical examples of host shifts in the context of ecological fitting. We conclude that host shifts via ecological fitting provide the fuel for the expansion phase of the recently proposed oscillation hypothesis of host range and speciation, and, more generally, the generation of novel combinations of interacting species within the geographic mosaic theory of coevolution. Finally, we conclude that taxon pulses, driven by climate change and large-scale ecological perturbation are drivers of biotic mixing and resultant ecological fitting, which leads to increased rates of rapid host switching, including the agents of Emerging Infectious Disease.
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                Author and article information

                Contributors
                gverocai@gmail.com
                knelson@sgvmosquito.org
                treycal@uga.edu
                wwekesa@cvmvcd.org
                hhassan@health.usf.edu
                geocolonizer@gmail.com
                Journal
                Parasit Vectors
                Parasit Vectors
                Parasites & Vectors
                BioMed Central (London )
                1756-3305
                16 October 2018
                16 October 2018
                2018
                : 11
                : 547
                Affiliations
                [1 ]ISNI 0000 0004 1936 738X, GRID grid.213876.9, Department of Infectious Diseases, College of Veterinary Medicine, , University of Georgia, ; 501 D.W. Brooks Drive, Athens, GA 30602 USA
                [2 ]ISNI 0000 0001 2353 285X, GRID grid.170693.a, Department of Global Health, College of Public Health, , University of South Florida, ; 3720 Spectrum Boulevard, Tampa, FL 33612 USA
                [3 ]San Gabriel Valley Mosquito and Vector Control District, 1145 N. Azusa Canyon Rd, West Covina, CA 91790 USA
                [4 ]Coachella Valley Mosquito and Vector Control District, 43420 Trader Place, Indio, CA 92201 USA
                [5 ]ISNI 0000 0001 0701 8607, GRID grid.28803.31, School of Veterinary Medicine, Department of Pathobiological Sciences, , University of Wisconsin, ; Madison, WI 53706 USA
                Article
                3133
                10.1186/s13071-018-3133-9
                6192150
                30326946
                7daae57c-7a9d-48f8-90d0-a9c122c92704
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

                History
                : 31 May 2018
                : 2 October 2018
                Funding
                Funded by: National Center for Veterinary Parasitology
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Parasitology
                cervidae,filarial parasites,filarioidea,onchocerciasis,parasite biodiversity,vector-borne diseases

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