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      Host specialization in ticks and transmission of tick-borne diseases: a review

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          Abstract

          Determining patterns of host use, and the frequency at which these patterns change, are of key importance if we are to understand tick population dynamics, the evolution of tick biodiversity, and the circulation and evolution of associated pathogens. The question of whether ticks are typically host specialists or host generalists has been subject to much debate over the last half-century. Indeed, early research proposed that morphological diversity in ticks was linked to host specific adaptations and that most ticks were specialists. Later work disputed this idea and suggested that ticks are largely limited by biogeographic conditions and tend to use all locally available host species. The work presented in this review suggests that the actual answer likely lies somewhere between these two extremes. Although recent observational studies support the view that phylogenetically diverse host species share ticks when found on similar ecological ranges, theory on host range evolution predicts that host specialization should evolve in ticks given their life history characteristics. Contemporary work employing population genetic tools to examine host-associated population structure in several tick systems support this prediction and show that simple species records are not enough to determine whether a parasite is a true host generalist; host specialization does evolve in ticks at local scales, but may not always lead to speciation. Ticks therefore seem to follow a pattern of being global generalists, local specialists. Given this, the notion of host range needs to be modified from an evolutionary perspective, where one simply counts the number of hosts used across the geographic distribution, to a more ecological view, where one considers host use at a local scale, if we are to better understand the circulation of tick-borne pathogens and exposure risks for humans and livestock.

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          The ecology of infectious disease: effects of host diversity and community composition on Lyme disease risk.

          The extent to which the biodiversity and community composition of ecosystems affect their functions is an issue that grows ever more compelling as human impacts on ecosystems increase. We present evidence that supports a novel function of vertebrate biodiversity, the buffering of human risk of exposure to Lyme-disease-bearing ticks. We tested the Dilution Effect model, which predicts that high species diversity in the community of tick hosts reduces vector infection prevalence by diluting the effects of the most competent disease reservoir, the ubiquitous white-footed mouse (Peromyscus leucopus). As habitats are degraded by fragmentation or other anthropogenic forces, some members of the host community disappear. Thus, species-poor communities tend to have mice, but few other hosts, whereas species-rich communities have mice, plus many other potential hosts. We demonstrate that the most common nonmouse hosts are relatively poor reservoirs for the Lyme spirochete and should reduce the prevalence of the disease by feeding, but rarely infecting, ticks. By accounting for nearly every host species' contribution to the number of larval ticks fed and infected, we show that as new host species are added to a depauperate community, the nymphal infection prevalence, a key risk factor, declines. We identify important "dilution hosts" (e.g., squirrels), characterized by high tick burdens, low reservoir competence, and high population density, as well as "rescue hosts" (e.g., shrews), which are capable of maintaining high disease risk when mouse density is low. Our study suggests that the preservation of vertebrate biodiversity and community composition can reduce the incidence of Lyme disease.
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            Ticks and tickborne bacterial diseases in humans: an emerging infectious threat.

            Ticks are currently considered to be second only to mosquitoes as vectors of human infectious diseases in the world. Each tick species has preferred environmental conditions and biotopes that determine the geographic distribution of the ticks and, consequently, the risk areas for tickborne diseases. This is particularly the case when ticks are vectors and reservoirs of the pathogens. Since the identification of Borrelia burgdorferi as the agent of Lyme disease in 1982, 15 ixodid-borne bacterial pathogens have been described throughout the world, including 8 rickettsiae, 3 ehrlichiae, and 4 species of the Borrelia burgdorferi complex. This article reviews and illustrate various aspects of the biology of ticks and the tickborne bacterial diseases (rickettsioses, ehrlichioses, Lyme disease, relapsing fever borrelioses, tularemia, Q fever), particularly those regarded as emerging diseases. Methods are described for the detection and isolation of bacteria from ticks and advice is given on how tick bites may be prevented and how clinicians should deal with patients who have been bitten by ticks.
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              Host Specialization in Phytophagous Insects

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                Author and article information

                Journal
                Front Cell Infect Microbiol
                Front Cell Infect Microbiol
                Front. Cell. Infect. Microbiol.
                Frontiers in Cellular and Infection Microbiology
                Frontiers Media S.A.
                2235-2988
                04 October 2013
                2013
                : 3
                : 57
                Affiliations
                [1] 1MiVEGEC, Mixed Research Unit 5290 CNRS-IRD-UM1-UM2, Centre IRD Montpellier, France
                [2] 2Department of Biology, Carleton University Ottawa, ON, Canada
                [3] 3Centre de Recherche et de Veille sur les Maladies Emergentes dans l'Océan Indien, GIP CYROI St. Clotilde, France
                [4] 4Department of Biology, Université de La Réunion St. Denis, France
                Author notes

                Edited by: Agustín Estrada-Peña, University of Zaragoza, Spain

                Reviewed by: Nicholas Ogden, Public Health Agency of Canada, Canada; Thierry De Meeus, Institut de Recherche pour le Développement, Burkina Faso

                *Correspondence: Karen D. McCoy, MiVEGEC UMR 5290 CNRS-IRD-UM1-UM2, Centre IRD, 911 Avenue Agropolis, BP 64501, 34394 Montpellier, France e-mail: karen.mccoy@ 123456ird.fr

                This article was submitted to the journal Frontiers in Cellular and Infection Microbiology.

                Article
                10.3389/fcimb.2013.00057
                3790072
                24109592
                3e4d0807-6146-4109-bfdb-b2f0bf2ea800
                Copyright © 2013 McCoy, Léger and Dietrich.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 01 May 2013
                : 13 September 2013
                Page count
                Figures: 3, Tables: 2, Equations: 0, References: 109, Pages: 12, Words: 11401
                Categories
                Microbiology
                Review Article

                Infectious disease & Microbiology
                adaptation,argasidae,borrelia burgdorferi sensu lato,community diversity,epidemiology,ixodidae,population genetic structure,transmission

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