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      Immune System Modulation and Viral Persistence in Bats: Understanding Viral Spillover

      review-article
      * , ,
      Viruses
      MDPI
      Immune response, flight, immune tolerance, viral persistence, spillover, bats, viruses

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          Abstract

          Bats harbor a myriad of viruses and some of these viruses may have spilled over to other species including humans. Spillover events are rare and several factors must align to create the “perfect storm” that would ultimately lead to a spillover. One of these factors is the increased shedding of virus by bats. Several studies have indicated that bats have unique defense mechanisms that allow them to be persistently or latently infected with viruses. Factors leading to an increase in the viral load of persistently infected bats would facilitate shedding of virus. This article reviews the unique nature of bat immune defenses that regulate virus replication and the various molecular mechanisms that play a role in altering the balanced bat–virus relationship.

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          Most cited references50

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          Ecological immunology: costly parasite defences and trade-offs in evolutionary ecology

          In the face of continuous threats from parasites, hosts have evolved an elaborate series of preventative and controlling measures - the immune system - in order to reduce the fitness costs of parasitism. However, these measures do have associated costs. Viewing an individual's immune response to parasites as being subject to optimization in the face of other demands offers potential insights into mechanisms of life history trade-offs, sexual selection, parasite-mediated selection and population dynamics. We discuss some recent results that have been obtained by practitioners of this approach in natural and semi-natural populations, and suggest some ways in which this field may progress in the near future.
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            DNA base damage by reactive oxygen species, oxidizing agents, and UV radiation.

            Emphasis has been placed in this article dedicated to DNA damage on recent aspects of the formation and measurement of oxidatively generated damage in cellular DNA in order to provide a comprehensive and updated survey. This includes single pyrimidine and purine base lesions, intrastrand cross-links, purine 5',8-cyclonucleosides, DNA-protein adducts and interstrand cross-links formed by the reactions of either the nucleobases or the 2-deoxyribose moiety with the hydroxyl radical, one-electron oxidants, singlet oxygen, and hypochlorous acid. In addition, recent information concerning the mechanisms of formation, individual measurement, and repair-rate assessment of bipyrimidine photoproducts in isolated cells and human skin upon exposure to UVB radiation, UVA photons, or solar simulated light is critically reviewed.
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              • Article: not found

              Host phylogeny constrains cross-species emergence and establishment of rabies virus in bats.

              For RNA viruses, rapid viral evolution and the biological similarity of closely related host species have been proposed as key determinants of the occurrence and long-term outcome of cross-species transmission. Using a data set of hundreds of rabies viruses sampled from 23 North American bat species, we present a general framework to quantify per capita rates of cross-species transmission and reconstruct historical patterns of viral establishment in new host species using molecular sequence data. These estimates demonstrate diminishing frequencies of both cross-species transmission and host shifts with increasing phylogenetic distance between bat species. Evolutionary constraints on viral host range indicate that host species barriers may trump the intrinsic mutability of RNA viruses in determining the fate of emerging host-virus interactions.
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                Author and article information

                Journal
                Viruses
                Viruses
                viruses
                Viruses
                MDPI
                1999-4915
                23 February 2019
                February 2019
                : 11
                : 2
                : 192
                Affiliations
                Department of Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK S7N 5B4, Canada; noreen.rapin@ 123456usask.ca (N.R.); vikram.misra@ 123456usask.ca (V.M.)
                Author notes
                [* ]Correspondence: sonu.subudhi@ 123456usask.ca ; Tel.: +1-306-966-6480
                Author information
                https://orcid.org/0000-0002-5937-1880
                https://orcid.org/0000-0001-6818-7156
                Article
                viruses-11-00192
                10.3390/v11020192
                6410205
                30813403
                a90d39fe-2fe6-4bd1-9984-642d9e3e345a
                © 2019 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 23 January 2019
                : 20 February 2019
                Categories
                Review

                Microbiology & Virology
                immune response,flight,immune tolerance,viral persistence,spillover,bats,viruses
                Microbiology & Virology
                immune response, flight, immune tolerance, viral persistence, spillover, bats, viruses

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