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      Hedgehogs and Squirrels as Hosts of Zoonotic Bartonella Species

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          Abstract

          Free-living animals frequently play a key role in the circulation of various zoonotic vector-borne pathogens. Bacteria of the genus Bartonella are transmitted by blood-feeding arthropods and infect a large range of mammals. Although only several species have been identified as causative agents of human disease, it has been proposed that any Bartonella species found in animals may be capable of infecting humans. Within a wide-ranging survey in various geographical regions of the Czech Republic, cadavers of accidentally killed synurbic mammalian species, namely Eurasian red squirrel ( Sciurus vulgaris), European hedgehog ( Erinaceus europaeus) and Northern white-breasted hedgehog ( Erinaceus roumanicus), were sampled and tested for Bartonella presence using multiple PCR reaction approach targeting several DNA loci. We demonstrate that cadavers constitute an available and highly useful source of biological material for pathogen screening. High infection rates of Bartonella spp., ranging from 24% to 76%, were confirmed for all three tested mammalian species, and spleen, ear, lung and liver tissues were demonstrated as the most suitable for Bartonella DNA detection. The wide spectrum of Bartonella spp. that were identified includes three species with previously validated zoonotic potential, B. grahamii, B. melophagi and B. washoensis, accompanied by ‘ Candidatus B. rudakovii’ and two putative novel species, Bartonella sp. ERIN and Bartonella sp. SCIER.

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          Ixodes ricinus and Its Transmitted Pathogens in Urban and Peri-Urban Areas in Europe: New Hazards and Relevance for Public Health

          Tick-borne diseases represent major public and animal health issues worldwide. Ixodes ricinus, primarily associated with deciduous and mixed forests, is the principal vector of causative agents of viral, bacterial, and protozoan zoonotic diseases in Europe. Recently, abundant tick populations have been observed in European urban green areas, which are of public health relevance due to the exposure of humans and domesticated animals to potentially infected ticks. In urban habitats, small and medium-sized mammals, birds, companion animals (dogs and cats), and larger mammals (roe deer and wild boar) play a role in maintenance of tick populations and as reservoirs of tick-borne pathogens. Presence of ticks infected with tick-borne encephalitis virus and high prevalence of ticks infected with Borrelia burgdorferi s.l., causing Lyme borreliosis, have been reported from urbanized areas in Europe. Emerging pathogens, including bacteria of the order Rickettsiales (Anaplasma phagocytophilum, “Candidatus Neoehrlichia mikurensis,” Rickettsia helvetica, and R. monacensis), Borrelia miyamotoi, and protozoans (Babesia divergens, B. venatorum, and B. microti) have also been detected in urban tick populations. Understanding the ecology of ticks and their associations with hosts in a European urbanized environment is crucial to quantify parameters necessary for risk pre-assessment and identification of public health strategies for control and prevention of tick-borne diseases.
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            Bartonella Species, an Emerging Cause of Blood-Culture-Negative Endocarditis.

            Since the reclassification of the genus Bartonella in 1993, the number of species has grown from 1 to 45 currently designated members. Likewise, the association of different Bartonella species with human disease continues to grow, as does the range of clinical presentations associated with these bacteria. Among these, blood-culture-negative endocarditis stands out as a common, often undiagnosed, clinical presentation of infection with several different Bartonella species. The limitations of laboratory tests resulting in this underdiagnosis of Bartonella endocarditis are discussed. The varied clinical picture of Bartonella infection and a review of clinical aspects of endocarditis caused by Bartonella are presented. We also summarize the current knowledge of the molecular basis of Bartonella pathogenesis, focusing on surface adhesins in the two Bartonella species that most commonly cause endocarditis, B. henselae and B. quintana. We discuss evidence that surface adhesins are important factors for autoaggregation and biofilm formation by Bartonella species. Finally, we propose that biofilm formation is a critical step in the formation of vegetative masses during Bartonella-mediated endocarditis and represents a potential reservoir for persistence by these bacteria.
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              Intruders below the radar: molecular pathogenesis of Bartonella spp.

              Bartonella spp. are facultative intracellular pathogens that employ a unique stealth infection strategy comprising immune evasion and modulation, intimate interaction with nucleated cells, and intraerythrocytic persistence. Infections with Bartonella are ubiquitous among mammals, and many species can infect humans either as their natural host or incidentally as zoonotic pathogens. Upon inoculation into a naive host, the bartonellae first colonize a primary niche that is widely accepted to involve the manipulation of nucleated host cells, e.g., in the microvasculature. Consistently, in vitro research showed that Bartonella harbors an ample arsenal of virulence factors to modulate the response of such cells, gain entrance, and establish an intracellular niche. Subsequently, the bacteria are seeded into the bloodstream where they invade erythrocytes and give rise to a typically asymptomatic intraerythrocytic bacteremia. While this course of infection is characteristic for natural hosts, zoonotic infections or the infection of immunocompromised patients may alter the path of Bartonella and result in considerable morbidity. In this review we compile current knowledge on the molecular processes underlying both the infection strategy and pathogenesis of Bartonella and discuss their connection to the clinical presentation of human patients, which ranges from minor complaints to life-threatening disease.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Pathogens
                Pathogens
                pathogens
                Pathogens
                MDPI
                2076-0817
                01 June 2021
                June 2021
                : 10
                : 6
                : 686
                Affiliations
                [1 ]Department of Parasitology, Faculty of Science, Charles University, 12800 Prague, Czech Republic; jan.votypka@ 123456natur.cuni.cz
                [2 ]Institute of Parasitology, Biology Center, Czech Academy of Sciences, 37005 Ceske Budejovice, Czech Republic; honig@ 123456paru.cas.cz (V.H.); ruzekd@ 123456paru.cas.cz (D.R.); modryd@ 123456vfu.cz (D.M.)
                [3 ]Military Health Institute, Military Medical Agency, 16200 Prague, Czech Republic
                [4 ]Koret School of Veterinary Medicine, The Hebrew University of Jerusalem, Rehovot 76100, Israel; ricardo.gutierrez@ 123456mail.huji.ac.il (R.G.); yaarit.biala@ 123456mail.huji.ac.il (Y.N.-B.); shimon.harrus@ 123456mail.huji.ac.il (S.H.)
                [5 ]Center for Infectious Disease Control, National Institute for Public Health and the Environment, 3721 Bilthoven, The Netherlands; manoj.fonville@ 123456rivm.nl (M.F.); hein.sprong@ 123456rivm.nl (H.S.)
                [6 ]Department of Infectious Diseases and Preventive Medicine, Veterinary Research Institute, 62100 Brno, Czech Republic
                [7 ]Department of Pathology and Parasitology, Faculty of Veterinary Medicine, University of Veterinary Sciences, 61242 Brno, Czech Republic; Reptimania@ 123456email.cz (P.P.); lada.hurkova@ 123456seznam.cz (L.H.); lesiczkapaulina@ 123456gmail.com (P.M.L.)
                [8 ]Central European Institute of Technology, University of Veterinary Sciences, 61242 Brno, Czech Republic
                [9 ]Department of Botany and Zoology, Faculty of Science, Masaryk University, 61137 Brno, Czech Republic
                Author notes
                Author information
                https://orcid.org/0000-0001-7701-5778
                https://orcid.org/0000-0001-6988-0251
                https://orcid.org/0000-0003-0469-4604
                https://orcid.org/0000-0003-1418-8879
                https://orcid.org/0000-0003-4655-2380
                https://orcid.org/0000-0002-0218-4320
                https://orcid.org/0000-0002-0552-9363
                Article
                pathogens-10-00686
                10.3390/pathogens10060686
                8229113
                34205901
                8cc1f0ba-4625-49ce-986b-73f610bc8d86
                © 2021 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 ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 11 May 2021
                : 29 May 2021
                Categories
                Article

                bartonella grahamii,b. melophagi,b. rochalimae,b. washoensis,‘candidatus b. rudakovii’,hedgehogs,squirrels,multiple pcr,vector-borne diseases,zoonoses

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