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      Detection of Rickettsiae, Borreliae, and Ehrlichiae in Ticks Collected from Walker County, Texas, 2017–2018

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          Abstract

          Cases of tick-borne diseases, including spotted fever rickettsioses, borreliosis, babesiosis, anaplasmosis and ehrlichiosis, in the United States and territories have more than doubled from 2004 to 2016 and account for 77% of all vector-borne disease reports. In an effort to inform control efforts, the presence of tick-borne pathogens and their vectors was assessed in a recreational park in Walker County, Texas. Here we report data from questing ticks collected on three dates from June 2017 to June 2018. The majority of ticks collected were Amblyomma americanum (96.69%) followed by three additional tick species: Dermacentor variabilis (2.59%), Ixodes scapularis (0.52%), and A. maculatum (0.21%). Ticks were pooled and tested for molecular evidence of bacterial and viral pathogens, respectively. All of the 68 pools of A. americanum had molecular evidence of the spotted fever group rickettsia, Rickettsia amblyommatis. Additionally, six (8.82%) of the A. americanum pools contained sequences matching Ehrlichia chaffeensis, the pathogen responsible for human monocytotropic ehrlichiosis, and 11 (16.18%) for E. ewingii. Three of the A. americanum pools demonstrated evidence of Borrelia lonestari. The presence of etiologic agents of known human disease in this study merits the continued surveillance efforts of ticks and their pathogens in areas where they could pose risks to public health.

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          Genotypic identification of rickettsiae and estimation of intraspecies sequence divergence for portions of two rickettsial genes.

          DNA sequences from specific genes, amplified by the polymerase chain reaction technique, were used as substrata for nonisotopic restriction endonuclease fragment length polymorphism differentiation of rickettsial species and genotypes. The products amplified using a single pair of oligonucleotide primers (derived from a rickettsial citrate synthase gene sequence) and cleaved with restriction endonucleases were used to differentiate almost all recognized species of rickettsiae. A second set of primers was used for differentiation of all recognized species of closely related spotted fever group rickettsiae. The procedure circumvents many technical obstacles previously associated with identification of rickettsial species. Multiple amplified DNA digest patterns were used to estimate the intraspecies nucleotide sequence divergence for the genes coding for rickettsial citrate synthase and a large antigen-coding gene of the spotted fever group rickettsiae. The estimated relationships deduced from these genotypic data correlate reasonably well with established rickettsial taxonomic schemes.
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            Phylogeny of hard- and soft-tick taxa (Acari: Ixodida) based on mitochondrial 16S rDNA sequences.

            Ticks are parasitiform mites that are obligate hematophagous ectoparasites of amphibians, reptiles, birds, and mammals. A phylogeny for tick families, subfamilies, and genera has been described based on morphological characters, life histories, and host associations. To test the existing phylogeny, we sequenced approximately 460 bp from the 3' end of the mitochondrial 16S rRNA gene (rDNA) in 36 hard- and soft-tick species; a mesostigmatid mite, Dermanyssus gallinae, was used as an outgroup. Phylogenies derived using distance, maximum-parsimony, or maximum-likelihood methods were congruent. The existing phylogeny was largely supported with four exceptions. In hard ticks (Ixodidae), members of Haemaphysalinae were monophyletic with the primitive Amblyomminae and members of Hyalomminae grouped within the Rhipicephalinae. In soft ticks (Argasidae), the derived phylogeny failed to support a monophyletic relationship among members of Ornithodorinae and supported placement of Argasinae as basal to the Ixodidae, suggesting that hard ticks may have originated from an Argas-like ancestor. Because most Argas species are obligate bird octoparasites, this result supports earlier suggestions that hard ticks did not evolve until the late Cretaceous.
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              The relevance of tick bites to the production of IgE antibodies to the mammalian oligosaccharide galactose-α-1,3-galactose.

              In 2009, we reported a novel form of delayed anaphylaxis to red meat that is related to serum IgE antibodies to the oligosaccharide galactose-α-1,3-galactose (alpha-gal). Most of these patients had tolerated meat for many years previously. The implication is that some exposure in adult life had stimulated the production of these IgE antibodies. We sought to investigate possible causes of this IgE antibody response, focusing on evidence related to tick bites, which are common in the region where these reactions occur. Serum assays were carried out with biotinylated proteins and extracts bound to a streptavidin ImmunoCAP. Prospective studies on IgE antibodies in 3 subjects after tick bites showed an increase in levels of IgE to alpha-gal of 20-fold or greater. Other evidence included (1) a strong correlation between histories of tick bites and levels of IgE to alpha-gal (χ(2) = 26.8, P < .001), (2) evidence that these IgE antibodies are common in areas where the tick Amblyomma americanum is common, and (3) a significant correlation between IgE antibodies to alpha-gal and IgE antibodies to proteins derived from A americanum (r(s) = 0.75, P < .001). The results presented here provide evidence that tick bites are a cause, possibly the only cause, of IgE specific for alpha-gal in this area of the United States. Both the number of subjects becoming sensitized and the titer of IgE antibodies to alpha-gal are striking. Here we report the first example of a response to an ectoparasite giving rise to an important form of food allergy. Copyright © 2011 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved.
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                Author and article information

                Journal
                Insects
                Insects
                insects
                Insects
                MDPI
                2075-4450
                25 September 2019
                October 2019
                : 10
                : 10
                : 315
                Affiliations
                [1 ]Department of Pathology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555, USA; nlmendel@ 123456utmb.edu
                [2 ]Department of Microbiology and Immunology, SUNY Upstate Medical University, 505 Irving Avenue, Syracuse, NY 13210, USA; ReynolEr@ 123456upstate.edu (E.S.R.); hermancm@ 123456upstate.edu (M.E.H.); chhart@ 123456utmb.edu (C.E.H.); atesterl@ 123456utmb.edu (A.T.E.)
                [3 ]Department of Internal Medicine, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555, USA; lsblanto@ 123456utmb.edu (L.S.B.); bequade@ 123456utmb.edu (B.R.Q.)
                [4 ]Department of Pathology, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA; aflondon@ 123456utmb.edu
                [5 ]The Institution for Translational Sciences, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555, USA
                [6 ]Department of Cell Biology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555, USA; cbrhendr@ 123456utmb.edu
                [7 ]Department of Entomology, Texas A&M AgriLife Research, College Station, TX 77843, USA; pteel@ 123456tamu.edu
                [8 ]Center for Biodefense and Emerging Infectious Diseases, Sealy Institute for Vaccine Studies, Center for Tropical Diseases, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555, USA
                [9 ]SUNY Center for Environmental Health and Medicine, SUNY Upstate Medical University, 505 Irving Avenue, Syracuse, NY 13210, USA
                Author notes
                [* ]Correspondence: dobouyer@ 123456utmb.edu (D.H.B.); thangams@ 123456upstate.edu (S.T.)
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-2847-0982
                https://orcid.org/0000-0002-4703-1387
                https://orcid.org/0000-0002-5043-9068
                Article
                insects-10-00315
                10.3390/insects10100315
                6836155
                31557808
                00f0b0e0-d3e0-4961-9c3f-e2347c8bf3bd
                © 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
                : 18 July 2019
                : 18 September 2019
                Categories
                Article

                rickettsiae,ehrlichiae,tick-borne disease,tick-borne disease surveillance,ixodid ticks,amblyomma americanum,amblyomma maculatum,dermacentor variabilis,ixodes scapularis,texas,usa

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