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      Observation of a novel Babesia spp. in Eastern Grey Kangaroos ( Macropus giganteus) in Australia

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          Abstract

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          Highlights

          ► New Babesia is identified in kangaroo. ► The origin is unknown. ► Caused severe anaemia and death in the infected kangaroos.

          Abstract

          The roles and epidemiological features of tick-borne protozoans are not well elicited in wildlife. Babesia spp. are documented in many domestic animals, including cattle, horses, pigs, dogs and cats. Three cases affecting eastern grey kangaroos are described. The kangaroos exhibited neurological signs, depression and marked anaemia, and microscopic examination of blood smears revealed intraerythrocytic piroplasms. One to seven intraerythrocytic spherical, oval, pyriform and irregularly-shaped parasites consistent with Babesia spp. were seen in the blood smears and the percentage of infected erythrocytes was estimated to be approximately 7% in each case. Data suggest that the tick vector for this kangaroo Babesia sp. is a Haemaphysalis species. For Case 2, ultrastructural examination of the erythrocytes of the renal capillaries showed parasites resembling Babesia spp. and 18 of 33 erythrocytes were infected. DNA sequencing of the amplified 18S rDNA confirmed that the observed intraerythrocytic piroplasms belong to the genus Babesia. The phylogenetic position of this new kangaroo Babesia sp. (de novo Babesia macropus), as a sister species to the new Australian woylie Babesia sp., suggests a close affinity to the described Afro–Eurasian species Babesia orientalis and Babesia occultans suggesting perhaps a common ancestor for the Babesia in kangaroos.

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          Most cited references48

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          MRBAYES: Bayesian inference of phylogenetic trees.

          The program MRBAYES performs Bayesian inference of phylogeny using a variant of Markov chain Monte Carlo. MRBAYES, including the source code, documentation, sample data files, and an executable, is available at http://brahms.biology.rochester.edu/software.html.
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            The characterization of enzymatically amplified eukaryotic 16S-like rRNA-coding regions.

            Polymerase chain reaction conditions were established for the in vitro amplification of eukaryotic small subunit ribosomal (16S-like) rRNA genes. Coding regions from algae, fungi, and protozoa were amplified from nanogram quantities of genomic DNA or recombinant plasmids containing rDNA genes. Oligodeoxynucleotides that are complementary to conserved regions at the 5' and 3' termini of eukaryotic 16S-like rRNAs were used to prime DNA synthesis in repetitive cycles of denaturation, reannealing, and DNA synthesis. The fidelity of synthesis for the amplification products was evaluated by comparisons with sequences of previously reported rRNA genes or with primer extension analyses of rRNAs. Fewer than one error per 2000 positions were observed in the amplified rRNA coding region sequences. The primary structure of the 16S-like rRNA from the marine diatom, Skeletonema costatum, was inferred from the sequence of its in vitro amplified coding region.
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              Zoonotic babesiosis: overview of the disease and novel aspects of pathogen identity.

              Babesiosis is a zoonosis caused by tick-transmitted intraerythrocytic protozoa of the Phylum Apicomplexa. The disease mostly occurs in the USA, but cases have also been reported in several European countries, in Egypt, India, Japan, Korea, Taiwan, and South Africa. The main pathological event is lysis of erythrocytes resulting in haemolytic anaemia, which in severe cases may lead to organ failure and death, particularly in immunocompromised patients. The 2 groups of parasites involved, Babesia microti-like and Babesia sensu stricto (s.s.) species, differ in their life cycle characteristics and susceptibility to antibabesial drugs. Molecular taxonomy is now making a major contribution to the identification of novel pathogens within both groups. Effective treatment of severe cases was initially hampered by the lack of specific antibabesial drugs for human use, but increased use of supportive measures and of the recently developed antimalarial, atovaquone, particularly in combination with azithromycin, has improved the prospects for management of acute disease especially when caused by Babesia s.s. species. Prevention should be based primarily on increasing the awareness of physicians and the public to the risks, but infection from blood transfusions is particularly difficult to prevent. Expanding deer populations, resulting in wider distribution and greater abundance of ticks, heightened medical awareness, and growing numbers of immunocompromised patients are likely to result in a continuing rise of reported cases. Copyright © 2009 Elsevier GmbH. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Int J Parasitol Parasites Wildl
                Int J Parasitol Parasites Wildl
                International Journal for Parasitology. Parasites and Wildlife
                Elsevier
                2213-2244
                31 December 2012
                31 December 2012
                December 2013
                : 2
                : 54-61
                Affiliations
                [a ]Elizabeth Macarthur Agricultural Institute, New South Wales Department of Primary Industries, Woodbridge Road, Menangle, NSW 2568, Australia
                [b ]Queensland Alliance for Agriculture & Food Innovation, The University of Queensland, 306 Carmody Road, St. Lucia, Qld 4072, Australia
                [c ]Moruya Veterinary Hospital, 86-88 Queens St. Moruya, NSW 2537, Australia
                [d ]Tick Fever Centre, Queensland Department of Agriculture, Fisheries & Forestry, 280 Grindle Road, Wacol, Qld 4076, Australia
                [e ]Biosecurity Queensland, Queensland Department of Agriculture, Fisheries & Forestry, 39 Kessels Road, Coopers Plains, Qld 4108, Australia
                [f ]Animal Science, Queensland Department of Agriculture, Fisheries & Forestry, 306 Carmody Road, St. Lucia, Qld 4072, Australia
                Author notes
                [* ]Corresponding author. Present address: School of Animal and Veterinary Sciences, Charles Sturt University, Wagga Wagga, NSW 2678, Australia. Postal address: P.O. Box: 895, Fairfield, NSW 1860, Australia. Tel.: +61 401930939. kaiser.dawood@ 123456gmail.com
                Article
                S2213-2244(12)00012-0
                10.1016/j.ijppaw.2012.12.001
                3862514
                24533316
                b20584a2-769d-4e0f-a5e7-aa5d09469363
                © 2013 Published by Elsevier Ltd on behalf of Australian Society for Parasitology.
                History
                : 27 September 2012
                : 4 December 2012
                : 13 December 2012
                Categories
                Article

                babesia,kangaroo,apicomplexan,haematology
                babesia, kangaroo, apicomplexan, haematology

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