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<art>
   <ui>1756-3305-2-S1-S5</ui>
   <ji>1756-3305</ji>
   <fm>
      <dochead>Review</dochead>
      <bibl>
         <title>
            <p>New developments in canine hepatozoonosis in North America: a review</p>
         </title>
         <aug>
            <au ca="yes" id="A1">
               <snm>Little</snm>
               <mi>E</mi>
               <fnm>Susan</fnm>
               <insr iid="I1"/>
               <email>susan.little@okstate.edu</email>
            </au>
            <au id="A2">
               <snm>Allen</snm>
               <mi>E</mi>
               <fnm>Kelly</fnm>
               <insr iid="I1"/>
               <email>kelly.allen@okstate.edu</email>
            </au>
            <au id="A3">
               <snm>Johnson</snm>
               <mi>M</mi>
               <fnm>Eileen</fnm>
               <insr iid="I1"/>
               <email>eileen.johnson@okstate.edu</email>
            </au>
            <au id="A4">
               <snm>Panciera</snm>
               <mi>J</mi>
               <fnm>Roger</fnm>
               <insr iid="I1"/>
               <email>roger.panciera@okstate.edu</email>
            </au>
            <au id="A5">
               <snm>Reichard</snm>
               <mi>V</mi>
               <fnm>Mason</fnm>
               <insr iid="I1"/>
               <email>mason.reichard@okstate.edu</email>
            </au>
            <au id="A6">
               <snm>Ewing</snm>
               <mi>A</mi>
               <fnm>Sidney</fnm>
               <insr iid="I1"/>
               <email>sidney.ewing@okstate.edu</email>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Department of Veterinary Pathobiology, Center for Veterinary Health Sciences, Oklahoma State University, Stillwater, OK, USA</p>
            </ins>
         </insg>
         <source>Parasites &amp; Vectors</source>
         <supplement>
            <title>
               <p>Proceedings of the 4th Symposium on Canine Vector-Borne Diseases</p>
            </title>
            <sponsor>
               <note>Publication of the supplement has been sponsored by Bayer Animal Health GmbH.</note>
            </sponsor>
            <note>Proceedings</note>
            <url>http://www.biomedcentral.com/content/pdf/1756-3305-2-S1-info.pdf</url>
         </supplement>
         <conference>
            <title>
               <p>4th International Canine Vector-Borne Disease Symposium</p>
            </title>
            <location>Seville, Spain</location>
            <date-range>25&#8211;28 March 2009</date-range>
            <url>http://www.cvbd.org/</url>
         </conference>
         <issn>1756-3305</issn>
         <pubdate>2009</pubdate>
         <volume>2</volume>
         <issue>Suppl 1</issue>
         <fpage>S5</fpage>
         <url>http://www.parasitesandvectors.com/content/2/S1/S5</url>
         <xrefbib>
            
         <pubidlist><pubid idtype="pmpid">19426444</pubid><pubid idtype="doi">10.1186/1756-3305-2-S1-S5</pubid></pubidlist></xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>26</day>
               <month>3</month>
               <year>2009</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2009</year>
         <collab>Little et al; licensee BioMed Central Ltd.</collab>
         <note>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</note>
      </cpyrt>
      <abs>
         <sec>
            <st>
               <p>Abstract</p>
            </st>
            <p>Canine hepatozoonosis is caused by <it>Hepatozoon canis </it>and <it>Hepatozoon americanum</it>, apicomplexan parasites transmitted to dogs by ingestion of infectious stages. Although the two agents are phylogenetically related, specific aspects, including characteristics of clinical disease and the natural history of the parasites themselves, differ between the two species. Until recently, <it>H. canis </it>infections had not been clearly documented in North America, and autochthonous infection with <it>H. americanum </it>has yet to be reported outside of the southern United States. However, recent reports demonstrate <it>H. canis </it>is present in areas of North America where its vector tick, <it>Rhipicephalus sanguineus</it>, has long been endemic, and that the range of <it>H. americanum </it>is likely expanding along with that of its vector tick, <it>Amblyomma maculatum</it>; co-infections with the two organisms have also been identified. Significant intraspecific variation has been reported in the 18S rRNA gene sequence of both <it>Hepatozoon </it>spp.-infecting dogs, suggesting that each species may represent a complex of related genogroups rather than well-defined species. Transmission of <it>H. americanum </it>to dogs via ingestion of cystozoites in muscle of infected vertebrates was recently demonstrated, supporting the concept of predation as a means of natural transmission. Although several exciting advances have occurred in recent years, much remains to be learned about patterns of infection and the nature of clinical disease caused by the agents of canine hepatozoonosis in North America.</p>
         </sec>
      </abs>
   </fm>
   <bdy>
      <sec>
         <st>
            <p>Background</p>
         </st>
         <p><it>Hepatozoon canis </it>has long been recognised to infect and cause disease in dogs in Asia, southern Europe, the Middle East, Africa and South America. In 1978, cases of hepatozoonosis were recognised for the first time in the southern United States and initially attributed to a more pathogenic strain of <it>H. canis </it><abbrgrp><abbr bid="B1">1</abbr></abbrgrp>. However, subsequent work demonstrated that the causative agent was a distinct species, <it>H. americanum</it>, and the disease induced became known as American canine hepatozoonosis <abbrgrp><abbr bid="B2">2</abbr><abbr bid="B3">3</abbr><abbr bid="B4">4</abbr><abbr bid="B5">5</abbr><abbr bid="B6">6</abbr></abbrgrp>. The life cycle of both <it>H. canis </it>and <it>H. americanum </it>involves a tick-definitive host, where fertilisation, oocyst formation and sporogony occur, and a canine or other mammalian intermediate host, in which merogony and gamont formation occurs <abbrgrp><abbr bid="B7">7</abbr></abbrgrp>. Gamonts are acquired by ticks during feeding, but sporozoites are released to infect the intermediate host only upon ingestion of the infected tick itself <abbrgrp><abbr bid="B8">8</abbr></abbrgrp>. Although somewhat similar in overall life cycle, the two <it>Hepatozoon </it>spp. reported from dogs differ in several ways, including aspects of the clinical disease they cause in dogs, the species of tick used as a definitive host and their geographic distribution.</p>
      </sec>
      <sec>
         <st>
            <p>Clinical features of canine hepatozoonoses</p>
         </st>
         <p>Dogs with American canine hepatozoonosis present with severe, febrile disease characterised by lethargy, myalgia, lameness and mucopurulent ocular discharge. Radiographs may reveal periosteal proliferation of long bones. A profound neutrophilic leukocytosis is often present, but gamonts are only rarely found in blood smears <abbrgrp><abbr bid="B9">9</abbr></abbrgrp>. In contrast, dogs with canine hepatozoonosis caused by <it>H. canis </it>are often clinically normal or develop only mild disease. With high parasitemia or in cases of co-infection with other tick-borne disease agents, dogs with <it>H. canis </it>may develop mild to severe clinical disease characterised by fever, lethargy and emaciation. Osteoproliferative lesions are only rarely described with <it>H. canis </it>infection <abbrgrp><abbr bid="B10">10</abbr></abbrgrp>, and thus radiographs are usually unremarkable. Leukocyte counts are also usually normal or only slightly elevated, and gamonts are numerous, infecting as many as 100% of neutrophils observed <abbrgrp><abbr bid="B7">7</abbr></abbrgrp>.</p>
      </sec>
      <sec>
         <st>
            <p>Tick vectors and geographic distribution of agents</p>
         </st>
         <sec>
            <st>
               <p>Hepatozoon americanum</p>
            </st>
            <p>The definitive host and tick vector of <it>H. americanum </it>is <it>Amblyomma maculatum</it>, the Gulf Coast tick, which in North America was historically limited to areas along the Gulf Coast and southern Atlantic coast <abbrgrp><abbr bid="B11">11</abbr></abbrgrp>. This tick has also been reported from Central America and northern South America <abbrgrp><abbr bid="B12">12</abbr></abbrgrp>. Reports of <it>H. americanum </it>infection in dogs outside of the U.S. are lacking, although one survey of wildlife described an 18S rDNA sequence 97% similar to that of <it>H. americanum </it>from a crab-eating fox from Brazil <abbrgrp><abbr bid="B13">13</abbr></abbrgrp>. In recent decades, the range of <it>A. maculatum </it>has expanded northward with populations now established in areas of Oklahoma, Kansas, Kentucky and some other states <abbrgrp><abbr bid="B12">12</abbr><abbr bid="B14">14</abbr></abbrgrp>. In addition, <it>H. americanum </it>has been reported from California, Washington and Vermont <abbrgrp><abbr bid="B15">15</abbr></abbrgrp>, states outside the recognised range of the tick vector, presumably due to relocation of infected dogs from endemic areas.</p>
         </sec>
         <sec>
            <st>
               <p>Hepatozoon canis</p>
            </st>
            <p>The main vector of <it>H. canis </it>is <it>Rhipicephalus sanguineus</it>, the brown dog tick, although other ticks have also been reported as hosts <abbrgrp><abbr bid="B16">16</abbr><abbr bid="B17">17</abbr><abbr bid="B18">18</abbr><abbr bid="B19">19</abbr><abbr bid="B20">20</abbr></abbrgrp>. <it>Rhipicephalus sanguineus </it>is found in temperate and tropical regions worldwide, and cases of <it>H. canis </it>have been reported from southern Europe, Asia, Africa, the Middle East and South America <abbrgrp><abbr bid="B7">7</abbr></abbrgrp>. However, prior to 2008, <it>H. canis </it>had not been definitively identified in dogs or wild canids in North America. Since that time, <it>H. canis </it>has been confirmed in 30 dogs in the United States by PCR, 14 of which were also infected with <it>H. americanum </it><abbrgrp><abbr bid="B15">15</abbr><abbr bid="B21">21</abbr></abbrgrp>, and identified in 5 dogs on the Caribbean island of Grenada <abbrgrp><abbr bid="B22">22</abbr></abbrgrp>. Gamonts, presumably <it>H. canis</it>, were also identified on blood smear from one dog from the U.S. that had been PCR-confirmed as infected with <it>H. canis</it>, but not <it>H. americanum </it><abbrgrp><abbr bid="B15">15</abbr></abbrgrp>. Infection has also been identified by sequence-confirmed PCR in a grey fox from Georgia (M. Yabsley, pers. comm.), further supporting the interpretation that this organism is present and actively transmitted to canids in North America.</p>
         </sec>
      </sec>
      <sec>
         <st>
            <p>Intraspecific variation</p>
         </st>
         <p>The only <it>Hepatozoon </it>species described from dogs to date are <it>H. canis </it>and <it>H. americanum</it>; both have variation in reported 18S rRNA gene sequences <abbrgrp><abbr bid="B21">21</abbr><abbr bid="B23">23</abbr></abbrgrp>. Although complete sequence data is available from only 2 dogs, identity among the 18S rDNA fragments reported from dogs infected with <it>H. americanum </it>ranges from 92.7&#8211;99.6% <abbrgrp><abbr bid="B21">21</abbr></abbrgrp>. Among <it>H. canis </it>sequences, the identity reported is 97&#8211;100% <abbrgrp><abbr bid="B21">21</abbr><abbr bid="B23">23</abbr></abbrgrp>. Although strain variations likely account for the differences in sequence of 18S rRNA gene, the genogroup clusters from the sequence data available to date do not appear to correspond with geographic location of the dogs or severity of disease seen (data not shown). Acquisition of larger data sets with detailed information on clinical and travel history of the dogs will be necessary to more fully understand the significance, if any, of the sequence variation seen.</p>
      </sec>
      <sec>
         <st>
            <p>Novel transmission routes</p>
         </st>
         <p>In both the <it>H. canis </it>and <it>H. americanum </it>systems, dogs have been shown capable of infecting immature ticks with gamonts that develop to infectious oocysts and are able to infect a new dog upon ingestion <abbrgrp><abbr bid="B24">24</abbr></abbrgrp>. For <it>H. canis</it>, dogs are likely the preeminent reservoir host because the preferred vector tick, <it>R. sanguineus</it>, feeds preferentially on dogs in all three active life stages <abbrgrp><abbr bid="B25">25</abbr></abbrgrp>. A variety of species of fox have also been reported infected with <it>H. canis </it><abbrgrp><abbr bid="B13">13</abbr></abbrgrp>, and thus wild canids may play a role in maintaining a source of infection in nature. In contrast, immature <it>A. maculatum </it>are more frequently found feeding on ground-dwelling birds, rodents and rabbits than on canids, although all three stages have been reported from coyotes <abbrgrp><abbr bid="B11">11</abbr></abbrgrp>. Infection of wild coyotes with <it>H. americanum </it>in <it>A. maculatum</it>-endemic areas has been documented <abbrgrp><abbr bid="B26">26</abbr><abbr bid="B27">27</abbr></abbrgrp>. Coyotes have been shown to be experimentally susceptible to infection and disease and are capable of infecting immature ticks <abbrgrp><abbr bid="B27">27</abbr><abbr bid="B28">28</abbr></abbrgrp>. However, the predominance of immature <it>A. maculatum </it>on other vertebrate species led to persistent questions about the role hosts other than canids may play in creating a source of infection for ticks <abbrgrp><abbr bid="B6">6</abbr><abbr bid="B9">9</abbr></abbrgrp>.</p>
         <p>Results from recent experiments confirm the validity of these suspicions. Ingestion of <it>H. americanum </it>sporozoites was shown to lead to the development of cystozoites in muscle tissue of cotton rats <abbrgrp><abbr bid="B29">29</abbr></abbrgrp>. Muscle from infected rats was infectious to a dog, inducing the characteristic clinical disease of American canine hepatozoonosis <abbrgrp><abbr bid="B30">30</abbr></abbrgrp>. Similar experiments with <it>H. americanum </it>in the past using muscle from infected dogs failed to result in transmission <abbrgrp><abbr bid="B2">2</abbr><abbr bid="B31">31</abbr></abbrgrp>, and although monozoic cysts have been described in dogs infected with <it>H. canis </it><abbrgrp><abbr bid="B32">32</abbr></abbrgrp>, to our knowledge no feeding experiments to evaluate their infectivity have been reported. Despite testing a number of animals in endemic areas, naturally occurring infection with <it>H. americanum </it>in wild rodents, rabbits or vertebrates other than canids has not yet been demonstrated (<abbrgrp><abbr bid="B33">33</abbr></abbrgrp>; K. Allen, unpub. data), but evidence is mounting to support the role of wild vertebrates as an important paratenic host for this parasite. Transplacental infection has also been shown to occur with <it>H. canis </it><abbrgrp><abbr bid="B34">34</abbr></abbrgrp>, but this transmission route has not been seen in <it>H. americanum</it>.</p>
      </sec>
      <sec>
         <st>
            <p>Conclusion</p>
         </st>
         <p>Although these new data are exciting, many important questions remain about canine hepatozoonosis in North America. The variation in 18S rDNA sequence reported from infected dogs suggests that multiple strains or species of <it>Hepatozoon</it>, which could vary in their pathogenicity and life history patterns, may be infecting and causing disease in dogs <abbrgrp><abbr bid="B21">21</abbr></abbrgrp>. Discovery of an infectious cystozoite stage in rodents suggests vertebrates other than canids could prove to be important in maintaining <it>H. americanum </it>infections in nature by serving as paratenic hosts that infect dogs through predation <abbrgrp><abbr bid="B29">29</abbr><abbr bid="B30">30</abbr></abbrgrp>; the ability of other vertebrates to infect immature ticks remains to be determined, as does the role, if any, of the monozoic cyst form described in dogs with <it>H. canis </it><abbrgrp><abbr bid="B32">32</abbr></abbrgrp> in transmitting infection. In addition, defining the extent to which <it>H. canis </it>infects dogs in North America is of great interest. In contrast to those caused by <it>H. americanum</it>, <it>H. canis </it>infections are often clinically inapparent, particularly in otherwise healthy dogs <abbrgrp><abbr bid="B7">7</abbr></abbrgrp>, and thus this agent may be more common in dogs in this region than currently realised. The presence of a number of other endemic tick-borne infections, including anaplasmosis, babesiosis, borreliosis, ehrlichiosis and Rocky Mountain spotted fever <abbrgrp><abbr bid="B35">35</abbr><abbr bid="B36">36</abbr><abbr bid="B37">37</abbr></abbrgrp>, provides ample opportunity for co-infection and more severe disease. The agents of hepatozoonosis, like those of other vector-borne diseases, present international challenges; these important questions can be addressed only through sustained collaboration between veterinarians and parasitologists worldwide with expertise in <it>H. canis </it>and <it>H. americanum</it>.</p>
      </sec>
      <sec>
         <st>
            <p>Competing interests</p>
         </st>
         <p>Dr. Little (SEL) receives financial support for her research on ticks and tick-borne diseases from the veterinary pharmaceutical industry, the National Institutes of Health (USA) and private foundations.</p>
      </sec>
      <sec>
         <st>
            <p>Authors' contributions</p>
         </st>
         <p>This work reviews recent findings from a collaborative effort among researchers at Oklahoma State University that identify and characterise <it>Hepatozoon </it>sp. infections in dogs and other animals with molecular techniques (SEL, KEA) and classical studies to describe lesions and parasite life stages in vertebrate and invertebrate hosts and identify the role of wild vertebrates in the maintenance and transmission of <it>H. americanum </it>(EMJ, MVR, RJP, SAE).</p>
      </sec>
   </bdy>
   <bm>
      <ack>
         <sec>
            <st>
               <p>Acknowledgements</p>
            </st>
            <p>The research findings reviewed in this article were supported by the Krull-Ewing Endowment in Veterinary Parasitology at Oklahoma State University as well as intramurally through the Center for Veterinary Health Sciences, Oklahoma State University.</p>
            <p>This article is published as part of <it>Parasites &amp; Vectors </it>Volume 2 Supplement 1, 2009: Proceedings of the 4th International Canine Vector-Borne Disease Symposium. The full contents of the supplement are available online at <url>http://www.parasitesandvectors.com/supplements/2/S1</url>.</p>
            <p>Publication of the supplement has been sponsored by Bayer Animal Health GmbH.</p>
         </sec>
      </ack>
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