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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Vet. Sci.</journal-id>
<journal-title-group>
<journal-title>Frontiers in Veterinary Science</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Vet. Sci.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2297-1769</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fvets.2025.1732337</article-id>
<article-version article-version-type="Version of Record" vocab="NISO-RP-8-2008"/>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Review</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>The impact of parasitic diseases on dromedary camel (<italic>Camelus dromedarius</italic>) welfare: a comprehensive review</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Nawaz</surname><given-names>Saqib</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="author-notes" rid="fn0001"><sup>&#x2020;</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/3333023"/>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Data curation" vocab-term-identifier="https://credit.niso.org/contributor-roles/data-curation/">Data curation</role>
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</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Tharwat</surname><given-names>Mohamed</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
<xref ref-type="author-notes" rid="fn0001"><sup>&#x2020;</sup></xref>
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<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="conceptualization" vocab-term-identifier="https://credit.niso.org/contributor-roles/conceptualization/">Conceptualization</role>
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<aff id="aff1"><label>1</label><institution>Anhui Province Key Laboratory of Veterinary Pathobiology and Disease Control, College of Veterinary Medicine, Anhui Agricultural University</institution>, <city>Hefei</city>, <country country="cn">China</country></aff>
<aff id="aff2"><label>2</label><institution>Department of Clinical Sciences, College of Veterinary Medicine, Qassim University</institution>, <city>Buraidah</city>, <country country="sa">Saudi Arabia</country></aff>
<author-notes>
<corresp id="c001"><label>&#x002A;</label>Correspondence: Mohamed Tharwat, <email xlink:href="mailto:atieh@qu.edu.sa">atieh@qu.edu.sa</email></corresp>
<fn fn-type="other" id="fn0001"><label>&#x2020;</label><p>ORCID: Saqib Nawaz, <uri xlink:href="https://orcid.org/0000-0002-9617-3074">orcid.org/0000-0002-9617-3074</uri>; Mohamed Tharwat, <uri xlink:href="https://orcid.org/0000-0002-3796-9590">orcid.org/0000-0002-3796-9590</uri></p></fn>
</author-notes>
<pub-date publication-format="electronic" date-type="pub" iso-8601-date="2026-01-23">
<day>23</day>
<month>01</month>
<year>2026</year>
</pub-date>
<pub-date publication-format="electronic" date-type="collection">
<year>2025</year>
</pub-date>
<volume>12</volume>
<elocation-id>1732337</elocation-id>
<history>
<date date-type="received">
<day>25</day>
<month>10</month>
<year>2025</year>
</date>
<date date-type="rev-recd">
<day>17</day>
<month>12</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>26</day>
<month>12</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2026 Nawaz and Tharwat.</copyright-statement>
<copyright-year>2026</copyright-year>
<copyright-holder>Nawaz and Tharwat</copyright-holder>
<license>
<ali:license_ref start_date="2026-01-23">https://creativecommons.org/licenses/by/4.0/</ali:license_ref>
<license-p>This is an open-access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License (CC BY)</ext-link>. The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</license-p>
</license>
</permissions>
<abstract>
<p>The dromedary camel (<italic>Camelus dromedarius</italic>) is a multifunctional animal indispensable for the livelihoods and food security of pastoralist communities residing in arid and semi-arid regions. Despite its socio-economic and cultural significance, the welfare of camels has garnered limited scientific scrutiny, particularly regarding the effects of parasitic diseases. These diseases pose a significant barrier to camel health, resulting in considerable production losses and severe welfare challenges. This review consolidates evidence on the impact of parasitic infections, which include hemoparasites (<italic>Trypanosoma evansi</italic>, <italic>Babesia</italic>, and <italic>Theileria</italic>), ectoparasites (ticks and mange mites), and endoparasites (gastrointestinal nematodes and <italic>coccidia</italic>) on the welfare of dromedary camels. We investigate the physiological and emotional repercussions of parasitism through the lenses of the Five Freedoms and the Five Domains model. This review demonstrates that parasitic diseases severely impact camel welfare, yet it highlights significant deficiencies in the species-specific assessment and surveillance systems needed to address these problems. Furthermore, it underscores the relationship between camel welfare, human health through zoonotic parasites, and the socio-economic stability of pastoral communities. The review concludes that an integrated, multidisciplinary approach combining veterinary parasitology, animal welfare science, and socioeconomics is urgently required. We advocate for the implementation of a cohesive One Health/One Welfare framework to establish validated welfare indicators, enhance diagnostic and control strategies, promote community engagement, and inform effective policies. This strategy is crucial for alleviating suffering, improving productivity, and sustaining livelihoods that depend on camels in the face of climate change.</p>
</abstract>
<kwd-group>
<kwd>animal welfare</kwd>
<kwd>dromedary camel</kwd>
<kwd>one health</kwd>
<kwd>parasitic diseases</kwd>
<kwd>pastoralism</kwd>
</kwd-group>
<funding-group>
<funding-statement>The author(s) declared that financial support was received for this work and/or its publication.</funding-statement>
</funding-group>
<counts>
<fig-count count="2"/>
<table-count count="3"/>
<equation-count count="0"/>
<ref-count count="119"/>
<page-count count="12"/>
<word-count count="10383"/>
</counts>
<custom-meta-group>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>One Health</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec1">
<label>1</label>
<title>Introduction</title>
<p>The dromedary camel (<italic>Camelus dromedarius</italic>) is a species specially adapted to thrive in arid and semi-arid environments, where it plays an essential role in providing resilience against water shortages, extreme temperatures, and limited grazing opportunities (<xref ref-type="bibr" rid="ref1">1</xref>). Its physiological adaptations, such as efficient water metabolism, exceptional heat tolerance, and specialized movement across sandy terrains, enable it to survive in conditions where other livestock cannot. These traits have supported the livelihoods of pastoralist communities across North Africa, the Middle East, and Asia for thousands of years (<xref ref-type="bibr" rid="ref2">2</xref>). Today, approximately 35 million dromedary camels are distributed across 47 countries, underscoring their enduring social and economic importance (<xref ref-type="bibr" rid="ref3">3</xref>). The camel&#x2019;s value extends beyond transport to being a crucial source of milk, meat, and income, thereby underpinning the food security and economic resilience of pastoralist communities (<xref ref-type="bibr" rid="ref4">4</xref>). Its deep cultural significance further cements its role in the social fabric of these regions (<xref ref-type="bibr" rid="ref5">5</xref>).</p>
<p>However, despite their socio-economic value, dromedary camel welfare remains a critically under-researched area, with parasitic diseases representing a particularly neglected aspect (<xref ref-type="bibr" rid="ref6">6</xref>). Key knowledge gaps persist, including: a lack of validated, species-specific welfare indicators tailored to camels; an incomplete understanding of the affective states (e.g., pain, itching, distress) induced by different parasites; and insufficient integration of parasitology and welfare science within a cohesive framework that also considers human and environmental health (<xref ref-type="bibr" rid="ref6">6</xref>, <xref ref-type="bibr" rid="ref7">7</xref>).</p>
<p>A major obstacle to dromedary camel welfare is their high susceptibility to a wide range of parasitic infections. Assessing welfare in this species is challenging due to extensive management systems and limited veterinary infrastructure (<xref ref-type="bibr" rid="ref8">8</xref>), creating a pressing need for validated, camel-specific assessment protocols (<xref ref-type="bibr" rid="ref9">9</xref>). Parasitic diseases exacerbate this challenge by causing not only production losses but also significant, often overlooked, welfare compromises (<xref ref-type="bibr" rid="ref8">8</xref>). This review, therefore, aims to synthesize current evidence on the multifaceted impact of parasitic diseases on dromedary camel welfare (<xref ref-type="bibr" rid="ref10">10</xref>). We will examine how parasitism influences key welfare domains (nutrition, physical health, behavior, and mental state) while also considering the broader implications for pastoralist livelihoods and public health through zoonotic transmission (<xref ref-type="bibr" rid="ref3">3</xref>). By integrating insights from disease ecology, welfare assessment, and socio-economics, this review is structured around a cohesive One Health/One Welfare approach, highlighting the inextricable links between animal, human, and environmental well-being (<xref ref-type="bibr" rid="ref11">11</xref>).</p>
</sec>
<sec id="sec2">
<label>2</label>
<title>Parasitic diseases and animal welfare</title>
<p>Animal welfare encompasses the overall well-being of an animal, including its physical health, mental state, and ability to perform natural behaviors. The Five Freedoms framework highlights essential rights, such as freedom from hunger and thirst, discomfort, pain, injury, and disease, as well as fear and distress, and the freedom to exhibit normal behavior (<xref ref-type="bibr" rid="ref4">4</xref>). Building on this, the more recent Five Domains model offers a detailed method to assess welfare through nutrition, environment, health, and behavior, with the fifth domain emphasizing the animal&#x2019;s mental state and subjective experiences (<xref ref-type="bibr" rid="ref12">12</xref>). Parasitic diseases pose a serious threat to each of the Five Freedoms in camels. First, the freedom from hunger and thirst is undermined as gastrointestinal nematodes compete for nutrients and can cause diarrhea, resulting in malnutrition and dehydration (<xref ref-type="bibr" rid="ref13">13</xref>, <xref ref-type="bibr" rid="ref14">14</xref>). Moreover, parasites like mange mites cause intense skin irritation, infringing on the freedom from discomfort by causing persistent itching. Even more concerning, infections such as <italic>Trypanosoma evansi</italic> can cause anemia and systemic weakness, challenging the freedom from pain, injury, and disease (<xref ref-type="bibr" rid="ref15">15</xref>, <xref ref-type="bibr" rid="ref16">16</xref>). The freedom to express normal behavior is also affected, as tick or mange mite infestations lead to excessive scratching and restlessness, reducing grazing time and possibly leading to social isolation (<xref ref-type="bibr" rid="ref16">16</xref>, <xref ref-type="bibr" rid="ref17">17</xref>). Lastly, the chronic pain and suffering from untreated parasitic infections, along with the stress of delayed treatment or culling, compromise the freedom from fear and distress (<xref ref-type="bibr" rid="ref18">18</xref>). Therefore, controlling parasites effectively is not just a production concern but an essential part of protecting the overall welfare of camelids (<xref ref-type="bibr" rid="ref19">19</xref>) (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p>Schematic illustration showing how parasitic infections compromise the five freedoms of animal welfare in camelids. The diagram emphasizes the direct pathways through which common parasites, especially gastrointestinal nematodes, impact welfare: causing discomfort (pruritus, skin irritation), pain and disease (anemia, systemic weakness), hunger and thirst (malnutrition, diarrhea, dehydration), and ultimately resulting in abnormal behaviors (scratching, restlessness, social isolation) as well as fear and distress.</p>
</caption>
<graphic xlink:href="fvets-12-1732337-g001.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Schematic diagram illustrating how parasitic infections compromise the Five Freedoms of animal welfare in camels. A central camel figure is linked to welfare impacts from common parasites like gastrointestinal nematodes. Pathways show: Freedom from Hunger/Thirst compromised by malnutrition, diarrhea, and dehydration. Freedom from Discomfort by pruritus and skin irritation. Freedom from Pain/Injury by anemia and systemic weakness. Freedom to Express Normal Behavior is hindered, leading to scratching, restlessness, reduced grazing, and social isolation. These combined effects ultimately violate the Freedom from Fear and Distress, resulting in stress and fear.</alt-text>
</graphic>
</fig>
<p>Implementing these models for dromedary camels requires context-specific modifications, which include extensive nomadic pastoralism, limited access to veterinary care, and ongoing exposure to parasites and extreme climates (<xref ref-type="bibr" rid="ref20">20</xref>). Parasitic infections cause a range of welfare concerns through both direct physiological harm and indirect behavioral effects. For example, gastrointestinal nematodes interfere with nutrient absorption, leading to weight loss, diarrhea, and chronic dehydration (<xref ref-type="bibr" rid="ref21">21</xref>). Ectoparasites, such as ticks and mange mites, cause severe itching, skin scratching, and lesions, which lead to restlessness and discomfort. These infestations trigger chronic stress responses that may weaken immune function and reduce overall resilience (<xref ref-type="bibr" rid="ref5">5</xref>). Hemoparasitic infections, like those caused by <italic>Trypanosoma evansi</italic>, result in anemia, significant lethargy, and generalized weakness, clearly indicating serious welfare problems (<xref ref-type="bibr" rid="ref22">22</xref>). The clinical signs of these parasitic infections often include decreased mobility, social withdrawal, and excessive scratching, which disrupt natural herd dynamics and social structures (<xref ref-type="bibr" rid="ref23">23</xref>). Chronic diseases, especially when combined with poor management practices, cause prolonged stress, further lowering both welfare and productivity (<xref ref-type="bibr" rid="ref9">9</xref>).</p>
<p>A comprehensive welfare assessment in dromedary camels requires developing and validating species-specific Animal-Based Measures (ABMs). Recent protocols highlight several important indicators (<xref ref-type="bibr" rid="ref24">24</xref>), including Body Condition Score (BCS), coat quality, and the presence of skin lesions or ocular discharge, which reflect nutritional status and parasite burden (<xref ref-type="bibr" rid="ref9">9</xref>, <xref ref-type="bibr" rid="ref25">25</xref>, <xref ref-type="bibr" rid="ref26">26</xref>). Also noted are signs such as abnormal scratching, reduced rumination, social withdrawal, and decreased grazing efficiency (<xref ref-type="bibr" rid="ref10">10</xref>, <xref ref-type="bibr" rid="ref25">25</xref>). Anemia, evaluated through packed cell volume, and the quantitative measurement of parasite load in blood or feces, are also crucial (<xref ref-type="bibr" rid="ref27">27</xref>, <xref ref-type="bibr" rid="ref28">28</xref>). Pastoralists often observe subtle signs of distress like decreased appetite, reduced milk production, or reluctance to walk, providing essential context (<xref ref-type="bibr" rid="ref29">29</xref>).</p>
<p>Nevertheless, the consistent implementation of these ABMs faces considerable obstacles within extensive camelid production systems. The nomadic management across expansive territories complicates regular clinical assessments. Moreover, the limited availability of veterinary services in remote regions leads to substantial underreporting and delays in the treatment of parasitic infections (<xref ref-type="bibr" rid="ref9">9</xref>, <xref ref-type="bibr" rid="ref30">30</xref>). Cultural attitudes that perceive parasites as an unavoidable burden often postpone intervention until clinical manifestations become severe (<xref ref-type="bibr" rid="ref23">23</xref>). A significant drawback is the absence of universally standardized and validated welfare protocols specific to camels, in contrast to those developed for cattle and small ruminants (<xref ref-type="bibr" rid="ref8">8</xref>, <xref ref-type="bibr" rid="ref31">31</xref>). This situation often renders the pain caused by chronic, debilitating conditions (<xref ref-type="bibr" rid="ref9">9</xref>) like hemoparasitism &#x2018;invisible,&#x2019; leading to a pervasive underestimation of suffering (<xref ref-type="bibr" rid="ref12">12</xref>, <xref ref-type="bibr" rid="ref32">32</xref>) (<xref ref-type="table" rid="tab1">Table 1</xref>).</p>
<table-wrap position="float" id="tab1">
<label>Table 1</label>
<caption>
<p>Validated and potential animal-based measures (ABMs) for welfare assessment in dromedary camels.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Welfare domain</th>
<th align="left" valign="top">Animal-based measure (ABM)</th>
<th align="left" valign="top">Description</th>
<th align="left" valign="top">Association with parasitic disease</th>
<th align="left" valign="top">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" rowspan="2">Nutrition</td>
<td align="left" valign="top">Body condition score (BCS)</td>
<td align="left" valign="top">5-point or 9-point scale assessing fat and muscle cover over ribs, spine, and pelvis.</td>
<td align="left" valign="top">Low BCS is directly linked to GI nematodes, trypanosomiasis (chronic form).</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref103">103</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Camel grimace scale (Potential)</td>
<td align="left" valign="top">Facial expression scoring for pain (e.g., orbital tightening, ear position, muzzle tension).</td>
<td align="left" valign="top">Validated in other livestock; high potential to assess pain from mange and lameness.</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref20">20</xref>, <xref ref-type="bibr" rid="ref104">104</xref>)</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="3">Health</td>
<td align="left" valign="top">Packed cell volume</td>
<td align="left" valign="top">Percentage of red blood cells in blood; measured via microhematocrit.</td>
<td align="left" valign="top">Key indicator for hemoparasites (e.g., <italic>T. evansi</italic>, <italic>Anaplasma</italic>) and hematophagous parasites.</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref105">105</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Skin lesion score</td>
<td align="left" valign="top">Quantitative assessment of area and severity of lesions (e.g., from mange, ticks).</td>
<td align="left" valign="top">Directly measures the impact of ectoparasites.</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref106">106</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Ocular/nasal discharge</td>
<td align="left" valign="top">Presence/absence or severity score of abnormal discharge.</td>
<td align="left" valign="top">It can indicate general systemic illness or specific infections.</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref107">107</xref>)</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="3">Behavior</td>
<td align="left" valign="top">Scratch index</td>
<td align="left" valign="top">Number of scratching bouts per unit time (e.g., per 15&#x202F;min).</td>
<td align="left" valign="top">Direct indicator of pruritus from mange mites, lice, or ticks.</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref108">108</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Grazing/rumination time</td>
<td align="left" valign="top">Duration of grazing and rumination is measured by observation or sensors.</td>
<td align="left" valign="top">Reduced time indicates lethargy (trypanosomiasis) or discomfort.</td>
<td align="left" valign="top" rowspan="2">(<xref ref-type="bibr" rid="ref109">109</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Posture and activity</td>
<td align="left" valign="top">Qualitative assessment (e.g., lethargic, alert) or time spent standing/lying.</td>
<td align="left" valign="top">Lethargy and recumbency are common in severe anemia or systemic illness.</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="2">Mental state</td>
<td align="left" valign="top">Avoidance distance</td>
<td align="left" valign="top">The distance at which a camel moves away from an approaching human.</td>
<td align="left" valign="top">Increased distance can indicate fear or distress due to chronic pain/poor handling.</td>
<td align="left" valign="top" rowspan="2">(<xref ref-type="bibr" rid="ref110">110</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Qualitative behavioral assessment (QBA) (Potential)</td>
<td align="left" valign="top">Holistic assessment of expressive behavior (e.g., &#x201C;content,&#x201D; &#x201C;agitated,&#x201D; &#x201C;depressed&#x201D;).</td>
<td align="left" valign="top">Can capture the affective state resulting from chronic parasitic burden.</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>A comprehensive assessment, viewed through the perspectives of the Five Freedoms and the Five Domains model, indicates that parasitic diseases pose a significant welfare issue, adversely affecting nutrition, health, behavioral expression, and mental well-being. The complex management systems inherent in camel husbandry exacerbate these shortcomings by hindering prompt diagnosis and effective intervention. Consequently, integrating the fields of veterinary parasitology and animal welfare science is not only advantageous but crucial for a complete understanding of camel health. Future initiatives should prioritize the development of validated, practical welfare assessment tools that are tailored to the unique physiological and ethological needs of the dromedary camel, ultimately facilitating improved management, timely treatment, and enhanced well-being within a One Welfare framework (<xref ref-type="bibr" rid="ref25">25</xref>, <xref ref-type="bibr" rid="ref33">33</xref>).</p>
</sec>
<sec id="sec3">
<label>3</label>
<title>Overview of parasitic diseases in dromedary camels</title>
<p>Parasitic infestations pose a significant challenge to the health of dromedary camels, severely restricting their productivity, physiological resilience, and overall welfare. These pathogens are typically categorized into hemoparasites, ectoparasites, and endoparasites, each causing unique yet frequently overlapping clinical and subclinical impacts. The resulting multifactorial impairments encompass reduced milk yield, suboptimal body condition, reproductive failures, and diminished work capacity, alongside direct welfare issues such as chronic pain, itching, anemia, and behavioral distress.</p>
<sec id="sec4">
<label>3.1</label>
<title>Hemoparasitic infections</title>
<sec id="sec5">
<label>3.1.1</label>
<title>Trypanosomiasis (Surra)</title>
<p><italic>Trypanosoma evansi</italic>, the causative agent of Surra, is a highly significant hemoparasite that is mechanically transmitted by blood-feeding flies such as <italic>Tabanus</italic> and <italic>Stomoxys</italic> spp. (<xref ref-type="bibr" rid="ref34">34</xref>). The clinical symptoms include progressive anemia, cachexia, intermittent fever, and dependent edema (<xref ref-type="bibr" rid="ref35 ref36 ref37">35&#x2013;37</xref>). The economic repercussions of Surra are substantial, primarily due to decreased productivity rather than elevated mortality rates. In untreated outbreaks, mortality can reach 10&#x2013;20%, but the morbidity is often significantly higher, impacting as much as 30&#x2013;50% of a herd, which leads to chronic debilitation (<xref ref-type="bibr" rid="ref2">2</xref>, <xref ref-type="bibr" rid="ref38">38</xref>). Infected camels experience severe weight loss, which can decrease meat and milk production by 15&#x2013;30%, and their draft capacity may be reduced by more than 50%, severely affecting the livelihoods of pastoralists (<xref ref-type="bibr" rid="ref39">39</xref>). Chronic infections often result in abortion, infertility, and high mortality if left untreated. From an animal welfare standpoint, Surra causes significant weakness, greatly diminishes foraging ability and mobility, and leads to chronic distress, making it one of the most debilitating diseases affecting camels worldwide (<xref ref-type="bibr" rid="ref35">35</xref>, <xref ref-type="bibr" rid="ref39">39</xref>).</p>
</sec>
<sec id="sec6">
<label>3.1.2</label>
<title>Babesiosis</title>
<p>Babesiosis is an emerging tick-borne disease in dromedary camels, caused by protozoan parasites belonging to the genus <italic>Babesia</italic> (for instance, <italic>Babesia caballi</italic> and <italic>B. canis</italic>). Serological and molecular investigations have uncovered a surprisingly high prevalence of the disease, with rates varying from 5% to over 20% in certain regions of Africa and the Middle East, suggesting that endemic transmission is frequently underestimated (<xref ref-type="bibr" rid="ref40">40</xref>). The pathogenicity of Babesia in camels can be considerable, although it differs depending on the species and the host&#x2019;s immune response. Clinical manifestations of babesiosis include high fever, hemolytic anemia, hemoglobinuria (characterized by reddish urine), icterus, and lethargy (<xref ref-type="bibr" rid="ref41">41</xref>). In acute instances, mortality rates can be significant, ranging from 10 to 30%, especially among young, elderly, or stressed animals, while morbidity within an exposed herd can also be elevated (<xref ref-type="bibr" rid="ref42">42</xref>). The economic implications are considerable, arising from direct mortality, treatment expenses, production losses due to anemia and weight reduction, and diminished work performance. Additionally, infected camels may become chronic carriers, acting as reservoirs for ticks and sustaining the infection cycle, which complicates control measures (<xref ref-type="bibr" rid="ref2">2</xref>, <xref ref-type="bibr" rid="ref43">43</xref>).</p>
</sec>
<sec id="sec7">
<label>3.1.3</label>
<title>Theileriosis</title>
<p>Theileriosis is an economically significant tick-borne hemoparasitosis in camels, caused by various <italic>Theileria</italic> species, such as <italic>Theileria camelensis</italic> and <italic>T. annulata</italic>. While certain infections may remain subclinical, pathogenic strains can lead to a severe condition known as tropical theileriosis (<xref ref-type="bibr" rid="ref34">34</xref>). Studies on prevalence indicate notable geographic differences, with infection rates ranging from 10 to 50% in endemic regions, as identified through molecular techniques (<xref ref-type="bibr" rid="ref44">44</xref>). The clinical manifestations are similar to those observed in bovids and include symptoms such as high fever, anorexia, lymphadenopathy, progressive anemia, and edema. The disease can be lethal, with mortality rates reported between 5 and 20% in naive herds, while morbidity can significantly impact a large segment of the herd, resulting in widespread debilitation. The economic ramifications are complex, encompassing mortality, decreased milk and meat production, loss of draft power, and costs associated with acaricides and chemotherapy (<xref ref-type="bibr" rid="ref45">45</xref>). The implications for animal welfare are severe, involving direct suffering from febrile illness and anemia, as well as the stress linked to clinical disease and its treatment.</p>
</sec>
<sec id="sec8">
<label>3.1.4</label>
<title>Anaplasmosis</title>
<p>Anaplasmosis is caused by <italic>Anaplasma marginale</italic> and related rickettsial species that infect erythrocytes, resulting in hemolytic anemia, icterus, and systemic debilitation (<xref ref-type="bibr" rid="ref46">46</xref>). Transmission is facilitated by tick vectors, with seroprevalence rates showing considerable geographic variation, ranging from 10% to over 60% in certain herds, indicating widespread exposure (<xref ref-type="bibr" rid="ref46">46</xref>, <xref ref-type="bibr" rid="ref47">47</xref>). While morbidity in naive herds can be significant, mortality rates are generally low, approximately 1&#x2013;2%; however, the economic impact arises from chronic production losses. Infected camels frequently become persistent carriers, experiencing reduced weight gain, lower milk production, and increased vulnerability to other diseases, which collectively impose considerable financial burdens on camel owners (<xref ref-type="bibr" rid="ref47">47</xref>, <xref ref-type="bibr" rid="ref48">48</xref>). The welfare consequences include chronically diminished stamina, suffering related to persistent anemia, and increased susceptibility to secondary infections.</p>
</sec>
</sec>
<sec id="sec9">
<label>3.2</label>
<title>Ectoparasites</title>
<sec id="sec10">
<label>3.2.1</label>
<title>Ticks</title>
<p>Ixodid ticks (<italic>Hyalomma</italic>, <italic>Rhipicephalus</italic>, <italic>Amblyomma</italic> spp.) are widespread ectoparasites and carriers of significant pathogen groups (<xref ref-type="bibr" rid="ref49 ref50 ref51 ref52">49&#x2013;52</xref>). Severe infestations result in direct harm through skin damage, abscess development, and severe irritation, leading to restlessness and excessive scratching (<xref ref-type="bibr" rid="ref53">53</xref>, <xref ref-type="bibr" rid="ref54">54</xref>). The economic repercussions are diverse. An individual adult tick can consume 0.5&#x2013;2&#x202F;mL of blood, and substantial infestations can result in considerable blood loss, leading to anemia and reduced productivity (<xref ref-type="bibr" rid="ref55">55</xref>, <xref ref-type="bibr" rid="ref56">56</xref>). Annual losses attributed to ticks are estimated to include a 16% decrease in milk yield and a 11% decline in weight gain, which critically impacts pastoralist economies (<xref ref-type="bibr" rid="ref57">57</xref>). Additionally, tick-borne diseases (such as theileriosis and anaplasmosis) exacerbate these losses (<xref ref-type="bibr" rid="ref58">58</xref>). The dual function of ticks as both direct parasites and disease vectors significantly enhances their welfare and economic consequences (<xref ref-type="bibr" rid="ref57">57</xref>).</p>
</sec>
<sec id="sec11">
<label>3.2.2</label>
<title>Mange mites</title>
<p>Sarcoptic mange (<italic>Sarcoptes scabiei</italic> var. <italic>cameli</italic>) is a highly debilitating and contagious skin disease. Its prevalence can reach up to 25% in affected herds, with morbidity soaring to 100% if not managed effectively (<xref ref-type="bibr" rid="ref59">59</xref>). Although direct mortality rates are low, the economic ramifications are severe due to substantial production losses. Camels affected by this condition may suffer a reduction of up to 40% in hide value, a 30% drop in milk production, and notable weight loss due to severe itching and stress (<xref ref-type="bibr" rid="ref59">59</xref>, <xref ref-type="bibr" rid="ref60">60</xref>). The intense itching can lead to alopecia, lichenification, and self-inflicted injuries that increase the risk of secondary bacterial infections. Affected camels experience considerable pain and discomfort, often resulting in social withdrawal from the herd due to changes in behavior. This condition is rightly considered one of the most pressing welfare concerns in the management of camelids (<xref ref-type="bibr" rid="ref59">59</xref>).</p>
</sec>
</sec>
<sec id="sec12">
<label>3.3</label>
<title>Other ectoparasites</title>
<p>Infestations caused by lice (<italic>Bovicola</italic> spp.) and flies that induce myiasis (such as <italic>Wohlfahrtia magnifica</italic>) play a significant role in dermatological issues, pruritus, and stress. Lice infestations may result in restlessness, severe cases can lead to anemia, and they can also damage hair fibers, thereby diminishing the quality of wool (<xref ref-type="bibr" rid="ref61">61</xref>). Myiasis, which refers to the invasion of living tissue by fly larvae, can result in painful lesions, secondary infections, and, if not treated, can be fatal (<xref ref-type="bibr" rid="ref49">49</xref>). Although often neglected, these parasites exacerbate welfare issues and lead to production losses, especially in animals that are already weakened by co-infections or inadequate nutrition (<xref ref-type="bibr" rid="ref62">62</xref>, <xref ref-type="bibr" rid="ref63">63</xref>).</p>
</sec>
<sec id="sec13">
<label>3.4</label>
<title>Endoparasites</title>
<sec id="sec14">
<label>3.4.1</label>
<title>Gastrointestinal nematodes</title>
<p>Strongylid nematodes, including <italic>Haemonchus</italic>, <italic>Trichostrongylus</italic>, and <italic>Ostertagia</italic>, along with whipworms (<italic>Trichuris</italic>), are notably widespread, with prevalence rates frequently surpassing 70&#x2013;90% in pastoral herds, thus establishing them as arguably the most prevalent parasitic challenge (<xref ref-type="bibr" rid="ref64">64</xref>). These parasites lead to gastroenteritis, diarrhea, weight loss, and anemia. The economic repercussions are considerable, primarily due to diminished feed conversion efficiency, stunted growth in juvenile camels, and reduced milk yield in lactating females. <italic>Haemonchus longistipes</italic>, a particularly virulent species, can induce significant blood loss, resulting in anemia and bottle jaw, which diminishes the market value of the affected animals (<xref ref-type="bibr" rid="ref61">61</xref>, <xref ref-type="bibr" rid="ref65">65</xref>). The main welfare issues arise from chronic malabsorption and protein depletion, which lead to ongoing hunger, dehydration, and decreased vitality, ultimately impairing mobility and reproductive behaviors (<xref ref-type="bibr" rid="ref2">2</xref>, <xref ref-type="bibr" rid="ref64">64</xref>).</p>
</sec>
<sec id="sec15">
<label>3.4.2</label>
<title>Coccidiosis</title>
<p>Coccidiosis, caused by <italic>Eimeria</italic> spp., is a leading factor in enteritis among young camels, leading to high rates of morbidity and mortality during severe outbreaks. Morbidity rates in calf populations can soar to 60&#x2013;80%, while mortality rates in untreated cases can vary from 5 to 20%, marking it as a significant contributor to pre-weaning losses (<xref ref-type="bibr" rid="ref38">38</xref>). Those that survive often endure prolonged episodes of diarrhea, which can result in malnutrition, growth retardation, and considerable distress, severely affecting the welfare of juvenile populations (<xref ref-type="bibr" rid="ref38">38</xref>, <xref ref-type="bibr" rid="ref66">66</xref>). The economic significance is associated with treatment costs, lost growth potential, and the mortality of future productive animals (<xref ref-type="table" rid="tab2">Table 2</xref>).</p>
<table-wrap position="float" id="tab2">
<label>Table 2</label>
<caption>
<p>Major parasitic diseases of dromedary camels: prevalence, clinical signs, and zoonotic potential.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Parasite</th>
<th align="left" valign="top">Species</th>
<th align="left" valign="top">Clinical signs</th>
<th align="left" valign="top">Prevalence (Range)</th>
<th align="left" valign="top">Zoonotic potential</th>
<th align="left" valign="top">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" rowspan="2">Hemoparasites</td>
<td align="left" valign="top"><italic>Trypanosoma evansi</italic> (Surra)</td>
<td align="left" valign="top">Fever, anemia, edema, lethargy, weight loss, abortion</td>
<td align="left" valign="top">10&#x2013;30% (seroprevalence can be &#x003E;50% in endemic areas)</td>
<td align="left" valign="top">Considered non-zoonotic, but rare human cases have been reported</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref2">2</xref>, <xref ref-type="bibr" rid="ref57">57</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>Anaplasma marginale</italic></td>
<td align="left" valign="top">Fever, anemia, jaundice, weight loss</td>
<td align="left" valign="top">5&#x2013;20% (varies by region)</td>
<td align="left" valign="top">Not a primary human pathogen, but related species are</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref3">3</xref>, <xref ref-type="bibr" rid="ref47">47</xref>)</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="2">Ectoparasites</td>
<td align="left" valign="top"><italic>Sarcoptes scabiei</italic> var. <italic>cameli</italic> (Mange)</td>
<td align="left" valign="top">Intense pruritus, alopecia, hyperkeratosis, skin thickening</td>
<td align="left" valign="top">Up to 25% in affected herds; highly contagious</td>
<td align="left" valign="top">Yes (causes transient scabies in humans)</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref111">111</xref>, <xref ref-type="bibr" rid="ref112">112</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>Hyalomma dromedarii</italic> (Tick)</td>
<td align="left" valign="top">Skin damage, anemia (heavy infestations), restlessness</td>
<td align="left" valign="top">Very high (&#x003E;80% in many pastoral systems)</td>
<td align="left" valign="top">Vectors for Crimean-Congo Hemorrhagic Fever (CCHF) virus</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref57">57</xref>, <xref ref-type="bibr" rid="ref72">72</xref>)</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="2">Gastrointestinal nematodes</td>
<td align="left" valign="top"><italic>Haemonchus longistipes</italic></td>
<td align="left" valign="top">Anemia, bottle jaw, submandibular edema, weight loss</td>
<td align="left" valign="top">Prevalence often &#x003E;60%; high burden common</td>
<td align="left" valign="top">No</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref54">54</xref>, <xref ref-type="bibr" rid="ref61">61</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>Trichostrongylus</italic> spp.</td>
<td align="left" valign="top">Diarrhea, weight loss, poor condition</td>
<td align="left" valign="top">Very common; often part of mixed infections</td>
<td align="left" valign="top">No</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref64">64</xref>, <xref ref-type="bibr" rid="ref65">65</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Protozoan endoparasites</td>
<td align="left" valign="top"><italic>Eimeria dromedarii</italic> (Coccidiosis)</td>
<td align="left" valign="top">Diarrhea (sometimes hemorrhagic), dehydration, and mortality in calves</td>
<td align="left" valign="top">Common in young camels; prevalence 20&#x2013;50%</td>
<td align="left" valign="top">No</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref3">3</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Zoonotic helminths</td>
<td align="left" valign="top"><italic>Echinococcus granulosus</italic></td>
<td align="left" valign="top">Often asymptomatic in camels; cysts found in lungs/liver</td>
<td align="left" valign="top">Variable; 5&#x2013;15% in slaughterhouse studies</td>
<td align="left" valign="top">Yes (Causes Cystic Echinococcosis in humans)</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref100">100</xref>, <xref ref-type="bibr" rid="ref113">113</xref>)</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
</sec>
</sec>
<sec id="sec16">
<label>4</label>
<title>Helminths of zoonotic importance</title>
<p>Gastrointestinal nematodes represent the primary helminthic concern for the health of camels; however, various cestode (tapeworm) and trematode (fluke) infections pose considerable zoonotic risks, thereby establishing a crucial connection between camel welfare and public health safety. Although the prevalence of these parasites in camels is generally lower than in other ruminants, their existence leads to productivity declines and remains a continuous threat to human populations.</p>
<sec id="sec17">
<label>4.1</label>
<title>Cestodes (tapeworms)</title>
<p>The most notable zoonotic cestode is <italic>Echinococcus granulosus</italic>, responsible for Cystic Echinococcosis (CE) or hydatid disease. Camels act as intermediate hosts, predominantly containing hydatid cysts within their lungs and liver. Surveys conducted in slaughterhouses within endemic areas, such as the Middle East and North Africa, indicate infection rates in camels that range from 5% to over 20% (<xref ref-type="bibr" rid="ref67">67</xref>, <xref ref-type="bibr" rid="ref68">68</xref>). Although camels often remain asymptomatic, significant cyst loads can result in organ condemnation, leading to direct economic repercussions for the meat industry. The more substantial impact, however, pertains to human health. Humans contract the infection by inadvertently ingesting eggs excreted in the feces of infected definitive hosts, usually dogs that have consumed infected camel offal. CE is classified as a neglected tropical disease that inflicts considerable morbidity and mortality within pastoral communities, with treatment being both complex and expensive (<xref ref-type="bibr" rid="ref69">69</xref>, <xref ref-type="bibr" rid="ref70">70</xref>).</p>
<p>Other cestodes, such as <italic>Moniezia</italic> spp., are prevalent yet non-zoonotic, leading to diarrhea, especially in young camels, which results in diminished growth rates and productivity (<xref ref-type="bibr" rid="ref71">71</xref>). Although trematode infections in camels are reported less frequently, they include species that possess both direct and indirect zoonotic potential. The liver flukes <italic>Fasciola hepatica</italic> and <italic>F. gigantica</italic> have been identified in camels. The prevalence of these infections varies but can be considerable in regions with appropriate wetland habitats for the intermediate snail host. Such infections lead to liver condemnation, fibrosis, and decreased weight gain. This represents a significant zoonosis, as humans can contract the infection through the ingestion of contaminated aquatic plants, such as watercress (<xref ref-type="bibr" rid="ref72">72</xref>, <xref ref-type="bibr" rid="ref73">73</xref>). <italic>Schistosoma</italic> spp. is capable of infecting camels, resulting in granulomatous lesions in the liver and intestines. Camels may act as reservoir hosts for species like <italic>S. japonicum</italic>, which complicates control measures in endemic regions. Human schistosomiasis is a debilitating condition acquired through exposure to cercariae-infested freshwater (<xref ref-type="bibr" rid="ref74">74</xref>).</p>
</sec>
<sec id="sec18">
<label>4.2</label>
<title>Nematodes (roundworms) with zoonotic potential</title>
<p>In addition to the primary gastrointestinal nematodes, certain species can lead to zoonotic infections. <italic>Trichuris</italic> (whipworm) is generally host-specific; however, close interaction with infected animals presents a 6 impact. The cumulative consequences of polyparasitism lead to a cycle of persistent suffering, economic detriment, and increased susceptibility, thereby jeopardizing the sustainability of livelihoods reliant on camels. An integrated One Health strategy that combines sophisticated diagnostics, established welfare evaluation methods, and customized control measures is critically needed to address these complex issues (<xref ref-type="bibr" rid="ref75">75</xref>, <xref ref-type="bibr" rid="ref76">76</xref>).</p>
</sec>
</sec>
<sec id="sec19">
<label>5</label>
<title>Welfare implications of parasitic diseases</title>
<p>Parasitic infestations create complex welfare challenges for dromedary camels, affecting not only their clinical health but also their behavioral, productive, and socio-economic aspects. These conditions disrupt normal physiological processes, lead to ongoing suffering, and hinder the camel&#x2019;s ability to flourish within its ecological and cultural environment. Importantly, the effects extend beyond the health of the animals, impacting the livelihoods of pastoralists, the dynamics of human-animal relationships, and public health through zoonotic transmission.</p>
<sec id="sec20">
<label>5.1</label>
<title>Pathophysiological and affective consequences</title>
<p>Chronic parasitism causes considerable pain, distress, and physical debilitation. Infestations by mange mites (<italic>Sarcoptes scabiei</italic> var. <italic>cameli</italic>) result in severe itching, which can lead to skin damage, lesions, and secondary bacterial infections. Camels suffering from these conditions often display signs of restlessness and social withdrawal, reflecting significant physical and psychological distress (<xref ref-type="bibr" rid="ref3">3</xref>). Likewise, hemoparasites like <italic>Trypanosoma evansi</italic> cause ongoing anemia, fever, and swelling, which contribute to lethargy and overall weakness (<xref ref-type="bibr" rid="ref22">22</xref>). The chronic nature of these ailments, frequently exacerbated by delayed interventions in isolated pastoralist communities, results in prolonged periods of aversion and diminished affective well-being. Continuous immune responses to parasitic antigens lead to a catabolic state, worsening weight loss and exhausting energy reserves. This metabolic burden, along with nutrient malabsorption due to gastrointestinal nematodes, results in poor body condition and chronic fatigue, which directly affects the camel&#x2019;s ability to engage in natural behaviors such as grazing, rumination, and social interaction (<xref ref-type="bibr" rid="ref77">77</xref>).</p>
</sec>
<sec id="sec21">
<label>5.2</label>
<title>Reduced productivity and work capacity</title>
<p>Parasitic diseases significantly reduce essential productive outputs, such as milk yield, meat production, and draft capacity. Trypanosomiasis is especially harmful to work performance due to fatigue caused by anemia (<xref ref-type="bibr" rid="ref22">22</xref>). Gastrointestinal helminths hinder nutrient absorption, resulting in decreased weight gain and growth stunting, which poses a threat to food security in communities that depend on camels (<xref ref-type="bibr" rid="ref78">78</xref>). Ectoparasite infestations (for instance, ticks and biting flies) lead to irritability and disrupt feeding and resting patterns, further diminishing productivity and welfare. The reduction in milk production not only impacts income generation but also jeopardizes the nutrition and health of suckling calves, raising concerns about intergenerational welfare.</p>
</sec>
<sec id="sec22">
<label>5.3</label>
<title>Reproductive and nutritional deficits</title>
<p>Parasitic infections have a significant detrimental impact on reproductive performance. <italic>T. evansi</italic> is linked to abortion, stillbirth, and decreased conception rates (<xref ref-type="bibr" rid="ref79">79</xref>). Chronic parasitism leads to poor body condition, which in turn delays puberty and prolongs postpartum anestrus in females, while also diminishing libido and semen quality in males. These issues pose a threat to herd sustainability and the resilience of pastoralists. Furthermore, nutritional status is adversely affected through various mechanisms: blood-feeding parasites (such as <italic>Haemonchus</italic> spp. and ticks) cause anemia and hypoproteinemia; protozoal infections like coccidiosis lead to diarrhea and dehydration, particularly in juveniles (<xref ref-type="bibr" rid="ref22">22</xref>). The camel&#x2019;s renowned ability to withstand drought is compromised by hyperthermia, panting, and cutaneous water loss induced by parasites, undermining a crucial adaptive advantage in arid regions (<xref ref-type="bibr" rid="ref80">80</xref>).</p>
</sec>
<sec id="sec23">
<label>5.4</label>
<title>Human-animal interactions and zoonotic risks</title>
<p>The welfare of camels is greatly affected by the responses of their owners to parasitism. Delays in treatment caused by limited access to veterinary care, financial limitations, or a lack of knowledge can prolong the suffering of these animals and may result in the culling of those that are severely weakened (<xref ref-type="bibr" rid="ref8">8</xref>). Restraint techniques employed during treatment (such as limb-tying and nose-pegging) can cause additional stress and injury if not executed with proper training. Numerous camel parasites pose zoonotic risks, including <italic>Toxoplasma gondii</italic> (found in milk), <italic>Cryptosporidium</italic> spp., <italic>Giardia</italic> spp., and <italic>Echinococcus granulosus</italic> (<xref ref-type="bibr" rid="ref3">3</xref>). Public apprehension regarding transmission can lead to the stigmatization of camel products, decrease their market value, and result in neglect or improper management practices, which indirectly worsen welfare issues (<xref ref-type="bibr" rid="ref81">81</xref>). These dynamics underscore the crucial interconnections between animal welfare, public health, and economic stability (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p>
<fig position="float" id="fig2">
<label>Figure 2</label>
<caption>
<p>The cascading impacts of parasitic diseases in camels on welfare, productivity, and socio-economic stability. The diagram outlines the pathway from initial infection by specific pathogens (e.g., mange mites, helminths, <italic>Trypanosoma evansi</italic>) through pathophysiological consequences (e.g., anemia, weight loss), to broader outcomes including reduced work capacity, reproductive deficits, and compromised human-animal interactions due to zoonotic risks and limited veterinary care.</p>
</caption>
<graphic xlink:href="fvets-12-1732337-g002.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Illustration depicting the cascading impacts of parasitic diseases on camel welfare, productivity, and socio-economics. Arrows flow from initial infections (e.g., mange mites, helminths, Trypanosoma evansi) to pathophysiological consequences like anemia, lethargy, and weight loss. These lead to four main outcome categories: 1) Reduced Productivity and Work Capacity, 2) Reproductive and Nutritional Deficits (e.g., from diarrhea and T. evansi), 3) Compromised Human-Animal Interactions, and 4) Zoonotic Risks to public health. The diagram emphasizes how these combined effects create a cycle that threatens both individual animal welfare and broader socio-economic stability.</alt-text>
</graphic>
</fig>
</sec>
</sec>
<sec id="sec24">
<label>6</label>
<title>Gaps in research, surveillance, and veterinary systems</title>
<sec id="sec25">
<label>6.1</label>
<title>Diagnostic limitations and the welfare consequences of underreporting</title>
<p>The effectiveness of surveillance and timely intervention is severely compromised by limited diagnostic capabilities in remote pastoralist areas (<xref ref-type="bibr" rid="ref82">82</xref>). Many diagnoses are based on clinical signs or low-sensitivity microscopy, which often fail to identify subclinical cases or co-infections, leading to considerable underreporting and misdiagnosis. This diagnostic gap has direct and severe welfare consequences: delayed or incorrect treatment results in the progression of preventable suffering (<xref ref-type="bibr" rid="ref20">20</xref>). Animals endure prolonged pain from conditions like mange, chronic debilitation from trypanosomiasis, and ongoing distress from gastrointestinal parasites, all of which could be alleviated with earlier, accurate detection (<xref ref-type="bibr" rid="ref2">2</xref>). Innovative field-applicable tools such as pen-side serological assays, loop-mediated isothermal amplification (LAMP, a simple, rapid DNA amplification technique that does not require a thermal cycler), and portable sequencing technologies present promising opportunities for enhanced, rapid diagnosis (<xref ref-type="bibr" rid="ref83">83</xref>, <xref ref-type="bibr" rid="ref84">84</xref>). However, their deployment faces significant hurdles, including cost, the need for a stable cold chain, and technical training, which currently limit their practicality in nomadic systems. The development of affordable, robust, and camel-specific point-of-care tests remains a critical unmet need (<xref ref-type="bibr" rid="ref82">82</xref>, <xref ref-type="bibr" rid="ref85">85</xref>).</p>
</sec>
<sec id="sec26">
<label>6.2</label>
<title>The impact of climate change on parasite ecology and distribution</title>
<p>Climate change is a significant driver modifying the distribution and intensity of parasitic diseases in camels (<xref ref-type="bibr" rid="ref3">3</xref>). Rising temperatures and altered precipitation patterns are broadening the geographical range of vectors, such as ticks and biting flies, for pathogens like <italic>Trypanosoma evansi</italic> and Anaplasma spp. (<xref ref-type="bibr" rid="ref81">81</xref>). Concurrently, desertification and shifts in land use are pushing camel husbandry into new areas, potentially exposing na&#x00EF;ve populations to unfamiliar parasite communities (<xref ref-type="bibr" rid="ref82">82</xref>, <xref ref-type="bibr" rid="ref83">83</xref>). Predictive ecological modeling and longitudinal studies are crucial for anticipating these changes and formulating proactive, welfare-focused mitigation strategies, such as targeted parasite control in emerging risk areas (<xref ref-type="bibr" rid="ref85">85</xref>).</p>
</sec>
<sec id="sec27">
<label>6.3</label>
<title>Strengthening veterinary capacity and community engagement</title>
<p>The critical shortage of formal veterinary services in nomadic and pastoralist systems remains a fundamental limitation to improving camel welfare (<xref ref-type="bibr" rid="ref7">7</xref>). While ethnoveterinary knowledge is valuable and culturally important, it is essential to complement it with evidence-based parasitology and welfare-oriented management practices (<xref ref-type="bibr" rid="ref82">82</xref>). A key strategy is educating and empowering community-based animal health workers (CAHWs) (<xref ref-type="bibr" rid="ref86">86</xref>, <xref ref-type="bibr" rid="ref87">87</xref>). Training CAHWs in rational drug use, basic diagnostics (e.g., fecal egg counts, recognizing clinical signs of major diseases), and low-stress handling techniques can dramatically improve early detection and enable more humane and timely interventions (<xref ref-type="bibr" rid="ref88">88</xref>). Such community-level programs bridge the gap between pastoralists and distant veterinary clinics (<xref ref-type="bibr" rid="ref9">9</xref>), fostering a proactive approach to camel health and welfare (<xref ref-type="bibr" rid="ref89">89</xref>, <xref ref-type="bibr" rid="ref90">90</xref>). Ultimately, increased investment in research and greater policy focus are necessary to elevate camel health (<xref ref-type="bibr" rid="ref83">83</xref>) and welfare on national and global veterinary and agricultural agendas (<xref ref-type="bibr" rid="ref80">80</xref>).</p>
</sec>
</sec>
<sec id="sec28">
<label>7</label>
<title>Strengthening diagnostic capacity and surveillance systems</title>
<sec id="sec29">
<label>7.1</label>
<title>Early diagnosis and surveillance</title>
<p>Accurate and prompt diagnosis serves as the foundation for effective management of parasites. Although microscopy is still extensively utilized in field environments, its shortcomings in identifying subclinical cases or co-infections highlight the need for more sensitive and specific diagnostic tools. Molecular diagnostics, such as PCR, LAMP, and next-generation sequencing, along with serological tests like ELISA, provide enhanced detection capabilities but must be tailored for pathogens specific to camels and the contexts of pastoralists (<xref ref-type="bibr" rid="ref91">91</xref>). Investing in point-of-care rapid testing, mobile laboratory units, and telemedicine solutions can help close diagnostic gaps in remote regions, facilitating earlier interventions and alleviating chronic suffering (<xref ref-type="bibr" rid="ref92">92</xref>). Additionally, integrating camel health into national surveillance systems is essential for producing comprehensive epidemiological data and guiding evidence-based control strategies (<xref ref-type="bibr" rid="ref93">93</xref>).</p>
</sec>
<sec id="sec30">
<label>7.2</label>
<title>Vaccination and vector control programs</title>
<p>Currently, there are no commercially available vaccines specifically for camel parasites; however, progress in immunoprophylaxis for similar livestock pathogens offers a promising path. Research into recombinant antigens, viral vector systems, and nanoparticle delivery methods could lead to effective vaccines against major pathogens such as <italic>Trypanosoma evansi</italic> or key tick species (<xref ref-type="bibr" rid="ref94">94</xref>). Meanwhile, integrated vector management, which includes rotating acaricides, using biological controls like entomopathogenic fungi, and making environmental adjustments, can help reduce ectoparasite populations while addressing concerns about chemical resistance and ecological impacts (<xref ref-type="bibr" rid="ref21">21</xref>). The targeted use of endectocides, such as ivermectin, should be carefully adjusted to minimize resistance risks and align with seasonal changes in parasite prevalence (<xref ref-type="bibr" rid="ref95">95</xref>).</p>
</sec>
<sec id="sec31">
<label>7.3</label>
<title>Education and training for camel owners and handlers</title>
<p>Improvements in sustainable welfare depend on the knowledge and practices of camel owners and handlers. Educational initiatives involving community participation, delivered through mobile technologies, workshops, and visual aids, can significantly improve understanding of parasite life cycles, zoonotic risks, and early disease detection (<xref ref-type="bibr" rid="ref83">83</xref>). Training programs for CAHWs should emphasize welfare-sensitive handling, rational drug use, and preventive strategies such as rotational grazing and improved sanitation (<xref ref-type="bibr" rid="ref96">96</xref>). Empowering local stakeholders promotes early intervention, reduces treatment delays, and encourages culturally sustainable practices.</p>
</sec>
<sec id="sec32">
<label>7.4</label>
<title>Welfare-sensitive treatment and handling protocols</title>
<p>Medical and procedural interventions must prioritize the well-being of animals. Stressful restraint techniques (such as forced recumbency and nose-pegging) ought to be substituted with low-stress alternatives that are informed by the ethology of camels (<xref ref-type="bibr" rid="ref22">22</xref>). Guidelines regarding drug administration, which include correct dosing, withdrawal periods, and the avoidance of toxic combinations, must be widely disseminated to avert iatrogenic harm (<xref ref-type="bibr" rid="ref97">97</xref>). Likewise, topical applications (for instance, acaricides) should be carefully formulated and applied to reduce cutaneous irritation and systemic side effects.</p>
</sec>
<sec id="sec33">
<label>7.5</label>
<title>Policy and legislative support</title>
<p>The welfare of camels is significantly overlooked in livestock policies and global welfare standards. It is crucial to achieve legislative acknowledgment to allocate resources for parasite management, subsidize veterinary services, and facilitate research projects (<xref ref-type="bibr" rid="ref98">98</xref>, <xref ref-type="bibr" rid="ref99">99</xref>). Furthermore, it is vital to incorporate camel health into One Health surveillance systems to effectively tackle zoonotic parasites (such as <italic>Echinococcus granulosus</italic> and <italic>Cryptosporidium</italic> spp.) at the intersection of human, animal, and environmental health (<xref ref-type="bibr" rid="ref86">86</xref>). As climate change and the expansion of agriculture exacerbate parasitic risks, policy frameworks should foster resilience through strategies that prioritize welfare (<xref ref-type="table" rid="tab3">Table 3</xref>).</p>
<table-wrap position="float" id="tab3">
<label>Table 3</label>
<caption>
<p>Integrated parasite control strategies in camelid management.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Strategy</th>
<th align="left" valign="top">Specific approach</th>
<th align="left" valign="top">Key advantage</th>
<th align="left" valign="top">Limitation</th>
<th align="left" valign="top">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" rowspan="2">Chemical control</td>
<td align="left" valign="top">Strategic Anthelmintic Use: Treating based on parasite monitoring (e.g., FEC) rather than a fixed schedule.</td>
<td align="left" valign="top">Reduces drug resistance and is more cost-effective.</td>
<td align="left" valign="top">Requires diagnostic capability and owner education.</td>
<td align="left" valign="top" rowspan="2">(<xref ref-type="bibr" rid="ref114">114</xref>, <xref ref-type="bibr" rid="ref115">115</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Acaricide Rotation: Rotating chemical classes (e.g., pyrethroids, amitraz) for tick control.</td>
<td align="left" valign="top">Slows the development of resistance in tick populations.</td>
<td align="left" valign="top">Logistically challenging in extensive systems; environmental contamination risk.</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="2">Management &#x0026; environmental</td>
<td align="left" valign="top">Rotational Grazing: Moving herds to fresh pastures to break parasite life cycles.</td>
<td align="left" valign="top">Reduces pasture contamination with infective larvae.</td>
<td align="left" valign="top">Requires sufficient land and management effort; not always feasible in arid zones.</td>
<td align="left" valign="top" rowspan="2">(<xref ref-type="bibr" rid="ref116">116</xref>, <xref ref-type="bibr" rid="ref117">117</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Biological Control: Use of entomopathogenic fungi (e.g., Metarhizium anisopliae) against ticks.</td>
<td align="left" valign="top">Environmentally friendly, target-specific.</td>
<td align="left" valign="top">Still in experimental stages for field use in camels; cost and application logistics.</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="2">Diagnostic &#x0026; technological</td>
<td align="left" valign="top">Point-of-Care Tests: Development of rapid tests for <italic>T. evansi</italic> or Fecal Egg Count (FEC) kits.</td>
<td align="left" valign="top">Enables early diagnosis and timely treatment in remote areas.</td>
<td align="left" valign="top">Limited commercial availability of camel-specific tests.</td>
<td align="left" valign="top" rowspan="2">(<xref ref-type="bibr" rid="ref118">118</xref>, <xref ref-type="bibr" rid="ref119">119</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Vaccine Development (Future)</td>
<td align="left" valign="top">Research into vaccines against <italic>T. evansi</italic> or tick antigens.</td>
<td align="left" valign="top">Would provide sustainable, long-term protection.</td>
</tr>
<tr>
<td align="left" valign="top">Community-based</td>
<td align="left" valign="top">Community Animal Health Workers (CAHWs): Training local handlers in basic health care and welfare assessment.</td>
<td align="left" valign="top">Improves access to basic care and early detection in remote pastoral systems.</td>
<td align="left" valign="top">Sustainability depends on continuous support and training.</td>
<td align="left" valign="top">(<xref ref-type="bibr" rid="ref96">96</xref>)</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
</sec>
<sec sec-type="conclusions" id="sec34">
<label>8</label>
<title>Conclusion</title>
<p>This review has synthesized evidence from veterinary parasitology and animal welfare science to elucidate the profound, multifaceted impact of parasitic diseases on dromedary camels. Our analysis demonstrates that pathogens such as <italic>Trypanosoma evansi</italic> (with seroprevalence exceeding 50% in endemic areas), mange mites (affecting up to 25% of herds), and gastrointestinal nematodes (prevalence &#x003E;70%) are not merely production constraints but direct causes of significant suffering (<xref ref-type="bibr" rid="ref22">22</xref>). These infections systematically compromise all domains of welfare, leading to chronic pain, debilitating anemia, severe pruritus, and behavioral distress, which in turn result in substantial production losses (e.g., up to 40% reduction in milk yield, 15&#x2013;30% decrease in meat production) (<xref ref-type="bibr" rid="ref23">23</xref>). The situation is exacerbated by critical gaps in species-specific welfare assessment, diagnostic capabilities in pastoralist systems, and a fundamental underappreciation of the affective states of camels (<xref ref-type="bibr" rid="ref3">3</xref>, <xref ref-type="bibr" rid="ref100">100</xref>). Furthermore, the presence of zoonotic parasites like <italic>Echinococcus granulosus</italic> creates an inseparable link between camel welfare and public health, necessitating an integrated One Health/One Welfare perspective (<xref ref-type="bibr" rid="ref101">101</xref>).</p>
</sec>
<sec id="sec35">
<label>9</label>
<title>Recommendations and future directions</title>
<p>To address these challenges, a coordinated, multi-stakeholder approach is urgently required. There is a critical need to develop and validate a set of practical, animal-based welfare indicators specific to dromedary camels for use in field conditions (<xref ref-type="bibr" rid="ref88">88</xref>). Capacity must be strengthened by training CAHWs in low-stress handling, rational anthelmintic use, and the recognition of common parasitic diseases (<xref ref-type="bibr" rid="ref94">94</xref>). Awareness campaigns should be implemented to educate pastoralists on the life cycles of parasites, zoonotic risks, and the economic and welfare benefits of early intervention (<xref ref-type="bibr" rid="ref102">102</xref>). Future research should focus on developing affordable, point-of-care diagnostic tests for key pathogens, such as <italic>T. evansi</italic> (<xref ref-type="bibr" rid="ref11">11</xref>). Investigations into the pathophysiology of parasitism should be expanded to better quantify the pain and distress associated with infections such as sarcoptic mange and trypanosomiasis (<xref ref-type="bibr" rid="ref102">102</xref>). Long-term studies are necessary to understand the impacts of climate change on parasite distribution and to explore the potential for vaccine development against major parasites (<xref ref-type="bibr" rid="ref20">20</xref>). Policy frameworks should formally incorporate camel welfare and parasitic disease control into national animal health strategies and One Health surveillance programs. Economic incentives, such as sustainable branding of parasite-free or high-welfare camel products, should be explored to reward good management practices. International collaboration and funding must be prioritized to support research and implementation programs in regions dependent on camel husbandry.</p>
<p>In summary, this review establishes that parasitic diseases are a central, yet often neglected, animal welfare crisis in dromedary camels. By moving beyond a purely production-centric view and integrating the principles of One Welfare, we can reframe effective parasite control as a moral imperative. The path forward requires translating this integrated understanding into practical tools, empowered communities, and supportive policies to safeguard the well-being of these essential animals, the livelihoods of the people who depend on them, and the public health of us all.</p>
</sec>
</body>
<back>
<sec sec-type="author-contributions" id="sec36">
<title>Author contributions</title>
<p>SN: Data curation, Software, Writing &#x2013; original draft. MT: Conceptualization, Data curation, Funding acquisition, Supervision, Validation, Writing &#x2013; review &#x0026; editing.</p>
</sec>
<ack>
<title>Acknowledgments</title>
<p>The researchers would like to thank the Deanship of Graduate Studies and Scientific Research at Qassim University for financial support (QU-APC-2026).</p>
</ack>
<sec sec-type="COI-statement" id="sec37">
<title>Conflict of interest</title>
<p>The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="ai-statement" id="sec38">
<title>Generative AI statement</title>
<p>The author(s) declared that Generative AI was not used in the creation of this manuscript.</p>
<p>Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.</p>
</sec>
<sec sec-type="disclaimer" id="sec39">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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<fn-group>
<fn fn-type="custom" custom-type="edited-by" id="fn0002">
<p>Edited by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2691309/overview">Mahamat Fayiz Abakar</ext-link>, Institut de recherche en &#x00E9;levage pour le d&#x00E9;veloppement (IRED), Chad</p>
</fn>
<fn fn-type="custom" custom-type="reviewed-by" id="fn0003">
<p>Reviewed by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/848346/overview">Giovanna Liguori</ext-link>, Azienda Sanitaria Locale di Foggia, Italy</p>
<p><ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/3270976/overview">Hadeel Albayati</ext-link>, University of Al-Qadisiyah, Iraq</p>
</fn>
</fn-group>
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