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Background <p><i>Babesia divergens</i> is a tick-borne apicomplexan parasite found predominantly in Europe, causing babesiosis in livestock and occasionally in humans, with severe disease reported in immunosuppressed or asplenic individuals. As populations of <i>Ixodes ricinus</i>, the principal vector, expand geographically, including into urban environments, there is a growing need for rapid, sensitive, and field-deployable surveillance tools. In this study, we aim to developed a Recombinase Polymerase Amplification Lateral Flow (RPA-LF) assay for the detection of <i>B. divergens</i>.</p> Methods <p>RPA assays targeting <i>B. divergens hsp70</i>, <i>cox1</i>, and <i>18S rRNA</i> genes were designed and evaluated for sensitivity and specificity using serial dilutions and control samples, including other apicomplexan parasites and tick samples spiked with <i>B. divergens</i> DNA. To assess field performance, 279 <i>I. ricinus</i> ticks were collected from urban parks in Greater London and screened by qPCR and a subset also tested using the new RPA-LF assays. <i>Anaplasma phagocytophilum</i> was screened by qPCR but not detected.</p> Results <p>The <i>cox1</i> and <i>18S rRNA</i> RPA-LF assays demonstrated high specificity, with detection limits of at least 10<sup>−5</sup>&#xa0;ng/μl and 10<sup>−3</sup>&#xa0;ng/μl, respectively, under isothermal conditions (39&#xa0;°C for 30&#xa0;min). No cross-reactivity was observed with non-target DNA. Field validation using pooled samples revealed a single sample positive for <i>Babesia divergens</i> by qPCR, indicating an estimated nymphal infection prevalence of 0.4–1.2%, as previously observed in UK tick studies. The <i>18S rRNA</i> RPA-LF assay successfully detected this pool, whereas the <i>cox1</i> RPA-LF did not. Sanger sequencing confirmed the presence of <i>B. divergens</i>/<i>B. capreoli</i>-like DNA, although species-level discrimination was limited due to high sequence similarity.</p> Conclusions <p>We report the first successful development of an RPA-LF assay for the detection in ticks of <i>B. divergens</i> or the closely related species <i>B. capreoli</i>. The assay demonstrates high sensitivity and specificity under isothermal conditions and provides a portable and reliable tool for field-based molecular surveillance of emerging tick-borne pathogens. Field validation revealed <i>B. divergens</i>/<i>B. capreoli</i> in questing ticks from urban green spaces in London, underscoring the importance of this tool for early detection and ongoing surveillance of tick-borne parasites in expanding urban ecosystems.</p> Graphical Abstract <p></p>

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A recombinase polymerase amplification lateral flow assay (RPA-LF) for detection of Babesia divergens-like parasites

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年7月27日

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  • Ernest Chin Jia Bin,
  • Keir Hughes,
  • Cheryl Whitehorn,
  • Mia White,
  • Kayleigh Hansford,
  • Jolyon Medlock,
  • Ellen Knuepfer,
  • Taane G. Clark,
  • Mojca Kristan,
  • Susana Campino

摘要

Background

Babesia divergens is a tick-borne apicomplexan parasite found predominantly in Europe, causing babesiosis in livestock and occasionally in humans, with severe disease reported in immunosuppressed or asplenic individuals. As populations of Ixodes ricinus, the principal vector, expand geographically, including into urban environments, there is a growing need for rapid, sensitive, and field-deployable surveillance tools. In this study, we aim to developed a Recombinase Polymerase Amplification Lateral Flow (RPA-LF) assay for the detection of B. divergens.

Methods

RPA assays targeting B. divergens hsp70, cox1, and 18S rRNA genes were designed and evaluated for sensitivity and specificity using serial dilutions and control samples, including other apicomplexan parasites and tick samples spiked with B. divergens DNA. To assess field performance, 279 I. ricinus ticks were collected from urban parks in Greater London and screened by qPCR and a subset also tested using the new RPA-LF assays. Anaplasma phagocytophilum was screened by qPCR but not detected.

Results

The cox1 and 18S rRNA RPA-LF assays demonstrated high specificity, with detection limits of at least 10−5 ng/μl and 10−3 ng/μl, respectively, under isothermal conditions (39 °C for 30 min). No cross-reactivity was observed with non-target DNA. Field validation using pooled samples revealed a single sample positive for Babesia divergens by qPCR, indicating an estimated nymphal infection prevalence of 0.4–1.2%, as previously observed in UK tick studies. The 18S rRNA RPA-LF assay successfully detected this pool, whereas the cox1 RPA-LF did not. Sanger sequencing confirmed the presence of B. divergens/B. capreoli-like DNA, although species-level discrimination was limited due to high sequence similarity.

Conclusions

We report the first successful development of an RPA-LF assay for the detection in ticks of B. divergens or the closely related species B. capreoli. The assay demonstrates high sensitivity and specificity under isothermal conditions and provides a portable and reliable tool for field-based molecular surveillance of emerging tick-borne pathogens. Field validation revealed B. divergens/B. capreoli in questing ticks from urban green spaces in London, underscoring the importance of this tool for early detection and ongoing surveillance of tick-borne parasites in expanding urban ecosystems.

Graphical Abstract