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Molecular methods are thus employed to measure gametocyte densities, particularly when assessing transmission epidemiology and the efficacy of transmission-blocking interventions. However, accurate quantification of male and female gametocytes with molecular methods requires pure male and female gametocytes as reference standards, which are not widely available.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      qRT-PCR assays were used to quantify levels of sex-specific mRNA transcripts in\n                      <jats:italic>Plasmodium falciparum<\/jats:italic>\n                      female and male gametocytes (\n                      <jats:italic>pfs25<\/jats:italic>\n                      and\n                      <jats:italic>pfMGET<\/jats:italic>\n                      , respectively) using synthetic complimentary RNA standards and in vitro cultured gametocytes. Assays were validated and assay performance was investigated in blood samples of clinical trial participants using these standards and compared to absolute quantification by droplet digital PCR (ddPCR).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The number of transcript copies per gametocyte were determined to be 279.3 (95% CI 253.5\u2013307.6) for the female-specific transcript\n                      <jats:italic>pfs25<\/jats:italic>\n                      , and 12.5 (95% CI 10.6\u201314.9) for the male-specific transcript\n                      <jats:italic>pfMGET<\/jats:italic>\n                      . These numbers can be used to convert from transcript copies\/mL to gametocyte\/mL. The reportable range was determined to be 5.71\u2009\u00d7\u200910\n                      <jats:sup>6<\/jats:sup>\n                      to 5.71 female\u00a0gametocytes\/mL for\n                      <jats:italic>pfs25<\/jats:italic>\n                      , and 1.73\u2009\u00d7\u200910\n                      <jats:sup>7<\/jats:sup>\n                      to 1.73\u2009\u00d7\u200910\n                      <jats:sup>1<\/jats:sup>\n                      male\u00a0gametocytes\/mL for\n                      <jats:italic>pfMGET.<\/jats:italic>\n                      The limit of detection was 3.9 (95% CI 2.5\u20138.2) female\u00a0gametocytes\/mL for\n                      <jats:italic>pfs25<\/jats:italic>\n                      , and 26.9 (95% CI 19.3\u201351.7) male\u00a0gametocytes\/mL for\n                      <jats:italic>PfMGET<\/jats:italic>\n                      . Both assays showed minimal intra-assay and inter-assay variability with coefficient of variation\u2009&lt;\u20093%. No cross-reactivity was observed in both assays in uninfected human blood samples. Comparison of results from ddPCR to qRT-PCR assays on clinical blood samples indicated a high-level agreement (ICC\u2009=\u20090.998 for\n                      <jats:italic>pfs25<\/jats:italic>\n                      and 0.995 for\n                      <jats:italic>pfMGET<\/jats:italic>\n                      ).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      This study reports the validation of qRT-PCR assays that are able to accurately quantify female and male\n                      <jats:italic>P. falciparum<\/jats:italic>\n                      gametocytes at sub-microscopic densities. The assays showed excellent reproducibility, sensitivity, precision, specificity, and accuracy. The methodology will enable the estimation of gametocyte density in the absence of pure female and male gametocyte standards, and will facilitate clinical trials and epidemiological studies.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1186\/s12936-020-03291-9","type":"journal-article","created":{"date-parts":[[2020,6,23]],"date-time":"2020-06-23T07:03:07Z","timestamp":1592895787000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":18,"title":["Assays for quantification of male and female gametocytes in human blood by qRT-PCR in the absence of pure sex-specific gametocyte standards"],"prefix":"10.1186","volume":"19","author":[{"given":"Claire Y. 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