Loading…

Extraordinary parasite multiplication rates in human malaria infections

Theory assumes that multiplication rates of pathogenic organisms have substantial influence on disease severity and spread.Malaria infections represent one of the most straightforward systems in which to measure parasite multiplication rates (PMRs), but PMRs have proven difficult to link to health o...

Full description

Saved in:
Bibliographic Details
Published in:Trends in parasitology 2023-08, Vol.39 (8), p.626-637
Main Authors: Greischar, Megan A., Childs, Lauren M.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c425t-239cde258946aeeaa779709c18023cd8136b5d0635dfb191888f38980d9e92a43
cites cdi_FETCH-LOGICAL-c425t-239cde258946aeeaa779709c18023cd8136b5d0635dfb191888f38980d9e92a43
container_end_page 637
container_issue 8
container_start_page 626
container_title Trends in parasitology
container_volume 39
creator Greischar, Megan A.
Childs, Lauren M.
description Theory assumes that multiplication rates of pathogenic organisms have substantial influence on disease severity and spread.Malaria infections represent one of the most straightforward systems in which to measure parasite multiplication rates (PMRs), but PMRs have proven difficult to link to health outcomes.Applied to human infection data, standard methods for estimating PMRs yield extraordinarily large values, far exceeding the maximum expansion rate (i.e., burst size) established in vitro.Spurious multiplication rates appear when some ages of parasites are more difficult to sample and when the age distribution of the parasite population changes through time, problems that are likely common among pathogenic organisms.Small changes in age distributions can lead to estimates of extraordinarily high multiplication rates that may explain why PMRs often fail to predict disease severity. For pathogenic organisms, faster rates of multiplication promote transmission success, the potential to harm hosts, and the evolution of drug resistance. Parasite multiplication rates (PMRs) are often quantified in malaria infections, given the relative ease of sampling. Using modern and historical human infection data, we show that established methods return extraordinarily – and implausibly – large PMRs. We illustrate how inflated PMRs arise from two facets of malaria biology that are far from unique: (i) some developmental ages are easier to sample than others; (ii) the distribution of developmental ages changes over the course of infection. The difficulty of accurately quantifying PMRs demonstrates a need for robust methods and a subsequent re-evaluation of what is known even in the well-studied system of malaria.
doi_str_mv 10.1016/j.pt.2023.05.006
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2827922569</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1471492223001241</els_id><sourcerecordid>2834280841</sourcerecordid><originalsourceid>FETCH-LOGICAL-c425t-239cde258946aeeaa779709c18023cd8136b5d0635dfb191888f38980d9e92a43</originalsourceid><addsrcrecordid>eNqNkLtLBDEQh4Movnsr2dLm1kmy2U3sRHyBYKN1yCWzmGNfJlnR_94cd9oJVjMM3_yY-Qg5o1BSoPXlqpxSyYDxEkQJUO-QQ1o1dCEAmt1tXynGDshRjCsAKppG7ZMD3nBeNwCH5P72MwUzBucHE76KyQQTfcKin7vkp85bk_w4FMEkjIUfire5N0PRm84Eb_KgRbsG4gnZa00X8XRbj8nr3e3LzcPi6fn-8eb6aWErJtKCcWUdMiFVVRtEY_I9DShLZX7COkl5vRQOai5cu6SKSilbLpUEp1AxU_FjcrHJncL4PmNMuvfRYteZAcc5aiZ5xSTIiv4DZU12I2qVUdigNowxBmz1FHyfhWgKem1ar_SU9Nq0BqGz6bxyvk2flz2634UftRm42gCYdXx4DDpaj4NF50OWpt3o_07_Bky6jRU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2827922569</pqid></control><display><type>article</type><title>Extraordinary parasite multiplication rates in human malaria infections</title><source>ScienceDirect Freedom Collection</source><creator>Greischar, Megan A. ; Childs, Lauren M.</creator><creatorcontrib>Greischar, Megan A. ; Childs, Lauren M.</creatorcontrib><description>Theory assumes that multiplication rates of pathogenic organisms have substantial influence on disease severity and spread.Malaria infections represent one of the most straightforward systems in which to measure parasite multiplication rates (PMRs), but PMRs have proven difficult to link to health outcomes.Applied to human infection data, standard methods for estimating PMRs yield extraordinarily large values, far exceeding the maximum expansion rate (i.e., burst size) established in vitro.Spurious multiplication rates appear when some ages of parasites are more difficult to sample and when the age distribution of the parasite population changes through time, problems that are likely common among pathogenic organisms.Small changes in age distributions can lead to estimates of extraordinarily high multiplication rates that may explain why PMRs often fail to predict disease severity. For pathogenic organisms, faster rates of multiplication promote transmission success, the potential to harm hosts, and the evolution of drug resistance. Parasite multiplication rates (PMRs) are often quantified in malaria infections, given the relative ease of sampling. Using modern and historical human infection data, we show that established methods return extraordinarily – and implausibly – large PMRs. We illustrate how inflated PMRs arise from two facets of malaria biology that are far from unique: (i) some developmental ages are easier to sample than others; (ii) the distribution of developmental ages changes over the course of infection. The difficulty of accurately quantifying PMRs demonstrates a need for robust methods and a subsequent re-evaluation of what is known even in the well-studied system of malaria.</description><identifier>ISSN: 1471-4922</identifier><identifier>EISSN: 1471-5007</identifier><identifier>DOI: 10.1016/j.pt.2023.05.006</identifier><identifier>PMID: 37336700</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; controlled human infection trial ; drug resistance ; human diseases ; Humans ; malaria ; Malaria - parasitology ; malaria therapy ; Malaria, Falciparum - parasitology ; Parasites ; parasitology ; Plasmodium falciparum ; replication rates ; within-host dynamics</subject><ispartof>Trends in parasitology, 2023-08, Vol.39 (8), p.626-637</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-239cde258946aeeaa779709c18023cd8136b5d0635dfb191888f38980d9e92a43</citedby><cites>FETCH-LOGICAL-c425t-239cde258946aeeaa779709c18023cd8136b5d0635dfb191888f38980d9e92a43</cites><orcidid>0000-0002-7521-9344 ; 0000-0003-3904-3895</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37336700$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Greischar, Megan A.</creatorcontrib><creatorcontrib>Childs, Lauren M.</creatorcontrib><title>Extraordinary parasite multiplication rates in human malaria infections</title><title>Trends in parasitology</title><addtitle>Trends Parasitol</addtitle><description>Theory assumes that multiplication rates of pathogenic organisms have substantial influence on disease severity and spread.Malaria infections represent one of the most straightforward systems in which to measure parasite multiplication rates (PMRs), but PMRs have proven difficult to link to health outcomes.Applied to human infection data, standard methods for estimating PMRs yield extraordinarily large values, far exceeding the maximum expansion rate (i.e., burst size) established in vitro.Spurious multiplication rates appear when some ages of parasites are more difficult to sample and when the age distribution of the parasite population changes through time, problems that are likely common among pathogenic organisms.Small changes in age distributions can lead to estimates of extraordinarily high multiplication rates that may explain why PMRs often fail to predict disease severity. For pathogenic organisms, faster rates of multiplication promote transmission success, the potential to harm hosts, and the evolution of drug resistance. Parasite multiplication rates (PMRs) are often quantified in malaria infections, given the relative ease of sampling. Using modern and historical human infection data, we show that established methods return extraordinarily – and implausibly – large PMRs. We illustrate how inflated PMRs arise from two facets of malaria biology that are far from unique: (i) some developmental ages are easier to sample than others; (ii) the distribution of developmental ages changes over the course of infection. The difficulty of accurately quantifying PMRs demonstrates a need for robust methods and a subsequent re-evaluation of what is known even in the well-studied system of malaria.</description><subject>Animals</subject><subject>controlled human infection trial</subject><subject>drug resistance</subject><subject>human diseases</subject><subject>Humans</subject><subject>malaria</subject><subject>Malaria - parasitology</subject><subject>malaria therapy</subject><subject>Malaria, Falciparum - parasitology</subject><subject>Parasites</subject><subject>parasitology</subject><subject>Plasmodium falciparum</subject><subject>replication rates</subject><subject>within-host dynamics</subject><issn>1471-4922</issn><issn>1471-5007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqNkLtLBDEQh4Movnsr2dLm1kmy2U3sRHyBYKN1yCWzmGNfJlnR_94cd9oJVjMM3_yY-Qg5o1BSoPXlqpxSyYDxEkQJUO-QQ1o1dCEAmt1tXynGDshRjCsAKppG7ZMD3nBeNwCH5P72MwUzBucHE76KyQQTfcKin7vkp85bk_w4FMEkjIUfire5N0PRm84Eb_KgRbsG4gnZa00X8XRbj8nr3e3LzcPi6fn-8eb6aWErJtKCcWUdMiFVVRtEY_I9DShLZX7COkl5vRQOai5cu6SKSilbLpUEp1AxU_FjcrHJncL4PmNMuvfRYteZAcc5aiZ5xSTIiv4DZU12I2qVUdigNowxBmz1FHyfhWgKem1ar_SU9Nq0BqGz6bxyvk2flz2634UftRm42gCYdXx4DDpaj4NF50OWpt3o_07_Bky6jRU</recordid><startdate>20230801</startdate><enddate>20230801</enddate><creator>Greischar, Megan A.</creator><creator>Childs, Lauren M.</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0002-7521-9344</orcidid><orcidid>https://orcid.org/0000-0003-3904-3895</orcidid></search><sort><creationdate>20230801</creationdate><title>Extraordinary parasite multiplication rates in human malaria infections</title><author>Greischar, Megan A. ; Childs, Lauren M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-239cde258946aeeaa779709c18023cd8136b5d0635dfb191888f38980d9e92a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>controlled human infection trial</topic><topic>drug resistance</topic><topic>human diseases</topic><topic>Humans</topic><topic>malaria</topic><topic>Malaria - parasitology</topic><topic>malaria therapy</topic><topic>Malaria, Falciparum - parasitology</topic><topic>Parasites</topic><topic>parasitology</topic><topic>Plasmodium falciparum</topic><topic>replication rates</topic><topic>within-host dynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Greischar, Megan A.</creatorcontrib><creatorcontrib>Childs, Lauren M.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Trends in parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Greischar, Megan A.</au><au>Childs, Lauren M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extraordinary parasite multiplication rates in human malaria infections</atitle><jtitle>Trends in parasitology</jtitle><addtitle>Trends Parasitol</addtitle><date>2023-08-01</date><risdate>2023</risdate><volume>39</volume><issue>8</issue><spage>626</spage><epage>637</epage><pages>626-637</pages><issn>1471-4922</issn><eissn>1471-5007</eissn><abstract>Theory assumes that multiplication rates of pathogenic organisms have substantial influence on disease severity and spread.Malaria infections represent one of the most straightforward systems in which to measure parasite multiplication rates (PMRs), but PMRs have proven difficult to link to health outcomes.Applied to human infection data, standard methods for estimating PMRs yield extraordinarily large values, far exceeding the maximum expansion rate (i.e., burst size) established in vitro.Spurious multiplication rates appear when some ages of parasites are more difficult to sample and when the age distribution of the parasite population changes through time, problems that are likely common among pathogenic organisms.Small changes in age distributions can lead to estimates of extraordinarily high multiplication rates that may explain why PMRs often fail to predict disease severity. For pathogenic organisms, faster rates of multiplication promote transmission success, the potential to harm hosts, and the evolution of drug resistance. Parasite multiplication rates (PMRs) are often quantified in malaria infections, given the relative ease of sampling. Using modern and historical human infection data, we show that established methods return extraordinarily – and implausibly – large PMRs. We illustrate how inflated PMRs arise from two facets of malaria biology that are far from unique: (i) some developmental ages are easier to sample than others; (ii) the distribution of developmental ages changes over the course of infection. The difficulty of accurately quantifying PMRs demonstrates a need for robust methods and a subsequent re-evaluation of what is known even in the well-studied system of malaria.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>37336700</pmid><doi>10.1016/j.pt.2023.05.006</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-7521-9344</orcidid><orcidid>https://orcid.org/0000-0003-3904-3895</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1471-4922
ispartof Trends in parasitology, 2023-08, Vol.39 (8), p.626-637
issn 1471-4922
1471-5007
language eng
recordid cdi_proquest_miscellaneous_2827922569
source ScienceDirect Freedom Collection
subjects Animals
controlled human infection trial
drug resistance
human diseases
Humans
malaria
Malaria - parasitology
malaria therapy
Malaria, Falciparum - parasitology
Parasites
parasitology
Plasmodium falciparum
replication rates
within-host dynamics
title Extraordinary parasite multiplication rates in human malaria infections
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T08%3A55%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Extraordinary%20parasite%20multiplication%20rates%20in%20human%20malaria%20infections&rft.jtitle=Trends%20in%20parasitology&rft.au=Greischar,%20Megan%20A.&rft.date=2023-08-01&rft.volume=39&rft.issue=8&rft.spage=626&rft.epage=637&rft.pages=626-637&rft.issn=1471-4922&rft.eissn=1471-5007&rft_id=info:doi/10.1016/j.pt.2023.05.006&rft_dat=%3Cproquest_cross%3E2834280841%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c425t-239cde258946aeeaa779709c18023cd8136b5d0635dfb191888f38980d9e92a43%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2827922569&rft_id=info:pmid/37336700&rfr_iscdi=true