Loading…
Apicoplast-Resident Processes: Exploiting the Chink in the Armour of Plasmodium falciparum Parasites
The discovery of a relict plastid, also known as an apicoplast (apicomplexan plastid), that houses housekeeping processes and metabolic pathways critical to Plasmodium parasites’ survival has prompted increased research on identifying potent inhibitors that can impinge on apicoplast-localised proces...
Saved in:
Published in: | Advances in pharmacological and pharmaceutical sciences 2024-05, Vol.2024, p.9940468-17 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c573t-4190d3d993eb439f9962597d2480e7749145d9e471eaf73d746cef036d84bc543 |
container_end_page | 17 |
container_issue | |
container_start_page | 9940468 |
container_title | Advances in pharmacological and pharmaceutical sciences |
container_volume | 2024 |
creator | Mamudu, Collins Ojonugwa Tebamifor, Mercy Eyitomi Sule, Mary Ohunene Dokunmu, Titilope Modupe Ogunlana, Olubanke Olujoke Iheagwam, Franklyn Nonso |
description | The discovery of a relict plastid, also known as an apicoplast (apicomplexan plastid), that houses housekeeping processes and metabolic pathways critical to Plasmodium parasites’ survival has prompted increased research on identifying potent inhibitors that can impinge on apicoplast-localised processes. The apicoplast is absent in humans, yet it is proposed to originate from the eukaryote’s secondary endosymbiosis of a primary symbiont. This symbiotic relationship provides a favourable microenvironment for metabolic processes such as haem biosynthesis, Fe-S cluster synthesis, isoprenoid biosynthesis, fatty acid synthesis, and housekeeping processes such as DNA replication, transcription, and translation, distinct from analogous mammalian processes. Recent advancements in comprehending the biology of the apicoplast reveal it as a vulnerable organelle for malaria parasites, offering numerous potential targets for effective antimalarial therapies. We provide an overview of the metabolic processes occurring in the apicoplast and discuss the organelle as a viable antimalarial target in light of current advances in drug discovery. We further highlighted the relevance of these metabolic processes to Plasmodium falciparum during the different stages of the lifecycle. |
doi_str_mv | 10.1155/2024/9940468 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_3e3a0bc5026842e190bc0dbd1a023cdf</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A794401555</galeid><doaj_id>oai_doaj_org_article_3e3a0bc5026842e190bc0dbd1a023cdf</doaj_id><sourcerecordid>A794401555</sourcerecordid><originalsourceid>FETCH-LOGICAL-c573t-4190d3d993eb439f9962597d2480e7749145d9e471eaf73d746cef036d84bc543</originalsourceid><addsrcrecordid>eNp9kt1v0zAUxSMEYtPYG88oEi8g6OavODEvqKoGVJpENeDZcu2b1iWJMzuB8d9zu5ZCEUJ-sH39u8fy8cmyp5RcUFoUl4wwcamUIEJWD7JTJjmfCKnIw8O6YifZeUobQghjSlIuH2cnvCplQSt5mrlp723oG5OGyQ0k76Ab8kUMFlKC9Ca_uuub4AffrfJhDfls7buvue_uN9PYhjHmoc4X2N8G58c2r01jfW8iLhcmmuQHSE-yR1hOcL6fz7Iv764-zz5Mrj--n8-m1xNblHyYCKqI404pDkvBVa2UZIUqHRMVgbIUiorCKRAlBVOX3JVCWqgJl64SS1sIfpbNd7oumI3uo29N_KGD8fq-EOJKmzh424DmwA3BJsJkJRjgzUtL3NJRQxi3rkattzutfly24Cz6Ek1zJHp80vm1XoVvmlJKKCskKrzYK8RwO0IadOuThaYxHYQxaU6KkpSMCIXo87_QDTrboVdbCr-q5Fz-plYGX-C7OuDFdiuqp6USgmAiCqQu_kHhcNDiV3dQe6wfNbw8akBmgLthZcaU9PzTzTH7esfaGFKKUB8MoURvE6m3idT7RCL-7E8TD_Cv_CHwagdgrpz57v8v9xMhIOU1</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3056517336</pqid></control><display><type>article</type><title>Apicoplast-Resident Processes: Exploiting the Chink in the Armour of Plasmodium falciparum Parasites</title><source>Publicly Available Content Database</source><source>Wiley Open Access Journals</source><source>PubMed Central</source><creator>Mamudu, Collins Ojonugwa ; Tebamifor, Mercy Eyitomi ; Sule, Mary Ohunene ; Dokunmu, Titilope Modupe ; Ogunlana, Olubanke Olujoke ; Iheagwam, Franklyn Nonso</creator><contributor>Pavadai, Parasuraman ; Parasuraman Pavadai</contributor><creatorcontrib>Mamudu, Collins Ojonugwa ; Tebamifor, Mercy Eyitomi ; Sule, Mary Ohunene ; Dokunmu, Titilope Modupe ; Ogunlana, Olubanke Olujoke ; Iheagwam, Franklyn Nonso ; Pavadai, Parasuraman ; Parasuraman Pavadai</creatorcontrib><description>The discovery of a relict plastid, also known as an apicoplast (apicomplexan plastid), that houses housekeeping processes and metabolic pathways critical to Plasmodium parasites’ survival has prompted increased research on identifying potent inhibitors that can impinge on apicoplast-localised processes. The apicoplast is absent in humans, yet it is proposed to originate from the eukaryote’s secondary endosymbiosis of a primary symbiont. This symbiotic relationship provides a favourable microenvironment for metabolic processes such as haem biosynthesis, Fe-S cluster synthesis, isoprenoid biosynthesis, fatty acid synthesis, and housekeeping processes such as DNA replication, transcription, and translation, distinct from analogous mammalian processes. Recent advancements in comprehending the biology of the apicoplast reveal it as a vulnerable organelle for malaria parasites, offering numerous potential targets for effective antimalarial therapies. We provide an overview of the metabolic processes occurring in the apicoplast and discuss the organelle as a viable antimalarial target in light of current advances in drug discovery. We further highlighted the relevance of these metabolic processes to Plasmodium falciparum during the different stages of the lifecycle.</description><identifier>ISSN: 2633-4682</identifier><identifier>ISSN: 2633-4690</identifier><identifier>EISSN: 2633-4690</identifier><identifier>DOI: 10.1155/2024/9940468</identifier><identifier>PMID: 38765186</identifier><language>eng</language><publisher>England: Hindawi</publisher><subject>Antiparasitic agents ; Autophagy ; Biosynthesis ; Chloroplasts ; DNA replication ; Drug discovery ; Endoplasmic reticulum ; Fatty acids ; Genes ; Genetic engineering ; Genetic transcription ; Genomes ; Heme ; Kinases ; Localization ; Malaria ; Metabolism ; Metabolites ; Parasites ; Physiological aspects ; Plasmodium falciparum ; Plastids ; Proteins ; Protozoa ; Review ; RNA polymerase ; Synthesis</subject><ispartof>Advances in pharmacological and pharmaceutical sciences, 2024-05, Vol.2024, p.9940468-17</ispartof><rights>Copyright © 2024 Collins Ojonugwa Mamudu et al.</rights><rights>COPYRIGHT 2024 John Wiley & Sons, Inc.</rights><rights>Copyright © 2024 Collins Ojonugwa Mamudu et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2024 Collins Ojonugwa Mamudu et al. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c573t-4190d3d993eb439f9962597d2480e7749145d9e471eaf73d746cef036d84bc543</cites><orcidid>0000-0002-5460-2643 ; 0000-0001-5781-592X ; 0000-0001-8487-4052</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3056517336/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3056517336?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771,74872</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38765186$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Pavadai, Parasuraman</contributor><contributor>Parasuraman Pavadai</contributor><creatorcontrib>Mamudu, Collins Ojonugwa</creatorcontrib><creatorcontrib>Tebamifor, Mercy Eyitomi</creatorcontrib><creatorcontrib>Sule, Mary Ohunene</creatorcontrib><creatorcontrib>Dokunmu, Titilope Modupe</creatorcontrib><creatorcontrib>Ogunlana, Olubanke Olujoke</creatorcontrib><creatorcontrib>Iheagwam, Franklyn Nonso</creatorcontrib><title>Apicoplast-Resident Processes: Exploiting the Chink in the Armour of Plasmodium falciparum Parasites</title><title>Advances in pharmacological and pharmaceutical sciences</title><addtitle>Adv Pharmacol Pharm Sci</addtitle><description>The discovery of a relict plastid, also known as an apicoplast (apicomplexan plastid), that houses housekeeping processes and metabolic pathways critical to Plasmodium parasites’ survival has prompted increased research on identifying potent inhibitors that can impinge on apicoplast-localised processes. The apicoplast is absent in humans, yet it is proposed to originate from the eukaryote’s secondary endosymbiosis of a primary symbiont. This symbiotic relationship provides a favourable microenvironment for metabolic processes such as haem biosynthesis, Fe-S cluster synthesis, isoprenoid biosynthesis, fatty acid synthesis, and housekeeping processes such as DNA replication, transcription, and translation, distinct from analogous mammalian processes. Recent advancements in comprehending the biology of the apicoplast reveal it as a vulnerable organelle for malaria parasites, offering numerous potential targets for effective antimalarial therapies. We provide an overview of the metabolic processes occurring in the apicoplast and discuss the organelle as a viable antimalarial target in light of current advances in drug discovery. We further highlighted the relevance of these metabolic processes to Plasmodium falciparum during the different stages of the lifecycle.</description><subject>Antiparasitic agents</subject><subject>Autophagy</subject><subject>Biosynthesis</subject><subject>Chloroplasts</subject><subject>DNA replication</subject><subject>Drug discovery</subject><subject>Endoplasmic reticulum</subject><subject>Fatty acids</subject><subject>Genes</subject><subject>Genetic engineering</subject><subject>Genetic transcription</subject><subject>Genomes</subject><subject>Heme</subject><subject>Kinases</subject><subject>Localization</subject><subject>Malaria</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Parasites</subject><subject>Physiological aspects</subject><subject>Plasmodium falciparum</subject><subject>Plastids</subject><subject>Proteins</subject><subject>Protozoa</subject><subject>Review</subject><subject>RNA polymerase</subject><subject>Synthesis</subject><issn>2633-4682</issn><issn>2633-4690</issn><issn>2633-4690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kt1v0zAUxSMEYtPYG88oEi8g6OavODEvqKoGVJpENeDZcu2b1iWJMzuB8d9zu5ZCEUJ-sH39u8fy8cmyp5RcUFoUl4wwcamUIEJWD7JTJjmfCKnIw8O6YifZeUobQghjSlIuH2cnvCplQSt5mrlp723oG5OGyQ0k76Ab8kUMFlKC9Ca_uuub4AffrfJhDfls7buvue_uN9PYhjHmoc4X2N8G58c2r01jfW8iLhcmmuQHSE-yR1hOcL6fz7Iv764-zz5Mrj--n8-m1xNblHyYCKqI404pDkvBVa2UZIUqHRMVgbIUiorCKRAlBVOX3JVCWqgJl64SS1sIfpbNd7oumI3uo29N_KGD8fq-EOJKmzh424DmwA3BJsJkJRjgzUtL3NJRQxi3rkattzutfly24Cz6Ek1zJHp80vm1XoVvmlJKKCskKrzYK8RwO0IadOuThaYxHYQxaU6KkpSMCIXo87_QDTrboVdbCr-q5Fz-plYGX-C7OuDFdiuqp6USgmAiCqQu_kHhcNDiV3dQe6wfNbw8akBmgLthZcaU9PzTzTH7esfaGFKKUB8MoURvE6m3idT7RCL-7E8TD_Cv_CHwagdgrpz57v8v9xMhIOU1</recordid><startdate>20240510</startdate><enddate>20240510</enddate><creator>Mamudu, Collins Ojonugwa</creator><creator>Tebamifor, Mercy Eyitomi</creator><creator>Sule, Mary Ohunene</creator><creator>Dokunmu, Titilope Modupe</creator><creator>Ogunlana, Olubanke Olujoke</creator><creator>Iheagwam, Franklyn Nonso</creator><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-5460-2643</orcidid><orcidid>https://orcid.org/0000-0001-5781-592X</orcidid><orcidid>https://orcid.org/0000-0001-8487-4052</orcidid></search><sort><creationdate>20240510</creationdate><title>Apicoplast-Resident Processes: Exploiting the Chink in the Armour of Plasmodium falciparum Parasites</title><author>Mamudu, Collins Ojonugwa ; Tebamifor, Mercy Eyitomi ; Sule, Mary Ohunene ; Dokunmu, Titilope Modupe ; Ogunlana, Olubanke Olujoke ; Iheagwam, Franklyn Nonso</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c573t-4190d3d993eb439f9962597d2480e7749145d9e471eaf73d746cef036d84bc543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antiparasitic agents</topic><topic>Autophagy</topic><topic>Biosynthesis</topic><topic>Chloroplasts</topic><topic>DNA replication</topic><topic>Drug discovery</topic><topic>Endoplasmic reticulum</topic><topic>Fatty acids</topic><topic>Genes</topic><topic>Genetic engineering</topic><topic>Genetic transcription</topic><topic>Genomes</topic><topic>Heme</topic><topic>Kinases</topic><topic>Localization</topic><topic>Malaria</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Parasites</topic><topic>Physiological aspects</topic><topic>Plasmodium falciparum</topic><topic>Plastids</topic><topic>Proteins</topic><topic>Protozoa</topic><topic>Review</topic><topic>RNA polymerase</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mamudu, Collins Ojonugwa</creatorcontrib><creatorcontrib>Tebamifor, Mercy Eyitomi</creatorcontrib><creatorcontrib>Sule, Mary Ohunene</creatorcontrib><creatorcontrib>Dokunmu, Titilope Modupe</creatorcontrib><creatorcontrib>Ogunlana, Olubanke Olujoke</creatorcontrib><creatorcontrib>Iheagwam, Franklyn Nonso</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Databases</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ: Directory of Open Access Journals</collection><jtitle>Advances in pharmacological and pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mamudu, Collins Ojonugwa</au><au>Tebamifor, Mercy Eyitomi</au><au>Sule, Mary Ohunene</au><au>Dokunmu, Titilope Modupe</au><au>Ogunlana, Olubanke Olujoke</au><au>Iheagwam, Franklyn Nonso</au><au>Pavadai, Parasuraman</au><au>Parasuraman Pavadai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Apicoplast-Resident Processes: Exploiting the Chink in the Armour of Plasmodium falciparum Parasites</atitle><jtitle>Advances in pharmacological and pharmaceutical sciences</jtitle><addtitle>Adv Pharmacol Pharm Sci</addtitle><date>2024-05-10</date><risdate>2024</risdate><volume>2024</volume><spage>9940468</spage><epage>17</epage><pages>9940468-17</pages><issn>2633-4682</issn><issn>2633-4690</issn><eissn>2633-4690</eissn><abstract>The discovery of a relict plastid, also known as an apicoplast (apicomplexan plastid), that houses housekeeping processes and metabolic pathways critical to Plasmodium parasites’ survival has prompted increased research on identifying potent inhibitors that can impinge on apicoplast-localised processes. The apicoplast is absent in humans, yet it is proposed to originate from the eukaryote’s secondary endosymbiosis of a primary symbiont. This symbiotic relationship provides a favourable microenvironment for metabolic processes such as haem biosynthesis, Fe-S cluster synthesis, isoprenoid biosynthesis, fatty acid synthesis, and housekeeping processes such as DNA replication, transcription, and translation, distinct from analogous mammalian processes. Recent advancements in comprehending the biology of the apicoplast reveal it as a vulnerable organelle for malaria parasites, offering numerous potential targets for effective antimalarial therapies. We provide an overview of the metabolic processes occurring in the apicoplast and discuss the organelle as a viable antimalarial target in light of current advances in drug discovery. We further highlighted the relevance of these metabolic processes to Plasmodium falciparum during the different stages of the lifecycle.</abstract><cop>England</cop><pub>Hindawi</pub><pmid>38765186</pmid><doi>10.1155/2024/9940468</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0002-5460-2643</orcidid><orcidid>https://orcid.org/0000-0001-5781-592X</orcidid><orcidid>https://orcid.org/0000-0001-8487-4052</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2633-4682 |
ispartof | Advances in pharmacological and pharmaceutical sciences, 2024-05, Vol.2024, p.9940468-17 |
issn | 2633-4682 2633-4690 2633-4690 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_3e3a0bc5026842e190bc0dbd1a023cdf |
source | Publicly Available Content Database; Wiley Open Access Journals; PubMed Central |
subjects | Antiparasitic agents Autophagy Biosynthesis Chloroplasts DNA replication Drug discovery Endoplasmic reticulum Fatty acids Genes Genetic engineering Genetic transcription Genomes Heme Kinases Localization Malaria Metabolism Metabolites Parasites Physiological aspects Plasmodium falciparum Plastids Proteins Protozoa Review RNA polymerase Synthesis |
title | Apicoplast-Resident Processes: Exploiting the Chink in the Armour of Plasmodium falciparum Parasites |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T23%3A37%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Apicoplast-Resident%20Processes:%20Exploiting%20the%20Chink%20in%20the%20Armour%20of%20Plasmodium%20falciparum%20Parasites&rft.jtitle=Advances%20in%20pharmacological%20and%20pharmaceutical%20sciences&rft.au=Mamudu,%20Collins%20Ojonugwa&rft.date=2024-05-10&rft.volume=2024&rft.spage=9940468&rft.epage=17&rft.pages=9940468-17&rft.issn=2633-4682&rft.eissn=2633-4690&rft_id=info:doi/10.1155/2024/9940468&rft_dat=%3Cgale_doaj_%3EA794401555%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c573t-4190d3d993eb439f9962597d2480e7749145d9e471eaf73d746cef036d84bc543%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3056517336&rft_id=info:pmid/38765186&rft_galeid=A794401555&rfr_iscdi=true |