Loading…
Epidemiology of Plasmodium falciparum infection and drug resistance markers in Ota Area, Southwestern Nigeria
Effective routine monitoring and surveillance of parasite genes is a necessary strategy in the control of parasites' resistance to antimalarial drugs, according to the WHO's recommendation. This cross-sectional study therefore aimed at carrying out an epidemiological analysis on malaria in...
Saved in:
Published in: | Infection and drug resistance 2019-07, Vol.12, p.1941-1949 |
---|---|
Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | 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-c573t-8a14fa2928cf792896dfd483ac7ba04e63361ffa7f9cd8c214dd2356fce924313 |
---|---|
cites | |
container_end_page | 1949 |
container_issue | |
container_start_page | 1941 |
container_title | Infection and drug resistance |
container_volume | 12 |
creator | Olasehinde, G I Diji-Geske, R I Fadina, I Arogundade, D Darby, P Adeleke, A Dokunmu, T M Adebayo, A H Oyelade, J |
description | Effective routine monitoring and surveillance of parasite genes is a necessary strategy in the control of parasites' resistance to antimalarial drugs, according to the WHO's recommendation. This cross-sectional study therefore aimed at carrying out an epidemiological analysis on malaria incidence in Ado-Odo/Ota, Ogun State.
Blood and corresponding saliva samples were collected from 1,243 subjects of all ages and sex presenting with fever and a parasitemia level ≥2,000 between September 2016 and March 2018. Samples were collected from selected health facilities in the study area of Ogun state to establish the prevalence of falciparum malaria and determine resistance genes harbored by the parasites. The overall prevalence of falciparum malaria in the study site by microscopic examination was 45.86%. The highest incidence of 57.42% was recorded among male subjects. Point mutations of K76T and N86Y in the
cr
and
mdr-1 genes, as well as non-synonymous mutations in
k13 genes, were screened for and sequenced for further analysis.
crt was detectable in 57.42% of blood and 51.02% of saliva samples, respectively. About 34.78% of the subjects that were confirmed microscopically harbored the
mdr
mutated gene while 26.67% of the saliva samples revealed
mdr
. Epidemiological studies identified the presence of wild-type
k13 genes in 21.84% of blood and 44.44% of saliva samples correspondingly. For each of the genes evaluated, saliva portrayed great diagnostic performance when compared with blood.
Findings from this study have established the prevalence of malaria and the resistance pattern of
in the study area. The findings may help in formulating drug policies and suggest the use of saliva as a noninvasive point-of-care method of diagnosing malaria potentially deployable to rural endemic areas. |
doi_str_mv | 10.2147/IDR.S190386 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_10d1456f59514aa48be439e2f2dc037e</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A602005288</galeid><doaj_id>oai_doaj_org_article_10d1456f59514aa48be439e2f2dc037e</doaj_id><sourcerecordid>A602005288</sourcerecordid><originalsourceid>FETCH-LOGICAL-c573t-8a14fa2928cf792896dfd483ac7ba04e63361ffa7f9cd8c214dd2356fce924313</originalsourceid><addsrcrecordid>eNptkt2L1DAUxYso7rLuk-9SEETQGZuPJu3LwrCuOrC44upzyCQ3nYxtMyatsv-9t864zogtJCH93dPknJtlT0kxp4TLN8u3n-e3pC5YJR5kp4TIaiZqyR4erE-y85Q2BT6sFlzSx9kJI6yoJOGnWXe19RY6H9rQ3OXB5Z9anbpg_djlTrfGb3XEpe8dmMGHPte9zW0cmzxC8mnQvYG80_EbxIRUfjPofBFBv85vwzisf0IaIPb5R99A9PpJ9ghFE5zv57Ps67urL5cfZtc375eXi-uZKSUbZpUm3Gla08o4iWMtrLO8YtrIlS44CMYEcU5LVxtbGTTCWspK4QzUlOPlzrLlTtcGvVHb6PGEdypor35vhNgoHQdvWlCksIRjaVmXhGvNqxVwVgN11JqCSUCti53Wdlx1YA30Q9Ttkejxl96vVRN-KCGIwBBQ4OVeIIbvIxqiOp8MtK3uIYxJUVpWkuM4nfv5P-gmjLFHq5ASsuSYNP9LNRovgNEE_K-ZRNVCFLQoSlpVSM3_Q-E7xW1CD87j_lHBi4OCNeh2WKfQjlPs6Rh8tQNNDClFcPdmkEJNXamwK9W-K5F-dujfPfunB9kvBh_bOQ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2267541904</pqid></control><display><type>article</type><title>Epidemiology of Plasmodium falciparum infection and drug resistance markers in Ota Area, Southwestern Nigeria</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>Taylor & Francis Open Access</source><source>PubMed Central Free</source><creator>Olasehinde, G I ; Diji-Geske, R I ; Fadina, I ; Arogundade, D ; Darby, P ; Adeleke, A ; Dokunmu, T M ; Adebayo, A H ; Oyelade, J</creator><creatorcontrib>Olasehinde, G I ; Diji-Geske, R I ; Fadina, I ; Arogundade, D ; Darby, P ; Adeleke, A ; Dokunmu, T M ; Adebayo, A H ; Oyelade, J</creatorcontrib><description>Effective routine monitoring and surveillance of parasite genes is a necessary strategy in the control of parasites' resistance to antimalarial drugs, according to the WHO's recommendation. This cross-sectional study therefore aimed at carrying out an epidemiological analysis on malaria incidence in Ado-Odo/Ota, Ogun State.
Blood and corresponding saliva samples were collected from 1,243 subjects of all ages and sex presenting with fever and a parasitemia level ≥2,000 between September 2016 and March 2018. Samples were collected from selected health facilities in the study area of Ogun state to establish the prevalence of falciparum malaria and determine resistance genes harbored by the parasites. The overall prevalence of falciparum malaria in the study site by microscopic examination was 45.86%. The highest incidence of 57.42% was recorded among male subjects. Point mutations of K76T and N86Y in the
cr
and
mdr-1 genes, as well as non-synonymous mutations in
k13 genes, were screened for and sequenced for further analysis.
crt was detectable in 57.42% of blood and 51.02% of saliva samples, respectively. About 34.78% of the subjects that were confirmed microscopically harbored the
mdr
mutated gene while 26.67% of the saliva samples revealed
mdr
. Epidemiological studies identified the presence of wild-type
k13 genes in 21.84% of blood and 44.44% of saliva samples correspondingly. For each of the genes evaluated, saliva portrayed great diagnostic performance when compared with blood.
Findings from this study have established the prevalence of malaria and the resistance pattern of
in the study area. The findings may help in formulating drug policies and suggest the use of saliva as a noninvasive point-of-care method of diagnosing malaria potentially deployable to rural endemic areas.</description><identifier>ISSN: 1178-6973</identifier><identifier>EISSN: 1178-6973</identifier><identifier>DOI: 10.2147/IDR.S190386</identifier><identifier>PMID: 31308714</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>Ado-Odo/Ota ; Amino acids ; Analysis ; Antimalarials ; Artemisinin ; Blood ; Diagnostic tests ; Disease ; Drug resistance ; Epidemiology ; Fever ; Fluids ; Gene mutation ; Genes ; Genetic research ; Halofantrine ; Health ; Health aspects ; Infections ; Malaria ; Microscopy ; Mutation ; Original Research ; Parasite resistance ; Parasitemia ; Parasites ; Plasmodium falciparum ; Prevalence ; Pyrimethamine ; Resistance ; Saliva ; Viral infections</subject><ispartof>Infection and drug resistance, 2019-07, Vol.12, p.1941-1949</ispartof><rights>COPYRIGHT 2019 Dove Medical Press Limited</rights><rights>2019. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 Olasehinde et al. 2019 Olasehinde et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c573t-8a14fa2928cf792896dfd483ac7ba04e63361ffa7f9cd8c214dd2356fce924313</citedby><orcidid>0000-0002-7166-3253 ; 0000-0002-5476-4992 ; 0000-0002-8751-3436 ; 0000-0002-5875-0985 ; 0000-0002-3410-1374</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2267541904/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2267541904?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31308714$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Olasehinde, G I</creatorcontrib><creatorcontrib>Diji-Geske, R I</creatorcontrib><creatorcontrib>Fadina, I</creatorcontrib><creatorcontrib>Arogundade, D</creatorcontrib><creatorcontrib>Darby, P</creatorcontrib><creatorcontrib>Adeleke, A</creatorcontrib><creatorcontrib>Dokunmu, T M</creatorcontrib><creatorcontrib>Adebayo, A H</creatorcontrib><creatorcontrib>Oyelade, J</creatorcontrib><title>Epidemiology of Plasmodium falciparum infection and drug resistance markers in Ota Area, Southwestern Nigeria</title><title>Infection and drug resistance</title><addtitle>Infect Drug Resist</addtitle><description>Effective routine monitoring and surveillance of parasite genes is a necessary strategy in the control of parasites' resistance to antimalarial drugs, according to the WHO's recommendation. This cross-sectional study therefore aimed at carrying out an epidemiological analysis on malaria incidence in Ado-Odo/Ota, Ogun State.
Blood and corresponding saliva samples were collected from 1,243 subjects of all ages and sex presenting with fever and a parasitemia level ≥2,000 between September 2016 and March 2018. Samples were collected from selected health facilities in the study area of Ogun state to establish the prevalence of falciparum malaria and determine resistance genes harbored by the parasites. The overall prevalence of falciparum malaria in the study site by microscopic examination was 45.86%. The highest incidence of 57.42% was recorded among male subjects. Point mutations of K76T and N86Y in the
cr
and
mdr-1 genes, as well as non-synonymous mutations in
k13 genes, were screened for and sequenced for further analysis.
crt was detectable in 57.42% of blood and 51.02% of saliva samples, respectively. About 34.78% of the subjects that were confirmed microscopically harbored the
mdr
mutated gene while 26.67% of the saliva samples revealed
mdr
. Epidemiological studies identified the presence of wild-type
k13 genes in 21.84% of blood and 44.44% of saliva samples correspondingly. For each of the genes evaluated, saliva portrayed great diagnostic performance when compared with blood.
Findings from this study have established the prevalence of malaria and the resistance pattern of
in the study area. The findings may help in formulating drug policies and suggest the use of saliva as a noninvasive point-of-care method of diagnosing malaria potentially deployable to rural endemic areas.</description><subject>Ado-Odo/Ota</subject><subject>Amino acids</subject><subject>Analysis</subject><subject>Antimalarials</subject><subject>Artemisinin</subject><subject>Blood</subject><subject>Diagnostic tests</subject><subject>Disease</subject><subject>Drug resistance</subject><subject>Epidemiology</subject><subject>Fever</subject><subject>Fluids</subject><subject>Gene mutation</subject><subject>Genes</subject><subject>Genetic research</subject><subject>Halofantrine</subject><subject>Health</subject><subject>Health aspects</subject><subject>Infections</subject><subject>Malaria</subject><subject>Microscopy</subject><subject>Mutation</subject><subject>Original Research</subject><subject>Parasite resistance</subject><subject>Parasitemia</subject><subject>Parasites</subject><subject>Plasmodium falciparum</subject><subject>Prevalence</subject><subject>Pyrimethamine</subject><subject>Resistance</subject><subject>Saliva</subject><subject>Viral infections</subject><issn>1178-6973</issn><issn>1178-6973</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkt2L1DAUxYso7rLuk-9SEETQGZuPJu3LwrCuOrC44upzyCQ3nYxtMyatsv-9t864zogtJCH93dPknJtlT0kxp4TLN8u3n-e3pC5YJR5kp4TIaiZqyR4erE-y85Q2BT6sFlzSx9kJI6yoJOGnWXe19RY6H9rQ3OXB5Z9anbpg_djlTrfGb3XEpe8dmMGHPte9zW0cmzxC8mnQvYG80_EbxIRUfjPofBFBv85vwzisf0IaIPb5R99A9PpJ9ghFE5zv57Ps67urL5cfZtc375eXi-uZKSUbZpUm3Gla08o4iWMtrLO8YtrIlS44CMYEcU5LVxtbGTTCWspK4QzUlOPlzrLlTtcGvVHb6PGEdypor35vhNgoHQdvWlCksIRjaVmXhGvNqxVwVgN11JqCSUCti53Wdlx1YA30Q9Ttkejxl96vVRN-KCGIwBBQ4OVeIIbvIxqiOp8MtK3uIYxJUVpWkuM4nfv5P-gmjLFHq5ASsuSYNP9LNRovgNEE_K-ZRNVCFLQoSlpVSM3_Q-E7xW1CD87j_lHBi4OCNeh2WKfQjlPs6Rh8tQNNDClFcPdmkEJNXamwK9W-K5F-dujfPfunB9kvBh_bOQ</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Olasehinde, G I</creator><creator>Diji-Geske, R I</creator><creator>Fadina, I</creator><creator>Arogundade, D</creator><creator>Darby, P</creator><creator>Adeleke, A</creator><creator>Dokunmu, T M</creator><creator>Adebayo, A H</creator><creator>Oyelade, J</creator><general>Dove Medical Press Limited</general><general>Taylor & Francis Ltd</general><general>Dove</general><general>Dove Medical Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-7166-3253</orcidid><orcidid>https://orcid.org/0000-0002-5476-4992</orcidid><orcidid>https://orcid.org/0000-0002-8751-3436</orcidid><orcidid>https://orcid.org/0000-0002-5875-0985</orcidid><orcidid>https://orcid.org/0000-0002-3410-1374</orcidid></search><sort><creationdate>20190701</creationdate><title>Epidemiology of Plasmodium falciparum infection and drug resistance markers in Ota Area, Southwestern Nigeria</title><author>Olasehinde, G I ; Diji-Geske, R I ; Fadina, I ; Arogundade, D ; Darby, P ; Adeleke, A ; Dokunmu, T M ; Adebayo, A H ; Oyelade, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c573t-8a14fa2928cf792896dfd483ac7ba04e63361ffa7f9cd8c214dd2356fce924313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Ado-Odo/Ota</topic><topic>Amino acids</topic><topic>Analysis</topic><topic>Antimalarials</topic><topic>Artemisinin</topic><topic>Blood</topic><topic>Diagnostic tests</topic><topic>Disease</topic><topic>Drug resistance</topic><topic>Epidemiology</topic><topic>Fever</topic><topic>Fluids</topic><topic>Gene mutation</topic><topic>Genes</topic><topic>Genetic research</topic><topic>Halofantrine</topic><topic>Health</topic><topic>Health aspects</topic><topic>Infections</topic><topic>Malaria</topic><topic>Microscopy</topic><topic>Mutation</topic><topic>Original Research</topic><topic>Parasite resistance</topic><topic>Parasitemia</topic><topic>Parasites</topic><topic>Plasmodium falciparum</topic><topic>Prevalence</topic><topic>Pyrimethamine</topic><topic>Resistance</topic><topic>Saliva</topic><topic>Viral infections</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Olasehinde, G I</creatorcontrib><creatorcontrib>Diji-Geske, R I</creatorcontrib><creatorcontrib>Fadina, I</creatorcontrib><creatorcontrib>Arogundade, D</creatorcontrib><creatorcontrib>Darby, P</creatorcontrib><creatorcontrib>Adeleke, A</creatorcontrib><creatorcontrib>Dokunmu, T M</creatorcontrib><creatorcontrib>Adebayo, A H</creatorcontrib><creatorcontrib>Oyelade, J</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest research library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Infection and drug resistance</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Olasehinde, G I</au><au>Diji-Geske, R I</au><au>Fadina, I</au><au>Arogundade, D</au><au>Darby, P</au><au>Adeleke, A</au><au>Dokunmu, T M</au><au>Adebayo, A H</au><au>Oyelade, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epidemiology of Plasmodium falciparum infection and drug resistance markers in Ota Area, Southwestern Nigeria</atitle><jtitle>Infection and drug resistance</jtitle><addtitle>Infect Drug Resist</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>12</volume><spage>1941</spage><epage>1949</epage><pages>1941-1949</pages><issn>1178-6973</issn><eissn>1178-6973</eissn><abstract>Effective routine monitoring and surveillance of parasite genes is a necessary strategy in the control of parasites' resistance to antimalarial drugs, according to the WHO's recommendation. This cross-sectional study therefore aimed at carrying out an epidemiological analysis on malaria incidence in Ado-Odo/Ota, Ogun State.
Blood and corresponding saliva samples were collected from 1,243 subjects of all ages and sex presenting with fever and a parasitemia level ≥2,000 between September 2016 and March 2018. Samples were collected from selected health facilities in the study area of Ogun state to establish the prevalence of falciparum malaria and determine resistance genes harbored by the parasites. The overall prevalence of falciparum malaria in the study site by microscopic examination was 45.86%. The highest incidence of 57.42% was recorded among male subjects. Point mutations of K76T and N86Y in the
cr
and
mdr-1 genes, as well as non-synonymous mutations in
k13 genes, were screened for and sequenced for further analysis.
crt was detectable in 57.42% of blood and 51.02% of saliva samples, respectively. About 34.78% of the subjects that were confirmed microscopically harbored the
mdr
mutated gene while 26.67% of the saliva samples revealed
mdr
. Epidemiological studies identified the presence of wild-type
k13 genes in 21.84% of blood and 44.44% of saliva samples correspondingly. For each of the genes evaluated, saliva portrayed great diagnostic performance when compared with blood.
Findings from this study have established the prevalence of malaria and the resistance pattern of
in the study area. The findings may help in formulating drug policies and suggest the use of saliva as a noninvasive point-of-care method of diagnosing malaria potentially deployable to rural endemic areas.</abstract><cop>New Zealand</cop><pub>Dove Medical Press Limited</pub><pmid>31308714</pmid><doi>10.2147/IDR.S190386</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-7166-3253</orcidid><orcidid>https://orcid.org/0000-0002-5476-4992</orcidid><orcidid>https://orcid.org/0000-0002-8751-3436</orcidid><orcidid>https://orcid.org/0000-0002-5875-0985</orcidid><orcidid>https://orcid.org/0000-0002-3410-1374</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1178-6973 |
ispartof | Infection and drug resistance, 2019-07, Vol.12, p.1941-1949 |
issn | 1178-6973 1178-6973 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_10d1456f59514aa48be439e2f2dc037e |
source | Publicly Available Content Database (Proquest) (PQ_SDU_P3); Taylor & Francis Open Access; PubMed Central Free |
subjects | Ado-Odo/Ota Amino acids Analysis Antimalarials Artemisinin Blood Diagnostic tests Disease Drug resistance Epidemiology Fever Fluids Gene mutation Genes Genetic research Halofantrine Health Health aspects Infections Malaria Microscopy Mutation Original Research Parasite resistance Parasitemia Parasites Plasmodium falciparum Prevalence Pyrimethamine Resistance Saliva Viral infections |
title | Epidemiology of Plasmodium falciparum infection and drug resistance markers in Ota Area, Southwestern Nigeria |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T20%3A34%3A11IST&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=Epidemiology%20of%20Plasmodium%20falciparum%20infection%20and%20drug%20resistance%20markers%20in%20Ota%20Area,%20Southwestern%20Nigeria&rft.jtitle=Infection%20and%20drug%20resistance&rft.au=Olasehinde,%20G%20I&rft.date=2019-07-01&rft.volume=12&rft.spage=1941&rft.epage=1949&rft.pages=1941-1949&rft.issn=1178-6973&rft.eissn=1178-6973&rft_id=info:doi/10.2147/IDR.S190386&rft_dat=%3Cgale_doaj_%3EA602005288%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c573t-8a14fa2928cf792896dfd483ac7ba04e63361ffa7f9cd8c214dd2356fce924313%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2267541904&rft_id=info:pmid/31308714&rft_galeid=A602005288&rfr_iscdi=true |