Loick P. Kojom Foko , Joseph Hawadak , Vineeta Singh
{"title":"对恶性疟原虫msp1和msp2候选疫苗多态性的调查显示,喀麦隆遗传多样性单克隆感染的比例很高","authors":"Loick P. Kojom Foko , Joseph Hawadak , Vineeta Singh","doi":"10.1016/j.genrep.2025.102348","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Antimalarial immunity is greatly modulated by the genetic structure of <em>Plasmodium</em> populations, which is an important hurdle to successful vaccine development.</div></div><div><h3>Methods</h3><div>Dried blood spots were collected from hospital patients living in four towns (Douala, Maroua, Mayo-Oulo, and Pette). Genomic DNA was extracted and used to genotype the merozoite surface protein 1 and 2 genes (<em>msp1</em> and <em>msp2</em>).</div></div><div><h3>Results</h3><div>K1 (76.3 %) and IC/3D7 (83.3 %) were the most frequently found <em>msp1</em> and <em>msp2</em> allelic types, respectively. The total number of genotypes was 24 <em>msp1</em> (11 K1; 8 Mad20; 5 RO33) and 43 <em>msp2</em> (29 IC/3D7; 14 FC27). Monoclonal infections were predominant: 68.4 % for <em>msp1</em> [K1 (46.1 %), Mad20 (18.4 %), and RO33 (3.9 %)], and 67.1 % for <em>msp2</em> [IC/3D7 (50.0 %), and FC27 (17.1 %)]. Individuals living in Pette had fewer chances to get <em>msp1</em>-related monoclonal infections than those living in Douala (OR = 0.22, <em>p</em> = 0.01). Regarding <em>msp2</em>, IC/3D7 and FC27 genotypes found in MI accounted for 58.6 % and 100 % of total IC/3D7 and FC27 genotypes found. No statistically significant association was found between MOI, age, parasite density, and geographical area.</div></div><div><h3>Conclusion</h3><div>This study reveals a high genetic diversity of <em>P. falciparum</em> infections, with a predominance of monoclonal infections.</div></div>","PeriodicalId":12673,"journal":{"name":"Gene Reports","volume":"41 ","pages":"Article 102348"},"PeriodicalIF":0.9000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Investigating polymorphism of Plasmodium falciparum msp1 and msp2 vaccine candidates reveals a high proportion of genetically diverse monoclonal infections in Cameroon\",\"authors\":\"Loick P. Kojom Foko , Joseph Hawadak , Vineeta Singh\",\"doi\":\"10.1016/j.genrep.2025.102348\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Antimalarial immunity is greatly modulated by the genetic structure of <em>Plasmodium</em> populations, which is an important hurdle to successful vaccine development.</div></div><div><h3>Methods</h3><div>Dried blood spots were collected from hospital patients living in four towns (Douala, Maroua, Mayo-Oulo, and Pette). Genomic DNA was extracted and used to genotype the merozoite surface protein 1 and 2 genes (<em>msp1</em> and <em>msp2</em>).</div></div><div><h3>Results</h3><div>K1 (76.3 %) and IC/3D7 (83.3 %) were the most frequently found <em>msp1</em> and <em>msp2</em> allelic types, respectively. The total number of genotypes was 24 <em>msp1</em> (11 K1; 8 Mad20; 5 RO33) and 43 <em>msp2</em> (29 IC/3D7; 14 FC27). Monoclonal infections were predominant: 68.4 % for <em>msp1</em> [K1 (46.1 %), Mad20 (18.4 %), and RO33 (3.9 %)], and 67.1 % for <em>msp2</em> [IC/3D7 (50.0 %), and FC27 (17.1 %)]. Individuals living in Pette had fewer chances to get <em>msp1</em>-related monoclonal infections than those living in Douala (OR = 0.22, <em>p</em> = 0.01). Regarding <em>msp2</em>, IC/3D7 and FC27 genotypes found in MI accounted for 58.6 % and 100 % of total IC/3D7 and FC27 genotypes found. No statistically significant association was found between MOI, age, parasite density, and geographical area.</div></div><div><h3>Conclusion</h3><div>This study reveals a high genetic diversity of <em>P. falciparum</em> infections, with a predominance of monoclonal infections.</div></div>\",\"PeriodicalId\":12673,\"journal\":{\"name\":\"Gene Reports\",\"volume\":\"41 \",\"pages\":\"Article 102348\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Gene Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2452014425002213\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gene Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2452014425002213","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Investigating polymorphism of Plasmodium falciparum msp1 and msp2 vaccine candidates reveals a high proportion of genetically diverse monoclonal infections in Cameroon
Background
Antimalarial immunity is greatly modulated by the genetic structure of Plasmodium populations, which is an important hurdle to successful vaccine development.
Methods
Dried blood spots were collected from hospital patients living in four towns (Douala, Maroua, Mayo-Oulo, and Pette). Genomic DNA was extracted and used to genotype the merozoite surface protein 1 and 2 genes (msp1 and msp2).
Results
K1 (76.3 %) and IC/3D7 (83.3 %) were the most frequently found msp1 and msp2 allelic types, respectively. The total number of genotypes was 24 msp1 (11 K1; 8 Mad20; 5 RO33) and 43 msp2 (29 IC/3D7; 14 FC27). Monoclonal infections were predominant: 68.4 % for msp1 [K1 (46.1 %), Mad20 (18.4 %), and RO33 (3.9 %)], and 67.1 % for msp2 [IC/3D7 (50.0 %), and FC27 (17.1 %)]. Individuals living in Pette had fewer chances to get msp1-related monoclonal infections than those living in Douala (OR = 0.22, p = 0.01). Regarding msp2, IC/3D7 and FC27 genotypes found in MI accounted for 58.6 % and 100 % of total IC/3D7 and FC27 genotypes found. No statistically significant association was found between MOI, age, parasite density, and geographical area.
Conclusion
This study reveals a high genetic diversity of P. falciparum infections, with a predominance of monoclonal infections.
Gene ReportsBiochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍:
Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.