Genetic Characterization of Plasmodium falciparum Histidine-Rich Protein 2 Deletions and Their Impact on Malaria Interventions in Odisha, India
Stuti Mohanty, Abbey M. Jones, Swagatika Dash, Satya Ranjan Chhatria, Timir Kanta Padhan, Sanjib Mohanty, Jane M. Carlton, Danielle C. Ompad, Anne Kessler, Praveen Kishore Sahu

TL;DR
This study examines how gene deletions in malaria parasites in India affect diagnostic tests and intervention programs, highlighting the need for better tools to achieve malaria elimination.
Contribution
The study identifies high prevalence of pfhrp2 gene deletions in subpatent infections and evaluates their impact on malaria interventions in Odisha, India.
Findings
61.6% of subpatent P. falciparum infections had pfhrp2 gene deletions, mostly in exon 2.
Mass screening and treatment with additional interventions reduced infection risk for both pfhrp2-deleted and intact parasites.
Novel amino acid repeat motifs were discovered in variant P. falciparum samples with intact pfhrp2 genes.
Abstract
Diagnostic escape via Plasmodium falciparum (P. falciparum) histidine-rich protein 2 (pfhrp2) gene deletions is a major potential hurdle for global malaria elimination efforts. We investigated the prevalence of pfhrp2 gene deletions in 15 malaria-endemic villages in the state of Odisha, India, and modeled their impact on an ongoing in-country malaria intervention program. We found that 61.6% of subpatent P. falciparum infections (i.e., rapid diagnostic test [RDT]-negative and positive by polymerase chain reaction [PCR]) had pfhrp2 gene deletions, which were predominantly located in the exon 2 region (96.2%) and largely identified in samples from febrile individuals (82.6%). DNA sequencing and protein diversity features were characterized in a subset of samples from individuals with subpatent infections carrying intact pfhrp2 exon 2 loci. Our analyses revealed novel amino acid repeat…
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Taxonomy
TopicsMalaria Research and Control · Mosquito-borne diseases and control · Computational Drug Discovery Methods
