Abstract

Panamá, together with all the nations in Mesoamerica, has committed to eliminate malaria from the region by 2020. As these countries approach malaria elimination and local transmission decreases, an active molecular surveillance to identify genotypes circulating along the border areas is particularly needed to accurately infer infection origin, drug resistance and disease propagation patterns in the region. This study evaluated the genetic diversity and allele frequencies of msp-1, msp-2 and glurp genes using different molecular analyses (nested PCR, PCR-restriction fragment length polymorphism (RFLP) and sequencing) from 106 autochthonous and imported P. falciparum isolates collected from different endemic areas in Panamá between 2003 and 2019. We also explored if P. falciparum genotypes assessed with these molecular markers were associated with relevant malaria epidemiological parameters using a multiple correspondence analysis. A strong association of certain local haplotypes with their geographic distribution in endemic areas, but also with parasite load and presence of gametocytes, was evidenced. Few multiclonal infections and low genetic diversity among locally transmitted P. falciparum samples were detected, consequent with the low transmission intensity of this parasite in Panamá, a pattern likely to be extended across Mesoamerica. In addition, several imported cases were genetically dissimilar to local infections and representative of more diverse extra-continental lineages.

Highlights

  • Malaria continues to be a major, though neglected, public health challenge for health authorities in Panamá

  • Parasites circulating at that time presented mutations associated with resistance to chloroquine (CQ) and partial resistance to sulfadoxine–pyrimethamine (SP) [8,9,10]. This situation prompted a change in the national malaria drug policy in Panamá from CQ to SP, and shortly after to mefloquine, as first-line treatments for uncomplicated P. falciparum infections [7,9,11]

  • To provide additional information to optimize the National Malaria Elimination Programme (NMEP) strategies, the present study evaluated the genetic diversity and allele frequencies of merozoite surface proteins 1 and 2 and the glutamate-rich protein genes from autochthonous and imported P. falciparum human isolates collected in different endemic areas from Panamá between 2003 and 2019

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Summary

Introduction

Malaria continues to be a major, though neglected, public health challenge for health authorities in Panamá. During a major malaria epidemic observed between 2002 and 2003, autochthonous P. falciparum transmission was reestablished east of the Panamá Canal, with several fatal cases—a situation not observed in the county since 1970 [7]. Parasites circulating at that time presented mutations associated with resistance to chloroquine (CQ) and partial resistance to sulfadoxine–pyrimethamine (SP) [8,9,10]. This situation prompted a change in the national malaria drug policy in Panamá from CQ to SP, and shortly after to mefloquine, as first-line treatments for uncomplicated P. falciparum infections [7,9,11]. Intensification of malaria control activities coupled with the change in drug policy was highly effective to control the 2002–2003 P. falciparum outbreak [3,5,6]

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