Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Malar J ; 13: 8, 2014 Jan 06.
Article in English | MEDLINE | ID: mdl-24393454

ABSTRACT

BACKGROUND: Despite the large burden of Plasmodium vivax, little is known about its transmission dynamics. This study explored the population structure and spatio-temporal dynamics of P. vivax recurrent infections after radical cure in a two-year cohort study carried out in a rural community of the Peruvian Amazon. METHODS: A total of 37 P. vivax participants recruited in San Carlos community (Peru) between April and December 2008 were treated radically with chloroquine and primaquine and followed up monthly for two years with systematic blood sampling. All samples were screened for malaria parasites and subsequently all P. vivax infections genotyped using 15 microsatellites. Parasite population structure and dynamics were determined by computing different genetic indices and using spatio-temporal statistics. RESULTS: After radical cure, 76% of the study participants experienced one or more recurrent P. vivax infections, most of them sub-patent and asymptomatic. The parasite population displayed limited genetic diversity (He = 0.49) and clonal structure, with most infections (84%) being monoclonal. Spatio-temporal clusters of specific haplotypes were found throughout the study and persistence of highly frequent haplotypes were observed over several months within the same participants/households. CONCLUSIONS: In San Carlos community, P. vivax recurrences were commonly observed after radical treatment, and characterized by asymptomatic, sub-patent and clustered infections (within and between individuals from a few neighbouring households). Moreover low genetic diversity as well as parasite inbreeding are likely to define a clonal parasite population which has important implications on the malaria epidemiology of the study area.


Subject(s)
Genetic Variation , Malaria, Vivax/epidemiology , Malaria, Vivax/transmission , Plasmodium vivax/genetics , Adolescent , Adult , Antimalarials/therapeutic use , Child , Child, Preschool , Chloroquine/therapeutic use , Cohort Studies , Female , Haplotypes , Humans , Malaria, Vivax/drug therapy , Malaria, Vivax/parasitology , Male , Middle Aged , Peru/epidemiology , Polymerase Chain Reaction , Primaquine/therapeutic use , Rural Population , Young Adult
2.
J Theor Biol ; 256(4): 561-73, 2009 Feb 21.
Article in English | MEDLINE | ID: mdl-19022263

ABSTRACT

There is increasing evidence showing that antimicrobial consumption provides a powerful selective force that promotes the emergence of resistance in pathogenic, commensal as well as zoonotic bacteria in animals. The main aim of this study was to develop a modeling framework that can be used to assess the impact of antimicrobial usage in pigs on the emergence and transmission of resistant bacteria within a finisher pig farm. The transmission dynamics of drug-sensitive and drug-resistant bacteria among pigs in the herd were characterized by studying the local and global stability properties of steady state solutions of the system. Numerical simulations demonstrating the influence of factors such as initial prevalence of infection, presence of pre-existing antimicrobial resistant mutants, and frequency of treatment on predicted prevalence were performed. Sensitivity analysis revealed that two parameters had a huge influence on the predicted proportion of pigs carrying resistant bacteria: (a) the transmission coefficient between uninfected pigs and those infected with drug-resistant bacteria during treatment (beta(2)) and after treatment stops (beta(3)), and (b) the spontaneous clear-out rate of drug-resistant bacteria during treatment (gamma(2)) and immediately after treatment stops (gamma(3)). Control measures should therefore be geared towards reducing the magnitudes of beta(2) and beta(3) or increasing those of gamma(2) and gamma(3).


Subject(s)
Anti-Bacterial Agents/administration & dosage , Bacterial Infections/transmission , Bacterial Infections/veterinary , Drug Resistance, Bacterial , Models, Biological , Swine Diseases/microbiology , Animal Husbandry/methods , Animals , Anti-Bacterial Agents/therapeutic use , Bacterial Infections/drug therapy , Bacterial Infections/microbiology , Disease Transmission, Infectious/veterinary , Drug Administration Schedule , Sus scrofa , Swine Diseases/drug therapy , Swine Diseases/transmission
SELECTION OF CITATIONS
SEARCH DETAIL
...