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1.
Article in English | MEDLINE | ID: mdl-32521653

ABSTRACT

Greece has been malaria-free since 1974. In October 2011, following an outbreak of 36 locally acquired malaria (LAM) cases in Evrotas Municipality, a Pro-Active Case Detection (PACD) program for malaria was implemented among migrants from malaria-endemic countries, to support early diagnosis and treatment of cases. We evaluated the PACD program for the years 2012-2017 using indicators such as the number of locally acquired cases, the detection rate/sensitivity and the timeliness of diagnosis and treatment. We visited each migrant home every 7-15 days to screen migrants for malaria symptoms, performing Rapid Diagnostic Tests (RDTs) and blood smears on symptomatic patients. We estimated: (i) the number of malaria cases detected by the PACD, divided by the total number of reported malaria cases during the same period among the same population; (ii) the time between onset of symptoms, diagnosis and initiation of treatment. The total number of migrants who were screened for malaria symptoms for the years 2012-2017 was 5057 with 84,169 fever screenings conducted, while 2288 RDTs and 1736 blood smears were performed. During the same period, 53 imported P. vivax malaria cases were detected, while incidence of malaria among migrants was estimated at 1.8% annually. Ten and one LAM cases were also reported in 2012 and 2015, respectively. Sensitivity of PACD ranged from 86% to 100%; median timeliness between onset of symptoms and diagnosis decreased from 72 h in 2012 to 12 h in 2017 (83% decrease), while timeliness between diagnosis and treatment initiation was 0 h. The implementation of PACD could be considered an effective prevention and response tool against malaria re-introduction.


Subject(s)
Disease Outbreaks , Malaria, Vivax , Malaria , Transients and Migrants , Fever , Greece , Humans , Male
3.
Emerg Infect Dis ; 24(3): 541-548, 2018 03.
Article in English | MEDLINE | ID: mdl-29460743

ABSTRACT

An influx of immigrants is contributing to the reemergence of Plasmodium vivax malaria in Greece; 1 persistent focus of transmission is in Laconia, Pelopónnese. We genotyped archived blood samples from a substantial proportion of malaria cases recorded in Greece in 2009-2013 using 8 microsatellite markers and a PvMSP-3α gene fragment and plotted their spatiotemporal distribution. High parasite genetic diversity with low multiplicity of infection was observed. A subset of genetically identical/related parasites was restricted to 3 areas in migrants and Greek residents, with some persisting over 2 consecutive transmission periods. We identified 2 hitherto unsuspected additional foci of local transmission: Kardhítsa and Attica. Furthermore, this analysis indicates that several cases in migrants initially classified as imported malaria were actually locally acquired. This study shows the potential for P. vivax to reestablish transmission and counsels public health authorities about the need for vigilance to achieve or maintain sustainable malaria elimination.


Subject(s)
Malaria, Vivax/epidemiology , Malaria, Vivax/parasitology , Plasmodium vivax/genetics , Alleles , Genetic Variation , Genome, Protozoan , Genotype , Geography , Greece/epidemiology , History, 21st Century , Humans , Malaria, Vivax/history , Malaria, Vivax/transmission , Spatio-Temporal Analysis
4.
PLoS One ; 10(3): e0120367, 2015.
Article in English | MEDLINE | ID: mdl-25803815

ABSTRACT

Greece, a malaria-free country since 1974, has experienced re-emergence of Plasmodium vivax autochthonous malaria cases in some agriculture areas over the last three years. In early 2012, an integrated control programme (MALWEST Project) was launched in order to prevent re-establishment of the disease. In the context of this project, the rapid diagnostic tests (RDT) of SD Bioline Malaria Ag Pf/Pan that detects hrp-2 and pan-LDH antigens were used. The aim of this study was to assess the field application of the RDT for the P. vivax diagnosis in comparison to light microscopy and polymerase chain reaction (PCR). A total of 955 samples were tested with all three diagnostic tools. Agreement of RDT against microscopy and PCR for the diagnosis of P. vivax was satisfactory (K value: 0.849 and 0.976, respectively). The sensitivity, specificity and positive predictive value of RDT against PCR was 95.6% (95% C.I.: 84.8-99.3), 100% (95% C.I.: 99.6-100.0) and 100% (95% CI: 91.7-100.0) respectively, while the sensitivity, specificity and positive predictive value of RDT against microscopic examination was 97.4% (95% C.I.: 86.1-99.6), 99.4% (95% C.I.: 98.6-99.8) and 86.1% (95% CI: 72.1-94.7), respectively. Our results indicate that RDT performed satisfactory in a non-endemic country and therefore is recommended for malaria diagnosis, especially in areas where health professionals lack experience on light microscopy.


Subject(s)
Diagnostic Tests, Routine/methods , Malaria, Vivax/diagnosis , Malaria, Vivax/epidemiology , Plasmodium vivax/isolation & purification , Adolescent , Adult , Aged , Aged, 80 and over , Antigens, Protozoan/analysis , Child , Child, Preschool , Diagnostic Tests, Routine/economics , Greece/epidemiology , Humans , Infant , Microscopy/economics , Microscopy/methods , Middle Aged , Polymerase Chain Reaction/economics , Polymerase Chain Reaction/methods , Sensitivity and Specificity , Young Adult
5.
Int J Environ Res Public Health ; 10(12): 6534-610, 2013 Dec 02.
Article in English | MEDLINE | ID: mdl-24317379

ABSTRACT

During the last three years Greece is experiencing the emergence of West Nile virus (WNV) epidemics. Within this framework, an integrated surveillance and control programme (MALWEST project) with thirteen associate partners was launched aiming to investigate the disease and suggest appropriate interventions. One out of seven work packages of the project is dedicated to the State of the Art report for WNV. Three expert working groups on humans, animals and mosquitoes were established. Medical databases (PubMed, Scopus) were searched together with websites: e.g., WHO, CDC, ECDC. In total, 1,092 relevant articles were initially identified and 258 of them were finally included as references regarding the current knowledge about WNV, along with 36 additional sources (conference papers, reports, book chapters). The review is divided in three sections according to the fields of interest: (1) WNV in humans (epidemiology, molecular characteristics, transmission, diagnosis, treatment, prevention, surveillance); (2) WNV in animals (epidemiological and transmission characteristics concerning birds, horses, reptiles and other animal species) and (3) WNV in mosquitoes (control, surveillance). Finally, some examples of integrated surveillance programmes are presented. The introduction and establishment of the disease in Greece and other European countries further emphasizes the need for thorough research and broadening of our knowledge on this viral pathogen.


Subject(s)
Bird Diseases/transmission , Culicidae/virology , Horse Diseases/transmission , Reptiles , West Nile Fever/transmission , Animals , Bird Diseases/epidemiology , Birds , Greece/epidemiology , Horse Diseases/epidemiology , Horses , Humans , Population Surveillance , West Nile Fever/epidemiology , West Nile Fever/prevention & control , West Nile virus/physiology
6.
Mol Cell Probes ; 25(2-3): 121-5, 2011.
Article in English | MEDLINE | ID: mdl-21458560

ABSTRACT

Human infection with the parasitic nematode Enterobius vermicularis occurs worldwide, particularly in children. Although its prevalence may exceed 35% in some parts of the world, molecular studies of E. vermicularis in humans are limited. The aim of the present study was to investigate the genetic variation within E. vermicularis in a human population. For this purpose, 77 adhesive tape samples taken from Greek children infested with E. vermicularis were tested. New primers were designed to amplify a segment of the mitochondrial cytochrome c oxidase subunit 1 (cox1) gene of E. vermicularis from adhesive tape samples. Thirty-six amplicons were sequenced and eleven different haplotypes were identified. All sequences clustered within the type previously characterized (type B), only reported to date from captive chimpanzees. To the best of our knowledge, this is the first study of E. vermicularis genotypes from a human population.


Subject(s)
DNA, Helminth/genetics , Enterobiasis/parasitology , Enterobius/genetics , Polymerase Chain Reaction/methods , Adhesives , Animals , Child , DNA Primers/genetics , DNA, Helminth/chemistry , Electron Transport Complex IV/classification , Electron Transport Complex IV/genetics , Enterobiasis/diagnosis , Geography , Greece , Helminth Proteins/genetics , Humans , Molecular Sequence Data , Phylogeny , Reproducibility of Results , Sensitivity and Specificity , Sequence Analysis, DNA
7.
Am J Clin Pathol ; 133(2): 251-8, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20093234

ABSTRACT

Blastocystis is a polymorphic intestinal parasite that is common in humans. A total of 51 asymptomatic and symptomatic patients positive for Blastocystis only were included in the study. Symptoms were mainly nonspecific gastrointestinal symptoms. Blastocystis isolates were xenically cultured and subtyped. Blastocystis species subtype 3 was the predominant subtype. Intrasubtype differences (vacuolar/amoeboid presence) in subtype 3 morphotypes were observed in 32 asymptomatic and symptomatic subtype 3 cases and could possibly be related to Blastocystis pathogenic potential. Diverse morphologic features (vacuolar transiting to amoeboid), probably reflecting the progression from an asymptomatic to a symptomatic state, were observed in an asymptomatic subtype 3 carrier who later had symptoms. Searching for amoeboid forms might be helpful to presumptively screen symptomatic patients with subtype 3 or to follow up an asymptomatic subtype 3 carrier in case symptoms become evident before antiprotozoal treatment was attempted. Further studies on the roles of morphologic features and variation within Blastocystis species subtypes as predictors of symptoms are encouraged.


Subject(s)
Blastocystis Infections/pathology , Intestinal Diseases, Parasitic/parasitology , Adult , Blastocystis/classification , Blastocystis/genetics , Blastocystis/isolation & purification , Blastocystis Infections/diagnosis , Blastocystis Infections/parasitology , DNA, Protozoan , Female , Genotype , Humans , Intestinal Diseases, Parasitic/diagnosis , Intestinal Diseases, Parasitic/pathology , Male
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