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1.
Eur Rev Med Pharmacol Sci ; 24(15): 8226-8231, 2020 08.
Article in English | MEDLINE | ID: mdl-32767354

ABSTRACT

OBJECTIVE: To explore whether the climate has played a role in the COVID-19 outbreak, we compared virus lethality in countries closer to the Equator with others. Lethality in European territories and in territories of some nations with a non-temperate climate was also compared. MATERIALS AND METHODS: Lethality was calculated as the rate of deaths in a determinate moment from the outbreak of the pandemic out of the total of identified positives for COVID-19 in a given area/nation, based on the COVID-John Hopkins University website. Lethality of countries located within the 5th parallels North/South on 6 April and 6 May 2020, was compared with that of all the other countries. Lethality in the European areas of The Netherlands, France and the United Kingdom was also compared to the territories of the same nations in areas with a non-temperate climate. RESULTS: A lower lethality rate of COVID-19 was found in Equatorial countries both on April 6 (OR=0.72 CI 95% 0.66-0.80) and on May 6 (OR=0.48, CI 95% 0.47-0.51), with a strengthening over time of the protective effect. A trend of higher risk in European vs. non-temperate areas was found on April 6, but a clear difference was evident one month later: France (OR=0.13, CI 95% 0.10-0.18), The Netherlands (OR=0.5, CI 95% 0.3-0.9) and the UK (OR=0.2, CI 95% 0.01-0.51). This result does not seem to be totally related to the differences in age distribution of different sites. CONCLUSIONS: The study does not seem to exclude that the lethality of COVID-19 may be climate sensitive. Future studies will have to confirm these clues, due to potential confounding factors, such as pollution, population age, and exposure to malaria.


Subject(s)
Climate , Coronavirus Infections/mortality , Pneumonia, Viral/mortality , Seasons , Weather , Betacoronavirus , Brunei/epidemiology , Burundi/epidemiology , COVID-19 , Congo/epidemiology , Coronavirus Infections/epidemiology , Ecuador/epidemiology , Equatorial Guinea/epidemiology , Europe , France/epidemiology , Gabon/epidemiology , Humans , Indian Ocean Islands/epidemiology , Indonesia/epidemiology , Kenya/epidemiology , Malaysia/epidemiology , Melanesia/epidemiology , Micronesia/epidemiology , Netherlands/epidemiology , Pandemics , Papua New Guinea/epidemiology , Pneumonia, Viral/epidemiology , Rwanda/epidemiology , SARS-CoV-2 , Samoa/epidemiology , Sao Tome and Principe/epidemiology , Seychelles/epidemiology , Singapore/epidemiology , Somalia/epidemiology , Timor-Leste/epidemiology , Tropical Climate , Uganda/epidemiology , United Kingdom/epidemiology
2.
Malar J ; 8: 97, 2009 May 11.
Article in English | MEDLINE | ID: mdl-19432958

ABSTRACT

BACKGROUND: Mannose binding lectin (MBL) has an important role in the activation of the complement system and opsonization of pathogenic microorganisms. Frequent polymorphisms found in the MBL2 gene affect the concentration and functionality of the protein and are associated with enhanced susceptibility to severe malaria in African children. Most MBL2 typing strategies were designed to the analysis of selected variants, the significance of whole haplotypes is poorly known. In this work, a new typing strategy was developed and validated in an association analysis of MBL2 with adult asymptomatic infection. METHODS: MBL2 allele-specific fragments of 144 healthy Gabonese adults were amplified by using haplotype-specific sequencing (HSS), a new strategy that combines sequence-specific PCR and sequence-based typing. The Gabonese were investigated for the presence of Plasmodium falciparum parasitaemia by the amplification of parasite genes, immunochromatographic antigen detection and microscopic analysis. HSS results were also compared with a previously used real-time PCR (RT-PCR) method in 72 Euro-Brazilians. RESULTS: Fourteen polymorphisms were identified beside the commonly investigated promoter (H, L; X, Y; P, Q) and exon 1 (A, O; O = B, C or D) variants. The MBL2*LYPA/LYPA genotype was associated with the absence of asymptomatic infection (P = 0.017), whereas the MBL2*LYQC haplotype and YA/YO + YO/YO genotypes were associated with positive parasite counts in asymptomatic adults (P = 0.033 and 0.018, respectively). The associations were specific to LYPA (identical to the reference sequence Y16577) and LYQC (Y16578) and would not have been revealed by standard genotyping, as there was no association with LYPA and LYQC haplotypes carrying new polymorphisms defined by sequence-based typing. In contrast, HSS and RT-PCR produced very similar results in the less diverse European-derived population. CONCLUSION: In this work, a new typing strategy for a highly polymorphic gene was developed and validated focusing on the asymptomatic status of P. falciparum-infected adults. In populations with high nucleotide diversity, it allowed for the identification of associations with fine-scaled haplotypes that would not have been found using common typing techniques. In this preliminary study, MBL2 haplotypes or SNPs linked to them were found associated with susceptibility to infection and parasitaemia control of asymptomatic adults.


Subject(s)
Genetic Predisposition to Disease/epidemiology , Haplotypes/genetics , Malaria, Falciparum/genetics , Mannose-Binding Lectin/genetics , Polymorphism, Genetic , Adolescent , Adult , Alleles , Animals , Base Sequence , Brazil/epidemiology , Female , Gabon/epidemiology , Genotype , Humans , Malaria, Falciparum/epidemiology , Male , Middle Aged , Parasitemia , Plasmodium falciparum , Polymerase Chain Reaction/methods , Promoter Regions, Genetic , Young Adult
3.
Virus Genes ; 23(3): 257-61, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11778693

ABSTRACT

An anomalous high frequency of ATL was observed in a remote 'noir maroons' village of French Guiana. Since it is not clear if HTLV-I is responsible for different frequencies of disease in different geographical areas, we undertook a comparison of the population with a similar one located in Gabon. We found a much higher degree of gp46 surface envelope glycoprotein sequence conservation in the Guianese village than in the Gabonese one.


Subject(s)
Genetic Variation , Human T-lymphotropic virus 1/genetics , Leukemia-Lymphoma, Adult T-Cell/virology , Base Sequence , Conserved Sequence , DNA, Viral , Female , French Guiana/epidemiology , Gabon/epidemiology , Gene Products, env/genetics , Humans , Leukemia-Lymphoma, Adult T-Cell/epidemiology , Male , Molecular Sequence Data , Phylogeny , Retroviridae Proteins, Oncogenic/genetics , Sequence Alignment
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