GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
Material
Language
Subjects(RVK)
  • 1
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 378, No. 6615 ( 2022-10-07)
    Abstract: Investment in Africa over the past year with regard to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) sequencing has led to a massive increase in the number of sequences, which, to date, exceeds 100,000 sequences generated to track the pandemic on the continent. These sequences have profoundly affected how public health officials in Africa have navigated the COVID-19 pandemic. RATIONALE We demonstrate how the first 100,000 SARS-CoV-2 sequences from Africa have helped monitor the epidemic on the continent, how genomic surveillance expanded over the course of the pandemic, and how we adapted our sequencing methods to deal with an evolving virus. Finally, we also examine how viral lineages have spread across the continent in a phylogeographic framework to gain insights into the underlying temporal and spatial transmission dynamics for several variants of concern (VOCs). RESULTS Our results indicate that the number of countries in Africa that can sequence the virus within their own borders is growing and that this is coupled with a shorter turnaround time from the time of sampling to sequence submission. Ongoing evolution necessitated the continual updating of primer sets, and, as a result, eight primer sets were designed in tandem with viral evolution and used to ensure effective sequencing of the virus. The pandemic unfolded through multiple waves of infection that were each driven by distinct genetic lineages, with B.1-like ancestral strains associated with the first pandemic wave of infections in 2020. Successive waves on the continent were fueled by different VOCs, with Alpha and Beta cocirculating in distinct spatial patterns during the second wave and Delta and Omicron affecting the whole continent during the third and fourth waves, respectively. Phylogeographic reconstruction points toward distinct differences in viral importation and exportation patterns associated with the Alpha, Beta, Delta, and Omicron variants and subvariants, when considering both Africa versus the rest of the world and viral dissemination within the continent. Our epidemiological and phylogenetic inferences therefore underscore the heterogeneous nature of the pandemic on the continent and highlight key insights and challenges, for instance, recognizing the limitations of low testing proportions. We also highlight the early warning capacity that genomic surveillance in Africa has had for the rest of the world with the detection of new lineages and variants, the most recent being the characterization of various Omicron subvariants. CONCLUSION Sustained investment for diagnostics and genomic surveillance in Africa is needed as the virus continues to evolve. This is important not only to help combat SARS-CoV-2 on the continent but also because it can be used as a platform to help address the many emerging and reemerging infectious disease threats in Africa. In particular, capacity building for local sequencing within countries or within the continent should be prioritized because this is generally associated with shorter turnaround times, providing the most benefit to local public health authorities tasked with pandemic response and mitigation and allowing for the fastest reaction to localized outbreaks. These investments are crucial for pandemic preparedness and response and will serve the health of the continent well into the 21st century. Expanse of SARS-CoV-2 sequencing capacity in Africa. ( A ) African countries (shaded in gray) and institutions (red circles) with on-site sequencing facilities that are capable of producing SARS-CoV-2 whole genomes locally. ( B ) The number of SARS-CoV-2 genomes produced per country and the proportion of those genomes that were produced locally, regionally within Africa, or abroad. ( C ) Decreased turnaround time of sequencing output in Africa to an almost real-time release of genomic data.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
    RVK:
    RVK:
    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2022
    detail.hit.zdb_id: 128410-1
    detail.hit.zdb_id: 2066996-3
    detail.hit.zdb_id: 2060783-0
    SSG: 11
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    In: BMJ Global Health, BMJ, Vol. 4, No. Suppl 3 ( 2019-04), p. A40.2-A40
    Abstract: New and re-emerging infectious disease outbreaks continue to cause much human suffering and loss of life worldwide. Since Africa has experienced repeated outbreaks of zoonotic infections, an important need exists to improve local and regional capacities to identify and respond to zoonotic outbreaks. PANDORA ID-NET is an EDCTP-supported ‘ONE Human and Animal HEALTH’ multidisciplinary consortium of 24 partner institutions (15 African and 9 European) in 9 African and 4 European countries. Methods Our overall aim is to strengthen regional and pan-African capacities and systems for enabling a rapid and effective response to infectious diseases with epidemic potential, arising from within Africa or imported from overseas. We aim to build laboratory and public health capabilites for rapid detection and surveillance of pathogens from human and animal sources. This will include obtaining accelerated evidence for optimal clinical management of patients, infection control measures, and public health response during outbreaks. Capacities will be built: a) for performing multisite clinical trials (evaluating rapid diagnostics, biomarkers, a range of treatments, vaccines and operational research studies) and, b) for timely collection, analysis and communication of information. Conclusion Our activities will be aligned to EDCTP regional Networks of Excellence, Africa CDC and other relevant global and regional initiatives, thus maximizing complementarity and achieving a multiplier effect, facilitating rapid policy implementation of outputs.
    Type of Medium: Online Resource
    ISSN: 2059-7908
    Language: English
    Publisher: BMJ
    Publication Date: 2019
    detail.hit.zdb_id: 2851843-3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    In: Epidemiology and Infection, Cambridge University Press (CUP), Vol. 148 ( 2020)
    Abstract: Global Health Security Index (GHSI) and Joint External Evaluation (JEE) are two well-known health security and related capability indices. We hypothesised that countries with higher GHSI or JEE scores would have detected their first COVID-19 case earlier, and would experience lower mortality outcome compared to countries with lower scores. We evaluated the effectiveness of GHSI and JEE in predicting countries' COVID-19 detection response times and mortality outcome (deaths/million). We used two different outcomes for the evaluation: (i) detection response time, the duration of time to the first confirmed case detection (from 31st December 2019 to 20th February 2020 when every country's first case was linked to travel from China) and (ii) mortality outcome (deaths/million) until 11th March and 1st July 2020, respectively. We interpreted the detection response time alongside previously published relative risk of the importation of COVID-19 cases from China. We performed multiple linear regression and negative binomial regression analysis to evaluate how these indices predicted the actual outcome. The two indices, GHSI and JEE were strongly correlated ( r = 0.82), indicating a good agreement between them. However, both GHSI ( r = 0.31) and JEE ( r = 0.37) had a poor correlation with countries' COVID-19–related mortality outcome. Higher risk of importation of COVID-19 from China for a given country was negatively correlated with the time taken to detect the first case in that country (adjusted R 2 = 0.63–0.66), while the GHSI and JEE had minimal predictive value. In the negative binomial regression model, countries' mortality outcome was strongly predicted by the percentage of the population aged 65 and above (incidence rate ratio (IRR): 1.10 (95% confidence interval (CI): 1.01–1.21) while overall GHSI score (IRR: 1.01 (95% CI: 0.98–1.01)) and JEE (IRR: 0.99 (95% CI: 0.96–1.02)) were not significant predictors. GHSI and JEE had lower predictive value for detection response time and mortality outcome due to COVID-19. We suggest introduction of a population healthiness parameter, to address demographic and comorbidity vulnerabilities, and reappraisal of the ranking system and methods used to obtain the index based on experience gained from this pandemic.
    Type of Medium: Online Resource
    ISSN: 0950-2688 , 1469-4409
    RVK:
    Language: English
    Publisher: Cambridge University Press (CUP)
    Publication Date: 2020
    detail.hit.zdb_id: 1470211-3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    In: Tropical Medicine & International Health, Wiley, Vol. 11, No. 9 ( 2006-09), p. 1350-1359
    Abstract: Para distinguir infecciones nuevas de recrudescentes se recomienda la genotipificación molecular de base, y el recurrente post tratamiento del Plasmodium falciparum . No obstante, la realización de la genotipificación y el ajuste de los resultados del tratamiento no han sido evaluados en ensayos a gran escala. Los resultados parasitológicos fueron evaluados en 9 ensayos doble ciego de malaria P. falciparum no complicada en niños africanos tratados con artesunato/placebo, más monoterapias estándar. Los índices de fallo en el día 28 fueron ajustados por genotipificación por etapas de la proteína rica en glutamato (GLURP) de Plasmodium falciparum , proteína 1 de superficie de merozoito ( msp1 ) y 2 ( msp2 ). Calculamos el desempeño general y de laboratorio de la genotipificación, y comparamos resultados no ajustados (bruto) y ajustados PCR. 3,455 (93.6%) de 3,691 pacientes enrolados que fueron evaluados en el día 28. 767 (22%) presentaron parasitemia recurrente posterior al día 14, de los cuales 686 podrían ser genotipificados: 246 eran recrudescencias, 286 nuevas infecciones, y 154 sin resolver. Los desempeños general y de laboratorio de la genotipificación fueron 69 (12–100)% y 78 (50–100)%, respectivamente. El índice de fallo parasitológicos bruto promedio en el día 28 fue 44 (rango 3–87)%. Los índices de PCR no ajustados fueron 36 (2–86)% si las infecciones sin resolver se contabilizaban como fallas, o 33 (2–86)% si se excluían del análisis. La diferencia general en los índices buto de fallo en el día 28 y el 14 fue de 22% (95% CI 20.3, 24.6) pero disminuía a 14% (12.1, 16.3) si las infecciones sin resolver se contaban como fallos, o a 11% (9.8, 16.3) si las infecciones sin resolver se excluían del análisis. Es necesario no solo refinar el resultado del tratamiento ginotipificado sino también la recolección y el análisis de las pruebas para mejorar el desempeño. Nuestros hallazgos reafirman las recomendaciones de la OMS de la genotipificación PCR en las pruebas clínicas de la malaria, y sugieren que la genotipificación por etapas de solo dos loci ( msp2 y msp1 o glurp ) puede discriminar de forma confiable las recrudescencias de las nuevas infecciones.
    Type of Medium: Online Resource
    ISSN: 1360-2276 , 1365-3156
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2006
    detail.hit.zdb_id: 2018112-7
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    In: Malaria Journal, Springer Science and Business Media LLC, Vol. 16, No. 1 ( 2017-12)
    Type of Medium: Online Resource
    ISSN: 1475-2875
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2017
    detail.hit.zdb_id: 2091229-8
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    In: Annals of Clinical Microbiology and Antimicrobials, Springer Science and Business Media LLC, Vol. 20, No. 1 ( 2021-12)
    Abstract: There is paucity of data on the prevalence and distribution of multidrug- Resistant-Tuberculosis (MDR-TB) in the Republic of Congo. Among the challenges resides the implementation of a robust TB resistance diagnostic program using molecular tools. In resource limited settings there is a need to gather data to enable prioritization of actions. The objective of this study was is to implement molecular tools as a best of diagnosing MDR and XDR-TB among presumptive tuberculosis patients referred to reference hospital of Makelekele in Brazzaville, Republic of the Congo. Methods We have conducted a cross-sectional study, including a total of 92 presumptive pulmonary tuberculosis patients and who had never received treatment recruited at the reference hospital of Makelekele from October 2018 to October 2019. The socio-demographic and clinical data were collected as well as sputum samples. Rifampicin resistance was investigated using Xpert (Cepheid) and second-line TB drugs Susceptibility testing were performed by the Brucker HAIN Line Probe Assay (GenoType MTBDRsl VER 2.0 assay) method. Results From the 92 recruited patients, 57 (62%) were found positive for the Mycobacterium tuberculosis complex. The prevalence of rifampicin-resistant tuberculosis (RR-TB) was 9.8% (9/92) and importantly 2.2% were pre-XDR/XDR. Conclusion This study showed a high rate of rifampicin resistance and the presence of extensively drug-resistant tuberculosis in the study area in new patients. This study highlights the need for further studies of TB drug resistance in the country.
    Type of Medium: Online Resource
    ISSN: 1476-0711
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2021
    detail.hit.zdb_id: 2097873-X
    SSG: 15,3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    In: Tropical Medicine & International Health, Wiley, Vol. 12, No. 10 ( 2007-10), p. 1164-1171
    Abstract: Hemos realizado un estudio de la eficacia de la sulfadoxina‐pirimetamina (SP) en Brazzaville durante el 2003, utilizando la prueba de 28‐días de la OMS y el análisis de mutaciones en los genes de la dihidrofolato reductasa de Plasmodium falciparum ( dhfrpf ) y la dihidropteroato sintetasa ( dhpspf ). Los niños menores de 5 años con malaria no complicada por falciparum fueron tratados con la dosis estándar de SP. De los 97 pacientes reclutados, a 83 se les siguió hasta el día 28. Hubo 7 (8.4%) fallos de tratamiento tempranos, 23 fallos de tratamiento tardíos (27.7%), 9 (10.8%) fallos parasitológicos tardíos y 44 (53%) respuestas clínicas y parasitológicas adecuadas (RCPA). Después del análisis mediante PCR de las 64 muestras disponibles, los resultados corregidos fueron los siguientes: 44 (68.8%) RCPA y 19 (31.2%) casos de recrudescencia. La prevalencia de mutaciones en dhfr fue muy alta, con un 97.5% de las muestras presentando la mutación Asn51Ile, 66.2% la mutación Cys59Arg, y 98.8% la mutación Ser108Asn. Las mutaciones de la dhps en las posiciones 437 (Ala a Gly) y 436 (Ser a Ala) se encontraron en un 85% y 12.5% de las muestras, respectivamente. Las mutaciones cuádruples (mutaciones triples dhfrpf en los codones 51, 59, y 108 + mutación dhpspf en 437) fueron halladas en 42 muestras (52.5%) y estaban asociadas con los casos de fallo terapéuticos. Este alto nivel de fallo terapéutico y las mutaciones en ambos genes hacen que sea urgente la aplicación de una nueva política para el tratamiento de la malaria, con el fin de retrasar la dispersión de la resistencia a SP.
    Type of Medium: Online Resource
    ISSN: 1360-2276 , 1365-3156
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2007
    detail.hit.zdb_id: 2018112-7
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 8
    In: Tropical Medicine & International Health, Wiley, Vol. 24, No. 12 ( 2019-12), p. 1427-1433
    Abstract: Evaluer la sévérité clinique de la diarrhée associée à la coinfection virale chez les enfants atteints de gastroentérite aiguë. Méthodes 461 enfants de moins de cinq ans hospitalisés pour une diarrhée aiguë (266 garçons et 187 filles) ont été inclus dans l'étude. Sur des échantillons de selles, les infections à rotavirus et à adénovirus ont été investiguées par ELISA et les infections à norovirus par RT‐PCR duplex imbriqué. Nous avons évalué les conditions sociales, démographiques, cliniques et comportementales susceptibles d'influencer la survenue d'infections à rotavirus, adénovirus et norovirus. Résultats Une infection mono virale a été détectée chez 49% des patients et une infection virale mixte chez 12% des patients. La prévalence des infections mixtes ne dépendait ni de l'âge ni du sexe. Trois échantillons étaient infectés par tous les trois virus. Une association significative a été observée entre la fièvre (température axillaire  〉  37,5 °C) et la double infection rotavirus‐norovirus (aOR (IC95%) = 2,1 (1,14–3,84), P  = 0,016; aOR (IC95%) = 0,37 (0,19–0,73), P  = 0,004). Les infections mixtes étaient les plus courantes pendant la saison sèche de juin à octobre (71,4% contre 54,7%, P  = 0,023). Conclusion La coinfection à la fois par le rotavirus et par le norovirus est fréquente chez les enfants de moins de cinq ans hospitalisés, mais ne contribue pas à la sévérité de la maladie.
    Type of Medium: Online Resource
    ISSN: 1360-2276 , 1365-3156
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 2018112-7
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 9
    In: Malaria Journal, Springer Science and Business Media LLC, Vol. 7, No. 1 ( 2008-12)
    Type of Medium: Online Resource
    ISSN: 1475-2875
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2008
    detail.hit.zdb_id: 2091229-8
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 10
    In: Malaria Journal, Springer Science and Business Media LLC, Vol. 11, No. 1 ( 2012-12)
    Abstract: In this first study conducted after the introduction of artemisinin-combination therapy (ACT), the major objective was to evaluate Plasmodium falciparum genetic diversity and multiplicity of infection in isolates from Congolese children between one and nine years of age enrolled and followed up for one year. The secondary objective was to characterize the msp2 profiles of P. falciparum isolates collected from successive malaria episodes in ten children who had four or more clinical episodes during the follow up. Methods Three-hundred and thirteen children residing in southern part of Brazzaville participated in this study. Blood samples were obtained from all children at enrollment and checked for P. falciparum infection. Based on the one year follow-up data, two clinical groups were considered according to the number of malaria episodes presented over the follow up period: “protected”(children who did not experience any episode) and “unprotected” (those who experienced more that two episodes). Therefore, the msp2 genetic diversity of P. falciparum isolates collected at enrollment in the two groups was characterized by allele-specific nested PCR and compared. The msp2 profiles of P. falciparum isolates collected from successive malaria episodes was also characterized by allele-specific nested PCR. Results Forty-three percent of FC27 and fifty-seven percent of 3D7 in protected vs fifty-six percent of FC27 and forty-four percent of 3D7 in isolates from unprotected children were detected. Seven and two alleles belonging to the FC27, and six and three alleles belonging to 3D7 families were distinguished in isolates from protected and unprotected children respectively. The mean multiplicity of infection (MOI) values at inclusion for the msp2 locus was 1.29 and 1.43 for protected and unprotected children respectively. 43 isolates were obtained from the ten children who had four or more clinical episodes during the follow up. A total of 63 alleles or fragments corresponding to 57% (36/63) FC27 and 43% (27/63) 3D7 were detected. The variant 400bp of FC27 was the most prevalent. 46% (20/43), 42% (18/43), 2% (1/43) and 2% (1/43) of isolates were found to have 1, 2, 3 and 4 parasite genotypes respectively and the mean MOI was 1.78. Conclusion This study shows that the introduction of ACT in the Republic of Congo has reduced the MOI but not the genetic diversity of P. falciparum isolates from children living in Southern districts of Brazzaville.
    Type of Medium: Online Resource
    ISSN: 1475-2875
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2012
    detail.hit.zdb_id: 2091229-8
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...