Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Fabiano L. Thompson is active.

Publication


Featured researches published by Fabiano L. Thompson.


Lancet Infectious Diseases | 2016

Detection and sequencing of Zika virus from amniotic fluid of fetuses with microcephaly in Brazil: a case study.

Guilherme Amaral Calvet; Renato S. Aguiar; Adriana Suely de Oliveira Melo; Simone Alves Sampaio; Ivano de Filippis; Allison Fabri; Eliane Saraiva Machado Araújo; Patrícia Carvalho de Sequeira; Marcos César Lima de Mendonça; Louisi de Oliveira; Diogo A. Tschoeke; Carlos G. Schrago; Fabiano L. Thompson; Patrícia Brasil; Flávia Barreto dos Santos; Rita Maria Ribeiro Nogueira; Amilcar Tanuri; Ana Maria Bispo de Filippis

BACKGROUNDnThe incidence of microcephaly in Brazil in 2015 was 20 times higher than in previous years. Congenital microcephaly is associated with genetic factors and several causative agents. Epidemiological data suggest that microcephaly cases in Brazil might be associated with the introduction of Zika virus. We aimed to detect and sequence the Zika virus genome in amniotic fluid samples of two pregnant women in Brazil whose fetuses were diagnosed with microcephaly.nnnMETHODSnIn this case study, amniotic fluid samples from two pregnant women from the state of Paraíba in Brazil whose fetuses had been diagnosed with microcephaly were obtained, on the recommendation of the Brazilian health authorities, by ultrasound-guided transabdominal amniocentesis at 28 weeks gestation. The women had presented at 18 weeks and 10 weeks gestation, respectively, with clinical manifestations that could have been symptoms of Zika virus infection, including fever, myalgia, and rash. After the amniotic fluid samples were centrifuged, DNA and RNA were extracted from the purified virus particles before the viral genome was identified by quantitative reverse transcription PCR and viral metagenomic next-generation sequencing. Phylogenetic reconstruction and investigation of recombination events were done by comparing the Brazilian Zika virus genome with sequences from other Zika strains and from flaviviruses that occur in similar regions in Brazil.nnnFINDINGSnWe detected the Zika virus genome in the amniotic fluid of both pregnant women. The virus was not detected in their urine or serum. Tests for dengue virus, chikungunya virus, Toxoplasma gondii, rubella virus, cytomegalovirus, herpes simplex virus, HIV, Treponema pallidum, and parvovirus B19 were all negative. After sequencing of the complete genome of the Brazilian Zika virus isolated from patient 1, phylogenetic analyses showed that the virus shares 97-100% of its genomic identity with lineages isolated during an outbreak in French Polynesia in 2013, and that in both envelope and NS5 genomic regions, it clustered with sequences from North and South America, southeast Asia, and the Pacific. After assessing the possibility of recombination events between the Zika virus and other flaviviruses, we ruled out the hypothesis that the Brazilian Zika virus genome is a recombinant strain with other mosquito-borne flaviviruses.nnnINTERPRETATIONnThese findings strengthen the putative association between Zika virus and cases of microcephaly in neonates in Brazil. Moreover, our results suggest that the virus can cross the placental barrier. As a result, Zika virus should be considered as a potential infectious agent for human fetuses. Pathogenesis studies that confirm the tropism of Zika virus for neuronal cells are warranted.nnnFUNDINGnConsellho Nacional de Desenvolvimento e Pesquisa (CNPq), Fundação de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ).


Nature | 2016

Lytic to temperate switching of viral communities

Ben Knowles; Cynthia B. Silveira; Barbara A. Bailey; Katie L. Barott; V. A. Cantu; A. G. Cobián-Güemes; Felipe H. Coutinho; E. A. Dinsdale; Ben Felts; Kathryn A. Furby; E. E. George; Kevin T. Green; Gustavo B. Gregoracci; Andreas F. Haas; John Matthew Haggerty; E. R. Hester; Nao Hisakawa; Linda Wegley Kelly; Yan Wei Lim; Mark Little; Antoni Luque; T. McDole-Somera; K. McNair; L. S. de Oliveira; Steven D. Quistad; N. L. Robinett; Enric Sala; Peter Salamon; Savannah E. Sanchez; Stuart A. Sandin

Microbial viruses can control host abundances via density-dependent lytic predator–prey dynamics. Less clear is how temperate viruses, which coexist and replicate with their host, influence microbial communities. Here we show that virus-like particles are relatively less abundant at high host densities. This suggests suppressed lysis where established models predict lytic dynamics are favoured. Meta-analysis of published viral and microbial densities showed that this trend was widespread in diverse ecosystems ranging from soil to freshwater to human lungs. Experimental manipulations showed viral densities more consistent with temperate than lytic life cycles at increasing microbial abundance. An analysis of 24 coral reef viromes showed a relative increase in the abundance of hallmark genes encoded by temperate viruses with increased microbial abundance. Based on these four lines of evidence, we propose the Piggyback-the-Winner model wherein temperate dynamics become increasingly important in ecosystems with high microbial densities; thus ‘more microbes, fewer viruses’.


Archives of Microbiology | 2015

Microbial taxonomy in the post-genomic era: Rebuilding from scratch?

Cristiane C. Thompson; Gilda Rose S. Amaral; Mariana E. Campeão; Robert Edwards; Martin F. Polz; Bas E. Dutilh; David W. Ussery; Tomoo Sawabe; Jean Swings; Fabiano L. Thompson

AbstractnMicrobial taxonomy should provide adequate descriptions of bacterial, archaeal, and eukaryotic microbial diversity in ecological, clinical, and industrial environments. Its cornerstone, the prokaryote species has been re-evaluated twice. It is time to revisit polyphasic taxonomy, its principles, and its practice, including its underlying pragmatic species concept. Ultimately, we will be able to realize an old dream of our predecessor taxonomists and build a genomic-based microbial taxonomy, using standardized and automated curation of high-quality complete genome sequences as the new gold standard.


BMC Genomics | 2014

Genomic and phenotypic attributes of novel salinivibrios from stromatolites, sediment and water from a high altitude lake

Marta Fabiana Gorriti; Graciela M. Dias; Luciane A. Chimetto; Amaro E. Trindade-Silva; Bruno Sergio de O. Silva; Milene Mesquita; Gustavo B. Gregoracci; Maria Eugenia Farias; Cristiane C. Thompson; Fabiano L. Thompson

BackgroundSalinivibrios are moderately halophilic bacteria found in salted meats, brines and hypersaline environments. We obtained three novel conspecific Salinivibrio strains closely related to S. costicola, from Socompa Lake, a high altitude hypersaline Andean lake (approx. 3,570 meters above the sea level).ResultsThe three novel Salinivibrio spp. were extremely resistant to arsenic (up to 200xa0mM HAsO42−), NaCl (up to 15%), and UV-B radiation (19 KJ/m2, corresponding to 240xa0minutes of exposure) by means of phenotypic tests. Our subsequent draft genome ionsequencing and RAST-based genome annotation revealed the presence of genes related to arsenic, NaCl, and UV radiation resistance. The three novel Salinivibrio genomes also had the xanthorhodopsin gene cluster phylogenetically related to Marinobacter and Spiribacter. The genomic taxonomy analysis, including multilocus sequence analysis, average amino acid identity, and genome-to-genome distance revealed that the three novel strains belong to a new Salinivibrio species.ConclusionsArsenic resistance genes, genes involved in DNA repair, resistance to extreme environmental conditions and the possible light-based energy production, may represent important attributes of the novel salinivibrios, allowing these microbes to thrive in the Socompa Lake.


Archives of Microbiology | 2015

Microbial community diversity and physical-chemical features of the Southwestern Atlantic Ocean

Nelson Alves Junior; Pedro M. Meirelles; Eidy de O. Santos; Bas E. Dutilh; Genivaldo G. Z. Silva; Rodolfo Paranhos; Anderson S. Cabral; Carlos Eduardo Rezende; Tetsuya Iida; Rodrigo L. Moura; Ricardo Henrique Kruger; Renato Crespo Pereira; Rogério Valle; Tomoo Sawabe; Cristiane C. Thompson; Fabiano L. Thompson

AbstractnMicrobial oceanography studies have demonstrated the central role of microbes in functioning and nutrient cycling of the global ocean. Most of these former studies including at Southwestern Atlantic Ocean (SAO) focused on surface seawater and benthic organisms (e.g., coral reefs and sponges). This is the first metagenomic study of the SAO. The SAO harbors a great microbial diversity and marine life (e.g., coral reefs and rhodolith beds). The aim of this study was to characterize the microbial community diversity of the SAO along the depth continuum and different water masses by means of metagenomic, physical–chemical and biological analyses. The microbial community abundance and diversity appear to be strongly influenced by the temperature, dissolved organic carbon, and depth, and three groups were defined [1. surface waters; 2. sub-superficial chlorophyll maximum (SCM) (48–82xa0m) and 3. deep waters (236–1,200xa0m)] according to the microbial composition. The microbial communities of deep water masses [South Atlantic Central water, Antarctic Intermediate water and Upper Circumpolar Deep water] are highly similar. Of the 421,418 predicted genes for SAO metagenomes, 36.7xa0% had no homologous hits against 17,451,486 sequences from the North Atlantic, South Atlantic, North Pacific, South Pacific and Indian Oceans. From these unique genes from the SAO, only 6.64xa0% had hits against the NCBI non-redundant protein database. SAO microbial communities share genes with the global ocean in at least 70 cellular functions; however, more than a third of predicted SAO genes represent a unique gene pool in global ocean. This study was the first attempt to characterize the taxonomic and functional community diversity of different water masses at SAO and compare it with the microbial community diversity of the global ocean, and SAO had a significant portion of endemic gene diversity. Microbial communities of deep water masses (236–1,200xa0m) are highly similar, suggesting that these water masses have very similar microbiological attributes, despite the common knowledge that water masses determine prokaryotic community and are barriers to microbial dispersal. The present study also shows that SCM is a clearly differentiated layer within Tropical waters with higher abundance of phototrophic microbes and microbial diversity.


PLOS ONE | 2015

Insights into the Microbial and Viral Dynamics of a Coastal Downwelling-Upwelling Transition.

Gustavo B. Gregoracci; Ana Carolina Soares; Milene Miranda; Ricardo Coutinho; Fabiano L. Thompson

Although previous studies have described opposing states in upwelling regions, i.e., the rise of cold nutrient-rich waters and prevalence of surface warm nutrient-poor waters, few have addressed the transition from one state to the other. This study aimed to describe the microbial and viral structure during this transition and was able to obtain the taxonomic and metabolic compositions as well as physical-chemical data. This integrated approach allowed for a better understanding of the dynamics of the downwelling upwelling transition, suggesting that a wealth of metabolic processes and ecological interactions are occurring in the minute fractions of the plankton (femto, pico, nano). These processes and interactions included evidence of microbial predominance during downwelling (with nitrogen recycling and aerobic anoxygenic photosynthesis), different viral predation pressures over primary production in different states (cyanobacteria vs eukaryotes), and a predominance of diatoms and selected bacterial and archaeal groups during upwelling (with the occurrence of a wealth of nitrogen metabolism involving ammonia). Thus, the results provided insights into which microbes, viruses and microbial-mediated processes are probably important in the functioning of upwelling systems.


BMC Medical Genomics | 2017

Pregnant women carrying microcephaly foetuses and Zika virus contain potentially pathogenic microbes and parasites in their amniotic fluid

Diogo Antonio Tschoeke; Louisi de Oliveira; Luciana Leomil; Amilcar Tanuri; Fabiano L. Thompson

BackgroundMicrocephaly has become a major public health problem in Brazil. The total number of newborns with microcephaly was reported to be >4000 in June 2016. Studies suggest that Zika Virus is a major cause of new microcephaly cases in Brazil. Inside the uterus, the foetus is surrounded by the Amniotic Fluid, a proximal fluid that contains foetal and maternal cells as well as microorganisms and where Zika Virus was already found.Case presentationA previous study reported the presence of the Zika Virus in the amniotic fluid (collected in the 28th gestational week) of two pregnant women carrying microcephaly foetuses in Brazil. The virus was detected by means of real-time PCR and metatranscriptomic analysis. We compared the microbiome of these two cases with metatranscriptomic sequences from 16 pregnant women collected at various times in their pregnanciesConclusionSeveral strains of bacteria (e.g., Streptococcus and Propionibacterium) found in Amniotic Fluid may be involved in neurological diseases. When the foetus is infected by the Zika Virus, due to neurological damage, they do not move inside the uterus, thus changing the Amniotic Fluid environment, potentially leading to secondary problems. Zika infection could also lead to an immunodeficient state, making bacterial colonization of the foetuses easier. An altered microbial composition during pregnancy may also result in harmful secondary metabolite production from certain microbes that further impair foetal brain development. However, these observations of potentially harmful microbial species are correlations and thus cannot be assumed to be causative agents of (microcephaly) disease. In our study, microbial and parasitic diversity of the Amniotic Fluid was lower in patients infected by ZIKV, compared to that of Prenatal and Preterm controls. The present study was a first attempt to shed light on the microbial and parasitic diversity associated with ZIKV-infected pregnant women bearing microcephaly foetuses, and the presence of diverse microbial and parasite communities in the Amniotic Fluid suggests a poor health status of both the pregnant women and the foetuses they carry.


Nature | 2016

Corrigendum: Lytic to temperate switching of viral communities.

Ben Knowles; Cynthia B. Silveira; Barbara A. Bailey; Katie L. Barott; V. A. Cantu; A. G. Cobián-Güemes; Felipe H. Coutinho; E. A. Dinsdale; Ben Felts; Kathryn A. Furby; E. E. George; Kevin T. Green; Gustavo B. Gregoracci; Andreas F. Haas; John Matthew Haggerty; E. R. Hester; Nao Hisakawa; Linda Wegley Kelly; Yan Wei Lim; Mark Little; Antoni Luque; T. McDole-Somera; K. McNair; L. S. de Oliveira; Steven D. Quistad; N. L. Robinett; Enric Sala; Peter Salamon; Savannah E. Sanchez; Stuart A. Sandin

This corrects the article DOI: 10.1038/nature17193


Journal of General Virology | 2018

An observational clinical case of Zika virus-associated neurological disease is associated with primary IgG response and enhanced TNF levels

Edson Delatorre; Milene Miranda; Diogo Antonio Tschoeke; Patrícia Carvalho de Sequeira; Simone Alves Sampaio; Giselle Barbosa-Lima; Yasmine Rangel Vieira; Luciana Leomil; Fernando A. Bozza; José Cerbino-Neto; Patricia T. Bozza; Rita Maria Ribeiro Nogueira; Patrícia Brasil; Fabiano L. Thompson; Ana Maria Bispo de Filippis; Thiago Moreno L. Souza

Descriptive clinical data help to reveal factors that may provoke Zika virus (ZIKV) neuropathology. The case of a 24-year-old female with a ZIKV-associated severe acute neurological disorder was studied. The levels of ZIKV in the cerebrospinal fluid (CSF) were 50 times higher than the levels in other compartments. An acute anti-flavivirus IgG, together with enhanced TNF-alpha levels, may have contributed to ZIKV invasion in the CSF, whereas the unbiased genome sequencing [obtained by next-generation sequencing (NGS)] of the CSF revealed that no virus mutations were associated with the anatomic compartments (CSF, serum, saliva and urine).


Microbial Resources#R##N#From Functional Existence in Nature to Applications | 2017

A Flavor of Prokaryotic Taxonomy: Systematics Revisited

Paul De Vos; Fabiano L. Thompson; Cristiane Thompson; Jean Swings

As a scientific discipline, prokaryotic taxonomy covers and puts order in prokaryotic diversity. Squeezed between conservatism and more progressive approaches, it is moving toward a second Renaissance after its modernization 50xa0years ago. Technology is clearly the driving force: the introduction of high throughput sequencing was instrumental, together with the newly developed bioinformatics tools. The challenge is to stick to a number of simple principles and develop appropriate procedures for genomic prokaryotic taxonomy to able to cope with the growing gap of sequenced biodiversity and to serve better the user community.

Collaboration


Dive into the Fabiano L. Thompson's collaboration.

Top Co-Authors

Avatar

Gustavo B. Gregoracci

Federal University of Rio de Janeiro

View shared research outputs
Top Co-Authors

Avatar

Cristiane C. Thompson

Federal University of Rio de Janeiro

View shared research outputs
Top Co-Authors

Avatar

Amaro E. Trindade-Silva

Federal University of Rio de Janeiro

View shared research outputs
Top Co-Authors

Avatar

Amilcar Tanuri

Federal University of Rio de Janeiro

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Cynthia B. Silveira

Federal University of Rio de Janeiro

View shared research outputs
Top Co-Authors

Avatar

E. A. Dinsdale

Federal University of Rio de Janeiro

View shared research outputs
Top Co-Authors

Avatar

Eidy de O. Santos

Federal University of Rio de Janeiro

View shared research outputs
Top Co-Authors

Avatar

Felipe H. Coutinho

Federal University of Rio de Janeiro

View shared research outputs
Top Co-Authors

Avatar

Louisi de Oliveira

Federal University of Rio de Janeiro

View shared research outputs
Researchain Logo
Decentralizing Knowledge