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1.
Cell Host Microbe ; 30(2): 248-259.e6, 2022 02 09.
Artigo em Inglês | MEDLINE | ID: mdl-34998466

RESUMO

The resurgence of yellow fever in South America has prompted vaccination against the etiologic agent, yellow fever virus (YFV). Current vaccines are based on a live-attenuated YF-17D virus derived from a virulent African isolate. The capacity of these vaccines to induce neutralizing antibodies against the vaccine strain is used as a surrogate for protection. However, the sensitivity of genetically distinct South American strains to vaccine-induced antibodies is unknown. We show that antiviral potency of the polyclonal antibody response in vaccinees is attenuated against an emergent Brazilian strain. This reduction was attributable to amino acid changes at two sites in central domain II of the glycoprotein E, including multiple changes at the domain I-domain II hinge, which are unique to and shared among most South American YFV strains. Our findings call for a reevaluation of current approaches to YFV immunological surveillance in South America and suggest approaches for updating vaccines.


Assuntos
Vacina contra Febre Amarela , Febre Amarela , Anticorpos Antivirais , Brasil , Genótipo , Humanos , Vacinas Atenuadas , Vírus da Febre Amarela/genética
2.
J Eukaryot Microbiol ; 66(5): 757-770, 2019 09.
Artigo em Inglês | MEDLINE | ID: mdl-30793409

RESUMO

Myxomycetes (plasmodial slime molds) are abundant protist predators that feed on bacteria and other microorganisms, thereby playing important roles in terrestrial nutrient cycling. Despite their significance, little is known about myxomycete communities and the extent to which they are affected by nutrient availability. We studied the influence of long-term addition of N, P, and K on the myxomycete community in a lowland forest in the Republic of Panama. In a previous study, microbial biomass increased with P but not N or K addition at this site. We hypothesized that myxomycetes would increase in abundance in response to P but that they would not respond to the sole addition of N or K. Moist chamber cultures of leaf litter and small woody debris were used to quantify myxomycete abundance. We generated the largest myxomycete dataset (3,381 records) for any single locality in the tropics comprised by 91 morphospecies. In line with our hypothesis, myxomycete abundance increased in response to P addition but did not respond to N or K. Community composition was unaffected by nutrient treatments. This work represents one of very few large-scale and long-term field studies to include a heterotrophic protist highlighting the feasibility and value in doing so.


Assuntos
Mixomicetos/metabolismo , Ecossistema , Florestas , Mixomicetos/crescimento & desenvolvimento , Nitrogênio/metabolismo , Nutrientes/metabolismo , Panamá , Fósforo/metabolismo , Folhas de Planta/parasitologia , Potássio/metabolismo , Solo/parasitologia , Madeira/parasitologia
3.
Mycologia ; 107(5): 1012-22, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26240305

RESUMO

A new species of myxomycete, Perichaena longipes, is described from 56 sporocarp specimens that appeared in moist chamber cultures prepared with samples of decaying plant materials collected in Panama, Costa Rica and Brazil. This new species is distinguished from the morphologically similar species P. pedata on the basis of the much longer stipe, lighter peridium and the unique ornamentation of the capillitium. The nuc 18S ribosomal DNA sequences obtained from four specimens of P. longipes support the distinction of this new taxon and its separation from P. pedata. Furthermore, maximum likelihood phylogeny supports earlier evidence that species currently within the genus Perichaena do not form a monophyletic clade. Instead they appear to form three separate branches within the bright-spored clade. The first clade includes P. longipes together with several species of Trichia and Metatrichia, the second includes P. pedata and P. chrysosperma, and the third clade is composed of P. corticalis, P. depressa and P. luteola.


Assuntos
DNA Fúngico/genética , Mixomicetos/classificação , Mixomicetos/genética , Microscopia Eletrônica de Varredura , Mixomicetos/ultraestrutura , Panamá , RNA Fúngico/genética , RNA Ribossômico 18S/genética , Especificidade da Espécie
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