Inhibition by Marine Algae of Chikungunya Virus Isolated From Patients in a Recent Disease Outbreak in Rio de Janeiro
Chikungunya virus (CHIKV) infection is one of the most challenging re-emergent diseases caused by a virus, and with no specific antiviral treatment it has now become a major public health concern. In this investigation, 25 blood samples were collected from patients with characteristic CHIKV symptoms...
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Veröffentlicht in: | Frontiers in microbiology 2019-10, Vol.10, p.2426-2426 |
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Sprache: | eng |
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Zusammenfassung: | Chikungunya virus (CHIKV) infection is one of the most challenging re-emergent diseases caused by a virus, and with no specific antiviral treatment it has now become a major public health concern. In this investigation, 25 blood samples were collected from patients with characteristic CHIKV symptoms and submitted to a virus isolation protocol, which detected 3 CHIKV isolates. These samples were evaluated by sequencing for the characterization of the strains and any homology to viruses circulating in Brazil during a recent outbreak. These viruses were used for the development of antiviral assays. Subsequently, the inhibitory effects of seaweed extracts on CHIKV replication were studied. The marine species of algae tested were
Bryothamnion triquetrum, Caulerpa racemosa, Laurencia dendroidea, Osmundaria obtusiloba
,
Ulva fasciata
, and
Kappaphycus alvarezii
, all of which are found in different countries including Brazil. The results revealed high levels of CHIKV inhibition, including extracts of
O. obtusiloba
with inhibition values of 1.25 μg/mL and a selectivity index of 420. Viral inhibition was dependent on the time of addition of extract of
O. obtusiloba
to the infected cells, with the optimal inhibition occurring up to 16 h after infection. Neuron evaluations with
O. obtusiloba
were performed and demonstrated low toxicity, and in infected neurons we observed high inhibitory activity in a dose-dependent manner. These results indicate that the algal extracts may be promising novel candidates for the development of therapeutic agents against CHIKV infections. |
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ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2019.02426 |