tetano
Editor, Senior Moderator
Medchemcomm. 2019 Jan 14;10(3):390-398. doi: 10.1039/c8md00508g. eCollection 2019 Mar 1.
[h=1]Potent antiviral activity of carbohydrate-specific algal and leguminous lectins from the Brazilian biodiversity.[/h] Gondim ACS[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP], Roberta da Silva S[SUP]4,[/SUP][SUP]5[/SUP], Mathys L[SUP]6[/SUP], Noppen S[SUP]6[/SUP], Liekens S[SUP]6[/SUP], Holanda Sampaio A[SUP]4[/SUP], Nagano CS[SUP]4[/SUP], Renata Costa Rocha C[SUP]7[/SUP], Nascimento KS[SUP]1[/SUP], Cavada BS[SUP]1[/SUP], Sadler PJ[SUP]2[/SUP], Balzarini J[SUP]6[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Brazil has one of the largest biodiversities in the world. The search for new natural products extracted from the Brazilian flora may lead to the discovery of novel drugs with potential to treat infectious and other diseases. Here, we have investigated 9 lectins extracted and purified from the Northeastern Brazilian flora, from both leguminous species: Canavalia brasiliensis (ConBr), C. maritima (ConM), Dioclea lasiocarpa (DLasiL) and D. sclerocarpa (DSclerL), and algae Amansia multifida (AML), Bryothamniom seaforthii (BSL), Hypnea musciformis (HML), Meristiella echinocarpa (MEL) and Solieria filiformis (SfL). They were exposed to a panel of 18 different viruses, including HIV and influenza viruses. Several lectins showed highly potent antiviral activity, often within the low nanomolar range. DSclerL and DLasiL exhibited EC[SUB]50[/SUB] values (effective concentration of lectin required to inhibit virus-induced cytopathicity by 50%) of 9 nM to 46 nM for HIV-1 and respiratory syncytial virus (RSV), respectively, DLasiL also inhibited feline corona virus at an EC[SUB]50[/SUB] of 5 nM, and DSclerL, ConBr and ConM showed remarkably low EC[SUB]50[/SUB] values ranging from 0.4 to 6 nM against influenza A virus strain H3N2 and influenza B virus. For HIV, evidence pointed to the blockage of entry of the virus into its target cells as the underlying mechanism of antiviral action of these lectins. Overall, the most promising lectins based on their EC[SUB]50[/SUB] values were DLasiL, DSclerL, ConBr, ConM, SfL and HML. These novel findings indicate that lectins from the Brazilian flora may provide novel antiviral compounds with therapeutic potential.
PMID: 30996857 PMCID: PMC6430086 [Available on 2020-01-14] DOI: 10.1039/c8md00508g
[h=1]Potent antiviral activity of carbohydrate-specific algal and leguminous lectins from the Brazilian biodiversity.[/h] Gondim ACS[SUP]1,[/SUP][SUP]2,[/SUP][SUP]3[/SUP], Roberta da Silva S[SUP]4,[/SUP][SUP]5[/SUP], Mathys L[SUP]6[/SUP], Noppen S[SUP]6[/SUP], Liekens S[SUP]6[/SUP], Holanda Sampaio A[SUP]4[/SUP], Nagano CS[SUP]4[/SUP], Renata Costa Rocha C[SUP]7[/SUP], Nascimento KS[SUP]1[/SUP], Cavada BS[SUP]1[/SUP], Sadler PJ[SUP]2[/SUP], Balzarini J[SUP]6[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Brazil has one of the largest biodiversities in the world. The search for new natural products extracted from the Brazilian flora may lead to the discovery of novel drugs with potential to treat infectious and other diseases. Here, we have investigated 9 lectins extracted and purified from the Northeastern Brazilian flora, from both leguminous species: Canavalia brasiliensis (ConBr), C. maritima (ConM), Dioclea lasiocarpa (DLasiL) and D. sclerocarpa (DSclerL), and algae Amansia multifida (AML), Bryothamniom seaforthii (BSL), Hypnea musciformis (HML), Meristiella echinocarpa (MEL) and Solieria filiformis (SfL). They were exposed to a panel of 18 different viruses, including HIV and influenza viruses. Several lectins showed highly potent antiviral activity, often within the low nanomolar range. DSclerL and DLasiL exhibited EC[SUB]50[/SUB] values (effective concentration of lectin required to inhibit virus-induced cytopathicity by 50%) of 9 nM to 46 nM for HIV-1 and respiratory syncytial virus (RSV), respectively, DLasiL also inhibited feline corona virus at an EC[SUB]50[/SUB] of 5 nM, and DSclerL, ConBr and ConM showed remarkably low EC[SUB]50[/SUB] values ranging from 0.4 to 6 nM against influenza A virus strain H3N2 and influenza B virus. For HIV, evidence pointed to the blockage of entry of the virus into its target cells as the underlying mechanism of antiviral action of these lectins. Overall, the most promising lectins based on their EC[SUB]50[/SUB] values were DLasiL, DSclerL, ConBr, ConM, SfL and HML. These novel findings indicate that lectins from the Brazilian flora may provide novel antiviral compounds with therapeutic potential.
PMID: 30996857 PMCID: PMC6430086 [Available on 2020-01-14] DOI: 10.1039/c8md00508g