Maria Letícia Duarte Lima , Paulo Ricardo da Silva Sanches , Dayla Bott Geraldini , Gabriela Miranda Ayusso , Pâmela Jóyce Previdelli da Conceição , Tamara Carvalho , Jorge Enrique Hernández González , Carolina Gismene , Cintia Bittar , Raghuvir Krishnaswamy Arni , Eduardo Maffud Cilli , Marilia de Freitas Calmon , Paula Rahal
{"title":"一个新的合成肽GA-KKALKKLKKALKKAL-CONH2在复制周期的多个阶段显示出抗病毒活性","authors":"Maria Letícia Duarte Lima , Paulo Ricardo da Silva Sanches , Dayla Bott Geraldini , Gabriela Miranda Ayusso , Pâmela Jóyce Previdelli da Conceição , Tamara Carvalho , Jorge Enrique Hernández González , Carolina Gismene , Cintia Bittar , Raghuvir Krishnaswamy Arni , Eduardo Maffud Cilli , Marilia de Freitas Calmon , Paula Rahal","doi":"10.1016/j.virol.2025.110650","DOIUrl":null,"url":null,"abstract":"<div><div>Zika virus (ZIKV) is an emerging arbovirus, and its infection is often asymptomatic or mild; however, it can lead to severe neurological disorders. Currently, there are no approved treatments or vaccines for ZIKV, highlighting the urgent need to explore potential therapeutic options. In this study, we evaluated the antiviral activity of a novel synthetic peptide (GA-peptide) against ZIKV in vitro. The GA-peptide exhibited dose-dependent inhibition of the virus, affecting multiple stages of the ZIKV replication cycle. It demonstrated virucidal activity and effectively protected Vero cells from ZIKV infection. Additionally, the GA-peptide disrupted viral entry by targeting both the attachment and internalization phases, as well as post-entry stages of the infection. <em>In silico</em> analyses identified potential viral targets that interact with the GA-peptide. These findings underscore the GA-peptide's promising potential as a therapeutic agent against ZIKV and its relevance in the development of new antiviral drugs.</div></div>","PeriodicalId":23666,"journal":{"name":"Virology","volume":"611 ","pages":"Article 110650"},"PeriodicalIF":2.4000,"publicationDate":"2025-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A new synthetic peptide GA-KKALKKLKKALKKAL-CONH2 exhibits antiviral activity against ZIKV in multiple stages of the replicative cycle\",\"authors\":\"Maria Letícia Duarte Lima , Paulo Ricardo da Silva Sanches , Dayla Bott Geraldini , Gabriela Miranda Ayusso , Pâmela Jóyce Previdelli da Conceição , Tamara Carvalho , Jorge Enrique Hernández González , Carolina Gismene , Cintia Bittar , Raghuvir Krishnaswamy Arni , Eduardo Maffud Cilli , Marilia de Freitas Calmon , Paula Rahal\",\"doi\":\"10.1016/j.virol.2025.110650\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Zika virus (ZIKV) is an emerging arbovirus, and its infection is often asymptomatic or mild; however, it can lead to severe neurological disorders. Currently, there are no approved treatments or vaccines for ZIKV, highlighting the urgent need to explore potential therapeutic options. In this study, we evaluated the antiviral activity of a novel synthetic peptide (GA-peptide) against ZIKV in vitro. The GA-peptide exhibited dose-dependent inhibition of the virus, affecting multiple stages of the ZIKV replication cycle. It demonstrated virucidal activity and effectively protected Vero cells from ZIKV infection. Additionally, the GA-peptide disrupted viral entry by targeting both the attachment and internalization phases, as well as post-entry stages of the infection. <em>In silico</em> analyses identified potential viral targets that interact with the GA-peptide. These findings underscore the GA-peptide's promising potential as a therapeutic agent against ZIKV and its relevance in the development of new antiviral drugs.</div></div>\",\"PeriodicalId\":23666,\"journal\":{\"name\":\"Virology\",\"volume\":\"611 \",\"pages\":\"Article 110650\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-07-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Virology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0042682225002636\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"VIROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0042682225002636","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"VIROLOGY","Score":null,"Total":0}
A new synthetic peptide GA-KKALKKLKKALKKAL-CONH2 exhibits antiviral activity against ZIKV in multiple stages of the replicative cycle
Zika virus (ZIKV) is an emerging arbovirus, and its infection is often asymptomatic or mild; however, it can lead to severe neurological disorders. Currently, there are no approved treatments or vaccines for ZIKV, highlighting the urgent need to explore potential therapeutic options. In this study, we evaluated the antiviral activity of a novel synthetic peptide (GA-peptide) against ZIKV in vitro. The GA-peptide exhibited dose-dependent inhibition of the virus, affecting multiple stages of the ZIKV replication cycle. It demonstrated virucidal activity and effectively protected Vero cells from ZIKV infection. Additionally, the GA-peptide disrupted viral entry by targeting both the attachment and internalization phases, as well as post-entry stages of the infection. In silico analyses identified potential viral targets that interact with the GA-peptide. These findings underscore the GA-peptide's promising potential as a therapeutic agent against ZIKV and its relevance in the development of new antiviral drugs.
期刊介绍:
Launched in 1955, Virology is a broad and inclusive journal that welcomes submissions on all aspects of virology including plant, animal, microbial and human viruses. The journal publishes basic research as well as pre-clinical and clinical studies of vaccines, anti-viral drugs and their development, anti-viral therapies, and computational studies of virus infections. Any submission that is of broad interest to the community of virologists/vaccinologists and reporting scientifically accurate and valuable research will be considered for publication, including negative findings and multidisciplinary work.Virology is open to reviews, research manuscripts, short communication, registered reports as well as follow-up manuscripts.