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Anti-SARS-CoV-2 Activity of Andrographis paniculata (Burm.f.) Nees Extract via Inhibition of Spike-mediated Syncytia Formation in HEK293T Cell Model

HAYATI Journal of Biosciences · Vol. 31 No. 5 (2024) · hlm. 996–1006

DOI
10.4308/hjb.31.5.996-1006
ISSN
2086-4094, 1978-3019
Terbit
2024-06-24
Penerbit
Bogor Agricultural University, Indonesia
Bahasa
eng

Abstrak

The resurgence of COVID-19 endemic cases at the end of 2023 has underscored the need for effective treatments. Some severe cases of COVID-19 are often characterized by the formation of multinucleated syncytial pneumocytes in the lungs. Therefore, our study aimed to explore the potential of Andrographis paniculata (Burm. f) Nees as an antivirus against SARS-CoV-2, which involves syncitia formation. We utilized the non-toxic concentrations of A. paniculata extract on HEK293T cells determined by MTT assay, which were 1 μg/ml (cell viability 97.96%) and 10 μg/ml (cell viability 95.24%) for further assays. First, we conducted a pseudovirus cellular entry assay as a model of SARS-CoV-2 infection in HEK293T cells expressing hACE2/TMPRSS2. The HEK293T cells were co-transfected with plasmids expressing hACE2 and TMPRSS2, then infected with pseudotyped spike*∆G-GFP rVSV with or without A. paniculata extract. The internalized pseudovirus would trigger GFP expression as a reporter of the infected cells. Next, we performed a syncytia assay by transfecting HEK293T cells with hACE2, TMPRSS2, and SARS-CoV-2 spike expression vectors to induce syncytia formation as a model of intercellular viral transmission. As the results, 10 μg/mL of the extract significantly lowered the number of SARS-CoV-2 pseudovirus-infected cells by 54.69% (P = 0.02) and spike-mediated syncytia formation by 42.39% (P<0.001). In conclusion, our results suggested that A. paniculata has a potential antiviral activity against SARS-CoV-2 by hindering virus infection and cell-to-cell transmission.

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  • National Research and Innovation Agency
  • Universitas Gadjah Mada
  • Indonesian Institute of Sciences
  • Indonesia International Institute for Life Sciences
  • Andalas University
  • PT Bio Farma (Indonesia)
  • Indonesia Defense University
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Rekan penulisOrganisasiArtikel bersama
Popi Hadi WisnuwardhaniNational Research and Innovation Agency10
Yana RubiyanaNational Research and Innovation Agency9
Ratna Dwi RamadaniNational Research and Innovation Agency8
Ahmad SuyokoNational Research and Innovation Agency8
Arizah KusumawatiIndonesian Institute of Sciences5
Ratih Asmana NingrumNational Research and Innovation Agency5
Neny NurainiPT Bio Farma (Indonesia)3
Komang Alit ParamitasariNational Research and Innovation Agency3
Alayna Lillahida Indri HimawanNational Research and Innovation Agency3
Salsabila Putri AzzahraIndonesia Defense University3
Khairul AnamNational Research and Innovation Agency3
Neng HerawatiNational Research and Innovation Agency3
Dadang SupriatnaNational Research and Innovation Agency2
Wien KusharyotoIndonesian Institute of Sciences2
Dian Fitria AgustiyantiNational Research and Innovation Agency2
Andri WardianaNational Research and Innovation Agency2
Gracia Christine Lembong PurwantoIndonesia International Institute for Life Sciences2
Fedric Intan DamaiIndonesia International Institute for Life Sciences2
Alfi Taufik FathurahmanNational Research and Innovation Agency2
Muhammad Khairul Lisan SidqiNational Research and Innovation Agency2
Ihsan Tria PramandaIndonesia International Institute for Life Sciences2
Eti YerizelAndalas University2
Dita FauziahAndalas University2
Larasati LarasatiUniversitas Gadjah Mada2
Ratih Asma NingrumAfiliasi tidak diketahui2
Retno Damajanti SoejoedonoIPB University1
Riris Istighfari JenieUniversitas Gadjah Mada1
Rohmad Yudi UtomoUniversitas Gadjah Mada1
Prisnu TirtanirmalaUniversitas Gadjah Mada1
Annisa NovarinaUniversitas Gadjah Mada1
Muthi IkawatiUniversitas Gadjah Mada1

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Sumber metadata: OAI-PMH (metadata jurnal) http://journal.ipb.ac.id/index.php/hayati/oai, pertama di-harvest 8 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (oai_dc)
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	<dc:title xml:lang="en">Anti-SARS-CoV-2 Activity of Andrographis paniculata (Burm.f.) Nees Extract via Inhibition of Spike-mediated Syncytia Formation in HEK293T Cell Model</dc:title>
	<dc:creator xml:lang="en">Prasetyaningrum, Pekik Wiji </dc:creator>
	<dc:creator xml:lang="en">Kastian, Ria Fajarwati</dc:creator>
	<dc:creator xml:lang="en">Novianti, Metta </dc:creator>
	<dc:creator xml:lang="en">Santoso, Adi </dc:creator>
	<dc:creator xml:lang="en">Septisetyani, Endah Puji </dc:creator>
	<dc:description xml:lang="en">The resurgence of COVID-19 endemic cases at the end of 2023 has underscored the need for effective treatments. Some severe cases of COVID-19 are often characterized by the formation of multinucleated syncytial pneumocytes in the lungs. Therefore, our study aimed to explore the potential of Andrographis paniculata (Burm. f) Nees as an antivirus against SARS-CoV-2, which involves syncitia formation. We utilized the non-toxic concentrations of A. paniculata extract on HEK293T cells determined by MTT assay, which were 1 μg/ml (cell viability 97.96%) and 10 μg/ml (cell viability 95.24%) for further assays. First, we conducted a pseudovirus cellular entry assay as a model of SARS-CoV-2 infection in HEK293T cells expressing hACE2/TMPRSS2. The HEK293T cells were co-transfected with plasmids expressing hACE2 and TMPRSS2, then infected with pseudotyped spike*∆G-GFP rVSV with or without A. paniculata extract. The internalized pseudovirus would trigger GFP expression as a reporter of the infected cells. Next, we performed a syncytia assay by transfecting HEK293T cells with hACE2, TMPRSS2, and SARS-CoV-2 spike expression vectors to induce syncytia formation as a model of intercellular viral transmission. As the results, 10 μg/mL of the extract significantly lowered the number of SARS-CoV-2 pseudovirus-infected cells by 54.69% (P = 0.02) and spike-mediated syncytia formation by 42.39% (P&amp;lt;0.001). In conclusion, our results suggested that A. paniculata has a potential antiviral activity against SARS-CoV-2 by hindering virus infection and cell-to-cell transmission.</dc:description>
	<dc:publisher xml:lang="en">Bogor Agricultural University, Indonesia</dc:publisher>
	<dc:date>2024-06-24</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:type xml:lang="en">Peer-reviewed Article</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>http://journal.ipb.ac.id/hayati/article/view/54522</dc:identifier>
	<dc:identifier>10.4308/hjb.31.5.996-1006</dc:identifier>
	<dc:source xml:lang="en">HAYATI Journal of Biosciences; Vol. 31 No. 5 (2024): September 2024; 996-1006</dc:source>
	<dc:source>2086-4094</dc:source>
	<dc:source>1978-3019</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>http://journal.ipb.ac.id/hayati/article/view/54522/28390</dc:relation>
	<dc:rights xml:lang="en">Copyright (c) 2024 Pekik Wiji  Prasetyaningrum, Ria Fajarwati Kastian, Metta  Novianti, Adi  Santoso, Endah Puji  Septisetyani</dc:rights>
</oai_dc:dc>