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Oil-Adjuvanted Polyvalent Formalin-killed Aeromonas hydrophila Vaccine Enhances Agglutinating Antibodies, Respiratory Burst, and Survival in Giant Gourami

Jurnal Ilmiah Perikanan dan Kelautan · Vol. 18 No. 1 (2025) · hlm. 17–40

DOI
10.20473/jipk.v18i1.82866
ISSN
2528-0759, 2085-5842
Terbit
2025-12-05
Penerbit
Faculty of Fisheries and Marine Universitas Airlangga
Bahasa
eng
Lisensi
creativecommons.org/licenses/by-nc-sa/4.0

Abstrak

Graphical Abstract Highlight Research Adjuvanted polyvalent FKC elicited the strongest and most sustained multi-arm immune response in Osphronemus goramy compared with monovalent and non-adjuvanted vaccines. The lead formulation combined high agglutinating antibody titres with enhanced NBT respiratory burst, indicating synergistic humoral–innate activation against Aeromonas hydrophila. Polyvalent vaccines did not dilute immunogenicity; instead, strain combination plus adjuvant broadened and amplified immune responsiveness. Longitudinal profiling of il-1β and ifn-γ revealed a stable pro-inflammatory/Th1-like cytokine signature uniquely associated with the adjuvanted polyvalent FKC. The integrated immunological “fingerprint” supports the adjuvanted polyvalent FKC as a rational lead candidate for motile Aeromonas septicaemia control in warm-water gourami aquaculture. Abstract Motile Aeromonas septicaemia (MAS), predominantly associated with Aeromonas hydrophila, remains a major constraint in giant gourami (Osphronemus goramy) aquaculture. This study evaluated formalin-inactivated A. hydrophila vaccines prepared from MAS-associated field isolates, comparing a monovalent formulation (P2), a non-adjuvanted polyvalent formulation (P3), and an oil-adjuvanted polyvalent formulation (P4) against PBS controls (P1). A total of 240 fish were used (60 per treatment) and assigned to two parallel cohorts (immunology and survival/challenge). Immune endpoints (agglutinating titres, NBT activity, and splenic il-1β and ifn-γ transcription) were assessed on days 7, 14, 21, 35, and 42 post-vaccination. The survival cohort was challenged intraperitoneally at day 21 with a homologous A. hydrophila strain and monitored for 14 days post-challenge. Vaccination was clinically well tolerated and improved survival relative to controls, with P4 showing the highest protection (RPS 81.8%). Agglutinating titres differed by treatment and time; at the peak sampling point (day 35), mean titres in P4 were ~200-fold higher than in P1, and model contrasts indicated significant differences versus controls (plt;0.001). Splenic il-1β and ifn-γ transcript levels were higher in vaccinated groups than in controls at later time points. These findings support further evaluation of an oil-adjuvanted polyvalent inactivated A. hydrophila vaccine for gourami, including dose optimisation, extended safety assessment, heterologous challenge, and field validation.

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  • Universitas Airlangga
  • Universiti Putra Malaysia
  • Universitas Borneo Tarakan
  • National Research and Innovation Agency
  • Diponegoro University
  • Institut Marin Borneo
  • Indonesia Defense University
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Rekan penulisOrganisasiArtikel bersama
Ratih Novita PrajaUniversitas Airlangga14
Maya Nurwartanti YunitaUniversitas Airlangga11
Agus IndarjoDiponegoro University8
Julian RansanganInstitut Marin Borneo6
Prima Ayu WibawatiUniversitas Airlangga6
Aswin Rafif KhairullahNational Research and Innovation Agency6
Lukman Yudho PrakosoIndonesia Defense University5
Mufasirin MufasirinUniversitas Airlangga5
Muhammad FirdausIPB University5
Aditya YudhanaUniversitas Airlangga5
Iwan Sahrial HamidUniversitas Airlangga5
Fedik Abdul RantamUniversitas Airlangga5
Lucia Tri SuwantiUniversitas Airlangga5
Mujiyanto MujiyantoNational Research and Innovation Agency4
Thonas Indra MaryantoBandung Institute of Technology4
Ina Salwany Md YasinUniversiti Putra Malaysia4
Permana Ari SoejarwoMinistry of Marine Affairs and Fisheries3
Christine Dyta NugraeniUniversitas Borneo Tarakan3
Yen Thi Hong PhamNational Kaohsiung University of Science and Technology3
Suryanie SarudjiUniversitas Airlangga3
Kusnoto KusnotoUniversitas Airlangga3
Zahidah ZahidahAfiliasi tidak diketahui2
Mochamad Candra Wirawan AriefPadjadjaran University2

Afiliasi berasal dari OpenAlex; metadata OAI-PMH jurnal tidak memuatnya. Penulis tanpa ID OpenAlex dicocokkan berdasarkan nama, sehingga dua orang bisa tergabung atau satu orang bisa terpisah.

Sumber metadata: OAI-PMH (metadata jurnal) https://e-journal.unair.ac.id/index.php/JIPK/oai, pertama di-harvest 9 Nov 2026, terakhir terlihat 9 Nov 2026.
Metadata asli (oai_dc)
<oai_dc:dc xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/  http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
	<dc:title xml:lang="en-US">Oil-Adjuvanted Polyvalent Formalin-killed Aeromonas hydrophila Vaccine Enhances Agglutinating Antibodies, Respiratory Burst, and Survival in Giant Gourami</dc:title>
	<dc:creator>Rozi</dc:creator>
	<dc:creator>Wiwiek Tyasningsih</dc:creator>
	<dc:creator>Jola Rahmahani</dc:creator>
	<dc:creator>Eduardus Bimo Aksono</dc:creator>
	<dc:creator>Muchammad Yunus </dc:creator>
	<dc:creator>Mohammad Anam Al-Arif</dc:creator>
	<dc:creator>Suryo Kuncorojakti</dc:creator>
	<dc:creator>Daruti Dinda Nindarwi</dc:creator>
	<dc:creator>Putri Desi Wulan Sari</dc:creator>
	<dc:creator>Nina Nurmalia Dewi</dc:creator>
	<dc:creator>Woro Hastuti Satyantini</dc:creator>
	<dc:creator>Muhammad Browijoyo Santanumurti</dc:creator>
	<dc:creator>Dita Wisudyawati</dc:creator>
	<dc:creator>Mohammad Noor Amal Azmai</dc:creator>
	<dc:creator>Annas Salleh</dc:creator>
	<dc:creator>Gazali Salim</dc:creator>
	<dc:creator>Suwarno, Suwarno</dc:creator>
	<dc:subject xml:lang="en-US">Aeromonas hydrophila vaccine Adjuvanted polyvalent FKC</dc:subject>
	<dc:description xml:lang="en-US">Graphical Abstract 

Highlight Research

Adjuvanted polyvalent FKC elicited the strongest and most sustained multi-arm immune response in Osphronemus goramy compared with monovalent and non-adjuvanted vaccines.
The lead formulation combined high agglutinating antibody titres with enhanced NBT respiratory burst, indicating synergistic humoral–innate activation against Aeromonas hydrophila.
Polyvalent vaccines did not dilute immunogenicity; instead, strain combination plus adjuvant broadened and amplified immune responsiveness.
Longitudinal profiling of il-1β and ifn-γ revealed a stable pro-inflammatory/Th1-like cytokine signature uniquely associated with the adjuvanted polyvalent FKC.
The integrated immunological “fingerprint” supports the adjuvanted polyvalent FKC as a rational lead candidate for motile Aeromonas septicaemia control in warm-water gourami aquaculture.

 
Abstract
Motile Aeromonas septicaemia (MAS), predominantly associated with Aeromonas hydrophila, remains a major constraint in giant gourami (Osphronemus goramy) aquaculture. This study evaluated formalin-inactivated A. hydrophila vaccines prepared from MAS-associated field isolates, comparing a monovalent formulation (P2), a non-adjuvanted polyvalent formulation (P3), and an oil-adjuvanted polyvalent formulation (P4) against PBS controls (P1). A total of 240 fish were used (60 per treatment) and assigned to two parallel cohorts (immunology and survival/challenge). Immune endpoints (agglutinating titres, NBT activity, and splenic il-1β and ifn-γ transcription) were assessed on days 7, 14, 21, 35, and 42 post-vaccination. The survival cohort was challenged intraperitoneally at day 21 with a homologous A. hydrophila strain and monitored for 14 days post-challenge. Vaccination was clinically well tolerated and improved survival relative to controls, with P4 showing the highest protection (RPS 81.8%). Agglutinating titres differed by treatment and time; at the peak sampling point (day 35), mean titres in P4 were ~200-fold higher than in P1, and model contrasts indicated significant differences versus controls (plt;0.001). Splenic il-1β and ifn-γ transcript levels were higher in vaccinated groups than in controls at later time points. These findings support further evaluation of an oil-adjuvanted polyvalent inactivated A. hydrophila vaccine for gourami, including dose optimisation, extended safety assessment, heterologous challenge, and field validation.</dc:description>
	<dc:publisher xml:lang="en-US">Faculty of Fisheries and Marine Universitas Airlangga</dc:publisher>
	<dc:date>2025-12-05</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:format>text/xml</dc:format>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://e-journal.unair.ac.id/JIPK/article/view/82866</dc:identifier>
	<dc:identifier>10.20473/jipk.v18i1.82866</dc:identifier>
	<dc:source xml:lang="en-US">Jurnal Ilmiah Perikanan dan Kelautan; Vol. 18 No. 1 (2026): JURNAL ILMIAH PERIKANAN DAN KELAUTAN; 17-40</dc:source>
	<dc:source>2528-0759</dc:source>
	<dc:source>2085-5842</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://e-journal.unair.ac.id/JIPK/article/view/82866/40589</dc:relation>
	<dc:relation>https://e-journal.unair.ac.id/JIPK/article/view/82866/35563</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2025 Jurnal Ilmiah Perikanan dan Kelautan</dc:rights>
	<dc:rights xml:lang="en-US">http://creativecommons.org/licenses/by-nc-sa/4.0</dc:rights>
</oai_dc:dc>