Microbiological Hazards in the Food Chain of the Asian Green Mussel (Perna viridis): A Review Focusing on Vibrio parahaemolyticus
Abstract
The Asian green mussel (Perna viridis) is an important aquaculture species in the Indo-Pacific region and, as a filter-feeding bivalve, can accumulate microorganisms from surrounding waters, including foodborne pathogens. This review synthesizes evidence on the occurrence, persistence, and control of Vibrio parahaemolyticus associated with P. viridis, with emphasis on pre-harvest environmental determinants, post-harvest survival, and processing interventions. Peer-reviewed literature and regulatory sources published between 2000 and 2026 were evaluated to characterize factors influencing pathogen prevalence and persistence and to assess control measures. Available evidence indicates that V. parahaemolyticus is frequently detected in filter-feeding bivalves, including populations from Southeast Asia, where strains carrying the tdh and trh virulence-associated genes have been reported. Environmental conditions, particularly temperature, influence pathogen occurrence and post-harvest persistence. Biofilm formation and the viable but non-culturable state may further contribute to pathogen persistence and complicate detection and control. Quantitative microbial risk assessment studies indicate that temperature abuse during post-harvest handling and transportation can increase the predicted risk of illness. Although seawater depuration can reduce bacterial loads under defined conditions, its efficacy may be limited by pathogen localization and physiological state. Alternative interventions, including high-pressure processing and emerging biochemical approaches such as chitooligosaccharide–polyphenol conjugates, have demonstrated potential for reducing V. parahaemolyticus contamination, although their effectiveness in P. viridis requires further validation. Overall, the evidence supports an integrated risk-management approach combining environmental monitoring, temperature control, validated post-harvest interventions, and pathogen-specific microbiological criteria. Further studies should validate emerging interventions under processing-relevant conditions and assess their feasibility for controlling V. parahaemolyticus in bivalve seafood.
Keywords:
Perna viridis, Vibrio parahaemolyticus, Microbial food safety, Bivalve aquaculture, Antimicrobial resistance, MicroplasticsReferences
Baker, G. (2016). Food safety impacts from post-harvest processing procedures of molluscan shellfish. Foods, 5, 29. https://doi.org/10.3390/foods5020029
Bechlars, S., Jäckel, C., Diescher, S., Wüstenhagen, D. A., Kubick, S., Dieckmann, R., & Strauch, E. (2015). Characterization of trh2 harbouring Vibrio parahaemolyticus strains isolated in Germany. PLOS ONE, 10, e0118559. https://doi.org/10.1371/journal.pone.0118559
Commission Regulation. (2005, November 15). Commission Regulation (EC) No 2073/2005 of 15 November 2005 on microbiological criteria for foodstuffs. https://eur-lex.europa.eu/eli/reg/2005/2073/oj/eng (accessed on September 6, 2026)
Destoumieux-Garzón, D., Duperthuy, M., Vanhove, A., Schmitt, P., & Wai, S. (2014). Resistance to antimicrobial peptides in vibrios. Antibiotics, 3, 540–563. https://doi.org/10.3390/antibiotics3040540
Di Salvo, E., Panebianco, F., Panebianco, A., & Ziino, G. (2023). Quantitative detection of viable but nonculturable Vibrio parahaemolyticus in frozen bivalve molluscs. Foods, 12, 2373. https://doi.org/10.3390/foods12122373
FAO/WHO. (2011). Risk assessment of Vibrio parahaemolyticus in seafood: Interpretative summary and technical report. Microbiological Risk Assessment Series No. 16. https://www.who.int/publications/i/item/9789241548175 (accessed on September 6, 2026)
Fernández, L., & Hancock, R. E. W. (2012). Adaptive and mutational resistance: Role of porins and efflux pumps in drug resistance. Clinical Microbiology Reviews, 25, 661–681. https://doi.org/10.1128/CMR.00043-12
Froelich, B. A., & Noble, R. T. (2016). Vibrio bacteria in raw oysters: managing risks to human health. Philosophical Transactions of the Royal Society B: Biological Sciences, 371, 20150209. https://doi.org/10.1098/rstb.2015.0209
Hara-Kudo, Y., Saito, S., Ohtsuka, K., Yamasaki, S., Yahiro, S., Nishio, T., Iwade, Y., Otomo, Y., Konuma, H., Tanaka, H., Nakagawa, H., Sugiyama, K., Sugita-Konishi, Y., & Kumagai, S. (2012). Characteristics of a sharp decrease in Vibrio parahaemolyticus infections and seafood contamination in Japan. International Journal of Food Microbiology, 157, 95–101. https://doi.org/10.1016/j.ijfoodmicro.2012.04.019
Hikmawati, F., Susilowati, A., & Setyaningsih, R. (2019). Colony morphology and molecular identification of Vibrio spp. on green mussels (Perna viridis) in Yogyakarta, Indonesia tourism beach areas. Biodiversitas Journal of Biological Diversity, 20, 2891-2899. https://doi.org/10.13057/biodiv/d201015
Hwang, C.-C., Lin, C.-S., Hsiao, Y.-T., Huang, Y.-L., Yen, F.-L., Lee, Y.-C., & Tsai, Y.-H. (2023). Inactivation kinetics of foodborne pathogens in carrot juice by high-pressure processing. Biology, 12, 1383. https://doi.org/10.3390/biology12111383
Indonesian National Agency of Drug and Food Control. (2019). Regulation of the National Agency of Drug and Food Control No. 13 of 2019 concerning maximum limits for microbial contaminants in processed food. https://peraturan.go.id/id/peraturan-bpom-no-13-tahun-2019 (accessed on September 6, 2026)
Koutsoumanis, K., Allende, A., Alvarez‐Ordóñez, A., Bolton, D., Bover‐Cid, S., Chemaly, M., De Cesare, A., Herman, L., Hilbert, F., Lindqvist, R., Nauta, M., Nonno, R., Peixe, L., Ru, G., Simmons, M., Skandamis, P., Baker‐Austin, C., Hervio‐Heath, D., Martinez‐Urtaza, J., … Suffredini, E. (2024). Public health aspects of Vibrio spp. related to the consumption of seafood in the EU. EFSA Journal, 22, e8896. https://doi.org/10.2903/j.efsa.2024.8896
Li, L., Meng, H., Gu, D., Li, Y., & Jia, M. (2019). Molecular mechanisms of Vibrio parahaemolyticus pathogenesis. Microbiological Research, 222, 43–51. https://doi.org/10.1016/j.micres.2019.03.003
Liu, J., Xiong, R., Wu, Q., Xu, T., Caridad, O. C. O., Zhu, Y., Pan, Y., Malakar, P. K., Zhao, Y., & Zhang, Z. (2025). Detection, assessment, and control strategies for managing Vibrio parahaemolyticus risk in seafood. Food Quality and Safety, 9, fyae051. https://doi.org/10.1093/fqsafe/fyae051
Martinez-Albores, A., Lopez-Santamarina, A., Rodriguez, J. A., Ibarra, I. S., Mondragón, A. del C., Miranda, J. M., Lamas, A., & Cepeda, A. (2020). Complementary methods to improve the depuration of bivalves: A review. Foods, 9, 129. https://doi.org/10.3390/foods9020129
Nakaguchi, Y. (2013). Contamination by Vibrio parahaemolyticus and its virulent strains in seafood marketed in Thailand, Vietnam, Malaysia, and Indonesia. Tropical Medicine and Health, 41, 95–102. https://doi.org/10.2149/tmh.2011-06
Ndraha, N., Huang, L., Wu, V. C., & Hsiao, H.-I. (2022). Vibrio parahaemolyticus in seafood: Recent progress in understanding influential factors at harvest and food-safety intervention approaches. Current Opinion in Food Science, 48, 100927. https://doi.org/10.1016/j.cofs.2022.100927
Nunal, S. N., Parcon, R. B., Logronio, S. B., Cartago, N. H. N., & Muegue, M. F. S. (2023). Nutritional evaluation of green mussel Perna viridis (Linnaeus, 1758) and brown mussel Modiolus modulaides (Röding, 1798) from Panay Island, Philippines. Asian Fisheries Science, 36, 152–163. https://doi.org/10.33997/j.afs.2023.36.3.004
Odeyemi, O. A. (2016). Incidence and prevalence of Vibrio parahaemolyticus in seafood: a systematic review and meta-analysis. SpringerPlus, 5, 464. https://doi.org/10.1186/s40064-016-2115-7
Odeyemi, O. A., Amin, M., Dewi, F. R., Kasan, N. A., Onyeaka, H., Stratev, D., & Odeyemi, O. A. (2023). Prevalence of antibiotic-resistant seafood-borne pathogens in retail seafood sold in Malaysia: A systematic review and meta-analysis. Antibiotics, 12, 829. https://doi.org/10.3390/antibiotics12050829
Ong, H. M. G., Zhong, Y., Hu, C., Ong, K. H., Khor, W. C., Schlundt, J., & Aung, K. T. (2023). Antimicrobial resistance risk assessment of Vibrio parahaemolyticus isolated from farmed green mussels in Singapore. Microorganisms, 11, 1498. https://doi.org/10.3390/microorganisms11061498
Palamae, S., Mittal, A., Yingkajorn, M., Saetang, J., Buatong, J., Tyagi, A., Singh, P., & Benjakul, S. (2022). Vibrio parahaemolyticus isolates from Asian green mussel: Molecular characteristics, virulence and their inhibition by chitooligosaccharide-tea polyphenol conjugates. Foods, 11, 4048. https://doi.org/10.3390/foods11244048
Puértolas, E., García-Muñoz, S., Caro, M., & Alvarez-Sabatel, S. (2023). Effect of different cold storage temperatures on the evolution of shucking yield and quality properties of offshore cultured Japanese oyster (Magallana gigas) treated by high pressure processing (HPP). Foods, 12, 1156. https://doi.org/10.3390/foods12061156
Sharma, M. H., Palamae, S., Yingkajorn, M., Benjakul, S., Singh, A., & Buatong, J. (2024). Multidrug-resistance of Vibrio species in bivalve mollusks from Southern Thailand: Isolation, identification, pathogenicity, and their sensitivity toward chitooligosaccharide-epigallocatechin-3-gallate conjugate. Foods, 13, 2375. https://doi.org/10.3390/foods13152375
Sharp, J. H., Clements, K., Diggens, M., McDonald, J. E., Malham, S. K., & Jones, D. L. (2021). E. coli is a poor end-product criterion for assessing the general microbial risk posed from consuming norovirus contaminated shellfish. Frontiers in Microbiology, 12, 608888. https://doi.org/10.3389/fmicb.2021.608888
Ulusoy, Ş., Üçok Alakavuk, D., Mol, S., & Coşansu, S. (2019). Effect of microwave cooking on foodborne pathogens in fish. Journal of Food Processing and Preservation, 43, e14045. https://doi.org/10.1111/jfpp.14045
US FDA. (2005). Quantitative risk assessment on the public health impact of pathogenic Vibrio parahaemolyticus in raw oysters. US FDA. https://www.fda.gov/food/risk-and-safety-assessments-food/quantitative-risk-assessment-public-health-impact-pathogenic-vibrio-parahaemolyticus-raw-oysters (accessed on September 6, 2026)
US FDA. (2023). National shellfish sanitation program (NSSP) - Guide for the control of molluscan shellfish. US FDA. https://www.fda.gov/food/federal-state-local-tribal-and-territorial-cooperative-human-food-programs/national-shellfish-sanitation-program-nssp (accessed on September 6, 2026)
Wang, R., Zhong, Y., Gu, X., Yuan, J., Saeed, A. F., & Wang, S. (2015a). The pathogenesis, detection, and prevention of Vibrio parahaemolyticus. Frontiers in Microbiology, 6, 144. https://doi.org/10.3389/fmicb.2015.00144
Wang, W., Li, M., & Li, Y. (2015b). Intervention strategies for reducing Vibrio parahaemolyticus in seafood: A review. Journal of Food Science, 80, R10-R19. https://doi.org/10.1111/1750-3841.12727
Data Availability Statement
No new data were created or analyzed in this study. Data sharing is not applicable to this article.
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Copyright (c) 2026 Fenny Crista Anastasia Panjaitan, Resti Nurmala Dewi, Nodali Ndraha

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