VETERİNER HEKİMLİK AÇISINDA ÖNEMLİ VİBRİO TÜRLERİ VE İNFEKSİYONLARI

Year 2022, Volume: 1 Issue: 191, 2 - 14, 18.05.2022

Banur Boynukara , Seyda Cengiz , Mehmet Cemal Adıguzel

Abstract

Su ürünleri yetiştiriciliği, dünya çapında hızlı bir büyüme trendine sahip yüksek proteinli kaynak pazarıdır. Su ürünleri yetiştiriciliğinde artan üretim, üretimin karlılığını ve sürdürülebilirliğini olumsuz etkileyen salgınları da beraberinde getirmektedir. Özellikle, kültürü yapılan kabuklu deniz ürünleri, karides ve balıklarda önemli ekonomik kayıplara neden olabilen önemli hastalıklardan vibriozis sorumludur. Vibrio türleri su ürünleri yetiştiriciliği için önemli derecede olumsuz etkilere sahiptir ve tedavi oldukça maliyetlidir. Ayrıca su ürünleri yetiştiriciliğinde vibriozise neden olan türlerin virülans, toksin genleri, konak hücreler üzerindeki etkileri ve sosyo-ekonomik etkileri ile ilgili çalışmalar sınırlıdır. Ayrıca Vibrio türleri, özellikle halk sağlığı için önemli olan zoonotik hastalıkları tetikleyebilen önemli patojenler içermektedir. Bu derleme, su ürünleri hastalıkları hakkında etiyoloji, epidemiyoloji, patogenez, klinik belirtiler, patolojik bulgular, tanı, bulaşma, risk faktörleri ve kontrol önlemleri dahil olmak üzere çeşitli güncellenmiş temel bilgileri vurgulamaktadır.

Keywords

Balık hastalıkları, kültür balıkçılığı, Vibrio, yetiştiricilik

Supporting Institution

yok

Project Number

yok

References

• Abushattal S, Vences A, Osorio CR (2020) A virulence gene typing scheme for Photobacterium damselae subsp. piscicida, the causative agent of fish photobacteriosis, reveals a high prevalence of plasmid-encoded virulence factors and of type III secretion system genes. Aquaculture, 521:735057. https://doi.org/10.1016/j.aquaculture.2020.735057
• Akayli T, Aydin B, Urku C, Kayalar O (2018) Diagnosis of Vibrio anguillarum in cultured rainbow trout (Oncorhynchus mykiss) by different methods. European Journal of Biology, 77:26-31.
• Austin B, Austin DA (2016) Bacterial Fish Pathogens: Disease of farmed and wild fish, 5th edn. Springer International Publishing, Switzerland.
• Balasubramanian D, Murcia S, Ogbunugafor CB, Gavilan R, Almagro-Moreno S (2021) Cholera dynamics: lessons from an epidemic. Journal of Medical Microbiology, 70:1-11. https://doi.org/10.1099/jmm.0.001298
• Balta F, Dengiz Balta Z (2017) Serotyping, genetic characterization and antimicrobial susceptibility determination of Vibrio anguillarum strains isolated from farmed rainbow trout (Oncorhynchus mykiss) in the eastern Black Sea. Ankara Üniversitesi Veteriner Fakültesi Dergisi, 64:321-328. https://doi.org/10.1501/Vetfak_0000002816
• Baumann P, Baumann L, Mandel M (1971) Taxonomy of marine bacteria: the genus Beneckea. Journal of Bacteriology, 107:268-294.
• Begum YA, Rydberg HA, Thorell K, Kwak YK, Sun L, Joffré E, Qadri F, Sjöling Å (2018) In situ analyses directly in diarrheal stool reveal large variations in bacterial load and active toxin expression of enterotoxigenic Escherichia coli and Vibrio cholerae. Msphere 3: e00517-17. https://doi.org/10.1128/msphere.00517-17
• Bergman AM (1909) Die rote beulenkrankheit des aals. Bericht aus der Koniglichen Bayerischen Versuchsstation 2:10-54.
• Bonnin-Jusserand M, Copin S, Le Bris C, Brauge T, Gay M, Brisabois A, Grard T, Midelet-Bourdin G (2019) Vibrio species involved in seafood-borne outbreaks (Vibrio cholerae, V. parahaemolyticus and V. vulnificus): Review of microbiological versus recent molecular detection methods in seafood products. Critical Reviews in Food Science and Nutrition, 59:597-610. https://doi.org/10.1080/10408398.2017.1384715
• Brenner DJ, Krieg NR, Staley JT (2007) The proteobacteria, Part B: The gammaproteobacteria. Garrity G. eds. Bergey’s Manual® of Systematic Bacteriology. Springer Science & Business Media, New York. pp. 491-555.
• Chong R, Bousfield B, Brown R (2011) Fish disease management. Veterinary Bulletin–Agriculture, Fisheries, and Conservation Depart-ment Newsletter (December 1) 1: 1–12.
• Davenport RJ, Satchell M, Shaw-Taylor LMW. (2019) Cholera as a ‘sanitary test’of British cities, 1831–1866. The History of the Family 24:404-438. https://dx.doi.org/10.1080%2F1081602X.2018.1525755
• Elbahnaswy S, Elshopakey GE (2020) Differential gene expression and immune response of Nile tilapia (Oreochromis niloticus) challenged intraperitoneally with Photobacterium damselae and Aeromonas hydrophila demonstrating immunosuppression. Aquaculture, 526:735364. https://doi.org/10.1016/j.aquaculture.2020.735364
• El‐Son MA, Elbahnaswy S, Ibrahim I (2020) Molecular and histopathological characterization of Photobacterium damselae in naturally and experimentally infected Nile tilapia (Oreochromis niloticus). Journal of Fish Diseases, 43:1505-1517. http://dx.doi.org/10.1111/jfd.13251
• Frans I, Michiels CW, Bossier P, Willems KA, Lievens B, Rediers H (2011) Vibrio anguillarum as a fish pathogen: virulence factors, diagnosis and prevention. Journal of Fish Diseases, 34:643-661. https://doi.org/10.1111/j.1365-2761.2011.01279.x
• Fuertes-Perez S, Hauschild P, Hilgarth M, Vogel RF (2019) Biodiversity of Photobacterium spp. isolated from meats. Frontiers in Microbiology, 10:2399. https://doi.org/10.3389/fmicb.2019.02399
• Gupta N, Partridge GJ, Buller NB, Pilmer L, Currie A, Lymbery AJ (2021) Genetic diversity of Australian isolates of Photobacterium damselae subsp. damselae is associated with virulence to yellowtail kingfish (Seriola lalandi). Aquaculture, 538:736552. https://doi.org/10.1016/j.aquaculture.2021.736552
• Hickey ME, Lee JL. (2018) A comprehensive review of Vibrio (Listonella) anguillarum: ecology, pathology and prevention. Reviews in Aquaculture, 10:585-610. https://doi.org/10.1111/raq.12188
• Huang JB, Wu YC, Chi SC (2014) Dietary supplementation of Pediococcus pentosaceus enhances innate immunity, physiological health and resistance to Vibrio anguillarum in orange-spotted grouper (Epinephelus coioides). Fish Shellfish Immunology, 39:196-205. https://doi.org/10.1016/j.fsi.2014.05.003
• Ina‐Salwany MY, Al‐saari N, Mohamad A, Mursidi FA, Mohd‐Aris A, Amal MNA, Kasai H, Mino S, Sawabe T, Zamri-Saad M (2019) Vibriosis in fish: a review on disease development and prevention. Journal of Aquatic Animal Health, 31: 3-22. https://doi.org/10.1002/aah.10045
• Kazazić SP, Topić Popović N, Strunjak-Perović I, Babić S, Florio D, Fioravanti M, Bojanić K, Čož-Rakovac R (2019) Matrix-assisted laser desorption/ionization time of flight mass spectrometry identification of Vibrio (Listonella) anguillarum isolated from sea bass and sea bream. Plos One, 14:e0225343. https://doi.org/10.1371/journal.pone.0225343
• MacDonell MT, Colwell RR (1985) Phylogeny of the Vibrionaceae, and recommendation for two new genera, Listonella and Shewanella. Systematic and Applied Microbiology, 6:171-182. https://doi.org/10.1016/S0723-2020(85)80051-5
• Matanza XM, Osorio CR (2020) Exposure of the opportunistic marine pathogen Photobacterium damselae subsp. damselae to human body temperature is a stressful condition that shapes the transcriptome, viability, cell morphology, and virulence. Frontiers in Microbiology, 11:1771. https://doi.org/10.3389/fmicb.2020.01771
• Mohamad N, Amal MNA, Yasin ISM, Saad MZ, Nasruddin NS, Al-saari N, Mino S, Sawabe T (2019) Vibriosis in cultured marine fishes: a review. Aquaculture, 512:734289. https://doi.org/10.1016/j.aquaculture.2019.734289
• Mohamad N, Mustafa M, Amal MN, Saad MZ, Yasin IS, Al‐saari N (2019) Environmental factors associated with the presence of Vibrionaceae in tropical cage‐cultured marine fishes. Journal of Aquatic Animal Health, 31:154-167. http://dx.doi.org/10.1002/aah.10062
• Moi IM, Roslan NN, Leow ATC, Ali MSM, Rahman RNZRA, Rahimpour A, Sabri S (2017) The biology and the importance of Photobacterium species. Applied Microbiology and Biotechnology, 101:4371-4385. https://doi.org/10.1007/s00253-017-8300-y
• Noga EJ (2010) Fish disease: diagnosis and treatment. 2 edn. John Wiley & Sons, Missouri.
• Onuk EE, Altun S, Duman M, Saticioglu İB, Mustak HK (2018) Phenotypic and genotypic characterization of Listonella anguillarum isolates from rainbow trout. Etlik Veteriner Mikrobiyoloji Dergisi, 29:143-150. https://doi.org/10.35864/evmd.513537
• Parin U, Erbas G, Savasan S, Yuksel HT, Gurpinar S, Kirkan S (2019) Antimicrobial resistance of Vibrio (Listonella) anguillarum isolated from rainbow trouts (Oncorhynchus mykiss). Indian Journal of Animal Research, 53:1522-1525. http://dx.doi.org/18805/ijar.v0iOF.7251
• Petchimuthu M (2020) Detection of virulence hemolysin gene (HlyA) in Photobacterium damselae subspecies damselae isolates. Journal of Entomology and Zoology Studies, 8:1326-1330. https://doi.org/10.22271/j.ento.2020.v8.i6r.8015
• Procop GW, Church DL, Hall GS, Janda WM (2017) Koneman’s Color Atlas and Textbook of Diagnostic Microbiology, Wolters Kluwer, Philedelphia. Sahu KK, Sherif AA, Davaro R. (2020) A rare cause of cellulitis: Photobacterium damselae. Journal of Microscopy and Ultrastructure, 8:25. https://doi.org/10.4103/ jmau.jmau_63_18
• Satitsri S, Pongkorpsakol P, Srimanote P, Chatsudthipong V, Muanprasat C (2016) Pathophysiological mechanisms of diarrhea caused by the Vibrio cholerae O1 El Tor variant: an in vivo study in mice. Virulence 7: 789-805. https://doi.org/10.1080/21505594.2016.1192743
• Singaravel V, Gopalakrishnan A, Dewangan NK, Kannan D, Shettu N, Martin GG (2020) Photobacterium damselae subsp. damselae associated with bacterial myonecrosis and hepatopancreatic necrosis in broodstock Pacific white leg shrimp, Litopenaeus vannamei (Boone, 1931). Aquaculture International, 28:1593-1608. https://link.springer.com/article/10.1007/s10499-020-00545-w
• Smith SK, Sutton DC, Fuerst JA, Reichelt JL (1991) Evaluation of the genus Listonella and reassignment of Listonella damsela (Love et al.) MacDonell and Colwell to the genus Photobacterium as Photobacterium damsela comb. nov. with an emended description. International Journal of Systematic and Evolutionary Microbiology, 41:529-534. https://doi.org/10.1099/00207713-41-4-529
• Sun X, Jin P, Liu Q, Wang Q, Zhang Y, Liu X. (2020) A CpG-riched plasmid as vaccine adjuvant reduce antigen dose of an inactivated Vibrio anguillarum vaccine in turbot (Scophthalmus maximus L.). Fish Shellfish immunology 98:312-317. http://doi.org/10.1016/j.fsi.2020.01.031
• Tanrıkul TT, Gultepe N (2011) Mix infections in rainbow trout (Oncorhynchus mykiss Walbaum): Lactococcus garvieae and Vibrio anguillarum O1. Journal of Animal and Veterinary Advances, 10:1019-1023. http://dx.doi.org/10.3923/javaa.2011.1019.1023
• Terceti MS, Vences A, Matanza XM, Barca AV, Noia M, Lisboa J, dos Santos NMS, do Vale A, Osorio CR (2019) The RstAB system impacts virulence, motility, cell morphology, penicillin tolerance and production of type II secretion system-dependent factors in the fish and human pathogen Photobacterium damselae subsp. damselae. Frontiers in Microbiology, 10:897. https://dx.doi.org/10.3389%2Ffmicb.2019.00897
• Thompson FL, Thompson CC, Dias GM, Naka H, Dubay C, Crosa JH (2011) The genus Listonella MacDonell and Colwell 1986 is a later heterotypic synonym of the genus Vibrio Pacini 1854 (Approved Lists 1980)–a taxonomic opinion. International Journal of Systematic and Evolutionary Microbiology, 61:3023. https://doi.org/10.1099/ijs.0.030015-0
• Touraki M, Karamanlidou G, Koziotis M, Christidis I (2013) Antibacterial effect of Lactococcus lactis subsp. lactis on Artemia franciscana nauplii and Dicentrarchus labrax larvae against the fish pathogen Vibrio anguillarum. Aquaculture International, 21:481-495. http://dx.doi.org/10.1007/s10499-012-9579-4
• Valderrama K, Balado M, Rey-Varela D, Rodríguez J, Vila-Sanjurjo A, Jiménez C, Lemos, ML (2019) Outer membrane protein FrpA, the siderophore piscibactin receptor of Photobacterium damselae subsp. piscicida, as a subunit vaccine against photobacteriosis in sole (Solea senegalensis). Fish Shellfish Immunology, 94:723-729. https://doi.org/10.1016/j.fsi.2019.09.066
• Vences A, Abushattal S, Matanza XM, Dubert J, Uzun E, Ogut H, Osorio CR (2020) Highly transferable pAQU-related plasmids encoding multidrug resistance are widespread in the human and fish pathogen Photobacterium damselae subsp. damselae in aquaculture areas in the Black Sea. Microbial Ecology, 80:507-518. https://doi.org/10.1007/s00248-020-01519-4
• Xie J, Mei H, Jin S, Bu L, Wang X, Wang C, Zhao Q, Ma R, Zhou S (2021) First report of Photobacterium damselae subsp. damselae infection in the mud crab Scylla paramamosain cultured in China. Aquaculture, 530:1-8. https://doi.org/10.1016/j.aquaculture.2020.735880
• Xing J, Jiang X, Xu H, Sheng X, Tang X, Chi H, Zhan W (2021) Local immune responses to VAA DNA vaccine against Listonella anguillarum in flounder (Paralichthys olivaceus). Molecular Immunology, 134:141-149. https://doi.org/10.1016/j.molimm.2021.03.012
• Yardımcı R, Turgay E, Steinum SK. (2020) Diagnosis of Photobacterium sanguinicancri in Smout-hound Shark (Mustelus mustelus, Linnaeus 1758). Acta Aquatica Turcica, 16:338-343. https://doi.org/10.22392/actaquatr.682155
• Yildiz FH, Visick KL (2009) Vibrio biofilms: so much the same yet so different. Trends in Microbiology, 17:109-118. https://doi.org/10.1016/j.tim.2008.12.004
• Zhang SD, Isbrandt T, Lindqvist LL, Larsen TO, Gram L (2021) Holomycin, an antibiotic secondary metabolite, is required for biofilm formation of the native producer Photobacterium galatheae S2753. Applied and Environmental Microbiology, 87:e00169-21. https://doi.org/10.1128/aem.00169-21
• Zhang Z, Yu YX, Wang K, Wang YG, Jiang Y, Liao MJ, Rong XJ (2019) First report of skin ulceration caused by Photobacterium damselae subsp. damselae in net-cage cultured black rockfish (Sebastes schlegeli). Aquaculture, 503: 1-7. https://doi.org/10.1016/j.aquaculture.2018.12.088