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Succession and Spread of Coral Diseases and Coral-Killing Sponges with Special Reference to Microbes in Southeast Asia and Adjacent Waters

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Coral Reefs of Eastern Asia under Anthropogenic Impacts

Part of the book series: Coral Reefs of the World ((CORW,volume 17))

Abstract

Corals and coral-associated organisms are threatened by repeated bleaching events and anthropogenic stresses, resulting in mass mortality and property loss (including foods, natural breakwater reefs, tourism resources, and landscapes). In addition to physical and chemical disturbances, the biological destruction caused by infectious diseases and encrusting/boring organisms exceeds our expectations. This chapter describes the present situation of coral diseases and coral-killing sponges in the region of Southeast Asia to East Asia. These areas maintain a wide array of coral reefs with highly diverse organisms, but there is limited information available compared to the Caribbean and Great Barrier Reef. Recent research focused on the pathological and microbiological perspectives of reefs in the Southeast Asian area are summarized in this chapter.

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References

  • Aeby G (2003) Corals in the genus Porites are susceptible to infection by a larval trematode. Coral Reefs 22:216–216

    Article  Google Scholar 

  • Aeby GS (2006) Baseline levels of coral disease in the Northwestern Hawaiian Islands. Atoll Res Bull 543:471–488

    Google Scholar 

  • Aini SN, Yamashiro H (2022) Densities of cyanobacterial cells, spicules, and particles in the coral-killing sponge Terpios hoshinota in Sesoko Island, Okinawa, Japan. Plankton Benthos Res 17:263–270

    Article  Google Scholar 

  • Aini SN, Tang S-L, Yamashiro H (2021) Monthly progression rates of the coral-killing sponge Terpios hoshinota in Sesoko Island, Okinawa, Japan. Coral Reefs 40:973–981

    Article  Google Scholar 

  • Ainsworth TD, Hoegh-Guldberg O (2008) Cellular processes of bleaching in the Mediterranean coral Oculina patagonica. Coral Reefs 27:593–597

    Article  Google Scholar 

  • Akmal KF, Shahbudin S (2020) Baseline assessment of coral health and disease in Tioman Island Marine Park, Malaysia. Community Ecol 21:285–301

    Article  Google Scholar 

  • Alvarado JJ, Grassian B, Cantera-Kintz JR, Carballo JL, Londoño-Cruz E (2017) Coral reef bioerosion in the Eastern Tropical Pacific. In: Glynn PW, Manzello DP, Enochs IC (eds) Coral reefs of the Eastern Tropical Pacific: persistence and loss in a dynamic environment. Springer, Dordrecht, pp 369–403

    Chapter  Google Scholar 

  • Anthony SL, Page CA, Bourne DG, Willis BL (2008) Newly characterized distinct phases of the coral disease ‘atramentous necrosis’ on the Great Barrier Reef. Dis Aquat Org 81:255–259

    Article  CAS  Google Scholar 

  • Antonius A (1973) New observations on coral destruction in reefs. Abs Assoc Isl Mar Lab Caribb 10:3

    Google Scholar 

  • Antonius A (1985) Coral diseases in the Indo-Pacific: a first record. Mar Ecol 6:197–218

    Article  Google Scholar 

  • Antonius A (1999) Halofolliculina corallasia, a new coral-killing ciliate on Indo-Pacific reefs. Coral Reefs 18:300

    Article  Google Scholar 

  • Arboleda M, Reichardt W (2009) Epizoic communities of prokaryotes on healthy and diseased scleractinian corals in Lingayen Gulf, Philippines. Microb Ecol 57:117–128

    Article  PubMed  Google Scholar 

  • Arboleda M, Reichardt W (2010) Vibrio sp. causing Porites ulcerative white spot disease. Dis Aquat Org 90:93–104

    Article  CAS  Google Scholar 

  • Arotsker L, Kushmaro A (2015) Vibriosis. In: Porter J, Woodley C (eds) Diseases of Coral. John Wiley & Sons, Ltd, pp 206–220

    Chapter  Google Scholar 

  • Arotsker L, Siboni N, Ben-Dov E, Kramarsky-Winter E, Loya Y, Kushmaro A (2009) Vibrio sp. as a potentially important member of the black band disease (BBD) consortium in Favia sp. corals. FEMS Microbiol Ecol 70:515–524

    Article  CAS  PubMed  Google Scholar 

  • Ashok AM, Schönberg CHL, Raj KD (2018) A sponge of the Cliona viridis complex invades and excavates corals of the Gulf of Mannar, south-eastern India. Mar Freshw Res 69:874–882

    Article  Google Scholar 

  • Ashok AM, Calcinai B, Edward JKP (2020) The coral-killing red sponge Clathria (Microciona) aceratoobtusa (Porifera: Demosponigiae) invades various coral communities of Gulf of Mannar Marine National Park, southeast India. European Zool J 87:1–11

    Article  Google Scholar 

  • Asoh K (2008) Loss of live tissue and exposure of coral skeleton in Porites cylindrica at Shiraho, Ishigaki Island, Japan. Galaxea J Coral Reef Stud 10:45–45

    Article  Google Scholar 

  • Ávila E, Carballo JL (2009) A preliminary assessment of the invasiveness of the Indo-Pacific sponge Chalinula nematifera on coral communities from the tropical Eastern Pacific. Biol Invasions 11:257–264

    Article  Google Scholar 

  • Bell JJ, Davy SK, Jones T, Taylor MW, Webster NS (2013) Could some coral reefs become sponge reefs as our climate changes? Glob Change Biol 19:2613–2624

    Article  Google Scholar 

  • Ben-Haim Y, Rosenberg E (2002) A novel Vibrio sp. pathogen of the coral Pocillopora damicornis. Mar Biol 141:47–55

    Article  Google Scholar 

  • Ben-Haim Y, Zicherman-Keren M (2003) Temperature-regulated bleaching and lysis of the coral Pocillopora damicornis by the novel pathogen Vibrio coralliilyticus. Appl Environ Microbiol 69:4236–4242

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Benzoni F, Calcinai B, Eisinger M, Klaus R (2008) Coral disease mimic: sponge attacks Porites lutea in Yemen. Coral Reefs 27:695–695

    Article  Google Scholar 

  • Beurmann S, Ushijima B, Videau P, Svoboda CM, Smith AM, Rivers OS, Aeby GS, Callahan SM (2017) Pseudoalteromonas piratica strain OCN003 is a coral pathogen that causes a switch from chronic to acute Montipora white syndrome in Montipora capitata. PLoS One 12:e0188319. https://doi.org/10.1371/journal.pone.0188319

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Biodiversity Center of Japan (2003) The annual report of the “Monitoring Sites 1000” in Japan: coral reefs. Biodiversity Center of Japan, Ministry of the Environment of Japan, Yamanashi

    Google Scholar 

  • Biodiversity Center of Japan (2004) The annual report of the “Monitoring Sites 1000” in Japan: coral reefs. Biodiversity Center of Japan, Ministry of the Environment of Japan, Japan. (in Japanese with English summary)

    Google Scholar 

  • Biodiversity Center of Japan (2013) The annual report of the “Monitoring Sites 1000” in Japan: coral reefs. Biodiversity Center of Japan, Ministry of the Environment of Japan, Yamanashi

    Google Scholar 

  • Biodiversity Center of Japan (2014) The annual report of the “Monitoring Sites 1000” in Japan: coral reefs. Biodiversity Center of Japan, Ministry of the Environment of Japan, Yamanashi

    Google Scholar 

  • Biodiversity Center of Japan (2015) The annual report of the “Monitoring Sites 1000” in Japan: coral reefs. Biodiversity Center of Japan, Ministry of the Environment of Japan, Yamanashi

    Google Scholar 

  • Biodiversity Center of Japan (2016) The annual report of the “Monitoring Sites 1000” in Japan: coral reefs. Biodiversity Center of Japan, Ministry of the Environment of Japan, Yamanashi

    Google Scholar 

  • Biodiversity Center of Japan (2017) The annual report of the “Monitoring Sites 1000” in Japan: coral reefs. Biodiversity Center of Japan, Ministry of the Environment of Japan, Yamanashi

    Google Scholar 

  • Biodiversity Center of Japan (2018) The annual report of the “Monitoring Sites 1000” in Japan: coral reefs. Biodiversity Center of Japan, Ministry of the Environment of Japan, Yamanashi

    Google Scholar 

  • Biodiversity Center of Japan (2019) The annual report of the “Monitoring Sites 1000” in Japan: coral reefs. Biodiversity Center of Japan, Ministry of the Environment of Japan, Yamanashi

    Google Scholar 

  • Biodiversity Center of Japan (2020) The annual report of the “Monitoring Sites 1000” in Japan: coral reefs. Biodiversity Center of Japan, Ministry of the Environment of Japan, Yamanashi

    Google Scholar 

  • Borneman E (2001) Aquarium corals: selection, husbandry, and natural history. T.F.H Publications, Inc

    Google Scholar 

  • Bourne D, Iida Y, Uthicke S, Smith-Keune C (2007) Changes in coral-associated microbial communities during a bleaching event. ISME J 2:350–363

    Article  PubMed  Google Scholar 

  • Bourne DG, Boyett HV, Henderson ME, Muirhead A, Willis BL (2008) Identification of a ciliate (Oligohymenophorea: Scuticociliatia) associated with brown band disease on corals of the Great Barrier Reef. Appl Environ Microbiol 74:883–888

    Article  CAS  PubMed  Google Scholar 

  • Bourne DG, Garren M, Work TM, Rosenberg E, Smith GW, Harvell CD (2009) Microbial disease and the coral holobiont. Trend Microbiol 17:554–562

    Article  CAS  Google Scholar 

  • Bourne DG, Ainsworth TD, Pollock FJ, Willis BL (2015) Towards a better understanding of white syndromes and their causes on Indo-Pacific coral reefs. Coral Reefs 34:233–242

    Article  Google Scholar 

  • Bourne DG, Morrow KM, Webster NS (2016) Insights into the coral microbiome: underpinning the health and resilience of reef ecosystems. Annu Rev Microbiol 70:317–340. https://doi.org/10.1146/annurev-micro-102215-095440

    Article  CAS  PubMed  Google Scholar 

  • Brown BE, Tissier MDA, Bythell JC (1995) Mechanisms of bleaching deduced from histological studies of reef corals sampled during a natural bleaching event. Mar Biol 122:655–663. https://doi.org/10.1007/BF00350687

    Article  Google Scholar 

  • Brownell AC, Richardson LL (2014) Sulfate reducing bacteria as secondary and necessary pathogens in black band disease of corals. Rev Biol Trop 62:249–257

    Google Scholar 

  • Bruno JF, Selig ER (2007) Regional decline of coral cover in the Indo-Pacific: timing, extent, and subregional comparisons. PLoS One 2:e711. https://doi.org/10.1371/journal.pone.0000711

    Article  PubMed  PubMed Central  Google Scholar 

  • Bruno JF, Selig ER, Casey KS, Page CA, Willis BL, Harvell CD, Sweatman H, Melendy AM (2007) Thermal stress and coral cover as drivers of coral disease outbreaks. PLoS Biol 5:e124. https://doi.org/10.1371/journal.pbio.0050124

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bruno JF, Côté IM, Toth LT (2019) Climate change, coral loss, and the curious case of the parrotfish paradigm: why don’t marine protected areas improve reef resilience? Annu Rev Mar Sci 11:307–334

    Article  Google Scholar 

  • Bryan PG (1973) Growth rate, toxicity, and distribution of the encrusting sponge Terpios sp. (Hadromerida: Suberitidae) in Guam, Mariana Islands. Micronesica 9:237–242

    Google Scholar 

  • Buerger P, Alvarez-Roa C, Weynberg KD, Baekelandt S, van Oppen MJH (2016) Genetic, morphological and growth characterisation of a new Roseofilum strain (Oscillatoriales, Cyanobacteria) associated with coral black band disease. PeerJ 4:e2110. https://doi.org/10.7717/peerj.2110

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Carballo JL, Bautista E, Nava H, Cruz-Barraza JA, Chávez JA (2013) Boring sponges, an increasing threat for coral reefs affected by bleaching events. Ecol Evol 3:872–886

    Article  PubMed  PubMed Central  Google Scholar 

  • Carlton RG, Richardson LL (1995) Oxygen and sulfide dynamics in a horizontally migrating cyanobacterial mat: black band disease of corals. FEMS Microbiol Ecol 18:155–162

    Article  CAS  Google Scholar 

  • Carpenter KE, Abrar M, Aeby G, Aronson RB, Banks S, Bruckner A, Chiriboga A, Cortés J, Delbeek JC, DeVantier L, Edgar GJ, Edwards AJ, Fenner D, Guzmán HM, Hoeksema BW, Hodgson G, Johan O, Licuanan WY, Livingstone SR, Lovell ER, Moore JA, Obura DO, Ochavillo D, Polidoro BA, Precht WF, Quibilan MC, Reboton C, Richards ZT, Rogers AD, Sanciangco J, Sheppard A, Sheppard C, Smith J, Stuart S, Turak E, Veron JEN, Wallace C, Weil E, Wood E (2008) One-third of reef-building corals face elevated extinction risk from climate change and local impacts. Science 321:560–563

    Article  CAS  PubMed  Google Scholar 

  • Casamatta D, Stanić D, Gantar M, Richardson LL (2012) Characterization of Roseofilum reptotaenium (Oscillatoriales, Cyanobacteria) gen. et sp. nov. isolated from Caribbean black band disease. Phycologia 51:489–499

    Article  Google Scholar 

  • Cervino JM, Thompson FL, Gomez-Gil B, Lorence EA, Goreau TJ, Hayes RL, Winiarski-Cervino KB, Smith GW, Hughen K, Bartels E (2008) The Vibrio core group induces yellow band disease in Caribbean and Indo-Pacific reef-building corals. J Appl Microbiol 105:1658–1671

    Article  CAS  PubMed  Google Scholar 

  • Chen Y-H, Chen H-J, Yang C-Y, Shiu J-H, Hoh DZ, Chiang P-W, Chow WS, Chen CA, Shih T-H, Lin S-H, Yang C-M, Reimer JD, Hirose E, Iskandar BH, Huang H, Schupp PJ, Tan CHJ, Yamashiro H, Liao M-H, Tang S-L (2021) Prevalence, complete genome, and metabolic potentials of a phylogenetically novel cyanobacterial symbiont in the coral-killing sponge, Terpios hoshinota. Environ Microbiol 24:1308–1325

    Article  PubMed  PubMed Central  Google Scholar 

  • Chiu JMY, Li S, Li A, Po B, Zhang R, Shin PKS, Qiu J-W (2012) Bacteria associated with skeletal tissue growth anomalies in the coral Platygyra carnosus. FEMS Microbiol Ecol 79:380–391

    Article  CAS  PubMed  Google Scholar 

  • Coles SL, Bolick H (2007) Invasive introduced sponge Mycale grandis overgrows reef corals in Kāne‘ohe Bay, O‘ahu, Hawai‘i. Coral Reefs 26:911–911

    Article  Google Scholar 

  • de Laubenfels M (1954) The sponges of the West-Central Pacific. Oregon State Monogr Stud Zool 7:1–306

    Google Scholar 

  • de Voogd NJ, Cleary DFR, Dekker F (2013) The coral-killing sponge Terpios hoshinota invades Indonesia. Coral Reefs 32:755. https://doi.org/10.1007/s00338-013-1030-4

    Article  Google Scholar 

  • Ding J-Y, Shiu J-H, Chen W-M, Chiang Y-R, Tang S-L (2016) Genomic insight into the host–endosymbiont relationship of Endozoicomonas montiporae CL-33T with its coral host. Front Microbiol 7:251. https://doi.org/10.3389/fmicb.2016.00251

    Article  PubMed  PubMed Central  Google Scholar 

  • Ekins M, Willis B, Bridge T, Srinivasan M, Rowley S, Hooper JNA (2017) The coral killing sponge Terpios hoshinota in Kimbe Bay, Papua New Guinea. Mem Queensl Mus Nat 60:174–175

    Article  Google Scholar 

  • Elliott J, Patterson M, Vitry E, Summers N, Miternique C (2016) Morphological plasticity allows coral to actively overgrow the aggressive sponge Terpios hoshinota (Mauritius, Southwestern Indian Ocean). Mar Biodivers 46:489–493

    Article  Google Scholar 

  • Fromont J, Richards ZT, Wilson NG (2019) First report of the coral-killing sponge Terpios hoshinota Rützler and Muzik, 1993 in Western Australia: A new threat to Kimberley coral reefs? Diversity 11:184. https://doi.org/10.3390/d11100184

    Article  Google Scholar 

  • Fujii T, Keshavmurthy S, Zhou W, Hirose E, Chen CA, Reimer JD (2011) Coral-killing cyanobacteriosponge (Terpios hoshinota) on the Great Barrier Reef. Coral Reefs 30:483. https://doi.org/10.1007/s00338-011-0734-6

    Article  Google Scholar 

  • Garren M, Raymundo L, Guest J, Harvell CD, Azam F (2009) Resilience of coral-associated bacterial communities exposed to fish farm effluent. PLoS One 4:e7319. https://doi.org/10.1371/journal.pone.0007319

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Garren M, Son K, Raina J-B, Rusconi R, Menolascina F, Shapiro OH, Tout J, Bourne DG, Seymour JR, Stocker R (2014) A bacterial pathogen uses dimethylsulfoniopropionate as a cue to target heat-stressed corals. ISME J 8:999–1007

    Article  CAS  PubMed  Google Scholar 

  • Garren M, Son K, Tout J, Seymour JR, Stocker R (2016) Temperature-induced behavioral switches in a bacterial coral pathogen. ISME J 10:1363–1372

    Article  CAS  PubMed  Google Scholar 

  • Geiser DM, Taylor JW, Ritchie KB (1998) Cause of sea fan death in the West Indies. Nature 394:137–138

    Article  CAS  Google Scholar 

  • Gignoux-Wolfsohn SA, Aronson FM, Vollmer SV (2017) Complex interactions between potentially pathogenic, opportunistic, and resident bacteria emerge during infection on a reef-building coral. FEMS Microbiol Ecol 93:7

    Article  Google Scholar 

  • Glas MS, Sato Y, Ulstrup KE, Bourne DG (2012) Biogeochemical conditions determine virulence of black band disease in corals. ISME J 6:1526–1534

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Glynn PW, Manzello DP (2015) Bioerosion and coral reef growth: a dynamic balance. In: Birkeland C (ed) Coral reefs in the anthropocene. Springer, pp 67–97

    Chapter  Google Scholar 

  • Guerra M, López MA, Estéves I, Zubillaga AL, Cróquer A (2014) Fourier-transformed infrared spectroscopy: a tool to identify gross chemical changes from healthy to yellow band disease tissues. Dis Aquat Org 107:249–258

    Article  CAS  Google Scholar 

  • Haapkylä J, Unsworth R, Seymour A, Melbourne-Thomas J, Flavell M, Willis B, Smith D (2009) Spatio-temporal coral disease dynamics in the Wakatobi Marine National Park, South-East Sulawesi, Indonesia. Dis Aquat Org 87:105–115

    Article  Google Scholar 

  • Harvell CD, Kim K, Burkholder JM, Colwell RR, Epstein PR, Grimes DJ, Hofmann EE, Lipp EK, Osterhaus ADME, Overstreet RM, Porter JW, Smith GW, Vasta GR (1999) Emerging marine diseases - climate links and anthropogenic factors. Science 285:1505–1510

    Article  CAS  PubMed  Google Scholar 

  • Harvell CD, Mitchell CE, Ward JR, Altizer S, Dobson AP, Ostfeld RS, Samuel MD (2002) Climate warming and disease risks for terrestrial and marine biota. Science 296:2158–2162

    Article  CAS  PubMed  Google Scholar 

  • Hatch WI (1980) The implication of carbonic anhydrase in the physiological mechanism of penetration of carbonate substrata by the marine burrowing sponge Cliona celata (demospongiae). Biol Bull 159:135–147

    Article  CAS  Google Scholar 

  • Higuchi T, Agostini S, Casareto BE, Yoshinaga K, Suzuki T, Nakano Y, Fujimura H, Suzuki Y (2013) Bacterial enhancement of bleaching and physiological impacts on the coral Montipora digitata. J Exp Mar Biol Ecol 440:54–60

    Article  Google Scholar 

  • Hirose E, Murakami A (2011) Microscopic anatomy and pigment characterization of coral-encrusting black sponge with cyanobacterial symbiont, Terpios hoshinota. Zool Sci 28:199–205

    Article  Google Scholar 

  • Hirose Y, Aini SN, Yamashiro H (2021) Contact reactions between individuals of the coral-killing sponge Terpios hoshinota. Zool Stud 60:41

    Google Scholar 

  • Hirose Y, Aini SN, Yamashiro H (2022) Coral-killing sponge Terpios hoshinota releases larvae at midnight. Coral Reefs 41:149–160

    Article  Google Scholar 

  • Hoegh-Guldberg O, Mumby PJ, Hooten AJ, Steneck RS, Greenfield P, Gomez E, Harvell CD, Sale PF, Edwards AJ, Caldeira K, Knowlton N, Eakin CM, Iglesias-Prieto R, Muthiga N, Bradbury RH, Dubi A, Hatziolos ME (2007) Coral reefs under rapid climate change and ocean acidification. Science 318:1737–1742

    Article  CAS  PubMed  Google Scholar 

  • Hoeksema BW, Waheed Z, de Voogd NJ (2014) Partial mortality in corals overgrown by the sponge Terpios hoshinota at Tioman Island, Peninsular Malaysia (South China Sea). Bull Mar Sci 90:989–990. https://doi.org/10.5343/bms.2014.1047

    Article  Google Scholar 

  • Hong M-J, Yu Y-T, Chen CA, Chiang P-W, Tang S-L (2009) Influence of species specificity and other factors on bacteria associated with the coral Stylophora pistillata in Taiwan. Appl Environ Microbiol 75:7797–7806

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Hsu C-M, Wang J-T, Chen CA (2013) Larval release and rapid settlement of the coral-killing sponge, Terpios hoshinota, at Green Island. Taiwan. Mar Biodiv 43:259–260. https://doi.org/10.1007/s12526-013-0176-1

    Article  Google Scholar 

  • Huang YM, de Voogd NJ, Cleary DFR, Li T-H, Mok H-K, Ueng J-P (2015) Biodiversity pattern of subtidal sponges (Porifera: Demospongiae) in the Penghu Archipelago (Pescadores), Taiwan. J Mar Biol Assoc U K 96:417–427

    Article  CAS  Google Scholar 

  • Huang C-Y, Hwang J-S, Yamashiro H, Tang S-L (2021) Spatial and cross-seasonal patterns of coral diseases in reefs of Taiwan: high prevalence and regional variation. Dis Aquat Org 146:145–156

    Article  Google Scholar 

  • Hughes TP, Baird AH, Bellwood DR, Card M, Connolly SR, Folke C, Grosberg R, Hoegh-Guldberg O, Jackson JBC, Kleypas J, Lough JM, Marshall P, Nyström M, Palumbi SR, Pandolfi JM, Rosen B, Roughgarden J (2003) Climate change, human impacts, and the resilience of coral reefs. Science 301:929–933

    Article  CAS  PubMed  Google Scholar 

  • Hughes TP, Kerry JT, Álvarez-Noriega M, Álvarez-Romero JG, Anderson KD, Baird AH, Babcock RC, Beger M, Bellwood DR, Berkelmans R, Bridge TC, Butler IR, Byrne M, Cantin NE, Comeau S, Connolly SR, Cumming GS, Dalton SJ, Diaz-Pulido G, Eakin CM, Figueira WF, Gilmour JP, Harrison HB, Heron SF, Hoey AS, Hobbs J-PA, Hoogenboom MO, Kennedy EV, Kuo C, Lough JM, Lowe RJ, Liu G, McCulloch MT, Malcolm HA, McWilliam MJ, Pandolfi JM, Pears RJ, Pratchett MS, Schoepf V, Simpson T, Skirving WJ, Sommer B, Torda G, Wachenfeld DR, Willis BL, Wilson SK (2017) Global warming and recurrent mass bleaching of corals. Nature 543:373–377

    Article  CAS  PubMed  Google Scholar 

  • Hutabarat PUB, Nguyen XH, Suda S (2018) Black band disease-related (BBD) cyanobacterium from Okinawan corals. J Appl Phycol 30:3197–3203

    Article  CAS  Google Scholar 

  • IPCC (2021) Climate Change 2021: the physical science basis, The Working Group I. https://www.ipcc.ch/assessment-report/ar6/

  • Irikawa A, Casareto BE, Suzuki Y, Agostini S, Hidaka M, van Woesik R (2011) Growth anomalies on Acropora cytherea corals. Mar Pollut Bull 62:1702–1707

    Article  CAS  PubMed  Google Scholar 

  • Johan O, Bengen DG, Zamani NP, Suharsono SMJ (2015) The distribution and abundance of black band disease and white syndrome in Kepulauan Seribu, Indonesia. HAYATI J Biosci 22:105–112. https://doi.org/10.1016/j.hjb.2015.09.001

    Article  Google Scholar 

  • Jones RJ, Bowyer J, Hoegh-Guldberg O, Blackall LL (2004) Dynamics of a temperature-related coral disease outbreak. Mar Ecol Prog Ser 281:63–77

    Article  Google Scholar 

  • Kaczmarsky LT (2006) Coral disease dynamics in the central Philippines. Dis Aqat Org 69:9–21. https://doi.org/10.3354/dao069009

    Article  Google Scholar 

  • Kaczmarsky L, Richardson LL (2007) Transmission of growth anomalies between Indo-Pacific Porites corals. J Invertebr Pathol 94:218–221

    Article  PubMed  Google Scholar 

  • Kaczmarsky LT, Draud M, Williams EH (2005) Is there a relationship between proximity to sewage effluent and the prevalence of coral disease. Caribb J Sci 41:124–137

    Google Scholar 

  • Kawamura K, Nishitsuji K, Shoguchi E, Fujiwara S, Satoh N (2021) Establishing sustainable cell lines of a coral, Acropora tenuis. Mar Biotechnol 23:373–388

    Article  CAS  Google Scholar 

  • Kelly M, Bell LJ, Herr B (2016) Splendid sponges of Palau. NIWA

    Google Scholar 

  • Kim I-H, Yamashiro H (2007) Two species of poecilostomatoid copepods inhabiting galls on scleractinian corals in Okinawa, Japan. J Crustac Biol 27:319–326

    Article  Google Scholar 

  • Kimes NE, Grim CJ, Johnson WR et al (2012) Temperature regulation of virulence factors in the pathogen Vibrio coralliilyticus. ISME J 6:835–846

    Article  CAS  PubMed  Google Scholar 

  • Kitamura R, Miura N, Ito M, Hasan NA, Tall BD, Kothary MH, Kiss H, Munk AC, Tapia R, Green L, Detter C, Bruce DC, Brettin TS, Colwell RR, Morris PJ (2021) Specific Detection of coral-associated Ruegeria, a potential probiotic bacterium, in corals and subtropical seawater. Mar Biotechnol 23:576–589

    Article  CAS  Google Scholar 

  • Koren O, Rosenberg E (2006) Bacteria associated with mucus and tissues of the coral Oculina patagonica in summer and winter. Appl Environ Microbiol 72:5254–5259

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kubomura T, Yamashiro H, Reimer JD (2018) Appearance of an anomalous black band disease at upper mesophotic depths after coral bleaching. Dis Aquat Org 131:245–250

    Article  Google Scholar 

  • Kubomura T, Wee HB, Reimer JD (2021) Investigating incidence and possible causes of pink and purple pigmentation response in hard coral genus Porites around Okinawajima Island, Japan. Reg Stud Mar Sci 41:101569

    Google Scholar 

  • Kushmaro A, Loya Y, Fine M, Rosenberg E (1996) Bacterial infection and coral bleaching. Nature 380:396

    Article  CAS  Google Scholar 

  • Kushmaro A, Rosenberg E, Fine M, Loya Y (1997) Bleaching of the coral Oculina patagonica by Vibrio AK-1. Mar Ecol Prog Ser 147:159–165

    Article  Google Scholar 

  • Kuta K, Richardson L (1997) Black band disease and the fate of diseased coral colonies in the Florida Keys. In: Proc 8th Int Coral Reef Symp. pp. 575–578

    Google Scholar 

  • Kuta K, Richardson L (2002) Ecological aspects of black band disease of corals: relationships between disease incidence and environmental factors. Coral Reefs 21:393–398

    Article  Google Scholar 

  • Kvennefors ECE, Sampayo E, Ridgway T, Barnes AC, Hoegh-Guldberg O (2010) Bacterial communities of two ubiquitous Great Barrier Reef corals reveals both site- and species-specificity of common bacterial associates. PLoS One 5:e10401. https://doi.org/10.1371/journal.pone.0010401

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lamb JB, Willis BL (2011) Using coral disease prevalence to assess the effects of concentrating tourism activities on offshore reefs in a tropical marine park. Conserv Biol 25:1044–1052

    Article  PubMed  Google Scholar 

  • Lamb JB, Water JAJM v d, Bourne DG, Altier C, Hein MY, Fiorenza EA, Abu N, Jompa J, Harvell CD (2017) Seagrass ecosystems reduce exposure to bacterial pathogens of humans, fishes, and invertebrates. Science 355:731–733

    Article  CAS  PubMed  Google Scholar 

  • Li H, Zhang X, Long H, Hu C, Zhou Y, Wang S, Ke S, Xie Z (2018) Vibrio alginolyticus 16S-23S intergenic spacer region analysis, and PCR assay for identification of coral pathogenic strain XSBZ03. Dis Aquat Org 129:71–83

    Article  CAS  Google Scholar 

  • Lobban CS, Raymundo LM, Montagnes DJS (2011) Porpostoma guamensis n. sp., a philasterine scuticociliate associated with brown-band disease of corals. J Eukaryot Microbiol 58:103–113

    Article  PubMed  Google Scholar 

  • Luna GM, Biavasco F, Danovaro R (2007) Bacteria associated with the rapid tissue necrosis of stony corals. Environ Microbiol 9:1851–1857

    Article  CAS  PubMed  Google Scholar 

  • Luna GM, Bongiorni L, Gili C, Biavasco F, Danovaro R (2010) Vibrio harveyi as a causative agent of the white syndrome in tropical stony corals. Environ Microbiol Rep 2:120–127

    Article  PubMed  Google Scholar 

  • Mera H, Bourne DG (2018) Disentangling causation: complex roles of coral-associated microorganisms in disease. Environ Microbiol 20:431–449

    Article  PubMed  Google Scholar 

  • Meyer JL, Paul VJ, Teplitski M (2014) Community shifts in the surface microbiomes of the coral Porites astreoides with unusual lesions. PLoS One 9:e100316. https://doi.org/10.1371/journal.pone.0100316

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Mills E, Shechtman K, Loya Y, Rosenberg E (2013) Bacteria appear to play important roles in both causing and preventing the bleaching of the coral Oculina patagonica. Mar Ecol Prog Ser 489:155–162

    Article  Google Scholar 

  • Miura N, Motone K, Takagi T, Aburaya S, Watanabe S, Aoki W, Ueda M (2019) Ruegeria sp. strains isolated from the reef-building coral Galaxea fascicularis inhibit growth of the temperature-dependent pathogen Vibrio coralliilyticus. Mar Biotechnol 21:1–8

    Article  CAS  Google Scholar 

  • Montano S, Chou WH, Chen CA, Galli P, Reimer JD (2015) First record of the coral-killing sponge Terpios hoshinota in the Maldives and Indian Ocean. Bull Mar Sci 91:97–98. https://doi.org/10.5343/bms.2014.1054

    Article  Google Scholar 

  • Moriarty T, Leggat W, Huggett MJ, Ainsworth TD (2020) Coral disease causes, consequences, and risk within coral restoration. Trends Microbiol 28:793–807

    Article  CAS  PubMed  Google Scholar 

  • Muller EM, Raymundo LJ, Willis BL, Haapkylä J, Yusuf S, WilsonJR HDC (2012) Coral Health and Disease in the Spermonde Archipelago and Wakatobi, Sulawesi. J Indonesia Coral Reefs 1:147–159

    Google Scholar 

  • Mumby PJ, Steneck RS (2008) Coral reef management and conservation in light of rapidly evolving ecological paradigms. Trends Ecol Evol 23:555–563

    Article  PubMed  Google Scholar 

  • Muscatine LR, McCloskey LE, Marian R (1981) Estimating the daily contribution of carbon from zooxanthellae to coral animal respiration. Limnol Oceanogr 26:601–611

    Article  CAS  Google Scholar 

  • Myers R, Raymundo L (2009) Coral disease in micronesian reefs: a link between disease prevalence and host abundance. Dis Aquat Org 87:97–104

    Article  Google Scholar 

  • Ng JCY, Chan Y, Tun HM, Leung FCC, Shin PKS, Chiu JMY (2015) Pyrosequencing of the bacteria associated with Platygyra carnosus corals with skeletal growth anomalies reveals differences in bacterial community composition in apparently healthy and diseased tissues. Front Microbiol 6:1142. https://doi.org/10.3389/fmicb.2015.01142

    Article  PubMed  PubMed Central  Google Scholar 

  • Nicolet KJ, Chong-Seng KM, Pratchett MS, Willis BL, Hoogenboom MO (2018) Predation scars may influence host susceptibility to pathogens: evaluating the role of corallivores as vectors of coral disease. Sci Rep 8:5258. https://doi.org/10.1038/s41598-018-23361-y

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Nozawa Y, Huang Y-S, Hirose E (2016) Seasonality and lunar periodicity in the sexual reproduction of the coral-killing sponge, Terpios hoshinota. Coral Reefs 35:1071–1081

    Article  Google Scholar 

  • Nugues MM, Smith GW, Hooidonk RJ, Seabra MI, Bak RPM (2004) Algal contact as a trigger for coral disease. Ecol Lett 7:919–923

    Article  Google Scholar 

  • Olson ND, Ainsworth TD, Gates RD, Takabayashi M (2009) Diazotrophic bacteria associated with Hawaiian Montipora corals: diversity and abundance in correlation with symbiotic dinoflagellates. J Exp Mar Biol Ecol 371:140–146

    Article  CAS  Google Scholar 

  • Page CA, Baker DM, Harvell CD, Golbuu Y (2009) Influence of marine reserves on coral disease prevalence. Dis Aquat Org 87:135–150. https://doi.org/10.3354/dao02112

  • Palmer C, Roth M, Gates R (2009) Red fluorescent protein responsible for pigmentation in trematode-infected Porites compressa tissues. Biol Bull 216:68–74

    Article  CAS  PubMed  Google Scholar 

  • Patterson KL, Porter JW, Ritche KB, Polson SW, Mueller E, Peters EC, Santavy DL, Smith GW (2002) The etiology of white pox, a lethal disease of the Caribbean elkhorn coral, Acropora palmata. Proc Natl Acad Sci U S A 99:8725–8730

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Plucer-Rosario G (1987) The effect of substratum on the growth of Terpios, an encrusting sponge which kills corals. Coral Reefs 5:197–200

    Article  Google Scholar 

  • Pollock FJ, Lamb JB, Field SN, Heron SF, Schaffelke B, Shedrawi G, Bourne DG, Willis BL (2016) Correction: sediment and turbidity associated with offshore dredging increase coral disease prevalence on Nearby Reefs. PLoS One 11:e0165541. https://doi.org/10.1371/journal.pone.0165541

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Pollock FJ, Wada N, Torda G, Willis BL, Bourne DG (2017) White syndrome-affected corals have a distinct microbiome at disease lesion fronts. Appl Environ Microbiol 83:e02799–e02716. https://doi.org/10.1128/AEM.02799-16

    Article  PubMed  Google Scholar 

  • Quang TM (2020) Morphology, abundance and the invasiveness of coral-killing sponge Chalinula nematifera (Porifera: Demosponigiae) from Con Dao National Park, Vietnam. Vietnam J Mar Sci Technol 20:95–103

    Article  Google Scholar 

  • Randall CJ, Jordán-Garza AG, van Woesik R (2015) Ciliates associated with signs of disease on two Caribbean corals. Coral Reefs 34:243–247

    Article  Google Scholar 

  • Rasoulouniriana D, Siboni N, Ben-Dov E, Kramarsky-Winter E, Loya Y, Kushmaro T (2009) Pseudoscillatoria coralii gen. nov., sp. nov., a cyanobacterium associated with coral black band disease (BBD). Dis Aquat Org 87:91–96

    Article  CAS  Google Scholar 

  • Raymundo LJ, Weil E (2015) Indo-Pacific colored-band diseases of corals. In: Porter J, Woodley C (eds) Diseases of coral. John Wiley & Sons, Ltd, pp 333–344

    Chapter  Google Scholar 

  • Raymundo LJH, Harvell CD, Reynolds TL (2003) Porites ulcerative white spot disease: description, prevalence, and host range of a new coral disease affecting Indo-Pacific reefs. Dis Aquat Org 56:95–104

    Article  Google Scholar 

  • Reimer JD, Nozawa Y, Hirose E (2010) Domination and disappearance of the black sponge: a quarter century after the initial Terpios outbreak in southern Japan. Zool Stud 50:394

    Google Scholar 

  • Reimer JD, Mizuyama M, Nakano M, Fujii T, Hirose E (2011) Current status of the distribution of the coral-encrusting cyanobacteriosponge Terpios hoshinota in southern Japan. Galaxea J Coral Reef Stud 13:35–44. https://doi.org/10.3755/galaxea.13.35

    Article  Google Scholar 

  • Reimer JD, Fourreau CJL, Fujii T, Ise Y, Kushida Y, Mizukami I, Nakano M (2022) Records and distribution of the coral-killing sponge Chalinula nematifera in the Ryukyu Islands, Japan. Plankton Benthos Res 17:249–254

    Article  Google Scholar 

  • Reshef L, Koren O, Loya Y, Zilber-Rosenberg I, Rosenberg E (2006) The coral probiotic hypothesis. Environ Microbiol 8:2068–2073

    Article  CAS  PubMed  Google Scholar 

  • Richardson LL (1998) Coral diseases: what is really known? Trends Ecol Evol 13:438–443

    Article  CAS  PubMed  Google Scholar 

  • Ritchie KB (2006) Regulation of microbial populations by coral surface mucus and mucus-associated bacteria. Mar Ecol Prog Ser 322:1–14

    Article  CAS  Google Scholar 

  • Roder C, Arif C, Bayer T, Aranda M, Daniels C, Shibl A, Chavanich S, Voolstra CR (2014) Bacterial profiling of white plague disease in a comparative coral species framework. ISME J 8:31–39

    Article  CAS  PubMed  Google Scholar 

  • Rodríguez S, Cróquer A (2008) Dynamics of black band disease in a Diploria strigosa population subjected to annual upwelling on the northeastern coast of Venezuela. Coral Reefs 27:381–388

    Article  Google Scholar 

  • Rohwer F, Seguritan V, Azam F, Knowlton N (2002) Diversity and distribution of coral-associated bacteria. Mar Ecol Prog Ser 243:1–10

    Article  Google Scholar 

  • Rossi G, Montori S, Cerrano C, Calcinai B (2015) The coral killing sponge Chalinula nematifera (Porifera: Haplosclerida) along the eastern coast of Sulawesi Island (Indonesia). Ital J Zool 82:143–148

    Article  Google Scholar 

  • Rubio-Portillo E, Martin-Cuadrado AB, Caraballo-Rodríguez AM, Rohwer F, Dorrestein PC, Antón J (2020) Virulence as a side effect of interspecies interaction in Vibrio coral pathogens. mBio 11:e00201–e00220. https://doi.org/10.1128/mBio.00201-20

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Rützler K, Muzik K (1993) Terpios hoshinota, a new cyanobacteriosponge threatening Pacific reefs. Sci Mar 57:395–403

    Google Scholar 

  • Rützler K, Rieger G (1973) Sponge burrowing: fine structure of Cliona lampa penetrating calcareous substrata. Mar Biol 21:144–162

    Article  Google Scholar 

  • Sato Y, Bourne DG, Willis BL (2009) Dynamics of seasonal outbreaks of black band disease in an assemblage of Montipora species at Pelorus Island (Great Barrier Reef, Australia). Proc R Soc B 276:2795–2803. https://doi.org/10.1098/rspb.2009.0481

    Article  PubMed  PubMed Central  Google Scholar 

  • Sato Y, Willis BL, Bourne DG (2010) Successional changes in bacterial communities during the development of black band disease on the reef coral, Montipora hispida. ISME J 4:203–214

    Article  PubMed  Google Scholar 

  • Sato Y, Civiello M, Bell SC, Willis BL, Bourne DG (2016) Integrated approach to understanding the onset and pathogenesis of black band disease in corals. Environ Microbiol 18:752–765

    Article  CAS  PubMed  Google Scholar 

  • Séré MG, Tortosa P, Chabanet P, Quod J-P, Sweet MJ, Schleyer MH (2015) Identification of a bacterial pathogen associated with Porites white patch syndrome in the Western Indian Ocean. Mol Ecol 24:4570–4581

    Article  PubMed  Google Scholar 

  • Shi Q, Liu GH, Yan HQ, Zhang HL (2012) Black disease (Terpios hoshinota): a probable cause for the rapid coral mortality at the northern reef of Yongxing Island in the South China Sea. Ambio 41:446–455. https://doi.org/10.1007/s13280-011-0245-2

    Article  PubMed  PubMed Central  Google Scholar 

  • Shiu J-H, Keshavmurthy S, Chiang P-W, Chen H-J, Lou S-P, Tseng C-H, Hsieh HJ, Chen CA, Tang S-L (2017) Dynamics of coral-associated bacterial communities acclimated to temperature stress based on recent thermal history. Sci Rep 7:14933. https://doi.org/10.1038/s41598-017-14927-3

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Squires DF (1965) Neoplasia in a coral? Science 148:503–505

    Article  CAS  PubMed  Google Scholar 

  • Subhan B, Arafat D, Rahmawati F, Dasmasela YH, Royhan QM, Madduppa H, Santoso P, Prabowo B (2020) Coral disease at Mansuar Island, Raja Ampat, Indonesia. IOP Conf Ser Earth Environ Sci 429:012027. https://doi.org/10.1088/1755-1315/429/1/012027

    Article  Google Scholar 

  • Sussman M, Loya Y, Fine M, Rosenberg E (2003) The marine fireworm Hermodice carunculata is a winter reservoir and spring-summer vector for the coral-bleaching pathogen Vibrio shiloi. Environ Microbiol 5:250–255

    Article  PubMed  Google Scholar 

  • Sussman M, Bourne DG, Willis BL (2006) A single cyanobacterial ribotype is associated with both red and black bands on diseased corals from Palau. Dis Aquat Org 69:111–118

    Article  Google Scholar 

  • Sussman M, Willis BL, Victor S, Bourne DG (2008) Coral pathogens identified for white syndrome (WS) epizootics in the Indo-Pacific. PLoS One 3:e2393. https://doi.org/10.1371/journal.pone.0002393

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sussman M, Mieog J, Doyle J, Victor S (2009) Vibrio zinc-metalloprotease causes photoinactivation of coral endosymbionts and coral tissue lesions. PLoS One 4:e4511. https://doi.org/10.1371/journal.pone.0004511

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sutherland K, Porter J, Torres C (2004) Disease and immunity in Caribbean and Indo-Pacific zooxanthellate corals. Mar Ecol Prog Ser 266:273–302

    Article  Google Scholar 

  • Sutherland KP, Berry B, Park A, Kemp DW, Kemp KM, Lipp EK, Porter JW (2016) Shifting white pox aetiologies affecting Acropora palmata in the Florida Keys, 1994–2014. Philos Trans R Soc B Biol Sci 371:20150205. https://doi.org/10.1098/rstb.2015.0205

    Article  CAS  Google Scholar 

  • Syue S-T, Hsu C-H, Soong K (2021) Testing of how and why the Terpios hoshinota sponge kills stony corals. Sci Rep 11:7661. https://doi.org/10.1038/s41598-021-87350-4

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Takagi T, Yoshioka Y, Zayasu Y, Satoh N, Shinzato C (2020) Transcriptome analyses of immune system behaviors in primary polyp of coral Acropora digitifera exposed to the bacterial pathogen Vibrio coralliilyticus under thermal loading. Mar Biotechnol 22:748–759. https://doi.org/10.1007/s10126-020-09984-1

    Article  CAS  Google Scholar 

  • Tandon K, Lu C-Y, Chiang P-W, Wada N, Yang S-H, Chan Y-F, Chen P-Y, Chang H-Y, Chiou Y-J, Chou M-S, Chen W-M, Tang S-L (2020) Comparative genomics: dominant coral-bacterium Endozoicomonas acroporae metabolizes dimethylsulfoniopropionate (DMSP). ISME J 14:1290–1303

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Tang S-L, Hong M, Liao M, Jane W, Chiang P, Chen C, Chen CA (2011) Bacteria associated with an encrusting sponge (Terpios hoshinota) and the corals partially covered by the sponge. Environ Microbiol 13:1179–1191

    Article  PubMed  Google Scholar 

  • Tang K, Zhan W, Zhou Y, Xu T, Chen X, Wang W, Zeng Z, Wang Y, Wang X (2020) Antagonism between coral pathogen Vibrio coralliilyticus and other bacteria in the gastric cavity of scleractinian coral Galaxea fascicularis. Sci China Earth Sci 63:157–166

    Article  CAS  Google Scholar 

  • Teplitski M, Krediet CJ, Meyer JL, Ritchie KB (2016) Microbial interactions on coral surfaces and within the coral holobiont. In: Goffredo S, Dubinsky Z (eds) The cnidaria, past, present and future: the world of medusa and her sisters. Springer, Cham, pp 331–346

    Chapter  Google Scholar 

  • Thinesh T, Meenatchi R, Pasiyappazham JPA, Selvan M, Kiran GS, Selvin J (2017) Short-term in situ shading effectively mitigates linear progression of coral-killing sponge Terpios hoshinota. PLoS One 12:e0182365. https://doi.org/10.1371/journal.pone.0182365

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Thompson FL, Barash Y, Sawabe T, Sharon G, Swings J, Rosenberg E (2006) Thalassomonas loyana sp. nov., a causative agent of the white plague-like disease of corals on the Eilat coral reef. Int J Syst Evol Microbiol 56:365–368

    Article  CAS  PubMed  Google Scholar 

  • Turicchia E, Hoeksema BW, Ponti M (2018) The coral-killing sponge Chalinula nematifera as a common substrate generalist in Komodo National Park, Indonesia. Mar Biol Res 14:827–833

    Article  Google Scholar 

  • Ushijima B, Smith A, Aeby GS, Callahan SM (2012) Vibrio owensii induces the tissue loss disease Montipora white syndrome in the Hawaiian reef coral Montipora capitata. PLoS One 7:e46717. https://doi.org/10.1371/journal.pone.0046717

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ushijima B, Videau P, Burger AH, Shore-Maggio A, Runyon CM, Sudek M, Aeby GS, Callahan SM (2014) Vibrio coralliilyticus Strain OCN008 Is an etiological agent of acute Montipora White Syndrome. Appl Environ Microbiol 80:2102–2109

    Article  PubMed  PubMed Central  Google Scholar 

  • Ushijima B, Videau P, Poscablo D, Stengel JW, Beurmann S, Burger AH, Aeby GS, Callahan SM (2016) Mutation of the toxR or mshA genes from Vibrio coralliilyticus strain OCN014 reduces infection of the coral Acropora cytherea. Environ Microbiol 18:4055–4067

    Article  CAS  PubMed  Google Scholar 

  • Van der Ent E, Hoeksema BW, de Voogd NJ (2015) Abundance and genetic variation of the coral-killing cyanobacteriosponge Terpios hoshinota in the Spermonde Archipelago, SW Sulawesi, Indonesia. J Mar Biol Assoc UK 96:453–463. https://doi.org/10.1017/S002531541500034X

    Article  Google Scholar 

  • van de Water JAJM, Chaib De Mares M, Dixon GB, Raina J-B, Willis BL, Bourne DG, van Oppen MJH (2018) Antimicrobial and stress responses to increased temperature and bacterial pathogen challenge in the holobiont of a reef-building coral. Mol Ecol 27:1065–1080

    Article  CAS  PubMed  Google Scholar 

  • Vargas-Angel B (2009) Coral health and disease assessment in the US Pacific remote Island areas. Bull Mar Sci 84:211–227

    Google Scholar 

  • Vega Thurber RL, Willner-Hall D, Rodriguez-Mueller B, Desnues C, Edwards RA, Angly F, Dinsdale E, Kelly L, Rohwer F (2009) Metagenomic analysis of stressed coral holobionts. Environ Microbiol 11:2148–2163

    Article  PubMed  Google Scholar 

  • Wada M, Nishihara G, Isomura N (2012) Probing stony coral rapid tissue necrosis with optical oxygen sensors. In: 12th Intern Coral Reef Symp. Cairns, Queensland, Australia

    Google Scholar 

  • Wada N, Ikeda S, Sekine S, Toizumi K, Nakamura R, Namba A, Uchida S, Nakamura K, Mano N (2015) Vibrio spp. isolated from scleractinian coral Acropora muricata with rapid tissue necrosis (RTN) and reared in aquarium. BioMicroWorld, Barcelona

    Google Scholar 

  • Wada N, Pollock FJ, Willis BL, Ainsworth T, Mano N, Bourne DG (2016) In situ visualization of bacterial populations in coral tissues: pitfalls and solutions. PeerJ 4:e2424. https://doi.org/10.7717/peerj.2424

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Wada N, Mano N, Yanagisawa Y, Mori T (2017) Occurrence of coral diseases at Akajima, Okinawa, Japan in 2010 and 2011. Galaxea J Coral Reef Stud 19:35–44. https://doi.org/10.3755/galaxea.19.1_35

    Article  Google Scholar 

  • Wada N, Ohdera A, Mano N (2018) Coral disease in Japan. In: Iguchi A, Hongo C (eds) Coral reef studies of Japan. Springer, Singapore, pp 41–62

    Chapter  Google Scholar 

  • Wang J-T, Chen Y-Y, Meng P-J, Sune Y-H, Hsu C-M, Wei K-Y, Chen CA (2012) Diverse interactions between corals and the coral-killing sponge, Terpios hoshinota (Suberitidae: Hadromerida). Zool Stud 10:150–159

    Google Scholar 

  • Webster NS, Thomas T (2016) The sponge hologenome. mBio 7:e00135–e00116. https://doi.org/10.1128/mBio.00135-16

    Article  PubMed  PubMed Central  Google Scholar 

  • Weil E, Irikawa A, Casareto B, Suzuki Y (2012) Extended geographic distribution of several Indo-Pacific coral reef diseases. Dis Aquat Org 98:163–170

    Article  CAS  Google Scholar 

  • West AG, Waite DW, Deines P et al (2019) The microbiome in threatened species conservation. Biol Conserv 229:85–98

    Article  Google Scholar 

  • Willis BL, Page CA, Dinsdale EA, Bourne DG, Digby A, McKenzie VJ, Taylor MW (2004) Coral disease on the Great Barrier Reef. In: Rosenberg PE, Loya Y (eds) Coral health and disease. Springer, Berlin, Heidelberg, pp 69–104

    Chapter  Google Scholar 

  • Wulff J (2016) Sponge contributions to the geology and biology of reefs: past, present, and future. In: Hubbard DK, Rogers CS, Lipps JH, Stanley Jr George D (eds) Coral reefs at the crossroads. Springer, Dordrecht, pp 103–126

    Chapter  Google Scholar 

  • Yamaguchi M (1986) Introduction to the study of coral reefs 4 Coral reef sponges (1) Sponges as destroyers of reef-building corals. Aquabiology 8:88–92. (in Japanese)

    Google Scholar 

  • Yamashiro H (2004) Coral diseases. In Coral Reefs of Japan. Ministry of the Environment and Japanese Coral Reef Society (ed). Ministry of the Environment, pp 56–59

    Google Scholar 

  • Yamano H, Hori K, Yamauchi M, Yamagawa O, Ohmura A (2001) Highest-latitude coral reef at Iki Island, Japan. Coral Reefs 20:9–12

    Article  Google Scholar 

  • Yamashiro H, Fukuda M (2009) White spot syndrome of Turbinaria peltata in the temperate region of Japan. Coral Reefs 28:893

    Article  Google Scholar 

  • Yamashiro H, Yamamoto M, van Woesik R (2000) Tumor formation on the coral Montipora informis. Dis Aquat Org 41:211–217

    Article  CAS  Google Scholar 

  • Yamashiro H, Oku H, Onaga K, Iwasaki H, Takara K (2001) Coral tumors store reduced level of lipids. J Exp Mar Biol Ecol 265:171–179

    Article  CAS  Google Scholar 

  • Yamashiro H, Isomura N, Sakai K (2014) Bloom of the cyanobacterium Moorea bouillonii on the gorgonian coral Annella reticulata in Japan. Sci Rep 4:6032. https://doi.org/10.1038/srep06032

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Yamashiro H, Fukuda M, Fukami H (2016) Outbreak of white syndrome in Acropora spp., temperate region of Japan. Mar Biodivers 46:321–322

    Article  Google Scholar 

  • Yamashiro H, Fukumori H, Aini SN, Hirose Y (2021) Snails associated with the coral-killing sponge Terpios hoshinota in Okinawa Island, Japan. Sci Rep 11:20709. https://doi.org/10.1038/s41598-021-00185-x

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Yang H, Shen J, Fu F, Wang Y, Zhao N (2014) Black band disease as a possible factor of the coral decline at the northern reef-flat of Yongxing Island, South China Sea. Sci China Earth Sci 57:569–578

    Article  CAS  Google Scholar 

  • Yang S-Y, Chen H-J, Ho M-J, Chen Y-J, Huang Y-Y, Chow WS, Tang S-L, Jeng M-S, Chen CA (2018) Outbreak of coral-killing cyanobacteriasponge, Terpios hoshinota, in Taiping Island (Itu Aba), Spratlys, South China Sea. Bull Mar Sci 94:1543–1544. https://doi.org/10.5343/bms.2018.0023

    Article  Google Scholar 

  • Yang S-H, Tandon K, Lu C-Y, Wada N, Shih C-J, Hsiao SS-Y, Jane W-N, Lee T-C, Yang C-M, Liu C-T, Denis V, Wu Y-T, Wang L-T, Huang L, Lee D-C, Wu Y-W, Yamashiro H, Tang S-L (2019) Metagenomic, phylogenetic, and functional characterization of predominant endolithic green sulfur bacteria in the coral Isopora palifera. Microbiome 7:3. https://doi.org/10.1186/s40168-018-0616-z

    Article  PubMed  PubMed Central  Google Scholar 

  • Yasuda N, Hidaka M (2012) Cellular kinetics in growth anomalies of the scleractinian corals Porites australiensis and Montipora informis. Dis Aquat Org 102:1–11

    Article  Google Scholar 

  • Yasuda N, Nakano Y, Yamashiro H, Hidaka M (2012) Skeletal structure and progression of growth ­anomalies in Porites australiensis in Okinawa, Japan. Dis Aquat Org 97:237–247

    Article  Google Scholar 

  • Yomogida M, Mizuyama M, Kubomura T, Reimer JD (2017) Disappearance and return of an outbreak of the coral-killing cyanobacteriosponge Terpios hoshinota in Southern Japan. Zool Stud 56:1–7. https://doi.org/10.6620/ZS.2017.56-07

    Article  Google Scholar 

  • Yu Q, Liu M, Su H, Xiao H, Wu S, Qin X, Li S, Mi H, Lu Z, Shi D, Li P (2019) Selection and characterization of ssDNA aptamers specifically recognizing pathogenic Vibrio alginolyticus. J Fish Dis 42:851–858

    Article  CAS  PubMed  Google Scholar 

  • Zaneveld JR, Burkepile DE, Shantz AA, Pritchard CE, McMinds R, Payet JP, Welsh R, Correa AMS, Lemoine NP, Rosales S, Fuchs C, Maynard JA, Thurber RV (2016) Overfishing and nutrient pollution interact with temperature to disrupt coral reefs down to microbial scales. Nat Commun 7:11833. https://doi.org/10.1038/ncomms11833

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Zhang Y, Sun J, Mu H, Lun JCY, Qiu J-W (2017) Molecular pathology of skeletal growth anomalies in the brain coral Platygyra carnosa: a meta-transcriptomic analysis. Mar Pollut Bull 124:660–667

    Article  CAS  PubMed  Google Scholar 

  • Zhenyu X, Shaowen K, Chaoqun H, Zhixiong Z, Shifeng W, Yongcan Z (2013) First characterization of bacterial pathogen, Vibrio alginolyticus, for Porites andrewsi white syndrome in the South China Sea. PLoS One 8:e75425. https://doi.org/10.1371/journal.pone.0075425

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Zvuloni A, Artzy-Randrup Y, Stone L, Kramarsky-Winter E, Barkan R, Loya Y (2009) Spatio-temporal transmission patterns of black-band disease in a coral community. PLoS One 4:e4993. https://doi.org/10.1371/journal.pone.0004993

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgments

This work was supported by the Japan Society for the Promotion of Science (JSPS) KAKENHI (grants 19 K06091 and 21H036191A).

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Yamashiro, H., Wada, N., Tang, SL. (2023). Succession and Spread of Coral Diseases and Coral-Killing Sponges with Special Reference to Microbes in Southeast Asia and Adjacent Waters. In: Takeuchi, I., Yamashiro, H. (eds) Coral Reefs of Eastern Asia under Anthropogenic Impacts. Coral Reefs of the World, vol 17. Springer, Cham. https://doi.org/10.1007/978-3-031-27560-9_5

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