Microbiome of Pacific Whiteleg shrimp reveals differential bacterial community composition between Wild, Aquacultured and AHPND/EMS outbreak conditions

QIIME allows analysis of high-throughput community sequencing data

Caporaso, J. G., Kuczynski, J., Stombaugh, J., Bittinger, K., Bushman, F. D., Costello, E. K., Fierer, N., Peña, A. G., Goodrich, J. K., Gordon, J. I., et al. (2010) · Nature Methods · doi:10.1038/nmeth.f.303 · Cited by 34,887

Metagenomic biomarker discovery and explanation

Segata, N., Izard, J., Waldron, L., Gevers, D., Miropolsky, L., Garrett, W. S., & Huttenhower, C. (2011) · Genome Biology · doi:10.1186/gb-2011-12-6-r60 · Cited by 16,192

Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences

Langille, M. G. I., Zaneveld, J., Caporaso, J. G., McDonald, D., Knights, D., Reyes, J. A., Clemente, J. C., Burkepile, D. E., Vega Thurber, R. L., Knight, R., et al. (2013) · Nature Biotechnology · doi:10.1038/nbt.2676 · Cited by 9,116

Quality-filtering vastly improves diversity estimates from Illumina amplicon sequencing

Bokulich, N. A., Subramanian, S., Faith, J. J., Gevers, D., Gordon, J. I., Knight, R. D., Mills, D. A., & Caporaso, J. G. (2012) · Nature Methods · doi:10.1038/nmeth.2276 · Cited by 4,525

A tale of three next generation sequencing platforms: comparison of Ion torrent, pacific biosciences and illumina MiSeq sequencers

Quail, M., Smith, M. E., Coupland, P., Otto, T. D., Harris, S. R., Connor, T. R., Bertoni, A., Swerdlow, H. P., & Gu, Y. (2012) · BMC Genomics · doi:10.1186/1471-2164-13-341 · Cited by 2,031

The Genus Aeromonas : Taxonomy, Pathogenicity, and Infection

Janda, J. M., & Abbott, S. L. (2010) · Clinical Microbiology Reviews · doi:10.1128/cmr.00039-09 · Cited by 1,766

How glycan metabolism shapes the human gut microbiota

Koropatkin, N. M., Cameron, E. A., & Martens, E. C. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2746 · Cited by 1,419

Performance comparison of benchtop high-throughput sequencing platforms

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Regulation of immune cell function by short‐chain fatty acids

Corrêa‐Oliveira, R., Fachi, J. L., Vieira, A., Sato, F. T., & Vinolo, M. A. R. (2016) · Clinical & Translational Immunology · doi:10.1038/cti.2016.17 · Cited by 1,346

A novel thymidylate synthase from theVibrionales,Alteromonadales,Aeromonadales, andPasteurellales(VAAP) clade with altered nucleotide and folate binding sites

López-Zavala, A. A., Guevara-Hernández, E., Vazquez-Lujan, L. H., Sánchez‐Paz, A., García‐Orozco, K. D., Contreras‐Vergara, C. A., López-Leal, G., Arvizu-Flores, A. A., Ochoa‐Leyva, A., & Sotelo‐Mundo, R. R. (2018) · PeerJ · doi:10.7717/peerj.5023 · Cited by 4

PRODUKTIVITAS BUDIDAYA UDANG VANAME (Litopenaeus vannamei) SUPER INTENSIF DI BAK TERPAL BUNDAR DENGAN PADAT TEBAR BERBEDA

Wahyudi, D., Prihutomo, A., & Mukhlis, A. (2022) · Jurnal Perikanan Unram · doi:10.29303/jp.v12i4.412 · Cited by 4

Metagenomic and metabolomic profiling of dried shrimp (Litopenaeus vannamei) prepared by a procedure traditional to the south China coastal area

Yu, M., Liu, J., Chen, J., Lin, C., Deng, S., & Wu, M.-F. (2024) · International Microbiology · doi:10.1007/s10123-023-00475-6 · Cited by 4

Bacterial Community Changes in Penaeus vannamei Boone, 1931 Surface and Rearing Water During Enterocytozoon hepatopenaei Infection

Baliga, P., Goolappa, P. T., Shekar, M., Girisha, S. K., RAMESH, K. S., Udyavara, V., & Venugopal, M. N. (2021) · Asian Fisheries Science · doi:10.33997/j.afs.2021.34.2.006 · Cited by 3

Preliminary investigation on the effect of Vibrio splendidus stimulation on the intestinal flora of Strongylocentrotus intermedius

Zhang, X., Li, Y., Liu, W., Zhang, H., Han, Y., Liu, Y., & Wang, X. (2024) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2024.150389 · Cited by 3

Effect of Dietary Restriction on Gut Microbiota and Brain–Gut Short Neuropeptide F in Mud Crab, Scylla paramamosain

Bao, C., Yang, Y., & Ye, H. (2024) · Animals · doi:10.3390/ani14162415 · Cited by 3

WSSV Infection in the Gut Microbiota of the Black Tiger Shrimp Penaeus monodon

Wang, Y., Wang, X., Gai, C., Li, Y., Xu, L., Wang, S., Li, L., Yu, X., Fu, R., Diao, J., et al. (2025) · Fishes · doi:10.3390/fishes10090440 · Cited by 3

Elevated water nutrient levels promote co-occurrence of sediment microbiota in white-leg shrimp (Litopenaeus vannamei) culture ponds

Wu, L., Shi, X., Wang, J., Zheng, X., Qian, X., Xie, S., Shi, B., Xiao, R., Wang, B., Lian, Y., et al. (2025) · Aquaculture Reports · doi:10.1016/j.aqrep.2025.103121 · Cited by 3

Antibacterial activity of four recombinant carbohydrate recognition domain proteins identified from the kuruma shrimp Marsupenaeus japonicus

Zheng, J., Ni, M., Mao, Y., & Su, Y. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.09.138 · Cited by 3

Comparative transcriptomic and metagenomic analyses reveal key factors affecting the growth rate of Red Swamp Crayfish (Procambarus clarkii)

Chen, D., Guo, L., Wang, C., Cao, H., Mo, W., Xin, Y., Zeng, Y., & Wang, H. (2022) · Aquaculture Reports · doi:10.1016/j.aqrep.2022.101098 · Cited by 3

Grazing by an endemic atyid shrimp controls microbial communities in the Hawaiian anchialine ecosystem

Havird, J. C., Brannock, P. M., Yoshioka, R. M., Vaught, R. C., Carlson, K. M., Edwards, C. B., Tracy, A. M., Twining, C. W., Zheng, Y., Chai, D., et al. (2022) · Limnology and Oceanography · doi:10.1002/lno.12184 · Cited by 3

Exploration of the candidate beneficial bacteria for Penaeus vannamei culture by core microbiome analysis using amplicon sequencing

Lalitha, N., Ronald, B. S. M., Chitra, M. A., Jangam, A. K., Katneni, V. K., Nathamuni, S. P., Senthilnayagam, H., Senthilkumar, T. M. A., & Muralidhar, M. (2023) · Letters in Applied Microbiology · doi:10.1093/lambio/ovad087 · Cited by 3

Gut microbiome variation based on 16S rRNA gene amplicon sequencing of the wild and domesticated broodstock populations of black tiger shrimp (Penaeus monodon) in the Indo-Pacific region

Wong, L. L., Deris, Z. M., Asaduzzaman, M., Wang, M., Liang, Y., Sung, Y. Y., & Iehata, S. (2023) · Ecological Genetics and Genomics · doi:10.1016/j.egg.2023.100204 · Cited by 3

Differences in diversity and community composition of the shell microbiome of apparently healthy lobsters Homarus americanus across Atlantic Canada

Koepper, S., Clark, K. F., McClure, J. T., Revie, C. W., Stryhn, H., & Thakur, K. K. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1320812 · Cited by 3

Interactions between the gut bacterial community of Exopalaemon carinicauda and infection by Enterocytozoon hepatopenaei

Li, W., Hua, S., Du, Z., Jiang, H., Jiang, S., Yu, M., Baloch, W. A., Noonari, S., Yan, B., & Gao, H. (2024) · Journal of Invertebrate Pathology · doi:10.1016/j.jip.2024.108115 · Cited by 3

Identification of the bacterial composition in the rockworm gut and biofloc-fed adult gut flora beneficial for integrated multitrophic aquaculture

Jung, H. Y., Kim, C. H., & Kim, J. K. (2021) · Fisheries and aquatic sciences · doi:10.47853/fas.2021.e29 · Cited by 3

A multi-angle analysis of injury induced by supplementation of soybean meal in Litopenaeus vannamei diets

Peng, K., Qiu, J., Li, C., Lü, H., Liu, Z., Liu, D., & Huang, W. L. (2023) · Frontiers in Microbiomes · doi:10.3389/frmbi.2023.1113635 · Cited by 2

Dietary Bromelain From Pineapple Extracts Enhanced Growth Performance and Modulated Stomach Microbiota Which Provided Longer‐Term Protection to Penaeus vannamei Against Acute Hepatopancreatic Necrosis Disease (AHPND) Caused by Vibrio parahaemolyticus

Ng, W., & Mong, M.-L. (2024) · Aquaculture Research · doi:10.1155/2024/6492170 · Cited by 2

Microbiome dynamics associated with Hematodinium sp. infection in Norway lobster (Nephrops norvegicus)

Martin, I., Elsheshtawy, A., Clokie, B. G. J., MacKenzie, S. A., Bateman, K. S., Bass, D. A., Stentiford, G. D., & Albalat, A. (2025) · Animal Microbiome · doi:10.1186/s42523-025-00416-w · Cited by 3

Exploring the gut microbiota of Pacific white shrimp (Litopenaeus vannamei) suffering pale shrimp disease

Kitsanayanyong, L., Chongprachavat, N., Rairat, T., Keetanon, A., Wimanhaemin, P., & Chuchird, N. (2025) · PLoS ONE · doi:10.1371/journal.pone.0336700 · Cited by 2

Probiotic Bacillus species to mitigate acute hepatopancreatic necrosis disease (AHPND) in shrimp aquaculture

Kashem, M. A., Haniswita, H., Sumon, T. A., Vandeputte, M., Drouillon, M., Declercq, A. M., Bossier, P., & Vanrompay, D. C. G. (2025) · Aquaculture · doi:10.1016/j.aquaculture.2025.743483 · Cited by 2

The innate immune IMD pathway is a key regulator of gut microbiome and metabolic homeostasis in the black tiger shrimp (Penaeus monodon)

Supungul, P., Tang, S., Uengwetwanit, T., Uawisetwathana, U., Angthong, P., Arayamethakorn, S., Bunphimpapha, P., Potibut, P., Jangsutthivorawat, W., Visudtiphole, V., et al. (2025) · PLoS ONE · doi:10.1371/journal.pone.0338796 · Cited by 2

Bacterial community of the shrimp (Litopenaeus vannamei) gut and its relationship with water quality in a recirculating aquaculture system (RAS)

Emmanuel, A., Raza, B., Ramzan, M. N., & Zheng, Z. (2025) · Aquaculture International · doi:10.1007/s10499-025-02349-2 · Cited by 2

Penaeus vannamei challenged with a Vibrio parahaemolyticus AHPND strain shows hepatopancreatic microbiota imbalance

Zermeño‐Cervantes, L. A., Barraza, A., González-Ponce, H. A., Martínez‐Díaz, S. F., & Cardona-Félix, C. S. (2023) · Ciencias Marinas · doi:10.7773/cm.y2023.3234 · Cited by 2

Shrimp Health and Microbiome

Kumar, S. H., Stephen, J., Jeena, K., Lekshmi, M., Sreedharan, K., & Valappil, R. K. (2023) · Springer eBooks · doi:10.1007/978-981-99-0852-3_9 · Cited by 2

Consistent responses of the shrimp Litopenaeus vannamei gut microbiota to Enterocytozoon hepatopenaei infection across spatially distant farms

Xu, S., Zhan, P., Li, J., Chen, J., Qiu, Q., & Xiong, J. (2024) · Aquaculture · doi:10.1016/j.aquaculture.2024.741447 · Cited by 2

Gut microbiota and functional metabolic predictions in white feces disease-infected Pacific white shrimp, Penaeus vannamei, from Indonesian farms

Amin, M. N. G., Rahardjo, K. K. E., Panosa, A. E., Satyantini, W. H., Mukti‬, ‪. T., Ali, M., Musdalifah, L., Akhyar, H., Yanuhar, U., Azmai, M. N. A., et al. (2025) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2025.110171 · Cited by 2

Alteration of Immune Function and Gut Microbiome Composition in Carassius auratus Challenged With Rahnella aquatilis

Huo, J., Li, X., Zhang, K., Fu, H. L., Hu, X., & Lv, A. (2024) · Journal of Fish Diseases · doi:10.1111/jfd.14054 · Cited by 2

Assessment of total bacterial diversity in whiteleg shrimps and its aquaculture environment in Pangkajene and Banyuwangi, Indonesia

Hastuti, Y. P., Fatma, Y. S., Pitoyo, H., Nurussalam, W., & Ruhyana, J. (2021) · Asia-Pacific Journal of Molecular Biology and Biotechnology · doi:10.35118/apjmbb.2021.029.3.04 · Cited by 2

Microbiome Interventions for the Prevention and Control of Disease Outbreaks in Shrimp Aquaculture

Rajeev, R., Seethalakshmi, P. S., Kiran, G. S., & Selvin, J. (2021) · Springer eBooks · doi:10.1007/978-981-16-5195-3_21 · Cited by 2

Genomic characterization of Vibrio parahaemolyticus from Pacific white shrimp and rearing water in Malaysia reveals novel sequence types and structural variation in genomic regions containing the Photorhabdus insect-related (Pir) toxin-like genesPreprint

Yan, C. Z. Y., Austin, C. M., Ayub, Q., Rahman, S., & Gan, H. M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/714626 · Cited by 2

Microbial Communities Associated With Stunted Growth Syndrome In Penaeus Vannamei FarmingPreprint

Jangam, A. K., Nathamuni, S. P., Katneni, V. K., Avunje, S., Angel, R. J., Grover, M., & Shekhar, M. S. (2021) · Research Square · doi:10.21203/rs.3.rs-1187880/v1 · Cited by 2

Gut McIrobiomeis Associated with Hepatopancreatic and Gonadal Transcriptomes and Together They Impact on Growth Traits in M. rosenbergiiPreprint

Xu, H., Ren, J., Xu, X., Lou, B., & Zhang, D. (2023) · Preprints.org · doi:10.20944/preprints202307.1150.v1 · Cited by 2

A novel SNW/SKIP domain-containing protein, Bx42, is involved in the antibacterial responses of Macrobrachium nipponense

Xu, L., Zhou, X., Wu, Y., Yang, J., & Xu, H. (2020) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2020.103788 · Cited by 1

The importance of gut microbes for nutrition and health

Piazzon, M. C., Ghosh, K., Ringø, E., & Kokou, F. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-21556-8.00013-2 · Cited by 2

Dietary silver nanoparticle effects on Penaeus vannamei growth, histopathology, faecal microbiome, and acute hepatopancreatic necrosis disease survival

Maldonado-Muñiz, M., Nieto-López, M. G., Tapia‐Salazar, M., Gómez‐Gil, B., Guerrero, A., Lozano‐Olvera, R., Cruz‐Suárez, L. E., & Soto-Rodríguez, S. A. (2025) · Diseases of Aquatic Organisms · doi:10.3354/dao03848 · Cited by 1

Effects of dietary flavone on growth performance and Omics profiles of Litopenaeus vannamei under high-temperature

Abraham, I. J., Huang, C., Lv, H., Yin, X., Park, J., Gao, Y., & Hur, J. (2025) · Aquaculture and Fisheries · doi:10.1016/j.aaf.2025.02.003 · Cited by 1

Comparative metagenomic analysis of core gut microbiome in white leg shrimp (Penaeus vannamei) cultivated in low-saline and saline farmland

Varatharajan, J., Dilipan, E., Sivaperumal, P., & Rajaram, R. (2025) · Ecological Genetics and Genomics · doi:10.1016/j.egg.2025.100359 · Cited by 1

Alterations in intestinal microbiota and host response in Penaeus monodon experimentally challenged with Enterocytozoon hepatopenaei (EHP)

Naveen Rajeshwar, B., Kumar, T. S., Jithendran, K. P., Suganya, P. N., Gangaraj, K. P., Bedekar, M. K., Sanath Kumar, H., Jeena, K., Pathan, M. A., & Rajendran, K. (2025) · Aquaculture International · doi:10.1007/s10499-025-02290-4 · Cited by 1

Emergence of decapod hepanhamaparvovirus genotype V and its co-infection with Enterocytozoon hepatopenaei in cultured Penaeus vannamei in Thailand: Evidence from epidemiological, pathogenicity, and microbiome analyses

Charoenwai, O., Tanpichai, P., Sukkarun, P., Jeon, H., Kim, B., Han, J. E., & Piamsomboon, P. (2025) · Veterinary World · doi:10.14202/vetworld.2025.3496-3508 · Cited by 1

Modulating Whiteleg Shrimp (Penaeus vannamei) Health from the Inside out: Effects of Xylooligosaccharides from Salicornia ramosissima on Gut Metabolites and Microbial Community

Garcia, A. D., Fernández-Boo, S., Barreto, A., Semedo, M., Thomsen, M. H., Stensballe, A., Monção, M., Μάτσακας, Λ., Christakopoulos, P., Kiron, V., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262411978 · Cited by 3

Breaking paradigms: Reconsidering the role of harmless vibrios in shrimp health

Pinos-Tamayo, E. A., Domínguez-Borbor, C., Morales, I., Ramírez, M., Sonnenholzner, S., & Rodríguez, J. A. (2026) · Journal of Invertebrate Pathology · doi:10.1016/j.jip.2026.108597 · Cited by 1

Thermal Stress Disrupts Gut Microbiota, Induces Oxidative DNA Damage, and Modulates Immune and Stress-Related Gene Expression in the Red Sea Urchin (Loxechinus albus)

Llanos-Azócar, K., Estrada, J. M., Oyarzún, P. A., Dettleff, P., Ugarte, G. D., & Valdés, J. A. (2026) · Biology · doi:10.3390/biology15120913 · Cited by 1

Shared temporal dynamics and high inter-individual variability in stomach microbiota of kuruma shrimp (Penaeus japonicus) across aquaculture farms

Imaizumi, K., Konishi, K., Yonashiro, Y., Kondo, H., & Hırono, I. (2026) · Fisheries Science · doi:10.1007/s12562-026-02011-7 · Cited by 1

From dysbiosis to resilience: Microbiome engineering for sustainable shrimp aquaculture

Imran, S., Junejo, Y., Ahmad, H. I., Ozaslan, M., & Safdar, M. (2026) · Comparative Biochemistry and Physiology Part D Genomics and Proteomics · doi:10.1016/j.cbd.2026.102024 · Cited by 1

Fish Microbiome and Metagenomics

Sannejal, A. D., Divyashree, M., Kumar, D. V., Sankappa, N. M., & Rai, P. (2023) · Springer eBooks · doi:10.1007/978-981-99-0852-3_4 · Cited by 1

GROWTH PERFORMANCES AND INTESTINAL BACTERIAL POPULATIONS OF PACIFIC WHITE SHRIMP (Penaeus vannamei) FED WITH DIFFERENT DIETARY PREBIOTICS-SUPPLEMENTED FEED

Utami, D. A. S., Wahyu, W., Insani, L., Yudana, I. G. R., & Harijono, T. (2024) · Jurnal Riset Akuakultur · doi:10.15578/jra.19.1.2024.1-13 · Cited by 1

Hemolymph microbiota and immune effectors’ expressions driven by geographical rearing acclimation of the aquacultured Penaeus stylirostris

Perez, V., Boulo, V., de Lorgeril, J., Pham, D., Ansquer, D., Plougoulen, G., Ballan, V., Lam, J.-S., Romatif, O., Luyer, J. L., et al. (2025) · Animal Microbiome · doi:10.1186/s42523-025-00376-1 · Cited by 1

Infection with White Spot Syndrome Virus Affects the Microbiota in the Stomachs and Intestines of Kuruma ShrimpPreprint

Wang, J., Niu, G.-J., Yan, M., Li, C., Lu, P.-Y., & Yu, Z. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4058416 · Cited by 1

Gut Microbiota Exhibits Discrete Patterns in the Presence of Wssv and Vpahpnd in Black Tiger Shrimp Penaeus MonodonPreprint

Akter, R., Punom, N. J., Eshik, M. M. E., Hossain, M. S., Momtaz, S., Sultana, S., & Rahman, M. S. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4846014 · Cited by 1

Peer Review #1 of "Microbiome differences between river-dwelling and cave-adapted populations of the fish Astyanax mexicanus (De Filippi, 1853) (v0.1)"

(2018) · PeerJ · doi:10.7287/peerj.5906v0.1/reviews/1

La microbiota del tracto digestivo de camarones peneidos: una perspectiva histórica y estado del arte//The gut microbiota of penaeid shrimp: a historical perspective and state of the art

Garibay-Valdéz, E., Martínez‐Porchas, M., Calderón, K., Gollas‐Galván, T., Martínez‐Córdova, L. R., Vargas‐Albores, F., & Arvayo, M. A. (2019) · BIOtecnia · doi:10.18633/biotecnia.v22i1.1119

Tình hình sử dụng thảo dược trong nuôi tôm vùng Đồng bằng sông Cửu Long

Huyền, H. M., Toàn, N. V., Hiền, H. V., & Hoa, T. T. T. (2020) · Can Tho University Journal of Science · doi:10.22144/ctu.jsi.2020.016

Effect of dietary protein and genetic line of Litopenaeus vannamei on its hepatopancreatic microbiota

Martínez‐Porchas, M., Vargas‐Albores, F., Casillas‐Hernández, R., Rodríguez-Anaya, L. Z., Lares‐Villa, F., Magdaleno-Moncayo, D., & González-Galavíz, J. R. (2020) · Scientia Agricola · doi:10.1590/1678-992x-2020-0096

Status of the Polar BSRN Sites Ny-Ålesund and Neumayer

Maturilli, M., & König‐Langlo, G. (2008) · Helmholtz-Zentrum für Polar-und Meeresforschung (Alfred-Wegener-Institut)

Peer Review #2 of "Longitudinal variations in the gastrointestinal microbiome of the white shrimp, Litopenaeus vannamei (v0.2)"

(2021) · PeerJ · doi:10.7287/peerj.11827v0.2/reviews/2

Peer Review #1 of "Longitudinal variations in the gastrointestinal microbiome of the white shrimp, Litopenaeus vannamei (v0.2)"

(2021) · PeerJ · doi:10.7287/peerj.11827v0.2/reviews/1

Peer Review #1 of "Longitudinal variations in the gastrointestinal microbiome of the white shrimp, Litopenaeus vannamei (v0.1)"

(2021) · PeerJ · doi:10.7287/peerj.11827v0.1/reviews/1

Distribution of Microbial Communities of Sediment and Relationship with Surrounding Environmental Factors in a Typical Rural River, Southwest ChinaPreprint

Yang, C., Zeng, Z., Zhang, H., Gao, D., Wang, Y., Guang-yi, H., Liu, Y., Wang, Y., & Du, X. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.3989498

Peer Review #3 of "Longitudinal variations in the gastrointestinal microbiome of the white shrimp, Litopenaeus vannamei (v0.1)"

(2021) · PeerJ · doi:10.7287/peerj.11827v0.1/reviews/3

Peer Review #2 of "Longitudinal variations in the gastrointestinal microbiome of the white shrimp, Litopenaeus vannamei (v0.1)"

(2021) · PeerJ · doi:10.7287/peerj.11827v0.1/reviews/2

The effect of “Fishery-PV Integration” on Penaeus monodon culture and Micro-ecological environmentPreprint

Sun, C., Liao, M., Long, X., He, Z., Zhao, J., Chen, X., & Zhu, D. (2022) · Research Square · doi:10.21203/rs.3.rs-1541781/v1

Peer Review #3 of "Microbiome analysis of Pacific white shrimp gut and rearing water from Malaysia and Vietnam: implications for aquaculture research and management (v0.2)"

(2018) · PeerJ · doi:10.7287/peerj.5826v0.2/reviews/3

Peer Review #1 of "Microbiome analysis of Pacific white shrimp gut and rearing water from Malaysia and Vietnam: implications for aquaculture research and management (v0.1)"

(2018) · PeerJ · doi:10.7287/peerj.5826v0.1/reviews/1

Peer Review #2 of "Microbiome analysis of Pacific white shrimp gut and rearing water from Malaysia and Vietnam: implications for aquaculture research and management (v0.1)"

(2018) · PeerJ · doi:10.7287/peerj.5826v0.1/reviews/2

Peer Review #3 of "Microbiome analysis of Pacific white shrimp gut and rearing water from Malaysia and Vietnam: implications for aquaculture research and management (v0.1)"

(2018) · PeerJ · doi:10.7287/peerj.5826v0.1/reviews/3

Peer Review #2 of "Microbiome differences between river-dwelling and cave-adapted populations of the fish Astyanax mexicanus (De Filippi, 1853) (v0.1)"

(2018) · PeerJ · doi:10.7287/peerj.5906v0.1/reviews/2

Peer Review #1 of "Microbiome analysis of Pacific white shrimp gut and rearing water from Malaysia and Vietnam: implications for aquaculture research and management (v0.2)"

(2018) · PeerJ · doi:10.7287/peerj.5826v0.2/reviews/1

Peer Review #1 of "Microbiome analysis of Pacific white shrimp gut and rearing water from Malaysia and Vietnam: implications for aquaculture research and management (v0.3)"

(2018) · PeerJ · doi:10.7287/peerj.5826v0.3/reviews/1

Intestinal Microbiota Differences in Penaeus Vannamei Shrimp between Greenhouse and Factory RearingPreprint

Shen, H., Jiang, G., Qiao, Y., Cheng, J., Dou, Y., Zhang, L., Zhang, S., He, X., Wan, X., Fan, X., et al. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4178944

Peer Review #1 of "Microbial signature profiles of Penaeus vannamei larvae in low-survival hatchery tanks affected by vibriosis (v0.1)"

(2023) · PeerJ · doi:10.7287/peerj.15795v0.1/reviews/1

Peer Review #3 of "Microbial signature profiles of Penaeus vannamei larvae in low-survival hatchery tanks affected by vibriosis (v0.1)"

(2023) · PeerJ · doi:10.7287/peerj.15795v0.1/reviews/3

Peer Review #3 of "Microbial signature profiles of Penaeus vannamei larvae in low-survival hatchery tanks affected by vibriosis (v0.2)"

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(2023) · PeerJ · doi:10.7287/peerj.15795v0.1/reviews/2

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Additional file 2 of In silico prediction of potential indigenous microbial biomarkers in Penaeus vannamei identified through meta-analysis and genome-scale metabolic modelling

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Additional file 4 of Microbial community characterization of shrimp survivors to AHPND challenge test treated with an effective shrimp probiotic (Vibrio diabolicus)

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Additional file 2 of Microbial community characterization of shrimp survivors to AHPND challenge test treated with an effective shrimp probiotic (Vibrio diabolicus)

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Additional file 1 of Microbial community characterization of shrimp survivors to AHPND challenge test treated with an effective shrimp probiotic (Vibrio diabolicus)

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Additional file 1 of In silico prediction of potential indigenous microbial biomarkers in Penaeus vannamei identified through meta-analysis and genome-scale metabolic modelling

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