Cited by 205Aquaculture disease management and microbiotaMicrobial Community Ecology and PhysiologyGut microbiota and health

The DOI matches its Crossref record, with a small difference in title or year; 35 of the 35 references it cites were found in a registry or an index.

Changes in the intestinal bacterial community during the growth of white shrimp, Litopenaeus vannamei

Huang, Zhaobin, Li, Xiaoyi, Wang, Liping, Shao, Zongze·2016·Aquaculture Research

DOI 10.1111/are.12628

Open this paper in CoChat — free account

Abstract

In this study, we documented the changes in the intestinal bacterial community at four stages in Litopenaeus vannamei: 14 days postlarvae (L14) and 1-, 2- and 3-month old juveniles (J1, J2, J3), using 454 pyrosequencing techniques. The intestinal bacterial community was dominated by three bacterial phyla, Proteobacteria, Bacteroidetes and Actinobacteria at all stages. However, the relative abundance and bacterial lineages varied at the family level. The intestinal bacterial community of L14 and J1 was similar, with dominant members belonging to the Comamonadaceae of Betaproteobacteria. Conversely, bacterial members affiliated to Flavobacteriaceae of Bacteroidetes were dominant in J2 and Vibrionaceae of Gammaproteobacteria was dominant in J3. The abundance of Microbacteriaceae of Actinobacteria also fluctuated during the four stages. Bacterial members of Flavobacteriaceae and Rhodobacteraceae (Alphaproteobacteria) were present through all growth stages, and likely form the intestinal core microbiome of L. vannamei. However, they varied at the operational taxonomic unit (OTU) level through the growth stages. The intestinal bacterial community of pond-rearing shrimp included the three main bacterial phyla identified above, and an additional group, Mycoplasmataceae of Mollicutes. Our results demonstrate that the intestinal bacterial community of L. vannamei was highly dynamic during the growth stages. Bacterial members belonging to Commamonadaceae dominated in the earlier growth stage of shrimp, possibly influenced by feeding with Artemia nauplii, but there was a shift to Flavobacteriaceae in the mid and Vibrionaceae in the late growth stages.

Integrity signals

Registry

Crossref · 10.1111/are.12628

Cites

35 of 35 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

MEGA6: Molecular Evolutionary Genetics Analysis version 6.0.
Tamura, K., Stecher, G., Peterson, D., Filipski, A., & Kumar, S. (2013) · Molecular biology and evolution · doi:10.1093/molbev/mst197 · Cited by 41,174
BLAST+: architecture and applications
Camacho, C., Coulouris, G., Avagyan, V., Ma, N., Papadopoulos, J., Bealer, K., & Madden, T. L. (2009) · BMC Bioinformatics · doi:10.1186/1471-2105-10-421 · Cited by 22,074
Introducing mothur: Open-Source, Platform-Independent, Community-Supported Software for Describing and Comparing Microbial Communities
Schloss, P. D., Westcott, S. L., Ryabin, T., Hall, J. R., Hartmann, M., Hollister, E. B., Lesniewski, R. A., Oakley, B. B., Parks, D. H., Robinson, C. J., et al. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01541-09 · Cited by 21,481
Naive Bayesian Classifier for Rapid Assignment of rRNA Sequences into the New Bacterial Taxonomy
Wang, Q., Garrity, G. M., Tiedje, J. M., & Cole, J. R. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.00062-07 · Cited by 20,145
PAST: PALEONTOLOGICAL STATISTICAL SOFTWARE PACKAGE FOR EDUCATION AND DATA ANALYSIS
Hammer, Ø., Harper, D. A. T., & Ryan, P. D. (2001) · Palaeontologia Electronica · Cited by 17,871
Diversity of the Human Intestinal Microbial Flora
Eckburg, P. B., Bik, E. M., Bernstein, C. N., Purdom, E., Dethlefsen, L., Sargent, M., Gill, S. R., Nelson, K. E., & Relman, D. A. (2005) · Science · doi:10.1126/science.1110591 · Cited by 7,913
A core gut microbiome in obese and lean twins
Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823
SILVA: a comprehensive online resource for quality checked and aligned ribosomal RNA sequence data compatible with ARB
Pruesse, E., Quast, C., Knittel, K., Fuchs, B. M., Ludwig, W., Peplies, J., & Glöckner, F. O. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm864 · Cited by 6,682
Microbial diversity in the deep sea and the underexplored “rare biosphere”
Sogin, M. L., Morrison, H. G., Huber, J. A., Welch, D. B. M., Huse, S. M., Neal, P. R., Arrieta, J. M., & Herndl, G. J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605127103 · Cited by 3,803
Evolution of mammals and their gut microbes
Ley, R. E., Hamady, M., Lozupone, C., Turnbaugh, P. J., Ramey, R. R., Bircher, J. S., Schlegel, M. L., Tucker, T. A., Schrenzel, M. D., Knight, R., et al. (2008) · Science · doi:10.1126/science.1155725 · Cited by 3,747

Flagged first, then by citations

Show all 35 references

Sorted by citations

Effect of dietary components on the gut microbiota of aquatic animals. A never‐ending story?
Ringø, E., Zhou, Z., Vecino, J. L. G., Wadsworth, S., Romero, J., Krogdahl, Å., Olsen, R. E., Dimitroglou, A., Foey, A., Davies, S. J., et al. (2015) · Aquaculture Nutrition · doi:10.1111/anu.12346 · Cited by 749
Understanding the role of the shrimp gut microbiome in health and disease
Holt, C. C., Bass, D., Stentiford, G. D., & van der Giezen, M. (2020) · Journal of Invertebrate Pathology · doi:10.1016/j.jip.2020.107387 · Cited by 368
Gut Microbiota and its Modulation for Healthy Farming of Pacific White ShrimpLitopenaeus vannamei
Li, E., Xu, C., Wang, X., Wang, S., Zhao, Q., Zhang, M., Qin, J. G., & Chen, L. (2018) · Reviews in Fisheries Science & Aquaculture · doi:10.1080/23308249.2018.1440530 · Cited by 304
Microbiome of Pacific Whiteleg shrimp reveals differential bacterial community composition between Wild, Aquacultured and AHPND/EMS outbreak conditions
Cornejo-Granados, F., Lopez-Zavala, A. A., Gallardo-Becerra, L., Mendoza-Vargas, A., Sánchez, F., Vichido, R., Brieba, L. G., Viana, M. T., Sotelo-Mundo, R. R., & Ochoa-Leyva, A. (2017) · Scientific Reports · doi:10.1038/s41598-017-11805-w · Cited by 302
Integrating gut microbiota immaturity and disease‐discriminatory taxa to diagnose the initiation and severity of shrimp disease
Xiong, J., Zhu, J., Dai, W., Dong, C., Qiu, Q., & Li, C. (2017) · Environmental Microbiology · doi:10.1111/1462-2920.13701 · Cited by 289
Microbiota assemblages of water, sediment, and intestine and their associations with environmental factors and shrimp physiological health
Huang, F., Pan, L., Song, M., Tian, C., & Gao, S. (2018) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-9229-5 · Cited by 177
Healthy microbiome: a key to successful and sustainable shrimp aquaculture
Rajeev, R., Adithya, K. K., Kiran, G. S., & Selvin, J. (2020) · Reviews in Aquaculture · doi:10.1111/raq.12471 · Cited by 186
Bacterial community associated with healthy and diseased pacific white shrimp (Litopenaeus vannamei) larvae and rearing water across different growth stages
Zheng, Y., Yu, M., Liu, J., Qiao, Y., Wang, L., Li, Z., Zhang, X.-H., & Yu, M. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01362 · Cited by 165
Self-citation
Changes in the Intestine Microbial, Digestive, and Immune-Related Genes of Litopenaeus vannamei in Response to Dietary Probiotic Clostridium butyricum Supplementation
Duan, Y., Wang, Y., Dong, H., Ding, X., Liu, Q., Li, H., Zhang, J., & Xiong, D. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02191 · Cited by 157
Aquaculture industry prospective from gut microbiome of fish and shellfish: An overview
Diwan, A. D., Harke, S. N., Gopalkrishna, & Panche, A. N. (2021) · Journal of Animal Physiology and Animal Nutrition · doi:10.1111/jpn.13619 · Cited by 157
A meta-analysis reveals the environmental and host factors shaping the structure and function of the shrimp microbiota
Cornejo‐Granados, F., Gallardo-Becerra, L., Leonardo-Reza, M., Ochoa‐Romo, J. P., & Ochoa‐Leyva, A. (2018) · PeerJ · doi:10.7717/peerj.5382 · Cited by 145
Metagenomic insights into the structure and function of intestinal microbiota of the farmed Pacific white shrimp (Litopenaeus vannamei)
Gao, S., Pan, L., Huang, F., Song, M., Tian, C., & Zhang, M. (2018) · Aquaculture · doi:10.1016/j.aquaculture.2018.09.026 · Cited by 141
Comparison of cultivable bacterial communities associated with Pacific white shrimp (Litopenaeus vannamei) larvae at different health statuses and growth stages
Zheng, Y., Yu, M., Liu, Y., Su, Y., Xu, T., Yu, M., & Zhang, X.-H. (2015) · Aquaculture · doi:10.1016/j.aquaculture.2015.09.020 · Cited by 133
Dynamics of the gut microbiota in developmental stages of Litopenaeus vannamei reveal its association with body weight
Fan, J., Chen, L., Mai, G., Zhang, H., Yang, J., Deng, D., & Ma, Y. (2019) · Scientific Reports · doi:10.1038/s41598-018-37042-3 · Cited by 133
Effects of dietary mixed probiotics on growth, non-specific immunity, intestinal morphology and microbiota of juvenile pacific white shrimp, Litopenaeus vannamei
Xie, J.-J., Liu, Q.-Q., Liao, S., Fang, H., Yin, P., Xie, S., Tian, L., Liu, Y., & Niu, J. (2019) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2019.04.301 · Cited by 131
Advances, challenges, and directions in shrimp disease control: the guidelines from an ecological perspective
Xiong, J., Dai, W., & Li, C. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-016-7679-1 · Cited by 132
Fine-scale succession patterns and assembly mechanisms of bacterial community of Litopenaeus vannamei larvae across the developmental cycle
Wang, Y., Wang, K., Huang, L., Dong, P., Wang, S., Chen, H., Lu, Z., Hou, D., & Zhang, D. (2020) · Microbiome · doi:10.1186/s40168-020-00879-w · Cited by 127
Microbiome analysis of Pacific white shrimp gut and rearing water from Malaysia and Vietnam: implications for aquaculture research and management
Zoqratt, M. Z. H. M., Eng, W. W. H., Thai, B. T., Austin, C. M., & Gan, H. M. (2018) · PeerJ · doi:10.7717/peerj.5826 · Cited by 126
Response of host–bacterial colonization in shrimp to developmental stage, environment and disease
Xiong, J., Dai, W., Qiu, Q., Zhu, J., Yang, W., & Li, C. (2018) · Molecular Ecology · doi:10.1111/mec.14822 · Cited by 125
Progress in the gut microbiota in exploring shrimp disease pathogenesis and incidence
Xiong, J. (2018) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-9199-7 · Cited by 108
Lactobacillus acidophilus and L. plantarum improve health status, modulate gut microbiota and innate immune response of marron (Cherax cainii)
Foysal, M. J., Fotedar, R. K., Siddik, M. A. B., & Tay, C. Y. (2020) · Scientific Reports · doi:10.1038/s41598-020-62655-y · Cited by 107
Harnessing the potentialities of probiotics, prebiotics, synbiotics, paraprobiotics, and postbiotics for shrimp farming
Goh, J. X. H., Tan, L. T., Law, J. W., Ser, H., Khaw, K. Y., Letchumanan, V., Lee, L., & Goh, B. H. (2022) · Reviews in Aquaculture · doi:10.1111/raq.12659 · Cited by 108
Habitat and indigenous gut microbes contribute to the plasticity of gut microbiome in oriental river prawn during rapid environmental change
Chen, C.-Y., Chen, P., Weng, F. C.-H., Shaw, G. T.-W., & Wang, D. (2017) · PLoS ONE · doi:10.1371/journal.pone.0181427 · Cited by 100
Host-microbiome interaction in fish and shellfish: An overview
Diwan, A. D., Harke, S. N., & Panche, A. N. (2023) · Fish and Shellfish Immunology Reports · doi:10.1016/j.fsirep.2023.100091 · Cited by 96
Changes in the intestine microbial, digestion and immunity of Litopenaeus vannamei in response to dietary resistant starch
Duan, Y., Wang, Y., Liu, Q., Dong, H., Li, H., Xiong, D., & Zhang, J. (2019) · Scientific Reports · doi:10.1038/s41598-019-42939-8 · Cited by 89
Effects of hypoxic stress and recovery on oxidative stress, apoptosis, and intestinal microorganisms in Pelteobagrus vachelli
Zheng, X., Fu, D., Cheng, J., Tang, R., Chu, M., Chu, P., Wang, T., & Yin, S. (2021) · Aquaculture · doi:10.1016/j.aquaculture.2021.736945 · Cited by 87
Toxic effect of chronic waterborne copper exposure on growth, immunity, anti-oxidative capacity and gut microbiota of Pacific white shrimp Litopenaeus vannamei
Qian, D., Xu, C., Chen, C., Qin, J. G., Chen, L., & Li, E. (2020) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2020.03.018 · Cited by 85
The bacteria from large-sized bioflocs are more associated with the shrimp gut microbiota in culture system
Huang, L., Guo, H., Chen, C., Huang, X., Chen, W., Bao, F., Liu, W., Wang, S., & Zhang, D. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735159 · Cited by 82
Growth and health responses to a long-term pH stress in Pacific white shrimp Litopenaeus vannamei
Yu, Q., Xie, J., Huang, M., Chen, C., Qian, D., Qin, J. G., Chen, L., Jia, Y., & Li, E. (2020) · Aquaculture Reports · doi:10.1016/j.aqrep.2020.100280 · Cited by 84
Strain-specific changes in the gut microbiota profiles of the white shrimp Litopenaeus vannamei in response to cold stress
Liu, J., Wang, K., Wang, Y., Chen, W., Jin, Z., Yao, Z., & Zhang, D. (2019) · Aquaculture · doi:10.1016/j.aquaculture.2019.01.026 · Cited by 77
Changes in the intestine barrier function of Litopenaeus vannamei in response to pH stress
Duan, Y., Wang, Y., Liu, Q., Zhang, J., & Xiong, D. (2019) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2019.02.047 · Cited by 75
Rapid Change of Microbiota Diversity in the Gut but Not the Hepatopancreas During Gonadal Development of the New Shrimp Model Neocaridina denticulata
Cheung, M. K., Yip, H. Y., Nong, W., Law, P. T. W., Chu, K. H., Kwan, H. S., & Hui, J. H. L. (2015) · Marine Biotechnology · doi:10.1007/s10126-015-9662-8 · Cited by 78
Metagenomics in bioflocs and their effects on gut microbiome and immune responses in Pacific white shrimp
Tepaamorndech, S., Nookaew, I., Higdon, S. M., Santiyanont, P., Phromson, M., Chantarasakha, K., Mhuantong, W., Plengvidhya, V., & Visessanguan, W. (2020) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2020.08.042 · Cited by 77
Disease outbreak accompanies the dispersive structure of shrimp gut bacterial community with a simple core microbiota
Yao, Z., Yang, K., Huang, L., Huang, X., Qiuqian, L., Wang, K., & Zhang, D. (2018) · AMB Express · doi:10.1186/s13568-018-0644-x · Cited by 78
Efficacy and variations in bacterial density in the gut of Litopenaeus vannamei reared in a BFT system and in clear water supplemented with a commercial probiotic mixture
Hostins, B., Lara, G., Decamp, O., Cesar, D. E., & Wasielesky, W. (2017) · Aquaculture · doi:10.1016/j.aquaculture.2017.07.036 · Cited by 75
Persistence and spatial variation of antibiotic resistance genes and bacterial populations change in reared shrimp in South China
Su, H., Hu, X., Xu, Y., Xu, W., Huang, X., Wen, G., Yang, K., Li, Z., & Cao, Y. (2018) · Environment International · doi:10.1016/j.envint.2018.07.007 · Cited by 74
Study of fermented feed by mixed strains and their effects on the survival, growth, digestive enzyme activity and intestinal flora of Penaeus vannamei
Zhang, M., Pan, L., Fan, D., He, J., Su, C., Gao, S., & Zhang, M. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735703 · Cited by 76
Dietary supplementation of black soldier fly ( Hermetica illucens) meal modulates gut microbiota, innate immune response and health status of marron ( Cherax cainii , Austin 2002) fed poultry-by-product and fishmeal based diets
Foysal, M. J., Fotedar, R. K., Tay, C. Y., & Gupta, S. K. (2019) · PeerJ · doi:10.7717/peerj.6891 · Cited by 76
Lactic Acid Bacteria in Shellfish: Possibilities and Challenges
Ringø, E., Doan, H. V., Lee, S., & Song, S. K. (2019) · Reviews in Fisheries Science & Aquaculture · doi:10.1080/23308249.2019.1683151 · Cited by 68
Paenibacillus polymyxa improves the growth, immune and antioxidant activity, intestinal health, and disease resistance in Litopenaeus vannamei challenged with Vibrio parahaemolyticus
Amoah, K., Huang, Q., Dong, X., Tan, B., Zhang, S., Chi, S., Yang, Q., Liu, H., & Yang, Y. (2019) · Aquaculture · doi:10.1016/j.aquaculture.2019.734563 · Cited by 67
Comparative analysis of the intestinal bacterial community and expression of gut immunity genes in the Chinese Mitten Crab (Eriocheir sinensis)
Dong, J., Li, X., Zhang, R., Zhao, Y., Wu, G., Liu, J., Zhu, X., & Li, L. (2018) · AMB Express · doi:10.1186/s13568-018-0722-0 · Cited by 64
Self-citation
Impact of Aquaculture Practices on Intestinal Bacterial Profiles of Pacific Whiteleg Shrimp Litopenaeus vannamei
Landsman, A., St‐Pierre, B., Rosales-Leija, M., Brown, M. L., & Gibbons, W. R. (2019) · Microorganisms · doi:10.3390/microorganisms7040093 · Cited by 64
Effects on development and microbial community of shrimp Litopenaeus vannamei larvae with probiotics treatment
Wang, R., Guo, Z., Tang, Y., Kuang, J., Duan, Y., Lin, H., Jiang, S., Shu, H., & Huang, J. (2020) · AMB Express · doi:10.1186/s13568-020-01041-3 · Cited by 62
Integrating molecular and ecological approaches to identify potential polymicrobial pathogens over a shrimp disease progression
Dai, W., Yu, W., Xuan, L., Tao, Z., & Xiong, J. (2018) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-8891-y · Cited by 62
Analysis of microbiota in the stomach and midgut of two penaeid shrimps during probiotic feeding
Imaizumi, K., Tinwongger, S., Kondo, H., & Hırono, I. (2021) · Scientific Reports · doi:10.1038/s41598-021-89415-w · Cited by 60
Change in the intestinal bacterial community structure associated with environmental microorganisms during the growth of Eriocheir sinensis
Wang, C., Zhou, Y., Lv, D., Ge, Y., Li, H., & You, Y. (2018) · MicrobiologyOpen · doi:10.1002/mbo3.727 · Cited by 59
Response of intestine microbiota, digestion, and immunity in Pacific white shrimp Litopenaeus vannamei to dietary succinate
Duan, Y., Wang, Y., Ding, X., Xiong, D., & Zhang, J. (2019) · Aquaculture · doi:10.1016/j.aquaculture.2019.734762 · Cited by 58
Bacterial population in intestines of white shrimp, Litopenaeus vannamei fed a synbiotic containing Lactobacillus plantarum and galactooligosaccharide
Huynh, T.-G., Hu, S., Chiu, C.-S., Truong, Q.-P., & Liu, C. (2019) · Aquaculture Research · doi:10.1111/are.13951 · Cited by 57
Effect of mannan oligosaccharides on the microbiota and productivity parameters of Litopenaeus vannamei shrimp under intensive cultivation in Ecuador
Gainza, O., & Romero, J. (2020) · Scientific Reports · doi:10.1038/s41598-020-59587-y · Cited by 58
Bacterial analysis in the early developmental stages of the black tiger shrimp (Penaeus monodon)
Angthong, P., Uengwetwanit, T., Arayamethakorn, S., Chaitongsakul, P., Karoonuthaisiri, N., & Rungrassamee, W. (2020) · Scientific Reports · doi:10.1038/s41598-020-61559-1 · Cited by 58
Analysis of the intestinal microbial community in healthy and diarrheal perinatal yaks by high-throughput sequencing
Han, Z., Li, K., Shahzad, M. A., Zhang, H., Luo, H., Qiu, G., Lan, Y., Wang, X., Mehmood, K., & Li, J. (2017) · Microbial Pathogenesis · doi:10.1016/j.micpath.2017.08.025 · Cited by 57
Effects of hypoxia stress on oxidative stress, apoptosis and microorganisms in the intestine of large yellow croaker (Larimichthys crocea)
Liu, Y., Wang, J., Ding, J., Zhang, Y., Hou, C.-C., Shen, W., Wu, X., & Zhu, J. (2023) · Aquaculture · doi:10.1016/j.aquaculture.2023.740444 · Cited by 54
Characterization of fungus microbial diversity in healthy and diarrheal yaks in Gannan region of Tibet Autonomous Prefecture
Li, K., Mehmood, K., Zhang, H., Jiang, X., Shahzad, M. A., Dong, X., & Li, J. (2018) · Acta Tropica · doi:10.1016/j.actatropica.2018.02.017 · Cited by 51
Impact of ocean acidification on the intestinal microflora of the Pacific oyster Crassostrea gigas
Kong, N., Han, S., Fu, Q., Yu, Z., Wang, L., & Song, L. (2021) · Aquaculture · doi:10.1016/j.aquaculture.2021.737365 · Cited by 50
Self-citation
Enhancement of growth, survival, immunity and disease resistance in Litopenaeus vannamei, by the probiotic, Lactobacillus plantarum Ep-M17
Du, Y., Xu, W., Wu, T., Li, H., Hu, X., & Chen, J. (2022) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2022.08.066 · Cited by 51
Developmental and gut-related changes to microbiomes of the cultured juvenile spiny lobster Panulirus ornatus
Ooi, M. C., Goulden, E. F., Smith, G. G., Nowak, B. F., & Bridle, A. R. (2017) · FEMS Microbiology Ecology · doi:10.1093/femsec/fix159 · Cited by 54
Effects on survival and bacterial community composition of the aquaculture water and gastrointestinal tract of shrimp (Litopenaeus vannamei) exposed to probiotic treatments after an induced infection of acute hepatopancreatic necrosis disease
Pinoargote, G., Flores, G. E., Cooper, K. K., & Ravishankar, S. (2018) · Aquaculture Research · doi:10.1111/are.13791 · Cited by 52
Intestinal microbiota of white shrimp, Litopenaeus vannamei, fed diets containing Bacillus subtilis E20‐fermented soybean meal (FSBM) or an antimicrobial peptide derived from B. subtilis E20‐FSBM
Cheng, A., Yeh, S., Hu, S., Lin, H., & Liu, C. (2019) · Aquaculture Research · doi:10.1111/are.14345 · Cited by 48
A review of shrimp aquaculture and factors affecting the gut microbiome
El‐Saadony, M. T., Shehata, A. M., Alagawany, M. M., Abdel‐Moneim, A. E., Selim, D. A.-F., Abdo, M., Khafaga, A. F., El-Tarabily, K. A., El-Shall, N. A., & El-Hack, M. E. A. (2022) · Aquaculture International · doi:10.1007/s10499-022-00936-1 · Cited by 52
Intestinal Microbiota of White Shrimp Penaeus vannamei Under Intensive Cultivation Conditions in Ecuador
Gainza, O., Ramírez, C., Ramos, A. S., & Romero, J. (2017) · Microbial Ecology · doi:10.1007/s00248-017-1066-z · Cited by 47
Altered intestinal microbiota induced by chronic hypoxia drives the effects on lipid metabolism and the immune response of oriental river prawn Macrobrachium nipponense
Sun, S., Yang, M., Fu, H., Ge, X., & Zou, J. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735431 · Cited by 47
Intestinal morphology and microflora to Vibrio alginolyticus in pacific white shrimp (Litopenaeus vannamei)
Liao, G., Wu, Q., Mo, B., Zhou, J. F., Li, J., Zou, J., & Fan, L. (2022) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2022.01.026 · Cited by 47
Comparative analysis of microbial community structure between healthy and Aeromonas veronii-infected Yangtze finless porpoise
Liu, Z., Li, J., Wang, Y., Iqbal, M., Zheng, A., Zhao, M., Li, Z., Wang, N., Wu, C., & Yu, D. (2020) · Microbial Cell Factories · doi:10.1186/s12934-020-01383-4 · Cited by 46
Effects of three probiotic strains (Bacillus coagulans, B. licheniformis and Paenibacillus polymyxa) on growth, immune response, gut morphology and microbiota, and resistance against Vibrio harveyi of northern whitings, Sillago sihama Forsskál (1775)
Amoah, K., Dong, X., Tan, B., Zhang, S., Chi, S., Yang, Q., Liu, H., Yang, Y., & Zhang, H. (2021) · Animal Feed Science and Technology · doi:10.1016/j.anifeedsci.2021.114958 · Cited by 47
Understanding the host-microbe-environment interactions: Intestinal microbiota and transcriptomes of black tiger shrimp Penaeus monodon at different salinity levels
Chaiyapechara, S., Uengwetwanit, T., Arayamethakorn, S., Bunphimpapha, P., Phromson, M., Jangsutthivorawat, W., Tala, S., Karoonuthaisiri, N., & Rungrassamee, W. (2021) · Aquaculture · doi:10.1016/j.aquaculture.2021.737371 · Cited by 43
Transcriptomic and microbiota response on Litopenaeus vannamei intestine subjected to acute sulfide exposure
Duan, Y., Wang, Y., Liu, Q., Xiong, D., & Zhang, J. (2019) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2019.02.021 · Cited by 43
Identifying Potential Polymicrobial Pathogens: Moving Beyond Differential Abundance to Driver Taxa
Lü, J., Zhang, X., Qiu, Q., Chen, J., & Xiong, J. (2020) · Microbial Ecology · doi:10.1007/s00248-020-01511-y · Cited by 43
Monascus purpureus M-32 improves growth performance, immune response, intestinal morphology, microbiota and disease resistance in Litopenaeus vannamei
Wang, P., Chen, S., Wei, C.-Y., Yan, Q., Sun, Y., Yi, G., Li, D., & Fu, W. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735947 · Cited by 44
Taxonomic and functional changes in the microbiota of the white shrimp (Litopenaeus vannamei) associated with postlarval ontogenetic development
Garibay-Valdéz, E., Martínez‐Porchas, M., Calderón, K., Vargas‐Albores, F., Gollas‐Galván, T., & Martínez‐Córdova, L. R. (2019) · Aquaculture · doi:10.1016/j.aquaculture.2019.734842 · Cited by 42
Dysbiosis of the shrimp ( Penaeus monodon ) gut microbiome with AHPND outbreaks revealed by 16S rRNA metagenomics analysis
Hossain, M. S., Dai, J., & Qiu, D. (2021) · Aquaculture Research · doi:10.1111/are.15178 · Cited by 41
Digestive microbiota of shrimp Penaeus vannamei and oyster Crassostrea gigas co-cultured in integrated multi-trophic aquaculture system
Omont, A., Elizondo‐González, R., Quiróz-Guzmán, E., Escobedo‐Fregoso, C., Hernández-Herrera, R., & Peña‐Rodríguez, A. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735059 · Cited by 41
A Review: Microbes and Their Effect on Growth Performance of Litopenaeus vannamei (White Leg Shrimps) during Culture in Biofloc Technology System
Raza, B., Zheng, Z., Zhu, J., & Yang, W. T. (2024) · Microorganisms · doi:10.3390/microorganisms12051013 · Cited by 40
Effect of stocking density of Crassostrea sp. in a multitrophic biofloc system with Litopenaeus vannamei in nursery
de Lima, P. C. M., Silva, A. D. N. E., Silva, D. A., da Silva, S. M. B. C., Brito, L. O., & Gálvez, A. O. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735913 · Cited by 40
You Are What You Eat: A Genomic Analysis of the Gut Microbiome of Captive and Wild Octopus vulgaris Paralarvae and Their Zooplankton Prey
Roura, Á., Doyle, S. R., Nande, M., & Strugnell, J. M. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00362 · Cited by 36
Complete replacement of fishmeal by soybean and poultry meals in Pacific whiteleg shrimp feeds: Growth and tolerance to EMS/AHPND and WSSV challenge
McLean, E., Barrows, F. T., Craig, S. R., Alfrey, K. B., & Tran, L. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735383 · Cited by 34
White spot syndrome virus (WSSV) disturbs the intestinal microbiota of shrimp (Penaeus vannamei) reared in biofloc and clear seawater
Valente, C. D. S., Rodiles, A., Marques, M. R. F., & Merrifield, D. L. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10816-4 · Cited by 34
Effects of live microalgae and algae powder on microbial community, survival, metamorphosis and digestive enzyme activity of Penaeus monodon larvae at different growth stages
Tang, Y., Wang, R., Tan, L., Guo, L., Duan, Y., Yang, L., Jiang, S., Zhou, F., Jiang, S., & Huang, J. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735344 · Cited by 35
Shrimp microbiome and immune development in the early life stages
Angthong, P., Chaiyapechara, S., & Rungrassamee, W. (2023) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2023.104765 · Cited by 33
Insights into the microbiota of larval and postlarval Pacific white shrimp (Penaeus vannamei) along early developmental stages: a case in pond level
Wang, H., Huang, J., Wang, P., & Li, T. (2020) · Molecular Genetics and Genomics · doi:10.1007/s00438-020-01717-2 · Cited by 32
Highly effective reduction of phosphate and harmful bacterial community in shrimp wastewater using short-term biological treatment with immobilized engineering microalgae
Krasaesueb, N., Boonnorat, J., Maneeruttanarungroj, C., & Khetkorn, W. (2022) · Journal of Environmental Management · doi:10.1016/j.jenvman.2022.116452 · Cited by 32
Partial Substitution of Fish Meal with Soy Protein Concentrate on Growth, Liver Health, Intestinal Morphology, and Microbiota in Juvenile Large Yellow Croaker (Larimichthys crocea)
Wang, X., Luo, H., Wang, D., Zheng, Y., Zhu, W., Zhang, W., Chen, Z., Chen, X., & Shao, J. (2023) · Aquaculture Nutrition · doi:10.1155/2023/3706709 · Cited by 32
Assessment of microbial dynamics and antioxidant enzyme gene expression following probiotic administration in farmed Pacific white shrimp (Litopenaeus vannamei)
Guzmán-Villanueva, L. T., Escobedo‐Fregoso, C., Barajas-Sandoval, D. R., Gómez‐Gil, B., Peña‐Rodríguez, A., Martínez‐Díaz, S. F., Balcázar, J. L., & Quiróz-Guzmán, E. (2019) · Aquaculture · doi:10.1016/j.aquaculture.2019.734907 · Cited by 32
Biases during DNA extraction affect characterization of the microbiota associated with larvae of the Pacific white shrimp,Litopenaeus vannamei
Xue, M., Wu, L., He, Y., Liang, H., & Wen, C. (2018) · PeerJ · doi:10.7717/peerj.5257 · Cited by 31
Microencapsulation of probiotics and its applications with prebiotic in Pacific white shrimp larvae through Artemia sp.
Ramadhani, D. E., Widanarni, W., & Sukenda, S. (2019) · Jurnal Akuakultur Indonesia · doi:10.19027/jai.18.2.130-140 · Cited by 31
Epimicrobiome Shifts With Bleaching Disease Progression in the Brown Seaweed Saccharina japonica
Fan, L., Egan, S., Zhuang, Y., Chang, L., Xiao, L., Qin, Y., & Wang, G. (2022) · Frontiers in Marine Science · doi:10.3389/fmars.2022.865224 · Cited by 30
Shrimp Intestinal Microbiota Homeostasis: Dynamic Interplay Between the Microbiota and Host Immunity
Zhou, K., Liu, P., Yao, J., Vasta, G. R., Wang, J., & Wang, X. (2024) · Reviews in Aquaculture · doi:10.1111/raq.12986 · Cited by 30
Changes of water, sediment, and intestinal bacterial communities in Penaeus japonicus cultivation and their impacts on shrimp physiological health
Song, M., Pan, L., Zhang, M., Huang, F., Gao, S., & Tian, C. (2020) · Aquaculture International · doi:10.1007/s10499-020-00562-9 · Cited by 30
Core microbiome involved in nitrite removal in shrimp culture ponds
Hu, D., Wang, L., Zhao, R., Zeng, J., & Shao, Z. (2021) · Aquaculture Research · doi:10.1111/are.15698 · Cited by 28
Self-citation
The Active Microbiota of the Eggs and the Nauplii of the Pacific Blue Shrimp Litopenaeus stylirostris Partially Shaped by a Potential Vertical Transmission
Giraud, C., Callac, N., Boulo, V., Lam, J.-S., Pham, D., Selmaoui-Folcher, N., & Wabete, N. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.886752 · Cited by 26
BALOs Improved Gut Microbiota Health in Postlarval Shrimp (Litopenaeus vannamei) After Being Subjected to Salinity Reduction Treatment
Cao, Q., Najnine, F., Han, H., Wu, B., & Cai, J. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01296 · Cited by 27
Modulation of gut microbiota, blood metabolites, and disease resistance by dietary β-glucan in rainbow trout (Oncorhynchus mykiss)
Menanteau‐Ledouble, S., Skov, J., Lukassen, M. B., Rolle-Kampczyk, U. E., Haange, S., Dalsgaard, I., von Bergen�, M., & Nielsen, J. L. (2022) · Animal Microbiome · doi:10.1186/s42523-022-00209-5 · Cited by 26
Investigation of the Potential Effects of Host Genetics and Probiotic Treatment on the Gut Bacterial Community Composition of Aquaculture-raised Pacific Whiteleg Shrimp, Litopenaeus vannamei
Landsman, A., St‐Pierre, B., Rosales-Leija, M., Brown, M. L., & Gibbons, W. R. (2019) · Microorganisms · doi:10.3390/microorganisms7080217 · Cited by 26
Interaction Between the Intestinal Microbial Community and Transcriptome Profile in Common Carp (Cyprinus carpio L.)
Su, S., Jing, X., Zhang, C., Hou, Y., Li, Z., Yang, X., Zhou, X., Xu, P., Tang, Y., & Zhu, J. X. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.659602 · Cited by 26
Characteristics of intestinal microbiota in male morphotypes of the giant freshwater prawn Macrobrachium rosenbergii
Gao, Q., Luo, J., Liu, P., Yi, S., Tang, Q., Jing-fen, L., Xia, Z., & Yang, G. (2022) · Aquaculture · doi:10.1016/j.aquaculture.2022.738200 · Cited by 25
Characterization and in-vivo evaluation of potential probiotics of the bacterial flora within the water column of a healthy shrimp larviculture system
Xue, M., Liang, H., He, Y., & Wen, C. (2015) · Chinese Journal of Oceanology and Limnology · doi:10.1007/s00343-016-5024-2 · Cited by 25
Biological filters regulate water quality, modulate health status, immune indices and gut microbiota of freshwater crayfish, marron (Cherax cainii, Austin, 2002)
Foysal, M. J., Fotedar, R. K., Tay, C. Y., & Gupta, S. K. (2020) · Chemosphere · doi:10.1016/j.chemosphere.2020.125821 · Cited by 24
Impact of dietary supplementation with Eleutherine bulbosa (Mill.) Urb. on intestinal microbiota diversity and growth of white shrimp, Litopenaeus vannamei
Munaeni, W., Widanarni, W., Yuhana, M., Setiawati, M., & Wahyudi, A. T. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735466 · Cited by 23
The implication of metabolically active Vibrio spp. in the digestive tract of Litopenaeus vannamei for its post-larval development
Garibay-Valdéz, E., Martínez‐Córdova, L. R., López‐Torres, M. A., Almendáriz-Tapia, F. J., Martínez‐Porchas, M., & Calderón, K. (2020) · Scientific Reports · doi:10.1038/s41598-020-68222-9 · Cited by 23
Absence of a microbiome in the midgut trunk of six representative Crustacea
Martin, G. G., Natha, Z., Henderson, N., Bang, S., Hendry, H., & Loera, Y. (2019) · Journal of Crustacean Biology · doi:10.1093/jcbiol/ruz087 · Cited by 23
Effects of different dietary copper sources on the growth and intestinal microbial communities of Pacific white shrimp ( Litopenaeus vannamei )
Yuan, Y., Jin, M., Luo, J., Xiong, J., Ward, T. L., Ji, F., Xu, G., Sun, M., & Zhou, Q. (2019) · Aquaculture Nutrition · doi:10.1111/anu.12901 · Cited by 22

Authors: Huang, Z., Li, X., Wang, L., & Shao, Z.
Affiliations: Third Institute of Oceanography (CN)
Ningbo University (CN)
Corresponding author: Shao, Zongze
ORCID: Li, Xiaoyi
Wang, Liping
Shao, Zongze
Venue: Aquaculture Research
Publisher: Wiley
Published: 2014-10-28
Volume: 47
Issue: 6
Pages: 1737-1746
ISSN: 1355-557X (ISSN-L)
DOI: 10.1111/are.12628
OpenAlex: W2116827175
Cited by: 205
References: 35
Citations by year: 2026: 7 · 2025: 15 · 2024: 22 · 2023: 21 · 2022: 21 · 2021: 20 · 2020: 37 · 2019: 25 · 2018: 19 · 2017: 13 · 2016: 1 · 2015: 4
FWCI: 2.74
Type: journal article
Language: en
Open access: closed
Licence: doi.wiley.com/10.1002/tdm_license_1.1 (tdm, 308 d)
Locations: Aquaculture Research (publishedVersion)
Funders: Public Welfare Project of SOA, China (201005032)
Topics: Life Sciences › Immunology and Microbiology › Immunology › Aquaculture disease management and microbiota
Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Keywords: Litopenaeus vannamei, white shrimp, intestinal bacterial community, gut microbiota, postlarvae, juveniles, Proteobacteria, Bacteroidetes, actinobacteria, Flavobacteriaceae, Vibrionaceae, Microbacteriaceae, Mycoplasmataceae, Artemia nauplii, bacterial community dynamics

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Changes in the intestinal bacterial community during the growth of white shrimp, Litopenaeus vannamei

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks