Integrating short- and full-length 16S rRNA gene sequencing to elucidate microbiome profiles in Pacific white shrimp ( Litopenaeus vannamei ) ponds
This interdisciplinary study investigated the influence of sequencing techniques on bacterial communities profiling within Pacific white shrimp ( Litopenaeus vannamei ) ponds. By integrating aquaculture, microbiology, and environmental science, we revealed the role of ecological niches and factors l...
Saved in:
Published in | Microbiology spectrum Vol. 12; no. 11; p. e0096524 |
---|---|
Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Microbiology
05.11.2024
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | This interdisciplinary study investigated the influence of sequencing techniques on bacterial communities profiling within Pacific white shrimp (
Litopenaeus vannamei
) ponds. By integrating aquaculture, microbiology, and environmental science, we revealed the role of ecological niches and factors like salinity and pH on microbiota diversity and composition in shrimp intestines, pond water, and sediment. Additionally, we compared the taxonomic resolution using partial versus full-length 16S rRNA gene sequences, highlighting the value of longer amplicons for precise identification of key taxa. These findings provide novel insights into microbial dynamics underlying environmental effects in shrimp aquaculture. Comprehensive characterization of the pond microbiome could lead to management strategies that promote shrimp health and productivity. Furthermore, the potential of a multi-omics approach for integrating complementary data streams to elucidate environment-microbiome-host interactions was highlighted. |
---|---|
AbstractList | ABSTRACT Despite their immense economic value as a key aquaculture species, the production of Pacific white shrimp (Litopenaeus vannamei) faces significant challenges from intensive farming practices and disease outbreaks. Routine microbial profiling for disease surveillance could be a promising approach to anticipate and control disease outbreaks. To achieve this, accuracy in microbial profiling in shrimp ponds is crucial for enabling targeted action and prevention. Extensive documentation emphasizes that, beyond biological factors (related to the host, diet, or health status during the rearing period), technical elements, including sequencing techniques significantly influence bacterial community profiling. This study investigated the influence of short- and long-read sequencing of 16S rRNA genes on the microbial profiles in shrimp intestines, water, and sediments. The origin of the samples (intestine or environmental) in shrimp culture ponds primarily drove the observed differences in core microbial species. The ecological niches accounted for 56% of bacterial community variations in culture ponds. Both sequencing approaches showed consistent results in identifying higher-rank taxa and assessing alpha and beta diversity. However, at the species level, full-length 16S rRNA gene sequences provided better resolution than V3–V4 sequences. For routine microbial profiling in shrimp culture ponds, our study suggests that short-read sequences were sufficient for determining overall bacterial community.IMPORTANCEThis interdisciplinary study investigated the influence of sequencing techniques on bacterial communities profiling within Pacific white shrimp (Litopenaeus vannamei) ponds. By integrating aquaculture, microbiology, and environmental science, we revealed the role of ecological niches and factors like salinity and pH on microbiota diversity and composition in shrimp intestines, pond water, and sediment. Additionally, we compared the taxonomic resolution using partial versus full-length 16S rRNA gene sequences, highlighting the value of longer amplicons for precise identification of key taxa. These findings provide novel insights into microbial dynamics underlying environmental effects in shrimp aquaculture. Comprehensive characterization of the pond microbiome could lead to management strategies that promote shrimp health and productivity. Furthermore, the potential of a multi-omics approach for integrating complementary data streams to elucidate environment-microbiome-host interactions was highlighted. Despite their immense economic value as a key aquaculture species, the production of Pacific white shrimp (Litopenaeus vannamei) faces significant challenges from intensive farming practices and disease outbreaks. Routine microbial profiling for disease surveillance could be a promising approach to anticipate and control disease outbreaks. To achieve this, accuracy in microbial profiling in shrimp ponds is crucial for enabling targeted action and prevention. Extensive documentation emphasizes that, beyond biological factors (related to the host, diet, or health status during the rearing period), technical elements, including sequencing techniques significantly influence bacterial community profiling. This study investigated the influence of short- and long-read sequencing of 16S rRNA genes on the microbial profiles in shrimp intestines, water, and sediments. The origin of the samples (intestine or environmental) in shrimp culture ponds primarily drove the observed differences in core microbial species. The ecological niches accounted for 56% of bacterial community variations in culture ponds. Both sequencing approaches showed consistent results in identifying higher-rank taxa and assessing alpha and beta diversity. However, at the species level, full-length 16S rRNA gene sequences provided better resolution than V3-V4 sequences. For routine microbial profiling in shrimp culture ponds, our study suggests that short-read sequences were sufficient for determining overall bacterial community.IMPORTANCEThis interdisciplinary study investigated the influence of sequencing techniques on bacterial communities profiling within Pacific white shrimp (Litopenaeus vannamei) ponds. By integrating aquaculture, microbiology, and environmental science, we revealed the role of ecological niches and factors like salinity and pH on microbiota diversity and composition in shrimp intestines, pond water, and sediment. Additionally, we compared the taxonomic resolution using partial versus full-length 16S rRNA gene sequences, highlighting the value of longer amplicons for precise identification of key taxa. These findings provide novel insights into microbial dynamics underlying environmental effects in shrimp aquaculture. Comprehensive characterization of the pond microbiome could lead to management strategies that promote shrimp health and productivity. Furthermore, the potential of a multi-omics approach for integrating complementary data streams to elucidate environment-microbiome-host interactions was highlighted.Despite their immense economic value as a key aquaculture species, the production of Pacific white shrimp (Litopenaeus vannamei) faces significant challenges from intensive farming practices and disease outbreaks. Routine microbial profiling for disease surveillance could be a promising approach to anticipate and control disease outbreaks. To achieve this, accuracy in microbial profiling in shrimp ponds is crucial for enabling targeted action and prevention. Extensive documentation emphasizes that, beyond biological factors (related to the host, diet, or health status during the rearing period), technical elements, including sequencing techniques significantly influence bacterial community profiling. This study investigated the influence of short- and long-read sequencing of 16S rRNA genes on the microbial profiles in shrimp intestines, water, and sediments. The origin of the samples (intestine or environmental) in shrimp culture ponds primarily drove the observed differences in core microbial species. The ecological niches accounted for 56% of bacterial community variations in culture ponds. Both sequencing approaches showed consistent results in identifying higher-rank taxa and assessing alpha and beta diversity. However, at the species level, full-length 16S rRNA gene sequences provided better resolution than V3-V4 sequences. For routine microbial profiling in shrimp culture ponds, our study suggests that short-read sequences were sufficient for determining overall bacterial community.IMPORTANCEThis interdisciplinary study investigated the influence of sequencing techniques on bacterial communities profiling within Pacific white shrimp (Litopenaeus vannamei) ponds. By integrating aquaculture, microbiology, and environmental science, we revealed the role of ecological niches and factors like salinity and pH on microbiota diversity and composition in shrimp intestines, pond water, and sediment. Additionally, we compared the taxonomic resolution using partial versus full-length 16S rRNA gene sequences, highlighting the value of longer amplicons for precise identification of key taxa. These findings provide novel insights into microbial dynamics underlying environmental effects in shrimp aquaculture. Comprehensive characterization of the pond microbiome could lead to management strategies that promote shrimp health and productivity. Furthermore, the potential of a multi-omics approach for integrating complementary data streams to elucidate environment-microbiome-host interactions was highlighted. Despite their immense economic value as a key aquaculture species, the production of Pacific white shrimp (Litopenaeus vannamei) faces significant challenges from intensive farming practices and disease outbreaks. Routine microbial profiling for disease surveillance could be a promising approach to anticipate and control disease outbreaks. To achieve this, accuracy in microbial profiling in shrimp ponds is crucial for enabling targeted action and prevention. Extensive documentation emphasizes that, beyond biological factors (related to the host, diet, or health status during the rearing period), technical elements, including sequencing techniques significantly influence bacterial community profiling. This study investigated the influence of short- and long-read sequencing of 16S rRNA genes on the microbial profiles in shrimp intestines, water, and sediments. The origin of the samples (intestine or environmental) in shrimp culture ponds primarily drove the observed differences in core microbial species. The ecological niches accounted for 56% of bacterial community variations in culture ponds. Both sequencing approaches showed consistent results in identifying higher-rank taxa and assessing alpha and beta diversity. However, at the species level, full-length 16S rRNA gene sequences provided better resolution than V3–V4 sequences. For routine microbial profiling in shrimp culture ponds, our study suggests that short-read sequences were sufficient for determining overall bacterial community.IMPORTANCEThis interdisciplinary study investigated the influence of sequencing techniques on bacterial communities profiling within Pacific white shrimp (Litopenaeus vannamei) ponds. By integrating aquaculture, microbiology, and environmental science, we revealed the role of ecological niches and factors like salinity and pH on microbiota diversity and composition in shrimp intestines, pond water, and sediment. Additionally, we compared the taxonomic resolution using partial versus full-length 16S rRNA gene sequences, highlighting the value of longer amplicons for precise identification of key taxa. These findings provide novel insights into microbial dynamics underlying environmental effects in shrimp aquaculture. Comprehensive characterization of the pond microbiome could lead to management strategies that promote shrimp health and productivity. Furthermore, the potential of a multi-omics approach for integrating complementary data streams to elucidate environment-microbiome-host interactions was highlighted. Despite their immense economic value as a key aquaculture species, the production of Pacific white shrimp ( Litopenaeus vannamei ) faces significant challenges from intensive farming practices and disease outbreaks. Routine microbial profiling for disease surveillance could be a promising approach to anticipate and control disease outbreaks. To achieve this, accuracy in microbial profiling in shrimp ponds is crucial for enabling targeted action and prevention. Extensive documentation emphasizes that, beyond biological factors (related to the host, diet, or health status during the rearing period), technical elements, including sequencing techniques significantly influence bacterial community profiling. This study investigated the influence of short- and long-read sequencing of 16S rRNA genes on the microbial profiles in shrimp intestines, water, and sediments. The origin of the samples (intestine or environmental) in shrimp culture ponds primarily drove the observed differences in core microbial species. The ecological niches accounted for 56% of bacterial community variations in culture ponds. Both sequencing approaches showed consistent results in identifying higher-rank taxa and assessing alpha and beta diversity. However, at the species level, full-length 16S rRNA gene sequences provided better resolution than V3–V4 sequences. For routine microbial profiling in shrimp culture ponds, our study suggests that short-read sequences were sufficient for determining overall bacterial community. Despite their immense economic value as a key aquaculture species, the production of Pacific white shrimp ( ) faces significant challenges from intensive farming practices and disease outbreaks. Routine microbial profiling for disease surveillance could be a promising approach to anticipate and control disease outbreaks. To achieve this, accuracy in microbial profiling in shrimp ponds is crucial for enabling targeted action and prevention. Extensive documentation emphasizes that, beyond biological factors (related to the host, diet, or health status during the rearing period), technical elements, including sequencing techniques significantly influence bacterial community profiling. This study investigated the influence of short- and long-read sequencing of 16S rRNA genes on the microbial profiles in shrimp intestines, water, and sediments. The origin of the samples (intestine or environmental) in shrimp culture ponds primarily drove the observed differences in core microbial species. The ecological niches accounted for 56% of bacterial community variations in culture ponds. Both sequencing approaches showed consistent results in identifying higher-rank taxa and assessing alpha and beta diversity. However, at the species level, full-length 16S rRNA gene sequences provided better resolution than V3-V4 sequences. For routine microbial profiling in shrimp culture ponds, our study suggests that short-read sequences were sufficient for determining overall bacterial community.IMPORTANCEThis interdisciplinary study investigated the influence of sequencing techniques on bacterial communities profiling within Pacific white shrimp ( ) ponds. By integrating aquaculture, microbiology, and environmental science, we revealed the role of ecological niches and factors like salinity and pH on microbiota diversity and composition in shrimp intestines, pond water, and sediment. Additionally, we compared the taxonomic resolution using partial versus full-length 16S rRNA gene sequences, highlighting the value of longer amplicons for precise identification of key taxa. These findings provide novel insights into microbial dynamics underlying environmental effects in shrimp aquaculture. Comprehensive characterization of the pond microbiome could lead to management strategies that promote shrimp health and productivity. Furthermore, the potential of a multi-omics approach for integrating complementary data streams to elucidate environment-microbiome-host interactions was highlighted. This interdisciplinary study investigated the influence of sequencing techniques on bacterial communities profiling within Pacific white shrimp ( Litopenaeus vannamei ) ponds. By integrating aquaculture, microbiology, and environmental science, we revealed the role of ecological niches and factors like salinity and pH on microbiota diversity and composition in shrimp intestines, pond water, and sediment. Additionally, we compared the taxonomic resolution using partial versus full-length 16S rRNA gene sequences, highlighting the value of longer amplicons for precise identification of key taxa. These findings provide novel insights into microbial dynamics underlying environmental effects in shrimp aquaculture. Comprehensive characterization of the pond microbiome could lead to management strategies that promote shrimp health and productivity. Furthermore, the potential of a multi-omics approach for integrating complementary data streams to elucidate environment-microbiome-host interactions was highlighted. |
Author | Sutheeworapong, Sawannee Jenjaroenpun, Piroon Rungrassamee, Wanilada Angthong, Pacharaporn Rajonhson, Dora M. Tapaneeyaworawong, Paveena Powtongsook, Sorawit Kruasuwan, Worarat Wongsurawat, Thidathip Chaiyapechara, Sage Thepsuwan, Timpika Satanwat, Penpicha |
Author_xml | – sequence: 1 givenname: Dora M. orcidid: 0000-0003-3247-4510 surname: Rajonhson fullname: Rajonhson, Dora M. organization: National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Khlong Luang, Pathum Thani, Thailand – sequence: 2 givenname: Pacharaporn orcidid: 0009-0008-4546-1915 surname: Angthong fullname: Angthong, Pacharaporn organization: National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Khlong Luang, Pathum Thani, Thailand – sequence: 3 givenname: Timpika surname: Thepsuwan fullname: Thepsuwan, Timpika organization: National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Khlong Luang, Pathum Thani, Thailand – sequence: 4 givenname: Sawannee orcidid: 0000-0002-1988-1624 surname: Sutheeworapong fullname: Sutheeworapong, Sawannee organization: Pilot Plant Development and Training Institute, King Mongkut’s University of Technology Thonburi, Bangkok, Thailand – sequence: 5 givenname: Penpicha surname: Satanwat fullname: Satanwat, Penpicha organization: National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Khlong Luang, Pathum Thani, Thailand, Center of Excellence for Marine Biotechnology, Department of Marine Science, Faculty of Science, Chulalongkorn University, Bangkok, Thailand – sequence: 6 givenname: Paveena surname: Tapaneeyaworawong fullname: Tapaneeyaworawong, Paveena organization: National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Khlong Luang, Pathum Thani, Thailand, Center of Excellence for Marine Biotechnology, Department of Marine Science, Faculty of Science, Chulalongkorn University, Bangkok, Thailand – sequence: 7 givenname: Sorawit surname: Powtongsook fullname: Powtongsook, Sorawit organization: National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Khlong Luang, Pathum Thani, Thailand, Center of Excellence for Marine Biotechnology, Department of Marine Science, Faculty of Science, Chulalongkorn University, Bangkok, Thailand – sequence: 8 givenname: Worarat orcidid: 0000-0002-0421-0211 surname: Kruasuwan fullname: Kruasuwan, Worarat organization: Division of Medical Bioinformatics, Research Department, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand, Siriraj Long-read Lab (Si-LoL), Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand – sequence: 9 givenname: Piroon orcidid: 0000-0002-1555-401X surname: Jenjaroenpun fullname: Jenjaroenpun, Piroon organization: Division of Medical Bioinformatics, Research Department, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand, Siriraj Long-read Lab (Si-LoL), Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand – sequence: 10 givenname: Thidathip orcidid: 0000-0002-3659-2074 surname: Wongsurawat fullname: Wongsurawat, Thidathip organization: Division of Medical Bioinformatics, Research Department, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand, Siriraj Long-read Lab (Si-LoL), Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand – sequence: 11 givenname: Sage orcidid: 0000-0002-6836-2759 surname: Chaiyapechara fullname: Chaiyapechara, Sage organization: National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Khlong Luang, Pathum Thani, Thailand – sequence: 12 givenname: Wanilada orcidid: 0000-0002-5802-4342 surname: Rungrassamee fullname: Rungrassamee, Wanilada organization: National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Khlong Luang, Pathum Thani, Thailand |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39329828$$D View this record in MEDLINE/PubMed |
BookMark | eNp1kstu1DAUhiNUREvpA7BBXpZFBl8TZ4WqistII0DQveU4JxmPEjvYTqs-R18YT6et2gUrH9mfPp1z_L8tjpx3UBTvCV4RQuWnOINJYZlWGDeVKCl_VZxQkivMm_roWX1cnMW4wxgTggUV9E1xzBpGG0nlSXG3dgmGoJN1A4pbH1KJtOtQv4xjOYIb0haR6g8Kv39coAEcoAh_F3BmzyePYFyM7XQCNFkTfGv9BGgOvrcjRGQd-qWN7a1BN1ubobgNdprROdrY5GdwGpaIrrVzegKLPqLZuy6-K173eoxw9nCeFldfv1xdfi83P7-tLy82peaiTmUrCQbSMCZFDRKLquM8j0g5E4Lw3mhtKimIJrzpmeTEAMOcY901bd0BZqfF-qDtvN6pOTemw63y2qr7Cx8GpUOyZgRVNaZjNeUaBOay7SUhgknZMU5BN6LPrs8H17y0E3QGXAp6fCF9-eLsVg3-Wu1FNa54Npw_GILPC45JTTYaGEftwC9RsTwax1VdNRldHVAdJ6p2fgkur0kRrPbBUI_BUPfBUHTv_vC8u6e2HmOQAXIA8hfGGKB_Qv4v_Qdw_MkO |
Cites_doi | 10.1016/j.jip.2020.107387 10.1038/sdata.2019.7 10.1111/are.13791 10.1186/s40168-020-00802-3 10.1111/j.1365-2095.2011.00865.x 10.1016/j.aquaculture.2021.737871 10.1093/bioinformatics/bty149 10.3389/fgene.2023.1213829 10.1038/s41598-020-61559-1 10.1016/j.aquaculture.2021.737371 10.1007/s00253-018-8855-2 10.1186/s13568-022-01423-9 10.1016/j.aquaculture.2016.01.011 10.1038/s41598-017-11805-w 10.1111/raq.12471 10.3389/fmicb.2017.01362 10.1038/s41598-017-09923-6 10.1007/s00248-011-9936-2 10.9734/AJEE/2017/35287 10.7717/peerj.5382 10.1111/are.14770 10.1016/j.aqrep.2024.101922 10.3390/w14244019 10.1007/s00284-022-02956-9 10.1007/s00253-024-13046-0 10.1016/j.aquaculture.2014.01.008 10.1111/are.15731 10.1093/bioinformatics/btad470 10.1371/journal.pone.0091853 10.3390/ijms150813663 10.3390/genes12010040 10.1371/journal.pone.0060802 10.1038/s41587-020-0548-6 10.1038/s41592-022-01520-4 10.1038/ismej.2017.119 10.1016/j.aquaculture.2016.02.008 10.1038/s41598-021-90067-z 10.3390/antiox11061143 10.1016/j.aquaculture.2015.12.014 10.4060/cc0461en 10.1038/s41587-019-0209-9 10.1093/nar/gks1219 10.1186/s40168-021-01043-8 10.1016/j.dci.2023.104765 10.1111/j.1444-2906.2005.01061.x 10.3147/jsfp.36.133 10.4172/2155-9910.S1-002 10.1007/s12562-014-0765-3 |
ContentType | Journal Article |
Copyright | Copyright © 2024 Rajonhson et al. Copyright © 2024 Rajonhson et al. 2024 Rajonhson et al. |
Copyright_xml | – notice: Copyright © 2024 Rajonhson et al. – notice: Copyright © 2024 Rajonhson et al. 2024 Rajonhson et al. |
DBID | AAYXX CITATION NPM 7X8 5PM DOA |
DOI | 10.1128/spectrum.00965-24 |
DatabaseName | CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic PubMed CrossRef |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
EISSN | 2165-0497 |
Editor | Connors, Bernadette J. |
Editor_xml | – sequence: 1 givenname: Bernadette J. surname: Connors fullname: Connors, Bernadette J. |
ExternalDocumentID | oai_doaj_org_article_69cd3724ae5048bf8115388d342ea95f PMC11537064 spectrum00965-24 39329828 10_1128_spectrum_00965_24 |
Genre | Journal Article |
GrantInformation_xml | – fundername: The NSRF via Program Management Unit for Human Resources and Institutional Development, Research, and Innovation Grant grantid: B05F640108 – fundername: The National Science, Research and Innovation Fund through Thailand Science Research, and Innovation (TSRI) – fundername: The National Research Council of Thailand (NRCT) and the National Science and Technology Development Agency (NSTDA) grantid: N42A670241 – fundername: The TWAS-BIOTEC Postdoctoral Fellowship Program – fundername: ; – fundername: ; grantid: B05F640108 – fundername: ; grantid: N42A670241 |
GroupedDBID | 53G AAGFI AAUOK AAYXX ADBBV AGVNZ ALMA_UNASSIGNED_HOLDINGS CITATION EJD FF~ FRP GROUPED_DOAJ H13 M~E OK1 RPM RSF NPM UCJ 7X8 5PM |
ID | FETCH-LOGICAL-a457t-b810e1933857e8056d441102435514fcaac6851a149f3841ce30440ad9b7de03 |
IEDL.DBID | DOA |
ISSN | 2165-0497 |
IngestDate | Wed Aug 27 01:21:31 EDT 2025 Thu Aug 21 18:43:42 EDT 2025 Thu Jul 10 19:00:55 EDT 2025 Wed Nov 06 04:45:17 EST 2024 Mon Jul 21 06:05:21 EDT 2025 Tue Jul 01 00:43:00 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 11 |
Keywords | full-length 16S rRNA gene sequencing intestinal microbiota Litopenaeus vannamei environmental microbiota short-read sequencing |
Language | English |
License | This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license. https://creativecommons.org/licenses/by/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-a457t-b810e1933857e8056d441102435514fcaac6851a149f3841ce30440ad9b7de03 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 The authors declare no conflict of interest. |
ORCID | 0000-0002-1988-1624 0000-0002-3659-2074 0000-0003-3247-4510 0000-0002-0421-0211 0000-0002-6836-2759 0009-0008-4546-1915 0000-0002-1555-401X 0000-0002-5802-4342 |
OpenAccessLink | https://doaj.org/article/69cd3724ae5048bf8115388d342ea95f |
PMID | 39329828 |
PQID | 3110406769 |
PQPubID | 23479 |
PageCount | 24 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_69cd3724ae5048bf8115388d342ea95f pubmedcentral_primary_oai_pubmedcentral_nih_gov_11537064 proquest_miscellaneous_3110406769 asm2_journals_10_1128_spectrum_00965_24 pubmed_primary_39329828 crossref_primary_10_1128_spectrum_00965_24 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2024-11-05 |
PublicationDateYYYYMMDD | 2024-11-05 |
PublicationDate_xml | – month: 11 year: 2024 text: 2024-11-05 day: 05 |
PublicationDecade | 2020 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States – name: 1752 N St., N.W., Washington, DC |
PublicationTitle | Microbiology spectrum |
PublicationTitleAbbrev | Spectrum |
PublicationTitleAlternate | Microbiol Spectr |
PublicationYear | 2024 |
Publisher | American Society for Microbiology |
Publisher_xml | – name: American Society for Microbiology |
References | e_1_3_4_9_2 e_1_3_4_7_2 e_1_3_4_40_2 e_1_3_4_5_2 Salayo ND (e_1_3_4_3_2) 2022 e_1_3_4_23_2 e_1_3_4_44_2 e_1_3_4_21_2 e_1_3_4_42_2 e_1_3_4_27_2 e_1_3_4_48_2 e_1_3_4_25_2 e_1_3_4_46_2 e_1_3_4_29_2 e_1_3_4_30_2 e_1_3_4_51_2 e_1_3_4_11_2 e_1_3_4_34_2 e_1_3_4_15_2 e_1_3_4_38_2 e_1_3_4_13_2 e_1_3_4_36_2 e_1_3_4_19_2 e_1_3_4_17_2 e_1_3_4_2_2 e_1_3_4_8_2 e_1_3_4_41_2 e_1_3_4_6_2 e_1_3_4_4_2 e_1_3_4_22_2 e_1_3_4_45_2 e_1_3_4_20_2 e_1_3_4_43_2 e_1_3_4_26_2 e_1_3_4_49_2 e_1_3_4_24_2 e_1_3_4_47_2 e_1_3_4_28_2 Di L (e_1_3_4_32_2) 1991 e_1_3_4_52_2 e_1_3_4_50_2 e_1_3_4_12_2 e_1_3_4_33_2 e_1_3_4_10_2 e_1_3_4_31_2 e_1_3_4_16_2 e_1_3_4_37_2 e_1_3_4_14_2 e_1_3_4_35_2 e_1_3_4_18_2 e_1_3_4_39_2 |
References_xml | – ident: e_1_3_4_18_2 doi: 10.1016/j.jip.2020.107387 – ident: e_1_3_4_39_2 doi: 10.1038/sdata.2019.7 – ident: e_1_3_4_36_2 doi: 10.1111/are.13791 – ident: e_1_3_4_42_2 doi: 10.1186/s40168-020-00802-3 – ident: e_1_3_4_22_2 doi: 10.1111/j.1365-2095.2011.00865.x – ident: e_1_3_4_6_2 doi: 10.1016/j.aquaculture.2021.737871 – ident: e_1_3_4_33_2 doi: 10.1093/bioinformatics/bty149 – ident: e_1_3_4_38_2 doi: 10.3389/fgene.2023.1213829 – ident: e_1_3_4_17_2 doi: 10.1038/s41598-020-61559-1 – ident: e_1_3_4_21_2 doi: 10.1016/j.aquaculture.2021.737371 – ident: e_1_3_4_41_2 doi: 10.1007/s00253-018-8855-2 – ident: e_1_3_4_52_2 doi: 10.1186/s13568-022-01423-9 – ident: e_1_3_4_8_2 doi: 10.1016/j.aquaculture.2016.01.011 – ident: e_1_3_4_19_2 doi: 10.1038/s41598-017-11805-w – ident: e_1_3_4_47_2 – ident: e_1_3_4_5_2 doi: 10.1111/raq.12471 – ident: e_1_3_4_46_2 doi: 10.3389/fmicb.2017.01362 – ident: e_1_3_4_43_2 doi: 10.1038/s41598-017-09923-6 – ident: e_1_3_4_16_2 doi: 10.1007/s00248-011-9936-2 – ident: e_1_3_4_11_2 doi: 10.9734/AJEE/2017/35287 – ident: e_1_3_4_23_2 doi: 10.7717/peerj.5382 – ident: e_1_3_4_20_2 doi: 10.1111/are.14770 – ident: e_1_3_4_26_2 doi: 10.1016/j.aqrep.2024.101922 – ident: e_1_3_4_12_2 doi: 10.3390/w14244019 – ident: e_1_3_4_40_2 doi: 10.1007/s00284-022-02956-9 – ident: e_1_3_4_49_2 doi: 10.1007/s00253-024-13046-0 – ident: e_1_3_4_37_2 doi: 10.1016/j.aquaculture.2014.01.008 – ident: e_1_3_4_24_2 doi: 10.1111/are.15731 – ident: e_1_3_4_35_2 doi: 10.1093/bioinformatics/btad470 – ident: e_1_3_4_15_2 doi: 10.1371/journal.pone.0091853 – ident: e_1_3_4_45_2 doi: 10.3390/ijms150813663 – volume-title: The Southeast Asian state of fisheries and aquaculture 2022 year: 2022 ident: e_1_3_4_3_2 – ident: e_1_3_4_13_2 doi: 10.3390/genes12010040 – ident: e_1_3_4_14_2 doi: 10.1371/journal.pone.0060802 – ident: e_1_3_4_34_2 doi: 10.1038/s41587-020-0548-6 – ident: e_1_3_4_28_2 doi: 10.1038/s41592-022-01520-4 – ident: e_1_3_4_30_2 doi: 10.1038/ismej.2017.119 – ident: e_1_3_4_48_2 doi: 10.1016/j.aquaculture.2016.02.008 – ident: e_1_3_4_27_2 doi: 10.1038/s41598-021-90067-z – ident: e_1_3_4_50_2 doi: 10.3390/antiox11061143 – ident: e_1_3_4_51_2 doi: 10.1016/j.aquaculture.2015.12.014 – ident: e_1_3_4_2_2 doi: 10.4060/cc0461en – ident: e_1_3_4_29_2 doi: 10.1038/s41587-019-0209-9 – ident: e_1_3_4_31_2 doi: 10.1093/nar/gks1219 – ident: e_1_3_4_25_2 doi: 10.1186/s40168-021-01043-8 – ident: e_1_3_4_4_2 doi: 10.1016/j.dci.2023.104765 – ident: e_1_3_4_9_2 doi: 10.1111/j.1444-2906.2005.01061.x – ident: e_1_3_4_7_2 doi: 10.3147/jsfp.36.133 – ident: e_1_3_4_44_2 doi: 10.4172/2155-9910.S1-002 – ident: e_1_3_4_10_2 doi: 10.1007/s12562-014-0765-3 – volume-title: Nucleic acid techniques in bacterial systematics year: 1991 ident: e_1_3_4_32_2 |
SSID | ssj0001105252 |
Score | 2.3052306 |
Snippet | This interdisciplinary study investigated the influence of sequencing techniques on bacterial communities profiling within Pacific white shrimp (
Litopenaeus... Despite their immense economic value as a key aquaculture species, the production of Pacific white shrimp ( ) faces significant challenges from intensive... Despite their immense economic value as a key aquaculture species, the production of Pacific white shrimp (Litopenaeus vannamei) faces significant challenges... Despite their immense economic value as a key aquaculture species, the production of Pacific white shrimp ( Litopenaeus vannamei ) faces significant challenges... ABSTRACT Despite their immense economic value as a key aquaculture species, the production of Pacific white shrimp (Litopenaeus vannamei) faces significant... |
SourceID | doaj pubmedcentral proquest asm2 pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database |
StartPage | e0096524 |
SubjectTerms | Environmental Microbiology environmental microbiota full-length 16S rRNA gene sequencing intestinal microbiota Litopenaeus vannamei Research Article short-read sequencing |
SummonAdditionalLinks | – databaseName: American Society for Microbiology Open Access dbid: AAUOK link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3ri9QwEA_nHYJfxLf1RQTBB_Rum6Rp-nEVj_N1gt7BfQvZZMoWbHbZ7iL-Gf7HTtJ0deUQv7YpUzKv32QmM4Q8kxbd2kSqfCJdgwGKNHmNjjIUrtlGQFNBHDbx6VSenIv3F-XFHpHjXZi0g_2h6buYyN9qNlNH8fLhatMdBuBd5kxcIQclqwUq5MF0ev75w-_TlSLMZ2MpjXnpt2iDkQbb8Uexbf9lWPPvksk_fNDxDXI9gUc6Hbh9k-yBv0WuDuMkf9wmP9-l3g_ojmg_R2CdU-MdDUfseZiYsp7TQn6lqy-nU4qCAzQVUof16wWFbxvbhhMA2rVDf6YOaBrq3dPW01TBR7-H3ANSWLXdkr74iEZhCd7ApqeIy73poH1Jlwvv-jvk7Pjt2ZuTPI1cyI0oq3U-U8UEENNxVVagEBw5hEtF6FoYkFVjjbESMZrBuKrhShQWeJhZbVw9qxxM-F2y7xce7hOKnJZGcu4AMGKxzNS1cE1luTTMKikz8jxsvx4ZrmM0wpQeGaUjozQTGXk1ckgvhxYc_1r8OvBwuzB0z44PUJZ0UkYta-t4xYSBEg3YrFFFsPvKccHA1GWTkaejBGjUtpBCMR4Wm15z3AwU6ErWGbk3SMSWFEcoXGMAmxG1Iys7_7L7xrfz2NE70K8QHD747015SK4xZEu8FVk-Ivv4Eh4jPFrPniRd-AVtxQ9c priority: 102 providerName: American Society for Microbiology |
Title | Integrating short- and full-length 16S rRNA gene sequencing to elucidate microbiome profiles in Pacific white shrimp ( Litopenaeus vannamei ) ponds |
URI | https://www.ncbi.nlm.nih.gov/pubmed/39329828 https://journals.asm.org/doi/10.1128/spectrum.00965-24 https://www.proquest.com/docview/3110406769 https://pubmed.ncbi.nlm.nih.gov/PMC11537064 https://doaj.org/article/69cd3724ae5048bf8115388d342ea95f |
Volume | 12 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1La9wwEBZlS6GX0qYv9xFUKPQBbtaSLcvHbUhIXym0CeQmtNKYNcTaZb1L6c_oP-6M7A27obSXXm2BxMw3mm-k0QxjL5VDtzZWOh0rX2OAomxaoaOkxDVX51CXEJtNfDlVJ-f5x4viYqvVF-WE9eWBe8EdqMp5WYrcQoFgm9Y6IxvVXuYCbFXUtPuiz9sKpuLpSkb92cRwjYl78EF8uLhct--ItBcpvXAf2a4VO_4olu3_E9e8njK55YOO77I7A3nkk37R99gNCHvsVt9O8ud99uvDUPsB3RHvZkisU26D53TEnlLHlNWMZ-o7X347nXAEDvAhkZrGr-YcLteuoRMA3jZ9faYW-NDUu-NN4EMGH_9Bdw84w7JpF_z1Z9wUFhAsrDuOvDzYFpo3fDEPvnvAzo6Pzg5P0qHlQmrzolylU52NATmd1EUJGsmRR7qUUdVCYla1s9Yp5GgW46pa6jxzIKlntfXVtPQwlg_ZKMwDPGYcNa2sktIDYMTihK2q3Nelk8oKp5VK2CsSvxlMpjMxGhHabBRloqKMyBP2dqMhs-hLcPxt8HvS4dVAqp4dPyCmzIAp8y9MJezFBgEGrY2uUGyA-bozEoWBgC5VlbBHPSKuppJIhSsMYBOmd7Cys5bdP6GZxYreNH-J5PDJ_1j9U3ZboMbig8niGRuhfOA5MqfVdJ_dnEzOv37aj8byG2ZmGNM |
linkProvider | Directory of Open Access Journals |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwELfGJgQviG8yvowEAiZlNHbiOA88lI-ppV2RoJP2ZrnJRc20pFXTatqfwZ_Bf8ld4g6KJsTLXlOrTnx3vt_5zvdj7KVK0a11lPY7KssxQFHWT9BRUuFamoeQx9CQTRyOVO8o_HIcHW-xn-u7MCfEy3ta79u6bPL4ZNh0EO34CPW75gLiYlXuE_iOfBG6gsoBnJ9huFa_739C2b4S4uDz-GPPd4wCvg2jeOlPdNABhCxSRzFo9P0ZooGAmvIRcMhTa1OFEMRi2JBLHQYpSKJktlkyiTPoSPzba2yHUpUY5-10u0dfB78PdAKihBMuc3rpq-K2j98lNlxgwxRwGbz9u0rzD7d3cJvdcniVd1sFu8O2oLrLrrcMluf32I--azeBHpDXU8TyPrdVxmkxfSJpWU55oL7zxbdRl6OuAne12zR-OeNwukoLOnTgZdG2hCqBOx7xmhcVd0WD_IzSHTjDoijn_M0Q96E5VBZWNcdQoLIlFG_5fFZl9X02vgqZPGDb1ayCR4yjcimrpMwAMEhKhU2SMMvjVCorUq2Ux17T8htnpbVpAiChzVpQphGUEaHH9tYSMvO268e_Bn8gGV4MpIbdzQPUX-Ps36gkzWQsQgsR7pmTXAfkanQmQwE2iXKPvVhrgEEDp6yNrWC2qo3ExUAbilXisYetRlxMJRF9Jxgze0xv6MrGu2z-UhXTpok4zR8jHt3970V5zm70xodDM-yPBo_ZTYEiai5lRk_YNg6Ep4jOlpNnzi44M1dsib8AzIhKxw |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwED-NTiBeEN8Ln0YC8SFla-zEcR54KIxqpaMg2KS9WW58USORtGpaTfsz-DP4Lzmn7qBoQrzsNbXqxHfn-53vfD-A5zInt9aVKuxKW1CAIk2YkaN0hWt5EWORYks28WkkD47jjyfJyRb8XN-F8SvY7JqmahP5zrJntvB8hGqvvYA4X1a7DnwnIY99QeUQz04pXGveDvZJti847384en8QekaB0MRJugjHKuoiQRahkhQV-X5LaCByTfkccChyY3JJEMRQ2FAIFUc5CkfJbGw2Ti12Bf3tFdhuc2Md2O71jj8Pfx_oRI4SjvvM6YWvSts-fRbfcIEtU8BF8PbvKs0_3F7_JtzweJX1Vgp2C7awvg1XVwyWZ3fgx8C3myAPyJoJYfmQmdoyd6ofOpKWxYRF8hubfx31GOkqMl-77cYvpgy_L_PSHTqwqly1hKqQeR7xhpU180WD7NSlO2iGeVnN2KtD2odmWBtcNoxCgdpUWL5ms2ltm7twdBkyuQedelrjDjBSLmmkEBaRgqScmyyLbZHmQhqeKykDeOmWX691TLcBEFd6LSjdCkrzOIA3awnp2arrx78Gv3MyPB_oGna3D0h9tbd_LbPcipTHBhPaM8eFipyrUVbEHE2WFAE8W2uAJgN3WRtT43TZaEGLQTaUyiyA-yuNOJ9KEPrOKGYOQG3oysa7bP5Sl5O2ibibPyU8-uC_F-UpXPuy39eHg9HwIVznJKH2TmbyCDo0Dh8TOFuMn3izYKAv2RB_AVS0SmM |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Integrating+short-+and+full-length+16S+rRNA+gene+sequencing+to+elucidate+microbiome+profiles+in+Pacific+white+shrimp+%28+Litopenaeus+vannamei+%29+ponds&rft.jtitle=Microbiology+spectrum&rft.au=Rajonhson%2C+Dora+M.&rft.au=Angthong%2C+Pacharaporn&rft.au=Thepsuwan%2C+Timpika&rft.au=Sutheeworapong%2C+Sawannee&rft.date=2024-11-05&rft.issn=2165-0497&rft.eissn=2165-0497&rft.volume=12&rft.issue=11&rft_id=info:doi/10.1128%2Fspectrum.00965-24&rft.externalDBID=n%2Fa&rft.externalDocID=10_1128_spectrum_00965_24 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2165-0497&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2165-0497&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2165-0497&client=summon |