Expression of the nirS, hzsA, and hdh genes and antibiotic resistance genes in response to recovery of anammox process inhibited by oxytetracycline
The inhibitory effects of oxytetracycline (OTC) on the anaerobic ammonium oxidation (anammox) performance were relieved by employing bio-augmentation (BA) tactics. However, the recovery mechanism was vague. The response of specific anammox activity (SAA), heme c, functional genes, extracellular poly...
Gespeichert in:
Veröffentlicht in: | The Science of the total environment 2019-09, Vol.681, p.56-65 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 65 |
---|---|
container_issue | |
container_start_page | 56 |
container_title | The Science of the total environment |
container_volume | 681 |
creator | Zhang, Qian-Qian Zhao, Yi-Heng Wang, Cheng-Jie Bai, Yu-Hui Wu, Dan Wu, Jing Tian, Guang-Ming Shi, Man-Ling Mahmood, Qaisar Jin, Ren-Cun |
description | The inhibitory effects of oxytetracycline (OTC) on the anaerobic ammonium oxidation (anammox) performance were relieved by employing bio-augmentation (BA) tactics. However, the recovery mechanism was vague. The response of specific anammox activity (SAA), heme c, functional genes, extracellular polymeric substance (EPS) and antibiotics resistance genes (ARGs) to OTC inhibition and BA aid were traced in the present study. The results indicated that response of SAA, heme c content and functional genes, such as nirS, hzsA and hdh to OTC inhibition were not synchronous. The presence of the tetC, tetG, tetX, and intI1 genes enhanced the resistance of anammox sludge to OTC, thus accelerating the performance recovery when aided by BA. A significant correlation existed between number of anammox 16S rRNA gene copies and protein level in the soluble microbial products (SMP), between tetG gene relative abundance and polysaccharose in SMP and between tetG gene relative abundance and protein in bound EPS (EPSs). In nutshell, the current findings provide the first description of a recovery mechanism regarding OTC-inhibited anammox performance aided by BA based on functional genes and highlights the contribution of ARGs and the self-resistance ability of EPS.
[Display omitted]
•The recovery mechanism for OTC-inhibited anammox was proposed for the first time.•Bioactivity and functional genes do not always coincide with each other.•The presence of ARGs improved the resistance of anammox sludge to OTC.•A significant correlation was observed between anammox, EPS composition and ARGs. |
doi_str_mv | 10.1016/j.scitotenv.2019.04.438 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2232048476</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0048969719319898</els_id><sourcerecordid>2232048476</sourcerecordid><originalsourceid>FETCH-LOGICAL-c371t-3bafa31c189671b074e509f9fc77b6126c0aee17f08cf60f8df665004d7f150c3</originalsourceid><addsrcrecordid>eNqFUcFuGyEURFWjxkn7Cy3HHrJb2F3D7tGK0qZSpB6anhHLPrpYXnABW3Z-Iz_ct7Gba7nA483MgxlCPnFWcsbFl3WZjMshg9-XFeNdyZqyqds3ZMFb2RWcVeItWTDWtEUnOnlJrlJaM1yy5e_IZc0R0XK5IM93h22ElFzwNFiaR6DexZ83dHxKqxuq_UDHYaS_wUN6qbTPrnchO0OR51LW3sC57_x8tw0-Ac0BzybsIR5nYe31NIUD3cZgcBxCR5TJMNAe-4djhhy1OZqN8_CeXFi9SfDhvF-TX1_vHm_vi4cf377frh4KU0uei7rXVtfc8LYTkvdMNrBkne2skbIXvBKGaQAuLWuNFcy2gxViiZ4M0vIlM_U1-XzSxUf92UHKanLJwGajPYRdUlVVV-hgIwVC5QlqYkgpglXb6CYdj4ozNSei1uo1ETUnolijMBFkfjwP2fUTDK-8fxEgYHUCAH517yDOQoCmDg4NzGoI7r9D_gKjkKSL</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2232048476</pqid></control><display><type>article</type><title>Expression of the nirS, hzsA, and hdh genes and antibiotic resistance genes in response to recovery of anammox process inhibited by oxytetracycline</title><source>Elsevier ScienceDirect Journals Complete</source><creator>Zhang, Qian-Qian ; Zhao, Yi-Heng ; Wang, Cheng-Jie ; Bai, Yu-Hui ; Wu, Dan ; Wu, Jing ; Tian, Guang-Ming ; Shi, Man-Ling ; Mahmood, Qaisar ; Jin, Ren-Cun</creator><creatorcontrib>Zhang, Qian-Qian ; Zhao, Yi-Heng ; Wang, Cheng-Jie ; Bai, Yu-Hui ; Wu, Dan ; Wu, Jing ; Tian, Guang-Ming ; Shi, Man-Ling ; Mahmood, Qaisar ; Jin, Ren-Cun</creatorcontrib><description>The inhibitory effects of oxytetracycline (OTC) on the anaerobic ammonium oxidation (anammox) performance were relieved by employing bio-augmentation (BA) tactics. However, the recovery mechanism was vague. The response of specific anammox activity (SAA), heme c, functional genes, extracellular polymeric substance (EPS) and antibiotics resistance genes (ARGs) to OTC inhibition and BA aid were traced in the present study. The results indicated that response of SAA, heme c content and functional genes, such as nirS, hzsA and hdh to OTC inhibition were not synchronous. The presence of the tetC, tetG, tetX, and intI1 genes enhanced the resistance of anammox sludge to OTC, thus accelerating the performance recovery when aided by BA. A significant correlation existed between number of anammox 16S rRNA gene copies and protein level in the soluble microbial products (SMP), between tetG gene relative abundance and polysaccharose in SMP and between tetG gene relative abundance and protein in bound EPS (EPSs). In nutshell, the current findings provide the first description of a recovery mechanism regarding OTC-inhibited anammox performance aided by BA based on functional genes and highlights the contribution of ARGs and the self-resistance ability of EPS.
[Display omitted]
•The recovery mechanism for OTC-inhibited anammox was proposed for the first time.•Bioactivity and functional genes do not always coincide with each other.•The presence of ARGs improved the resistance of anammox sludge to OTC.•A significant correlation was observed between anammox, EPS composition and ARGs.</description><identifier>ISSN: 0048-9697</identifier><identifier>EISSN: 1879-1026</identifier><identifier>DOI: 10.1016/j.scitotenv.2019.04.438</identifier><identifier>PMID: 31102817</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Anammox ; Antibiotic resistance genes ; Bio-augmentation ; Functional genes ; Oxytetracycline</subject><ispartof>The Science of the total environment, 2019-09, Vol.681, p.56-65</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright © 2019 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-3bafa31c189671b074e509f9fc77b6126c0aee17f08cf60f8df665004d7f150c3</citedby><cites>FETCH-LOGICAL-c371t-3bafa31c189671b074e509f9fc77b6126c0aee17f08cf60f8df665004d7f150c3</cites><orcidid>0000-0003-0978-7594 ; 0000-0003-2685-1367</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.scitotenv.2019.04.438$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31102817$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Qian-Qian</creatorcontrib><creatorcontrib>Zhao, Yi-Heng</creatorcontrib><creatorcontrib>Wang, Cheng-Jie</creatorcontrib><creatorcontrib>Bai, Yu-Hui</creatorcontrib><creatorcontrib>Wu, Dan</creatorcontrib><creatorcontrib>Wu, Jing</creatorcontrib><creatorcontrib>Tian, Guang-Ming</creatorcontrib><creatorcontrib>Shi, Man-Ling</creatorcontrib><creatorcontrib>Mahmood, Qaisar</creatorcontrib><creatorcontrib>Jin, Ren-Cun</creatorcontrib><title>Expression of the nirS, hzsA, and hdh genes and antibiotic resistance genes in response to recovery of anammox process inhibited by oxytetracycline</title><title>The Science of the total environment</title><addtitle>Sci Total Environ</addtitle><description>The inhibitory effects of oxytetracycline (OTC) on the anaerobic ammonium oxidation (anammox) performance were relieved by employing bio-augmentation (BA) tactics. However, the recovery mechanism was vague. The response of specific anammox activity (SAA), heme c, functional genes, extracellular polymeric substance (EPS) and antibiotics resistance genes (ARGs) to OTC inhibition and BA aid were traced in the present study. The results indicated that response of SAA, heme c content and functional genes, such as nirS, hzsA and hdh to OTC inhibition were not synchronous. The presence of the tetC, tetG, tetX, and intI1 genes enhanced the resistance of anammox sludge to OTC, thus accelerating the performance recovery when aided by BA. A significant correlation existed between number of anammox 16S rRNA gene copies and protein level in the soluble microbial products (SMP), between tetG gene relative abundance and polysaccharose in SMP and between tetG gene relative abundance and protein in bound EPS (EPSs). In nutshell, the current findings provide the first description of a recovery mechanism regarding OTC-inhibited anammox performance aided by BA based on functional genes and highlights the contribution of ARGs and the self-resistance ability of EPS.
[Display omitted]
•The recovery mechanism for OTC-inhibited anammox was proposed for the first time.•Bioactivity and functional genes do not always coincide with each other.•The presence of ARGs improved the resistance of anammox sludge to OTC.•A significant correlation was observed between anammox, EPS composition and ARGs.</description><subject>Anammox</subject><subject>Antibiotic resistance genes</subject><subject>Bio-augmentation</subject><subject>Functional genes</subject><subject>Oxytetracycline</subject><issn>0048-9697</issn><issn>1879-1026</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFUcFuGyEURFWjxkn7Cy3HHrJb2F3D7tGK0qZSpB6anhHLPrpYXnABW3Z-Iz_ct7Gba7nA483MgxlCPnFWcsbFl3WZjMshg9-XFeNdyZqyqds3ZMFb2RWcVeItWTDWtEUnOnlJrlJaM1yy5e_IZc0R0XK5IM93h22ElFzwNFiaR6DexZ83dHxKqxuq_UDHYaS_wUN6qbTPrnchO0OR51LW3sC57_x8tw0-Ac0BzybsIR5nYe31NIUD3cZgcBxCR5TJMNAe-4djhhy1OZqN8_CeXFi9SfDhvF-TX1_vHm_vi4cf377frh4KU0uei7rXVtfc8LYTkvdMNrBkne2skbIXvBKGaQAuLWuNFcy2gxViiZ4M0vIlM_U1-XzSxUf92UHKanLJwGajPYRdUlVVV-hgIwVC5QlqYkgpglXb6CYdj4ozNSei1uo1ETUnolijMBFkfjwP2fUTDK-8fxEgYHUCAH517yDOQoCmDg4NzGoI7r9D_gKjkKSL</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Zhang, Qian-Qian</creator><creator>Zhao, Yi-Heng</creator><creator>Wang, Cheng-Jie</creator><creator>Bai, Yu-Hui</creator><creator>Wu, Dan</creator><creator>Wu, Jing</creator><creator>Tian, Guang-Ming</creator><creator>Shi, Man-Ling</creator><creator>Mahmood, Qaisar</creator><creator>Jin, Ren-Cun</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0978-7594</orcidid><orcidid>https://orcid.org/0000-0003-2685-1367</orcidid></search><sort><creationdate>20190901</creationdate><title>Expression of the nirS, hzsA, and hdh genes and antibiotic resistance genes in response to recovery of anammox process inhibited by oxytetracycline</title><author>Zhang, Qian-Qian ; Zhao, Yi-Heng ; Wang, Cheng-Jie ; Bai, Yu-Hui ; Wu, Dan ; Wu, Jing ; Tian, Guang-Ming ; Shi, Man-Ling ; Mahmood, Qaisar ; Jin, Ren-Cun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-3bafa31c189671b074e509f9fc77b6126c0aee17f08cf60f8df665004d7f150c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Anammox</topic><topic>Antibiotic resistance genes</topic><topic>Bio-augmentation</topic><topic>Functional genes</topic><topic>Oxytetracycline</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Qian-Qian</creatorcontrib><creatorcontrib>Zhao, Yi-Heng</creatorcontrib><creatorcontrib>Wang, Cheng-Jie</creatorcontrib><creatorcontrib>Bai, Yu-Hui</creatorcontrib><creatorcontrib>Wu, Dan</creatorcontrib><creatorcontrib>Wu, Jing</creatorcontrib><creatorcontrib>Tian, Guang-Ming</creatorcontrib><creatorcontrib>Shi, Man-Ling</creatorcontrib><creatorcontrib>Mahmood, Qaisar</creatorcontrib><creatorcontrib>Jin, Ren-Cun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Science of the total environment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Qian-Qian</au><au>Zhao, Yi-Heng</au><au>Wang, Cheng-Jie</au><au>Bai, Yu-Hui</au><au>Wu, Dan</au><au>Wu, Jing</au><au>Tian, Guang-Ming</au><au>Shi, Man-Ling</au><au>Mahmood, Qaisar</au><au>Jin, Ren-Cun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of the nirS, hzsA, and hdh genes and antibiotic resistance genes in response to recovery of anammox process inhibited by oxytetracycline</atitle><jtitle>The Science of the total environment</jtitle><addtitle>Sci Total Environ</addtitle><date>2019-09-01</date><risdate>2019</risdate><volume>681</volume><spage>56</spage><epage>65</epage><pages>56-65</pages><issn>0048-9697</issn><eissn>1879-1026</eissn><abstract>The inhibitory effects of oxytetracycline (OTC) on the anaerobic ammonium oxidation (anammox) performance were relieved by employing bio-augmentation (BA) tactics. However, the recovery mechanism was vague. The response of specific anammox activity (SAA), heme c, functional genes, extracellular polymeric substance (EPS) and antibiotics resistance genes (ARGs) to OTC inhibition and BA aid were traced in the present study. The results indicated that response of SAA, heme c content and functional genes, such as nirS, hzsA and hdh to OTC inhibition were not synchronous. The presence of the tetC, tetG, tetX, and intI1 genes enhanced the resistance of anammox sludge to OTC, thus accelerating the performance recovery when aided by BA. A significant correlation existed between number of anammox 16S rRNA gene copies and protein level in the soluble microbial products (SMP), between tetG gene relative abundance and polysaccharose in SMP and between tetG gene relative abundance and protein in bound EPS (EPSs). In nutshell, the current findings provide the first description of a recovery mechanism regarding OTC-inhibited anammox performance aided by BA based on functional genes and highlights the contribution of ARGs and the self-resistance ability of EPS.
[Display omitted]
•The recovery mechanism for OTC-inhibited anammox was proposed for the first time.•Bioactivity and functional genes do not always coincide with each other.•The presence of ARGs improved the resistance of anammox sludge to OTC.•A significant correlation was observed between anammox, EPS composition and ARGs.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31102817</pmid><doi>10.1016/j.scitotenv.2019.04.438</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-0978-7594</orcidid><orcidid>https://orcid.org/0000-0003-2685-1367</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0048-9697 |
ispartof | The Science of the total environment, 2019-09, Vol.681, p.56-65 |
issn | 0048-9697 1879-1026 |
language | eng |
recordid | cdi_proquest_miscellaneous_2232048476 |
source | Elsevier ScienceDirect Journals Complete |
subjects | Anammox Antibiotic resistance genes Bio-augmentation Functional genes Oxytetracycline |
title | Expression of the nirS, hzsA, and hdh genes and antibiotic resistance genes in response to recovery of anammox process inhibited by oxytetracycline |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T17%3A05%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Expression%20of%20the%20nirS,%20hzsA,%20and%20hdh%20genes%20and%20antibiotic%20resistance%20genes%20in%20response%20to%20recovery%20of%20anammox%20process%20inhibited%20by%20oxytetracycline&rft.jtitle=The%20Science%20of%20the%20total%20environment&rft.au=Zhang,%20Qian-Qian&rft.date=2019-09-01&rft.volume=681&rft.spage=56&rft.epage=65&rft.pages=56-65&rft.issn=0048-9697&rft.eissn=1879-1026&rft_id=info:doi/10.1016/j.scitotenv.2019.04.438&rft_dat=%3Cproquest_cross%3E2232048476%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2232048476&rft_id=info:pmid/31102817&rft_els_id=S0048969719319898&rfr_iscdi=true |