Quantification of multiple respiratory viruses in wastewater in the Kathmandu Valley, Nepal: Potential implications of wastewater-based epidemiology for community disease surveillance in developing countries
Despite being the major cause of death, clinical surveillance of respiratory viruses at the community level is very passive, especially in developing countries. This study focused on the surveillance of three respiratory viruses [severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), influenz...
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Veröffentlicht in: | The Science of the total environment 2024-04, Vol.920, p.170845-170845, Article 170845 |
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creator | Raya, Sunayana Malla, Bikash Shrestha, Sadhana Sthapit, Niva Kattel, Hari Sharma, Sangita Tara Tuladhar, Reshma Maharjan, Rabin Takeda, Tomoko Kitajima, Masaaki Tandukar, Sarmila Haramoto, Eiji |
description | Despite being the major cause of death, clinical surveillance of respiratory viruses at the community level is very passive, especially in developing countries. This study focused on the surveillance of three respiratory viruses [severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), influenza A virus (IFV-A), and respiratory syncytial virus (RSV)] in the Kathmandu Valley, Nepal, by implication of wastewater-based epidemiology (WBE). Fifty-one untreated wastewater samples were from two wastewater treatment plants (WWTPs) between April and October 2022. Among eight combinations of the pre-evaluated methods, the combination of concentration by simple centrifugation, pretreatment by DNA/RNA Shield (Zymo Research), and extraction by the QIAamp Viral RNA Mini Kit (QIAGEN) showed the best performance for detecting respiratory viruses. Using this method with a one-step reverse transcription-quantitative polymerase chain reaction (RT-qPCR), SARS-CoV-2 RNA was successfully detected from both WWTPs (positive ratio, 100 % and 81 %) at concentrations of 5.6 ± 0.6 log10 copies/L from each WWTP. Forty-six SARS-CoV-2 RNA-positive samples were further tested for three mutation site-specific one-step RT-qPCR (L452R, T478K, and E484A/G339D), where G339D/E484A mutations were frequently detected in both WWTPs (96 %). IFV-A RNA was more frequently detected in WWTP A (84 %) compared to WWTP B (38 %). RSV RNA was also detected in both WWTPs (28 % and 8 %, respectively). This is the first study on detecting IFV-A and RSV in wastewater in Nepal, showing the applicability and importance of WBE for respiratory viruses in developing countries where clinical data are lacking.
[Display omitted]
•The simple centrifugation method was used to concentrate viruses in wastewater.•SARS-CoV-2 RNA was detected from both wastewater treatment plants.•IFV-A RNA was frequently detected when SARS-CoV-2 RNA concentrations were low.•RSV RNA was detected from both WWTPs at the end of the study period.•WBE using the simple centrifugation method is recommended to reduce the cost. |
doi_str_mv | 10.1016/j.scitotenv.2024.170845 |
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[Display omitted]
•The simple centrifugation method was used to concentrate viruses in wastewater.•SARS-CoV-2 RNA was detected from both wastewater treatment plants.•IFV-A RNA was frequently detected when SARS-CoV-2 RNA concentrations were low.•RSV RNA was detected from both WWTPs at the end of the study period.•WBE using the simple centrifugation method is recommended to reduce the cost.</description><identifier>ISSN: 0048-9697</identifier><identifier>EISSN: 1879-1026</identifier><identifier>DOI: 10.1016/j.scitotenv.2024.170845</identifier><identifier>PMID: 38340866</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>centrifugation ; death ; disease surveillance ; DNA ; environment ; epidemiology ; Influenza A virus ; monitoring ; mutation ; Nepal ; polymerase chain reaction ; Respiratory syncytial virus ; RNA ; RT-qPCR ; SARS-CoV-2 ; Severe acute respiratory syndrome coronavirus 2 ; wastewater ; Wastewater-based epidemiology</subject><ispartof>The Science of the total environment, 2024-04, Vol.920, p.170845-170845, Article 170845</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-4a10673f22467baeb8c76d07f8ee1d184356dbab9a0d392e51bafdb18b3331073</citedby><cites>FETCH-LOGICAL-c404t-4a10673f22467baeb8c76d07f8ee1d184356dbab9a0d392e51bafdb18b3331073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0048969724009847$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38340866$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Raya, Sunayana</creatorcontrib><creatorcontrib>Malla, Bikash</creatorcontrib><creatorcontrib>Shrestha, Sadhana</creatorcontrib><creatorcontrib>Sthapit, Niva</creatorcontrib><creatorcontrib>Kattel, Hari</creatorcontrib><creatorcontrib>Sharma, Sangita Tara</creatorcontrib><creatorcontrib>Tuladhar, Reshma</creatorcontrib><creatorcontrib>Maharjan, Rabin</creatorcontrib><creatorcontrib>Takeda, Tomoko</creatorcontrib><creatorcontrib>Kitajima, Masaaki</creatorcontrib><creatorcontrib>Tandukar, Sarmila</creatorcontrib><creatorcontrib>Haramoto, Eiji</creatorcontrib><title>Quantification of multiple respiratory viruses in wastewater in the Kathmandu Valley, Nepal: Potential implications of wastewater-based epidemiology for community disease surveillance in developing countries</title><title>The Science of the total environment</title><addtitle>Sci Total Environ</addtitle><description>Despite being the major cause of death, clinical surveillance of respiratory viruses at the community level is very passive, especially in developing countries. This study focused on the surveillance of three respiratory viruses [severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), influenza A virus (IFV-A), and respiratory syncytial virus (RSV)] in the Kathmandu Valley, Nepal, by implication of wastewater-based epidemiology (WBE). Fifty-one untreated wastewater samples were from two wastewater treatment plants (WWTPs) between April and October 2022. Among eight combinations of the pre-evaluated methods, the combination of concentration by simple centrifugation, pretreatment by DNA/RNA Shield (Zymo Research), and extraction by the QIAamp Viral RNA Mini Kit (QIAGEN) showed the best performance for detecting respiratory viruses. Using this method with a one-step reverse transcription-quantitative polymerase chain reaction (RT-qPCR), SARS-CoV-2 RNA was successfully detected from both WWTPs (positive ratio, 100 % and 81 %) at concentrations of 5.6 ± 0.6 log10 copies/L from each WWTP. Forty-six SARS-CoV-2 RNA-positive samples were further tested for three mutation site-specific one-step RT-qPCR (L452R, T478K, and E484A/G339D), where G339D/E484A mutations were frequently detected in both WWTPs (96 %). IFV-A RNA was more frequently detected in WWTP A (84 %) compared to WWTP B (38 %). RSV RNA was also detected in both WWTPs (28 % and 8 %, respectively). This is the first study on detecting IFV-A and RSV in wastewater in Nepal, showing the applicability and importance of WBE for respiratory viruses in developing countries where clinical data are lacking.
[Display omitted]
•The simple centrifugation method was used to concentrate viruses in wastewater.•SARS-CoV-2 RNA was detected from both wastewater treatment plants.•IFV-A RNA was frequently detected when SARS-CoV-2 RNA concentrations were low.•RSV RNA was detected from both WWTPs at the end of the study period.•WBE using the simple centrifugation method is recommended to reduce the cost.</description><subject>centrifugation</subject><subject>death</subject><subject>disease surveillance</subject><subject>DNA</subject><subject>environment</subject><subject>epidemiology</subject><subject>Influenza A virus</subject><subject>monitoring</subject><subject>mutation</subject><subject>Nepal</subject><subject>polymerase chain reaction</subject><subject>Respiratory syncytial virus</subject><subject>RNA</subject><subject>RT-qPCR</subject><subject>SARS-CoV-2</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>wastewater</subject><subject>Wastewater-based epidemiology</subject><issn>0048-9697</issn><issn>1879-1026</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkUtv1TAQhS0EopfCXwAvWZCLHSdxwq6qykNUPCRgaznxpJ0rJw5-pMqv5C-R6F7Kst6MLH1zzugcQl5xtueMV28P-9BhdBHGeZ-zvNhzyeqifER2vJZNxllePSY7xoo6a6pGnpFnIRzY-mTNn5IzUYuC1VW1I3--Jz1G7LHTEd1IXU-HZCNOFqiHMKHX0fmFzuhTgEBxpHc6RLjTEfz2i7dAP-t4O-jRJPpLWwvLG_oFJm3f0W_bhRG1pThM9uQRNpP_IlmrAxgKExoY0Fl3s9Deedq5YUgjxoUaDLAyNCQ_A1qrxw42awMzWDfheLPCaYweITwnT3ptA7w4zXPy8_3Vj8uP2fXXD58uL66zrmBFzArNWSVFn-dFJVsNbd3JyjDZ1wDc8LoQZWVa3TaaGdHkUPJW96bldSuE4EyKc_L6qDt59ztBiGrA0MF2HLgUlOClyNf8WfMgmjd5yYRo-KYqj2jnXQgeejV5HLRfFGdqK14d1H3xaiteHYtfN1-eTFI7gLnf-9f0ClwcAVhTmRH8JgRrkgY9dFEZhw-a_AUdvMrR</recordid><startdate>20240410</startdate><enddate>20240410</enddate><creator>Raya, Sunayana</creator><creator>Malla, Bikash</creator><creator>Shrestha, Sadhana</creator><creator>Sthapit, Niva</creator><creator>Kattel, Hari</creator><creator>Sharma, Sangita Tara</creator><creator>Tuladhar, Reshma</creator><creator>Maharjan, Rabin</creator><creator>Takeda, Tomoko</creator><creator>Kitajima, Masaaki</creator><creator>Tandukar, Sarmila</creator><creator>Haramoto, Eiji</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20240410</creationdate><title>Quantification of multiple respiratory viruses in wastewater in the Kathmandu Valley, Nepal: Potential implications of wastewater-based epidemiology for community disease surveillance in developing countries</title><author>Raya, Sunayana ; Malla, Bikash ; Shrestha, Sadhana ; Sthapit, Niva ; Kattel, Hari ; Sharma, Sangita Tara ; Tuladhar, Reshma ; Maharjan, Rabin ; Takeda, Tomoko ; Kitajima, Masaaki ; Tandukar, Sarmila ; Haramoto, Eiji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-4a10673f22467baeb8c76d07f8ee1d184356dbab9a0d392e51bafdb18b3331073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>centrifugation</topic><topic>death</topic><topic>disease surveillance</topic><topic>DNA</topic><topic>environment</topic><topic>epidemiology</topic><topic>Influenza A virus</topic><topic>monitoring</topic><topic>mutation</topic><topic>Nepal</topic><topic>polymerase chain reaction</topic><topic>Respiratory syncytial virus</topic><topic>RNA</topic><topic>RT-qPCR</topic><topic>SARS-CoV-2</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>wastewater</topic><topic>Wastewater-based epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raya, Sunayana</creatorcontrib><creatorcontrib>Malla, Bikash</creatorcontrib><creatorcontrib>Shrestha, Sadhana</creatorcontrib><creatorcontrib>Sthapit, Niva</creatorcontrib><creatorcontrib>Kattel, Hari</creatorcontrib><creatorcontrib>Sharma, Sangita Tara</creatorcontrib><creatorcontrib>Tuladhar, Reshma</creatorcontrib><creatorcontrib>Maharjan, Rabin</creatorcontrib><creatorcontrib>Takeda, Tomoko</creatorcontrib><creatorcontrib>Kitajima, Masaaki</creatorcontrib><creatorcontrib>Tandukar, Sarmila</creatorcontrib><creatorcontrib>Haramoto, Eiji</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>The Science of the total environment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raya, Sunayana</au><au>Malla, Bikash</au><au>Shrestha, Sadhana</au><au>Sthapit, Niva</au><au>Kattel, Hari</au><au>Sharma, Sangita Tara</au><au>Tuladhar, Reshma</au><au>Maharjan, Rabin</au><au>Takeda, Tomoko</au><au>Kitajima, Masaaki</au><au>Tandukar, Sarmila</au><au>Haramoto, Eiji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantification of multiple respiratory viruses in wastewater in the Kathmandu Valley, Nepal: Potential implications of wastewater-based epidemiology for community disease surveillance in developing countries</atitle><jtitle>The Science of the total environment</jtitle><addtitle>Sci Total Environ</addtitle><date>2024-04-10</date><risdate>2024</risdate><volume>920</volume><spage>170845</spage><epage>170845</epage><pages>170845-170845</pages><artnum>170845</artnum><issn>0048-9697</issn><eissn>1879-1026</eissn><abstract>Despite being the major cause of death, clinical surveillance of respiratory viruses at the community level is very passive, especially in developing countries. This study focused on the surveillance of three respiratory viruses [severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), influenza A virus (IFV-A), and respiratory syncytial virus (RSV)] in the Kathmandu Valley, Nepal, by implication of wastewater-based epidemiology (WBE). Fifty-one untreated wastewater samples were from two wastewater treatment plants (WWTPs) between April and October 2022. Among eight combinations of the pre-evaluated methods, the combination of concentration by simple centrifugation, pretreatment by DNA/RNA Shield (Zymo Research), and extraction by the QIAamp Viral RNA Mini Kit (QIAGEN) showed the best performance for detecting respiratory viruses. Using this method with a one-step reverse transcription-quantitative polymerase chain reaction (RT-qPCR), SARS-CoV-2 RNA was successfully detected from both WWTPs (positive ratio, 100 % and 81 %) at concentrations of 5.6 ± 0.6 log10 copies/L from each WWTP. Forty-six SARS-CoV-2 RNA-positive samples were further tested for three mutation site-specific one-step RT-qPCR (L452R, T478K, and E484A/G339D), where G339D/E484A mutations were frequently detected in both WWTPs (96 %). IFV-A RNA was more frequently detected in WWTP A (84 %) compared to WWTP B (38 %). RSV RNA was also detected in both WWTPs (28 % and 8 %, respectively). This is the first study on detecting IFV-A and RSV in wastewater in Nepal, showing the applicability and importance of WBE for respiratory viruses in developing countries where clinical data are lacking.
[Display omitted]
•The simple centrifugation method was used to concentrate viruses in wastewater.•SARS-CoV-2 RNA was detected from both wastewater treatment plants.•IFV-A RNA was frequently detected when SARS-CoV-2 RNA concentrations were low.•RSV RNA was detected from both WWTPs at the end of the study period.•WBE using the simple centrifugation method is recommended to reduce the cost.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>38340866</pmid><doi>10.1016/j.scitotenv.2024.170845</doi><tpages>1</tpages></addata></record> |
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subjects | centrifugation death disease surveillance DNA environment epidemiology Influenza A virus monitoring mutation Nepal polymerase chain reaction Respiratory syncytial virus RNA RT-qPCR SARS-CoV-2 Severe acute respiratory syndrome coronavirus 2 wastewater Wastewater-based epidemiology |
title | Quantification of multiple respiratory viruses in wastewater in the Kathmandu Valley, Nepal: Potential implications of wastewater-based epidemiology for community disease surveillance in developing countries |
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