Identification of eukaryotic microorganisms with 18S rRNA next-generation sequencing in wastewater treatment plants, with a more targeted NGS approach required for Cryptosporidium detection
dc.contributor.author | Zahedi, A. | |
dc.contributor.author | Greay, T.L. | |
dc.contributor.author | Paparini, A. | |
dc.contributor.author | Linge, Kathryn | |
dc.contributor.author | Joll, Cynthia | |
dc.contributor.author | Ryan, U.M. | |
dc.date.accessioned | 2023-03-14T08:27:53Z | |
dc.date.available | 2023-03-14T08:27:53Z | |
dc.date.issued | 2019 | |
dc.identifier.citation | Zahedi, A. and Greay, T.L. and Paparini, A. and Linge, K.L. and Joll, C.A. and Ryan, U.M. 2019. Identification of eukaryotic microorganisms with 18S rRNA next-generation sequencing in wastewater treatment plants, with a more targeted NGS approach required for Cryptosporidium detection. Water Research. 158: pp. 301-312. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/90970 | |
dc.identifier.doi | 10.1016/j.watres.2019.04.041 | |
dc.description.abstract |
While some microbial eukaryotes can improve effluent quality in wastewater treatment plants (WWTPs), eukaryotic waterborne pathogens are a threat to public health. This study aimed to identify Eukarya, particularly faecal pathogens including Cryptosporidium, in different treatment stages (influent, intermediate and effluent) from four WWTPs in Western Australia (WA). Three WWTPs that utilise stabilisation ponds and one WWTP that uses activated sludge (oxidation ditch) treatment technologies were sampled. Eukaryotic 18S rRNA (18S) was targeted in the wastewater samples (n = 26) for next-generation sequencing (NGS), and a mammalian-blocking primer was used to reduce the amplification of mammalian DNA. Overall, bioinformatics analyses revealed 49 eukaryotic phyla in WWTP samples, and three of these phyla contained human intestinal parasites, which were primarily detected in the influent. These human intestinal parasites either had a low percent sequence composition or were not detected in the intermediate and effluent stages and included the amoebozoans Endolimax sp., Entamoeba sp. and Iodamoeba sp., the human pinworm Enterobius vermicularis (Nematoda), and Blastocystis sp. subtypes (Sarcomastigophora). Six Blastocystis subtypes and four Entamoeba species were identified by eukaryotic 18S NGS, however, Cryptosporidium sp. and Giardia sp. were not detected. Real-time polymerase chain reaction (PCR) also failed to detect Giardia, but Cryptosporidium-specific NGS detected Cryptosporidium in all WWTPs, and a total of nine species were identified, including five zoonotic pathogens. Although eukaryotic 18S NGS was able to identify some faecal pathogens, this study has demonstrated that more specific NGS approaches for pathogen detection are more sensitive and should be applied to future wastewater pathogen assessments. | |
dc.language | English | |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | |
dc.relation.sponsoredby | http://purl.org/au-research/grants/arc/LP130100602 | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | Science & Technology | |
dc.subject | Technology | |
dc.subject | Life Sciences & Biomedicine | |
dc.subject | Physical Sciences | |
dc.subject | Engineering, Environmental | |
dc.subject | Environmental Sciences | |
dc.subject | Water Resources | |
dc.subject | Engineering | |
dc.subject | Environmental Sciences & Ecology | |
dc.subject | Wastewater | |
dc.subject | Cryptosporidium | |
dc.subject | Blastotystis | |
dc.subject | Entamoeba | |
dc.subject | Next-generation sequencing | |
dc.subject | ZOONOTIC CRYPTOSPORIDIUM | |
dc.subject | ENTAMOEBA-MOSHKOVSKII | |
dc.subject | BLASTOCYSTIS SUBTYPES | |
dc.subject | GENETIC DIVERSITY | |
dc.subject | GIARDIA-CYSTS | |
dc.subject | PROTOZOA | |
dc.subject | PREVALENCE | |
dc.subject | GENOTYPES | |
dc.subject | HOMINIS | |
dc.subject | PARVUM | |
dc.subject | Blastocystis | |
dc.subject | Cryptosporidium | |
dc.subject | Entamoeba | |
dc.subject | Next-generation sequencing | |
dc.subject | Wastewater | |
dc.subject | Animals | |
dc.subject | Cryptosporidium | |
dc.subject | Eukaryota | |
dc.subject | Feces | |
dc.subject | High-Throughput Nucleotide Sequencing | |
dc.subject | Humans | |
dc.subject | RNA, Ribosomal, 18S | |
dc.subject | Wastewater | |
dc.subject | Western Australia | |
dc.subject | Feces | |
dc.subject | Animals | |
dc.subject | Humans | |
dc.subject | Cryptosporidium | |
dc.subject | RNA, Ribosomal, 18S | |
dc.subject | Western Australia | |
dc.subject | Eukaryota | |
dc.subject | High-Throughput Nucleotide Sequencing | |
dc.subject | Wastewater | |
dc.title | Identification of eukaryotic microorganisms with 18S rRNA next-generation sequencing in wastewater treatment plants, with a more targeted NGS approach required for Cryptosporidium detection | |
dc.type | Journal Article | |
dcterms.source.volume | 158 | |
dcterms.source.startPage | 301 | |
dcterms.source.endPage | 312 | |
dcterms.source.issn | 0043-1354 | |
dcterms.source.title | Water Research | |
dc.date.updated | 2023-03-14T08:27:52Z | |
curtin.department | School of Molecular and Life Sciences (MLS) | |
curtin.accessStatus | Open access | |
curtin.faculty | Faculty of Science and Engineering | |
curtin.contributor.orcid | Joll, Cynthia [0000-0003-4761-7350] | |
curtin.contributor.orcid | Linge, Kathryn [0000-0002-3743-0640] | |
curtin.contributor.researcherid | Linge, Kathryn [B-8095-2008] | |
dcterms.source.eissn | 1879-2448 | |
curtin.contributor.scopusauthorid | Joll, Cynthia [6602547584] | |
curtin.contributor.scopusauthorid | Linge, Kathryn [6603758942] | |
curtin.repositoryagreement | V3 |