Microbial Diversity of the Hell Creek Watershed at the Tri-Faith Community in Nebraska, Based on 16S rRNA Gene Amplicon Sequencing John A. Kyndt a a College of Science and Technology, Bellevue University, Bellevue, Nebraska, USA ABSTRACT Hell Creek’s watershed is a historically important native land area lo- cated in Omaha, Nebraska, that includes Hell Creek and an adjacent flood plain. This initial microbial analysis showed that even though samples were isolated from the same watershed area, there were significant differences between the creek itself and the nearby pond. T he Hell Creek watershed area was once an established prairie, savanna, and forest, before development of homes and business roads caught up with the watershed in the past two decades. This significantly reduced the ability to absorb rainwater, making Hell Creek more flood-prone and a possible source of harmful coliform bacteria (1, 2). The Hell Creek area is also the location of the globally unique Tri-Faith Commons (https://www.tenxtenstudio.com/trifaith; 3), and with this new establishment, a restoration of the native watershed area has been started. This includes selected plantings that promote local wildlife and rain gardens that reduce runoff. Hell Creek runs north to south diagonally through the area, which also includes a nearby stand-alone reservoir pond (Fig. 1). We isolated samples from both the creek and the nearby pond in April 2020. Two pond samples were taken from the center of the pond, 6 m apart (HC1 and HC2), while a third pond sample was taken near the edge of the pond (HC3). A fourth sample (HC4) was taken from Hell Creek itself, near the pond (41°14=37.15N, 96°7=2.42W) (Fig. 1). Samples were collected in sterile collection tubes and imme- diately transferred to the lab, where they were stored at 4°C. The next day, 10 ml of each sample was centrifuged for 15 min at 16,000  g to form a biomass pellet. Total DNA was extracted using the PureLink microbiome DNA purification kit (Invitrogen). Utilizing Qubit and NanoDrop technologies, we determined the quality and quantity of DNA, showing A 260 /A 280 ratios of 1.76 (HC3) to 1.94 (HC4). A 16S rRNA amplicon sequencing library was prepared for each sample, following the 16S Metagenomic Sequencing Library Preparation protocol (Illumina; https://support .illumina.com/documents/documentation/chemistry_documentation/16s/16s -metagenomic-library-prep-guide-15044223-b.pdf). Amplicon primers targeting the V3 and V4 region (4) including the Illumina adapter overhang sequences are described in the Illumina library prep protocol and were synthesized by Sigma. The samples were sequenced using a 1.8-pM library with an Illumina MiniSeq instrument. Paired-end (2  150 bp) sequencing generated 1,714,184 (HC1), 1,744,434 (HC2), 1,649,932 (HC3), and 1,539,232 (HC4) reads. The primer sequences were removed, and reads with a low quality score (average score, 20) were filtered out using the FASTQ toolkit within BaseSpace version 2.2.0 (Illumina). The 16S Metagenomics application (version 1.0.1) within BaseSpace was used to perform a taxonomic classification, which uses an Illumina-curated version of the GreenGenes taxonomic database and the RDP naive Bayes taxonomic classification algorithm with an accuracy of 98.2% at the species Citation Kyndt JA. 2020. Microbial diversity of the Hell Creek watershed at the Tri-Faith community in Nebraska, based on 16S rRNA gene amplicon sequencing. Microbiol Resour Announc 9:e00467-20. https://doi.org/10.1128/ MRA.00467-20. Editor Frank J. Stewart, Georgia Institute of Technology Copyright © 2020 Kyndt. This is an open- access article distributed under the terms of the Creative Commons Attribution 4.0 International license. Address correspondence to jkyndt@bellevue.edu. Received 27 April 2020 Accepted 11 May 2020 Published 28 May 2020 AMPLICON SEQUENCE COLLECTIONS crossm Volume 9 Issue 22 e00467-20 mra.asm.org 1 Downloaded from https://journals.asm.org/journal/mra on 12 December 2021 by 18.209.15.134.