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Evaluation of the bacterial diversity in the feces of cattle using 16S rDNA bacterial tag-encoded FLX amplicon pyrosequencing (bTEFAP)
Open accessAbstract
BACKGROUND: The microbiota of an animal's intestinal tract plays important roles in the animal's overall health, productivity and well-being. There is still a scarcity of information on the microbial diversity in the gut of livestock species such as cattle. The primary reason for this lack of data relates to the expense of methods needed to generate such data. Here we have utilized a bacterial tag-encoded FLX 16s rDNA amplicon pyrosequencing (bTEFAP) approach that is able to perform diversity analyses of gastrointestinal populations. bTEFAP is relatively inexpensive in terms of both time and labor due to the implementation of a novel tag priming method and an efficient bioinformatics pipeline. We have evaluated the microbiome from the feces of 20 commercial, lactating dairy cows. RESULTS: Ubiquitous bacteria detected from the cattle feces included Clostridium, Bacteroides, Porpyhyromonas, Ruminococcus, Alistipes, Lachnospiraceae, Prevotella, Lachnospira, Enterococcus, Oscillospira, Cytophage, Anaerotruncus, and Acidaminococcus spp. Foodborne pathogenic bacteria were detected in several of the cattle, a total of 4 cows were found to be positive for Salmonella spp (tentative enterica) and 6 cows were positive for Campylobacter spp. (tentative lanienae). CONCLUSION: Using bTEFAP we have examined the microbiota in the feces of cattle. As these methods continue to mature we will better understand the ecology of the major populations of bacteria the lower intestinal tract. This in turn will allow for a better understanding of ways in which the intestinal microbiome contributes to animal health, productivity and wellbeing.
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“Prevotella, Bacteroides, Ruminococcus, Faecalibacterium, Roseburia and Clostridium are consistently identified in fecal samples from ruminants and are considered part of the core microbiota (Dowd et al., 2008; Durso et al., 2012).”
From Addressing global ruminant agricultural challenges through understanding the rumen microbiome: past, present, and future (2018) · cites this paper as Dowd et al., 2008
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Distribution of Bacteria and Archaea in meromictic tropical Lake Kivu (Africa)
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“DNA extractions from each water depth and sampling site were analysed by means of bacterial and archaeal tag-encoded FLX amplicon pyrosequencing (bTEFAP and aTEFAP, respectively) as previously described (Dowd et al. 2008, Callaway et al. 2010).”
MethodLiu, T., Ahn, H., Sun, W., McGuinness, L. R., Kerkhof, L. J., & Häggblom, M. M. (2016) · Environmental Science & Technology · doi:10.1021/acs.est.5b04731 · Cited by 24
Fungal dysbiosis predicts the diagnosis of pediatric Crohn’s disease
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First insight into the faecal microbiota of the high Arctic muskoxen (Ovibos moschatus)
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“The Firmicutes and Bacteroidetes are also dominant in faeces from the cattle and horse hindgut (Dowd et al. , 2008; Steelman et al. , 2012).”
Whipple, B., Agar, J., Zhao, J., Pearce, D. A., & Kovács, A. (2021) · Scientific Reports · doi:10.1038/s41598-021-82570-0 · Cited by 24
Microbiome diversity of cotton aphids (Aphis gossypii) is associated with host alternation
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“UNIVERSAL EUBACTERIAL GENES [17] 530F (5′-GTC CCA GCM GCN GCG G) 1100R (5′-GGG TTN CGN TCG TTG)”
BackgroundLactic acid fermentation of human excreta for agricultural application
Andreev, N., Ronteltap, M., Boincean, B. P., & Lens, P. N. L. (2017) · Journal of Environmental Management · doi:10.1016/j.jenvman.2017.11.072 · Cited by 25
“monosaccharides, oligosaccharides, polysaccharides and lignocelluloses (Dowd et al., 2008).”
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“The resulting PCR product was used as template in a second PCR reaction with fusion primers [42].”
MethodMetagenomic investigation of faecal microbiota in sheep and goats of the same ages
Shabana, I., Albakri, N. N., & Bouqellah, N. A. (2020) · Journal of Taibah University for Science · doi:10.1080/16583655.2020.1864930 · Cited by 23
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“Two previous studies examined Holstein feces using 16S rDNA gene sequence analysis (Dowd et al., 2008; Ozutsumi et al., 2005).”
MethodResultLow pH reduces the virulence of black band disease on Orbicella faveolata
Muller, E. M., Leporacci, N. M., Macartney, K. J., Shea, A. G., Crane, R. E., Hall, E. R., & Ritchie, K. B. (2017) · PLoS ONE · doi:10.1371/journal.pone.0178869 · Cited by 22
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The impact of different diets and genders on fecal microbiota in Hanwoo cattle
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Ready-To-Eat Rocket Salads as Potential Reservoir of Bacteria for the Human Microbiome
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“Amplicons were then sequenced using primer 1100R (59-G GGTTNCGNTCGTTG-39) (53).”
MethodFunctional-Structural Analysis of Nitrogen-Cycle Bacteria in a Hypersaline Mat from the Omani Desert
Abed, R. M. M., de Beer, D., & Stief, P. (2014) · Geomicrobiology Journal · doi:10.1080/01490451.2014.932033 · Cited by 22
“Tag-encoded FLX amplicon pyrosequencing (bTEFAP) was performed as described before (Dowd et al. 2008a,b) using the GS FLX titanium sequencing kit XLR70.”
MethodBradley, R. L., Chroňáková, A., Elhottová, D., & Šimek, P. (2012) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2012.04.025 · Cited by 22
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Raw milk and fecal microbiota of commercial Alpine dairy cows varies with herd, fat content and diet
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“High molecular weight DNA was then sent to the Molecular Research LP (MR DNA; Texas, USA) for 16S rRNA gene based bar-coded pyrosequencing [32].”
MethodSupplementary Materials and Methods
Groenendijk, F. H., Zwart, W. T., Floore, A. N., Akbari, S., & Bernards, R. (2013) · Cited by 22
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Determination of adsorption and desorption of DNA molecules on freshwater and marine sediments
Xue, J., & Feng, Y. (2018) · Journal of Applied Microbiology · doi:10.1111/jam.13739 · Cited by 21
“…by faecal Journal of Applied Microbiology 124, 1480--1492 © 2018 The Society for Applied Microbiology1480 contamination in environmental waters (Bernhard and Field 2000a, 2000b; Eckburg et al. 2005; Layton et al. 2006; Dowd et al. 2008; Hattori and Taylor 2009; Durso et al. 2010; Kim et al. 2011).”
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“The reference primers were 16S universal eubacterial genes 530F (5′-GTC CCA GCM GCN GCG G) and 1100R (5′-GGG TTN CGN TCG TTG) [29], for the Firmicutes phylum these were 16S 928F-Firm (5′-TGA AAC TYA AAG GAA TTG ACG) and 1040FirmR (5′-ACC ATG CAC CAC CTG TC), and for Bacteroidetes these were 16S 798cfbF (5′-CRA ACA GGA…”
BackgroundMicrobial community composition in the dung of five sympatric European herbivore species
Sun, X., Sitters, J., Ruytinx, J., Wassen, M. J., & Venterink, H. O. (2024) · Ecology and Evolution · doi:10.1002/ece3.11071 · Cited by 21
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“The reverse fusion primer was constructed (5 ′-3 ′) with a biotin molecule, the Roche B linker (CCTATCCCCTGTGTGCCTTGGCAGTCTCAG), and the 519R primer (GTNTTACNGCGGCKGCTG) (Dowd et al. 2008; Ishak et al. 2011; Medina et al. 2011).”
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“Other minor phyla include Proteobacteria, Actinobacteria, Verrucomicrobia, Fusobacteria, Fibrobacteres, TM7, and Cyanobacteria (Ley et al. 2008; Dowd et al. 2008).”
BackgroundSeasonal variation in an acid mine drainage microbial community
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“The extracted DNA was sent to Research and Testing Laboratories (http://researchandtesting.com/) for sequencing on a Roche 454 FLX/FLX + pyrosequencing platform following a modified version of the amplicon pyrosequencing (bTEFAP) process (Dowd et al. 2008).”
MethodLondono, N., Donovan, A. R., Shi, H., Geisler, M. J., & Liang, Y. (2019) · Chemosphere · doi:10.1016/j.chemosphere.2019.05.110 · Cited by 21
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Invasive willows drive instream community structure
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“Values are mean ± SE of three replications, and same letters in each treatment are not significantly different from each other at P\ 0.05 according to DMRT cow dung, which includes cultivable and non-cultivable bacteria (Dowd et al. 2008).”
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Higgins, D., Pal, C., Sulaiman, I. M., Jia, C., Zerwekh, T., Dowd, S. E., & Banerjee, P. (2017) · Food Research International · doi:10.1016/j.foodres.2017.10.057 · Cited by 20
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“Operational taxonomic units (OTUs) were defined after removal of singleton sequences, clustering at 3% divergence (97% similarity) (Dowd et al. 2008a, c; Capone et al. 2011).”
BackgroundMethodHydraulic Fracturing Fluid Compositions Induce Differential Enrichment of Soil Bacterial Communities
Lozano, T. M., McCutchan, A. L., & Krzmarzick, M. J. (2018) · Environmental Engineering Science · doi:10.1089/ees.2018.0271 · Cited by 20
“Illumina MiSeq 2 · 300 bp barcoded amplicon sequencing (Dowd et al. , 2008).”
Vela-Cano, M., Cervera‐Mata, A., Purswani, J., Pozo, C., Delgado, G. A., & González-López, J. (2019) · Applied Soil Ecology · doi:10.1016/j.apsoil.2019.01.006 · Cited by 20
The shape and speciation of Ag nanoparticles drive their impacts on organisms in a lotic ecosystem
Auffan, M., Santaella, C., Brousset, L., Tella, M., Morel, E., Ortet, P., Barakat, M., Chanéac, C., Issartel, J., Angeletti, B., et al. (2020) · Environmental Science Nano · doi:10.1039/d0en00442a · Cited by 20
Dynamics of Seawater Bacterial Communities in a Shellfish Hatchery
Powell, S. M., Chapman, C. C., Bermudes, M., & Tamplin, M. L. (2013) · Microbial Ecology · doi:10.1007/s00248-013-0183-6 · Cited by 20
“Tag-encoded FLX amplicon pyrosequencing of the V1 and V2 regions was carried out by Research and Testing Laboratories (Lubbock, TX) using a Roche 454 FLX instrument with titanium reagents and the primers 28F (5 ′TTTGATCNTGGCTCAG) and 519R (5 ′ GTNTTACNGCGGCKGCTG) as described in [17, 18].”
Ueno, Y., & Kitajima, Y. (2014) · Advances in Microbiology · doi:10.4236/aim.2014.45032 · Cited by 20
“Pyrotag Sequencing of 16S rRNA Gene Amplicons PCR amplification of 16S rRNA gene fragments (V4 region) was performed using the primers ad-tag-515F (5’-CGTATCGCCTCCCTCGCGCCATCAGXXXXXX GTGCCAGCMGCCGCGGTAA-3’) and ad-806R (5’CTATGCGCCTTGCCAGCCCGCTCAG GGACTACHVGGGTWTCTAAT) [13], where the underlined sequences are adaptors…”
MethodZhang, D., Luo, J., Lee, Z. M. P., Gersberg, R. M., Liu, Y., Tan, S. K., & Ng, W. J. (2016) · Environmental Science and Pollution Research · doi:10.1007/s11356-016-6586-4 · Cited by 20
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Eckley, C. S., Luxton, T. P., Knightes, C. D., & Shah, V. (2021) · Environmental Toxicology and Chemistry · doi:10.1002/etc.5041 · Cited by 19
“and appropriate primers, Illumina miSeq protocols, sequence analysis, and pipelines were performed as described in the literature (Dowd et al. 2008; Chiodini et al. 2015; Garcia‐Mazcorro et al. 2017).”
MethodSyropoulou, F., Anagnostopoulos, D. A., Parlapani, F. F., Karamani, E. A., Stamatiou, A., Tzokas, K., Nychas, G. E., & Boziaris, I. S. (2022) · Microorganisms · doi:10.3390/microorganisms10091870 · Cited by 19
González‐Martínez, A., Rodríguez–Sánchez, A., Rodelas, B., Abbas, B. A., Martinez-Toledo, M. V., van Loosdrecht, M. C. M., Osorio, F., & González-López, J. (2015) · BioMed Research International · doi:10.1155/2015/892013 · Cited by 19
“For the purposes of pyrosequencing, reverse primer 1100R was taken, following the literature that has utilized primer 530F for pyrosequencing analysis [21].”
MethodInfluentialOmer, M. K., Hauge, S. J., Østensvik, Ø., Moen, B., Alvseike, O. A., Røtterud, O.-J., Maradona, M. P., Dommersnes, S., Nesteng, O. H., & Nesbakken, T. (2014) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2014.11.002 · Cited by 19
Microbial Flora of Cochlear Implants by Gene Pyrosequencing
Antonelli, P. J., & Ojano-Dirain, C. P. (2013) · Otology & Neurotology · doi:10.1097/mao.0b013e3182941101 · Cited by 19
“Amplicon pyrosequencing (bTEFAP) was performed as previously described (10).”
BackgroundMethodTracking Bacteria through the Entire Gastrointestinal Tract of a Beef Steer
Durso, L. M., Miller, D. N., Schmidt, T. B., & Callaway, T. R. (2017) · Agricultural & Environmental Letters · doi:10.2134/ael2017.05.0016 · Cited by 19
“Chimeras were removed following denoising and operational taxonomic unit (OTU) generation (97%), and BLASTn was used against a curated GreenGenes database (DeSantis et al., 2006) to assign taxonomies (Dowd et al., 2008).”
MethodCorrelated production and consumption of chloromethane in the Arabidopsis thaliana phyllosphere
Haque, M. F. U., Besaury, L., Nadalig, T., Bringel, F., Mutterer, J., Schaller, H., & Vuilleumier, S. (2017) · Scientific Reports · doi:10.1038/s41598-017-17421-y · Cited by 19
Rotini, A., Conte, C., Seveso, D., Montano, S., Galli, P., Vai, M., Migliore, L., & Mejia, A. Y. (2019) · Journal of Sea Research · doi:10.1016/j.seares.2019.101835 · Cited by 19
Ran, T., Jiao, P., AlZahal, O., Xie, X., Beauchemin, K. A., Niu, D. X., & Yang, W. Z. (2020) · Journal of Animal Science · doi:10.1093/jas/skaa058 · Cited by 19
Cholewińska, P., Wołoszyńska, M., Michalak, M., Czyż, K., Rant, W., & Janczak, M. (2020) · Animals · doi:10.3390/ani10101901 · Cited by 19
“The reference genes were 16S universal eubacterial genes 530F (5′-GTC CCA GCM GCN GCG G) and 1100R (5′-GGG TTN CGN TCG TTG) [14], for the Firmicutes phylum these were 16S 928F-Firm (5′-TGA AAC TYA AAG GAA TTG ACG) and 1040FirmR (5′-ACC ATG CAC CAC CTG TC), and for Bacteroidetes these were 16S 798cfbF (5′-CRA ACA GGA T…”
BackgroundKoo, H., Mojib, N., THACKER, R. W., & Bej, A. K. (2014) · Antonie van Leeuwenhoek · doi:10.1007/s10482-014-0268-3 · Cited by 19
“Pyrosequencing was performed on hypervariable V3–V5 segment of the bacterial 16S rRNA gene (Dowd et al. 2008), which was first PCR amplified”
BackgroundMethodGuass, O., Haapanen, L. M., Dowd, S. E., Širović, A., & McLaughlin, R. W. (2016) · Antonie van Leeuwenhoek · doi:10.1007/s10482-016-0698-1 · Cited by 19
“Pyrosequencing for bacterial and fungal organisms bTEFAP Ò was originally described by Dowd et al. (2008) and has been used to determine the bacteria present in the faecal material of a variety of animals, including cattle (Dowd et al. 2008; Callaway et al. 2010; Hristov et al. 2012), cats and dogs…”
MethodGou, Y., Nan, Z.-B., & Hou, F.-J. (2015) · Genetics and Molecular Research · doi:10.4238/2015.december.15.5 · Cited by 16
Marcatili, P., Nielsen, M. W., Sicheritz‐Pontén, T., Jensen, T. K., Schafer‐Nielsen, C., Boyé, M., Nielsen, M., & Schou, K. K. (2016) · BMC Genomics · doi:10.1186/s12864-016-3341-7 · Cited by 19
“At the genus level, Bacteroidetes core genes were primarily composed of the genera Alistipes, Odoribacter, Bacteroides, Cytophaga, and Porphyromonas, most of which are ubiquitously found in cattle feces [28] (Additional file 1: Figure S1).”
BackgroundAssessment of fecal pollution in Lake Pontchartrain, Louisiana
Xue, J., Lin, S., Lamar, F. G., Lamori, J. G., & Sherchan, S. P. (2017) · Marine Pollution Bulletin · doi:10.1016/j.marpolbul.2017.10.053 · Cited by 19
Giang, H., Zhang, J., Zhu, Z., Suni, I. I., & Liang, Y. (2017) · International Journal of Energy Research · doi:10.1002/er.3931 · Cited by 19
“Operational taxonomic units were defined as clusters at 3% divergence (97% similarity).(27)”
BackgroundChen, W. L., Tang, S. G. H., Jahromi, M. F., Candyrine, S. C. L., Idrus, Z., Abdullah, N., & Liang, J. B. (2018) · Poultry Science · doi:10.3382/ps/pey366 · Cited by 19
Bellou, N., Garcia, J. A. L., Colijn, F., & Herndl, G. J. (2019) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2019.104703 · Cited by 18
“Callaway TR. Wolcott RD. Sun Y. McKeehan T. Hagevoort RG. Edrington TS. 2008.”
BackgroundMohammadi-Aragh, M. K., Linhoss, J. E., & Evans, J. D. (2022) · The Journal of Applied Poultry Research · doi:10.1016/j.japr.2022.100278 · Cited by 18
Hollister, E. B., Hammett, A. J. M., Holtzapple, M. T., Gentry, T. J., & Wilkinson, H. H. (2010) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2010.04919.x · Cited by 18
“…Clostridium-like organisms are frequently associated with mammalian gut microbial communities and the decomposition of crop residues, municipal solid waste, and other lignocellulosic materials (Chynoweth and Pullammanappallil 1996; Akasaka et al. 2003; Burrell et al. 2004; Dowd et al. 2008).”
BackgroundHuang, C., Shi, Y., El‐Din, M. G., & Liu, Y. (2016) · International Biodeterioration & Biodegradation · doi:10.1016/j.ibiod.2016.04.037 · Cited by 18
Fugle, C. W., Zhang, Y., Hong, F., Sun, S., Westwater, C., Rachidi, S., Yu, H. H., Garret-Mayer, E., Kirkwood, K. L., Liu, B., et al. (2016) · OncoImmunology · doi:10.1080/2162402x.2016.1226719 · Cited by 18
“Operational taxonomic units (OTUs) were defined after removal of singleton sequences, clustering at 3% divergence (97% similarity).(58,64) OTUs were then taxonomically classified using BLASTn against a curated Green Genes database(65) and compiled into each taxonomic level into both “counts” and “percentage” files.”
MethodTeki̇n, Ş., Dowd, S. E., Davinic, M., Bursalı, A., & Keskin, A. (2017) · Parasitology Research · doi:10.1007/s00436-017-5387-0 · Cited by 18
“These ticks were sent to a laboratory where the DNA was extracted as described by Dowd et al. (2008), and diversity analysis performed using 28F-519R primers.”
BackgroundMethodWang, L., Wu, D., Yan, T., & Wang, L. (2017) · Journal of Animal Physiology and Animal Nutrition · doi:10.1111/jpn.12676 · Cited by 18
Jiang, X. P., Liu, X., Liu, S., Li, Y., Zhao, H. B., & Zhang, Y. (2019) · Animal Feed Science and Technology · doi:10.1016/j.anifeedsci.2019.01.012 · Cited by 18
Abundance and diversity of diazotrophs in the surface sediments of Kongsfjorden, an Arctic fjord
Jabir, T., Vipindas, P. V., Krishnan, K. P., & Hatha, A. A. M. (2021) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-020-02993-1 · Cited by 18
Callaway, T. R., Edrington, T. S., & Nisbet, D. J. (2014) · Journal of Animal Science · doi:10.2527/jas.2013-7308 · Cited by 18
Gatica, J., Yang, K., Pagaling, E., Jurkevitch, É., Yan, T., & Cytryn, E. J. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01233 · Cited by 18
“DNA was extracted from the microcosm samples with the PowerSoil DNA Isolation kit (MoBio, Laboratories, Carlsbad, CA, USA) using the protocol described by the manufacturer, and amplified with the universal bacterial 16S rRNA gene primers 530F and 1100R as previously described (Dowd et al., 2008a,b).”
MethodAbdel-Wahab, M. A., Bahkali, A. H., Elgorban, A. M., & Jones, E. B. G. (2021) · Mycological Progress · doi:10.1007/s11557-021-01744-2 · Cited by 17
Stockler, R. M., Hallowell, H. A., Higgins, K. V., Groover, E. S., Hiltbold, E. M., Newcomer, B. W., & Walz, P. H. (2022) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.799063 · Cited by 17
“16S rDNA Sequencing and Bioinformatic Analysis The bacterial microbiome was analyzed using 16S rRNA gene V4 variable region PCR primers 515/806 in a single-step 30 cycle PCR using a commercially available kit following a published protocol (22).”
MethodMähler, B., Janssen, K., Lönartz, M. I., Lagos, M., Geisler, T., Rust, J., & Bierbaum, G. (2023) · Scientific Reports · doi:10.1038/s41598-023-28713-x · Cited by 14
Bartak, D., Bedrníková, E., Kašpar, V., Říha, J., Hlaváčková, V., Večerník, P., Šachlová, Š., & Černá, K. (2023) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-023-03849-0 · Cited by 17
“For both PCR runs, EliZyme HS HIFI MIX polymerase (Elizabeth Pharmacon, Czech Republic) and the universal primers 515 F (Dowd et al. 2008) and 802R (Claesson et al. 2010) were used for amplification of the hypervariable V4 region of the 16S rDNA gene.”
MethodLinking Microbial Community Structure to Function in Representative Simulated Systems
Marcus, I. M., Wilder, H., Quazi, S. J., & Walker, S. L. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.03461-12 · Cited by 17
“These DNA samples were then shipped to the Research and Testing Laboratory (Lubbock, TX) for bacterial tag-encoded FLX amplicon pyrosequencing (bTEFAP) using Gray28F (5= GAGTTTGATCNTGGCTCAG) and Gray519r (5= GTNTTA CNGCGGCKGCTG) (39).”
MethodDudhagara, P. R., Ghelani, A., Patel, R. K., Chaudhari, R., & Bhatt, S. (2015) · Genomics Data · doi:10.1016/j.gdata.2015.01.010 · Cited by 17
“Metagenome sequencing was done by the 16S rDNA bacterial tag-encoded FLX amplicon pyrosequencing (bTEFAP) method [19].”
MethodLiu, Z., & Liu, S. (2015) · Environmental Science & Technology · doi:10.1021/acs.est.5b03039 · Cited by 18
The stable microbiome of inter and sub-tidal anemone species under increasing pCO2
Muller, E. M., Fine, M., & Ritchie, K. B. (2016) · Scientific Reports · doi:10.1038/srep37387 · Cited by 17
Calumba, K. F., Reyes, V., Bonilla, F., Villasmil, E., & Sathivel, S. (2021) · Food Production Processing and Nutrition · doi:10.1186/s43014-021-00051-3 · Cited by 17
“Beer samples with FLB and ILB were analyzed for bacterial and fungal diversity using bacterial tag-encoded FLX amplicon pyrosequencing (bTEFAP) as described previously by Dowd et al. (2008) (MR DNA, Shallowater, TX, USA).”
MethodInfluentialEmerson, D., Scott, J. J., Leavitt, A., Fleming, E. J., & Moyer, C. L. (2017) · Deep Sea Research Part I Oceanographic Research Papers · doi:10.1016/j.dsr.2017.05.011 · Cited by 17
PCR-RFLP Detection and Genogroup Identification of Piscirickettsia salmonis in Field Samples
Aravena, P., Pulgar, R., Ortíz-Severín, J., Maza, F. R., Gaete, A., Martínez, S., Serón, E., González, M., & Cambiazo, V. (2020) · Pathogens · doi:10.3390/pathogens9050358 · Cited by 17
“The 16S rDNA raw amplicon sequences were processed and analyzed following the previously described protocols [61,62].”
Method
Metadata
- Authors
- Dowd, S. E., Callaway, T. R., Wolcott, R. D., Sun, Y., McKeehan, T., Hagevoort, R. G., & Edrington, T. S.
- Affiliations
- Agricultural Research Service (US)
- Corresponding author
- Dowd, Scot E
- Venue
- BMC Microbiology
- Published
- 2008
- Volume
- 8
- Issue
- 1
- Pages
- 125
- ISSN
- 1471-2180 (ISSN-L)
- PMC
- PMC2515157
- OpenAlex
- W2105807803
- Cited by
- 1,121
- References
- 80
- Citations by year
- 2026: 16 · 2025: 23 · 2024: 32 · 2023: 32 · 2022: 45 · 2021: 65 · 2020: 52 · 2019: 60 · 2018: 68 · 2017: 105 · 2016: 116 · 2015: 121 · 2014: 129 · 2013: 99 · 2012: 75
- FWCI
- 11.37
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- BMC Microbiology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- U.S. Department of Agriculture
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Ruminant Nutrition and Digestive Physiology
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Nutrition and Physiology
- Keywords
- fecal microbiota, bacterial diversity, dairy cattle, Clostridium, Bacteroides, Ruminococcus, Lachnospiraceae, foodborne pathogens, Salmonella, Campylobacter, gut microbiota
- MeSH terms
- Animals, Bacteria, Cattle, DNA, Bacterial, DNA, Ribosomal, Feces, Female, RNA, Ribosomal, 16S, Polymerase Chain Reaction, Sequence Analysis, DNA, Gastrointestinal Tract, Biodiversity
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