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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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Light Structures Phototroph, Bacterial and Fungal Communities at the Soil Surface
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MethodMir, R. A., Weppelmann, T. A., Elzo, M. A., Ahn, S., Driver, J., & Jeong, K. C. (2016) · PLoS ONE · doi:10.1371/journal.pone.0148518 · Cited by 43
Competition-based screening helps to secure the evolutionary stability of a defensive microbiome
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“This genus comprises Gram-negative and anaerobic bacteria commonly identified in the bovine GIT microbiome (Dowd et al., 2008; Holman and Gzyl, 2019).”
BackgroundPyrosequencing-Based Analysis of the Microbiome Associated with the Horn Fly, Haematobia irritans
Azhahianambi, P., Guerrero, F. D., Heekin, A. M., Wang, J., Dowd, S. E., Sun, Y., Foil, L. D., & de León, A. Á. P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044390 · Cited by 42
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“…by PCR using barcoded primers (i.e., 27Fmod 5 -AGRGTTTGATCMTGGCTCAG-3 and 519Rmodbio 5 -GTNTTACNGCGGCKGCTG-3 ) and the product sequence determined by bacterial tag-encoded FLX (non-titanium chemistry) amplicon pyrosequencing (Roche, Nutley, NJ) as reported previously (Dowd et al., 2008a,b).”
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“This primer pair was tailored for bacterial tag-encoded FLX amplicon pyrosequencing (bTEFAP) by adding a fusion linker and a proprietary 12 base-pair barcode sequence at the 5′ end of the forward primer, and a biotin and fusion linker sequence at the 5′ end of the reverse primer (Dowd et al., 2008).”
MethodLondono, N., Donovan, A. R., Shi, H., Geisler, M. J., & Liang, Y. (2017) · Nanotoxicology · doi:10.1080/17435390.2017.1401141 · Cited by 42
“Final operational taxonomic units (OTUs) defined by clustering at 3% divergence (97% similarity) (Dowd et al. 2008; Edgar, 2010) were taxonomically classified using BLASTn against a database derived from RDPII and NCBI and compiled into each taxonomic level into both “count” and “percentage” files.”
MethodLiu, Z., Klümper, U., Shi, L., Ye, L., & Li, M. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00043 · Cited by 42
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“Amplicon pyrosequencing generates large quantities of sequence data without the need for cloning, thereby allowing for in-depth assessment of bacterial community composition without the bias of culture based methods [13, 20].”
Belkin, N., Rahav, E., Elifantz, H., Kress, N., & Berman‐Frank, I. (2015) · Environmental Microbiology · doi:10.1111/1462-2920.12979 · Cited by 41
“For initial amplification, the broadly conserved bacterial primers 27F and 1100R were used to amplify the 16S rRNA gene region (Lane, 1991; Dowd et al., 2008), and eukaryotic primers 360F and 1492R for 18S rRNA gene region (Edgcomb et al., 2011).”
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“Operational taxonomic units were defined after removal of singleton sequences, clustering at 3% divergence (97% similarity) (Dowd et al., 2008a, 2008b, 2011; Edgar, 2010; Capone et al., 2011; Eren et al., 2011; Swanson et al., 2011).”
MethodDoblin, M. A., Petrou, K., Sinutok, S., Seymour, J. R., Messer, L. F., Brown, M. V., Norman, L., Everett, J. D., McInnes, A. S., Ralph, P. J., et al. (2016) · PeerJ · doi:10.7717/peerj.1973 · Cited by 41
“To determine bacterial community composition, the 224 V1-V3 region of the 16S rRNA gene was amplified using the primer sets in Table S1, and 225 sequenced by 454 pyrosequencing (Roche, FLX Titanium; Molecular Research LP) following 226 previously published protocols (Acosta-Martínez et al. 2008; Dowd et al. 2008).”
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“of metagenomic 16S rRNA amplicons was performed by Research and Testing Laboratory (RTL; Lubbock, TX, USA) as previously described [75] based upon RTL protocols [76].”
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“454-Pyrosequencing To identify the microbial community in the parent enrichment, the extracted DNA was pyrosequenced using 454-FLX (Dowd et al., 2008) using universal primers 926F (5′-AAA CTY AAA KGA ATT GRC GG-3′) and 1392R (5′-ACG GGC GGT GTG TRC-3′) (Matsuki et al., 2002).”
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“Barcoded 16S amplicon sequencing was performed using the trademark service bTEFAP R© as described by Dowd et al. (2008).”
MethodNovel facultative Methylocella strains are active methane consumers at terrestrial natural gas seeps
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An eight-year investigation of bovine livestock fecal microbiota
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“Our study is based on samples from Wales, United Kingdom, while the other referred studies are from the United States of America (Dowd et al., 2008; Durso et al., 2010).”
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The Effect of Freeze-Thaw Conditions on Arctic Soil Bacterial Communities
Kumar, N., Grogan, P., Chu, H., Christiansen, C. T., & Walker, V. K. (2013) · Biology · doi:10.3390/biology2010356 · Cited by 39
“TX, USA) with tag-encoded FLX amplicon pyrosequencing (TEFAP) performed in accordance with established protocols [66,67].”
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“The bacterial tag-encoded FLX amplicon pyrosequencing (bTEFAP) used Eubacterial primers 28F 5′TTTGATCNTGGCTCAG-3′ and 519R 5′GTNTTACNGCGGCKGCTG-3′ to amplify the 500 bp region of 16S rRNA gene (Dowd et al., 2008; Smith et al., 2010).”
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Warren, L. A., Kendra, K. E., Brady, A. L., & Slater, G. F. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01533 · Cited by 39
“Fe concentrations associated with each sequential extraction step were determined in triplicate using the Ferrover HACH method (Ultraspec 2000, UV/visible spectrophotometer, Pharmacia Biotech, Cambridge, UK).”
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Nutrient cycling potential within microbial communities on culturally important stoneworks
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“, 2016) and from previous studies on rock and stone habitats which also highlighted a number of these phyla (Sorlini et al., 1987; Zanardini et al., 1997; Ettenauer et al., 2014; Marnocha and Dixon, 2014; Gutarowska et al., 2015; Wu et al., 2015).”
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“454 tag-encoded amplicon pyrosequencing was performed by the Research and Testing Laboratory (Lubbock, Texas, USA) as previously described (Dowd et al., 2008).”
MethodSibley, C. D., Church, D. L., Surette, M. G., Dowd, S. E., & Parkins, M. D. (2012) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-012-1614-x · Cited by 38
“Sequence collections were depleted of any non-bacterial ribosome sequences and chimeras using B2C2 [22], as previously described [9, 10, 16, 20, 21].”
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The microbiome of neotropical ticks parasitizing on passerine migratory birds
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“Furthermore, the sequences with ambiguous base calls and homopolymer runs exceeding 6 base pairs in length were deleted (Acosta-Martinez et al., 2008; Dowd et al., 2011, 2008; Eren et al., 2011).”
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“As described previously [26, 27], next generation technology (bTEFAP®) can be utilized to examine a broad range of microbiomes.”
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Smoking related environmental microbes affecting the pulmonary microbiome in Chinese population
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“Bacterial tag-encoded FLX amplicon pyrosequencing (bTEFAP) (Dowd et al. 2008) was performed at the Research and Testing Laboratory, Lubbock, TX, USA (www.researchandtesting.com).”
BackgroundMethodNecrotizing Enterocolitis and Cytomegalovirus Infection in a Premature Infant
Tran, L., Ferris, M. J., Norori, J., Stark, M. W., Craver, R. D., Dowd, S. E., & Penn, D. (2012) · PEDIATRICS · doi:10.1542/peds.2011-1971 · Cited by 37
Role of Diatoms in the Spatial-Temporal Distribution of Intracellular Nitrate in Intertidal Sediment
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“PCR, sequencing, and initial quality checking were carried out as described in [32] at the Research and Testing Laboratory (RTL, Lubbock, TX, USA).”
MethodThe ecological controls on the prevalence of candidate division TM7 in polar regions
Winsley, T. J., Snape, I., McKinlay, J. P., Stark, J., van Dorst, J. M., Ji, M., Ferrari, B. C., & Siciliano, S. D. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00345 · Cited by 37
“…were sent to a sequencing facility in Lubbock, Texas (Research and Testing Lab, Lubbock, TX, USA) for 16S rRNA gene amplicon sequencing using the PCR primers 27F and 519R (Lane, 1991) on the 454 FLX titanium platform as described by Dowd et al. (2008) (Roche Life Sciences, Branford, CT, USA).”
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“The DNA samples were submitted to Research and Testing Laboratory (Lubbock, TX) for bacterial tag-encoded FLX amplicon pyrosequencing (bTEFAP) (Dowd et al., 2008).”
MethodHameed, S. A., Riffat, R., Li, B., Naz, I., Badshah, M., Ahmed, S., & Ali, N. (2019) · Journal of Chemical Technology & Biotechnology · doi:10.1002/jctb.5955 · Cited by 37
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“Amplification of the 16 S rDNA gene itself was undertaken using the primers 530F [43] and 802R [44].”
MethodRubin‐Blum, M., Antler, G., Turchyn, A. V., Tsadok, R., Goodman‐Tchernov, B., Shemesh, E., Austin, J. A., Coleman, D. F., Makovsky, Y., Sivan, O., et al. (2013) · FEMS Microbiology Ecology · doi:10.1111/1574-6941.12264 · Cited by 38
Liu, M., Bischoff, K. M., Gill, J. J., Mire-Criscione, M. D., Berry, J. D., Young, R., & Summer, E. J. (2015) · Biotechnology for Biofuels · doi:10.1186/s13068-015-0325-9 · Cited by 37
“DNA was subject to bacterial tag-encoded FLX amplicon pyrosequencing (bTEFAP) using primers 939F-TTGACGGGGGCCCGCAC and 1492R-TACCTTGTTACGACTT, and resulting sequences were analyzed as previously described [35, 36].”
MethodBose, A., Rogers, D. R., Adams, M. M., Joye, S. B., & Girguis, P. R. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00386 · Cited by 38
“The extracted DNA was subjected to massively parallel sequencing of the 16S ribosomal RNA (rRNA) gene using Roche 454 Titanium™ chemistry and the primer pairs 27F/519R and 340F/806R for the bacterial V1–V3 and archaeal V3–V4 regions, respectively (Dowd et al., 2008; Acosta-Martinez et al., 2010).”
MethodNovel Culturing Techniques Select for Heterotrophs and Hydrocarbon Degraders in a Subantarctic Soil
van Dorst, J. M., Hince, G., Snape, I., & Ferrari, B. C. (2016) · Scientific Reports · doi:10.1038/srep36724 · Cited by 37
Zouch, H., Karray, F., Armougom, F., Chifflet, S., Hirschler-Réa, A., Kharrat, H., Kamoun, L., Ben Hania, W., Ollivier, B., Sayadi, S., et al. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01583 · Cited by 37
“The mixtures of 16S rRNA gene amplicons were generated using a 341F/815R primer set, as previously described by Dowd et al. (2008), and were sequenced by the MiSeq Illumina (paired-end 2 × 300 bp) platform of the Molecular Research Laboratory (Texas, USA).”
MethodPartners to survive: Hoffmannseggia doellii root‐associated microbiome at the Atacama Desert
Maldonado, J. E., Gaete, A., Mandaković, D., Aguado‐Norese, C., Aguilar, M., Gutiérrez, R. A., & González, M. (2022) · New Phytologist · doi:10.1111/nph.18080 · Cited by 38
Ramírez, H., NESTOR, K. E., Tedeschi, L. O., Callaway, T. R., Dowd, S. E., Fernando, S. C., & Kononoff, P. J. (2012) · Canadian Journal of Animal Science · doi:10.4141/cjas2011-133 · Cited by 36
Hubert, J., Kopecký, J., Ságová‐Marečková, M., Nesvorná, M., Žůrek, L., & Erban, T. (2016) · Journal of Economic Entomology · doi:10.1093/jee/tow089 · Cited by 37
Spungin, D., Pfreundt, U., Berthelot, H., Bonnet, S., AlRoumi, D., Natale, F., Hess, W. R., Bidle, K. D., & Berman‐Frank, I. (2016) · Biogeosciences · doi:10.5194/bg-13-4187-2016 · Cited by 36
“The 16S rRNA genes within community genomic DNA were initially amplified with conserved bacterial primers 27F and 1100R (Dowd et al., 2008) using a high-fidelity polymerase (Phusion DNA polymerase, Thermo Scientific) with an initial denaturation step of 95 ◦C for 3 min followed by 20 cycles of 95…”
MethodMiller, H. C., Morgan, M. J., Wylie, J. T., Kaksonen, A. H., Sutton, D. C., Braun, K., & Puzon, G. J. (2016) · Water Research · doi:10.1016/j.watres.2016.11.061 · Cited by 36
“…of biofilm samples (Table 2) at pre-RCl and post-RCl sites before and after the activation of the chlorinator were assessed by amplicon pyrosequencing of 16S rRNA genes using the total DNA extracted from a subset of field samples as previously described (Dowd et al., 2008; Morgan et al., 2016).”
MethodSchou, K. K., Strube, M. L., Isbrand, A., Jensen, T. K., & Nielsen, M. W. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.00244-17 · Cited by 36
“Most of these families are ubiquitously present in bovine rumen material or feces (8, 10, 16).”
BackgroundNěmeček, J., Dolinová, I., Macháčková, J., Špánek, R., Ševců, A., Lederer, T., & Černík, M. (2017) · Chemosphere · doi:10.1016/j.chemosphere.2017.06.100 · Cited by 36
Probiotic Yeast: Mode of Action and Its Effects on Ruminant Nutrition
Ghazanfar, S., Khalid, N., Ahmed, I., & Imran, M. (2017) · InTech eBooks · doi:10.5772/intechopen.70778 · Cited by 39
Nguyen, N. H. A., Špánek, R., Kasalický, V., Ribas, D. L., Vlková, D., Řeháková, H., Kejzlar, P., & Ševců, A. (2018) · Environmental Science Nano · doi:10.1039/c7en01120b · Cited by 36
Minich, J. J., Zhu, Q., Xu, Z. Z., Amir, A., Ngochera, M. J., Simwaka, M., Allen, E. E., Zidana, H., & Knight, R. D. (2018) · MicrobiologyOpen · doi:10.1002/mbo3.716 · Cited by 36
“Many animal gut associated microbes are anaerobic (Dowd et al., 2008), occupying a unique niche (Thompson et al., 2017) and thus may not be capable of surviving in an aerobic water environment.”
BackgroundLee, C. H., Morris, D. L., Copelin, J. E., Hettick, J. M., & Kwon, I. (2019) · Journal of Dairy Science · doi:10.3168/jds.2018-15777 · Cited by 36
“Whole ruminal samples collected 4 h after feeding were analyzed for bacterial populations at Molecular Research DNA (Shallowater, TX) using 16S rDNA bacterial tag-encoded FLX amplicon pyrosequencing (Dowd et al., 2008; Hristov et al., 2012).”
MethodKibegwa, F. M., Bett, R. C., Gachuiri, C. K., Stomeo, F., & Mujibi, F. D. N. (2020) · BioMed Research International · doi:10.1155/2020/2348560 · Cited by 36
“abundance of these phototrophic oxygenic bacteria in dairy and beef cattle rumen [40, 41].”
BackgroundAcuña-Amador, L., & Barloy-Hubler, F. (2020) · Anaerobe · doi:10.1016/j.anaerobe.2020.102280 · Cited by 35
Worsley, S. F., Macey, M. C., Prudence, S. M. M., Wilkinson, B. M., Murrell, J. C., & Hutchings, M. I. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.686110 · Cited by 36
Aricha, H., Simujide, H., Wang, C., Zhang, J., Lv, W., Jimisi, X., Liu, B., Chen, H., Zhang, C., He, L., et al. (2021) · Animals · doi:10.3390/ani11071938 · Cited by 36
Wagner, R. D., Johnson, S. J., Cerniglia, C. E., & Erickson, B. D. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00008-11 · Cited by 36
“isolated in the present study are components of the normal bovine intestinal microbiota, and they are generally considered to be commensal organisms (14).”
BackgroundLhotský, O., Krákorová, E., Linhartová, L., Křesinová, Z., Steinová, J., Dvořák, L., Rødsand, T., Filipová, A., Kroupová, K., Wimmerová, L., et al. (2017) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2017.06.193 · Cited by 36
“Two consecutive PCR reactions per sample were performed to amplify the V4 region of the bacterial 16S rRNA gene using primers 530F (Dowd et al., 2008) and 802R (Claesson et al.”
MethodHeadd, B., & Engel, A. S. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.02812-12 · Cited by 35
“tag-encoded FLX amplicon pyrosequences (bTEFAP), as described previously (41, 42), with the forward primer 28F (5=-TTTGATCNTGGCTCA G-3=) and reverse primer 519r (5=-GTNTTACNGCGGCKGCTG-3=).”
MethodAnaerobic toxicity of cationic silver nanoparticles
Gitipour, A., Thiel, S. W., Scheckel, K. G., & Tolaymat, T. M. (2016) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2016.02.190 · Cited by 35
Prokaryotic and diazotrophic population dynamics within a large oligotrophic inverse estuary
Messer, L. F., Doubell, M. J., JEFFRIES, T. W., Brown, M., & Seymour, J. R. (2014) · Aquatic Microbial Ecology · doi:10.3354/ame01726 · Cited by 39
Gut microbiota may predict host divergence time during Glires evolution
Li, H., Qu, J., Li, T., Yao, M., Li, J., & Li, X. (2017) · FEMS Microbiology Ecology · doi:10.1093/femsec/fix009 · Cited by 34
Diversity and Activity of Diazotrophs in Great Barrier Reef Surface Waters
Messer, L. F., Brown, M. V., Furnas, M. J., Carney, R. L., McKinnon, A. D., & Seymour, J. R. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00967 · Cited by 35
“…Titanium; Molecular Research LP) after an additional 10 PCR cycles with custom barcoded nifH1 and nifH2 primers under the same reaction conditions (Dowd et al., 2008; Messer et al., 2015a), with between 5110 and 10860 sequences retrieved per sample (3561–7939 high quality sequences; Supplementary…”
Diversity and Persistence of the Gut Microbiome of the Giant Neotropical Bullet Ant
Moreau, C. S., & Rubin, B. E. R. (2017) · Integrative and Comparative Biology · doi:10.1093/icb/icx037 · Cited by 35
“Bacterial tag-encoded FLX titanium amplicon pyrosequencing (bTEFAP) was performed by the Research and Testing Laboratory (Lubbock, TX, USA) as described in Dowd et al. (2008).”
MethodHuang, Q., Holman, D. B., Alexander, T. W., Hu, T., Jin, L., Xu, Z., McAllister, T. A., Acharya, S. N., Zhao, G., & Wang, Y. (2017) · Archives of Microbiology · doi:10.1007/s00203-017-1427-5 · Cited by 35
“2014) and therefore the large number of unclassified sequences within these families may explain why the proportion of sequences identified as Clostridium were relatively low compared to some reports in bovine feces (Callaway et al. 2010; Dowd et al. 2008).”
BackgroundResultFacultative methanotrophs are abundant at terrestrial natural gas seeps
Haque, M. F. U., Crombie, A. T., Ensminger, S., Baciu, C. L., & Murrell, J. C. (2018) · Microbiome · doi:10.1186/s40168-018-0500-x · Cited by 35
Comparison of Bacterial Diversity in Air and Water of a Major Urban Center
Dueker, M. E., French, S. R., & O'Mullan, G. D. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02868 · Cited by 36
“Amplicon pyrosequencing was then performed on extracted environmental DNA at Molecular Research DNA labs (1MRDNA, Shallowater, TX, United States), using a protocol described by Dowd et al. (2008) to determine bacterial community composition.”
MethodVongsa, R., Hoffman, D., Shepard, K., & Koenig, D. W. (2019) · BMC Microbiology · doi:10.1186/s12866-019-1391-0 · Cited by 37
Gut Microbiome Perturbations in Patients with Hidradenitis Suppurativa: A Case Series
Kam, S. A., Collard, M., Lam, J., & Alani, R. M. (2020) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2020.04.017 · Cited by 35
Kirk, M. F., Santillan, E. F. U., Sanford, R. A., & Altman, S. J. (2013) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2013.08.018 · Cited by 35
“After PCR, amplicon pyrosequencing 227 (bTEFAP) as described by Dowd et al. (2008) was used to sequence 16S rRNA genes.”
MethodThe dynamics of biofilm bacterial communities is driven by flow wax and wane in a temporary stream
Timoner, X., Borrego, C., Acuña, V., & Sabater, S. (2014) · Limnology and Oceanography · doi:10.4319/lo.2014.59.6.2057 · Cited by 35
“Raw sequence data set was preprocessed at RTL facilities to reduce noise and sequencing artifacts as previously described (Dowd et al. 2008).”
MethodBiogeographic congruency among bacterial communities from terrestrial sulfidic springs
Headd, B., & Engel, A. S. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00473 · Cited by 35
“The V1-V3 region of the 16S rRNA gene was amplified and all sequencing was done by the Research and Testing Laboratories (Lubbock, Texas, USA), using previously described methods (Dowd et al., 2008a,b).”
MethodPetri, R. M., Mapiye, C., Dugan, M. E. R., & McAllister, T. A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104167 · Cited by 36
“Bacterial tag-encoded FLX-Titanium amplicon pyrosequencing (bTEFAP) of the pooled DNA, [23], was performed at MR DNA (Shallowater, TX, USA).”
MethodRodríguez–Sánchez, A., Purswani, J., Lotti, T., Maza‐Márquez, P., van Loosdrecht, M. C. M., Vahala, R., & González‐Martínez, A. (2016) · Environmental Technology · doi:10.1080/09593330.2016.1147613 · Cited by 34
“Dowd et al.[17] by the Research & Testing Laboratory (Lubbock, TX, USA).”
BackgroundSalem, F. B., Saïd, O. B., Cravo‐Laureau, C., Mahmoudi, E., Bru, N., Monperrus, M., & Duran, R. (2019) · Environmental Pollution · doi:10.1016/j.envpol.2019.05.146 · Cited by 37
Murray, E., Smith, K. B., Stoby, K. S., Thomas, B. J., Swenson, M. J., Arber, L., Frenette, E., & Ismail, N. (2019) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2019.104481 · Cited by 34
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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