Evaluation of Physiological Parameters of Intestinal Sulfate-Reducing Bacteria Isolated from Patients Suffering from IBD and Healthy People
Background: Inflammatory bowel diseases (IBDs) are multifactorial illnesses of the intestine, to which microorganisms are contributing. Among the contributing microorganisms, sulfate-reducing bacteria (SRB) are suggested to be involved in the process of bowel inflammation due to the production of hy...
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Published in | Journal of clinical medicine Vol. 9; no. 6; p. 1920 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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MDPI AG
19.06.2020
MDPI |
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ISSN | 2077-0383 2077-0383 |
DOI | 10.3390/jcm9061920 |
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Abstract | Background: Inflammatory bowel diseases (IBDs) are multifactorial illnesses of the intestine, to which microorganisms are contributing. Among the contributing microorganisms, sulfate-reducing bacteria (SRB) are suggested to be involved in the process of bowel inflammation due to the production of hydrogen sulfide (H2S) by dissimilatory sulfate reduction. The aims of our research were to physiologically examine SRB in fecal samples of patients with IBD and a control group, their identification, the study of the process of dissimilatory sulfate reduction (sulfate consumption and H2S production) and biomass accumulation. Determination of biogenic elements of the SRB and evaluation of obtained parameters by using statistical methods were also included in the research. The material for the research consisted of 14 fecal samples, which was obtained from patients and control subjects. Methods: Microscopic techniques, microbiological, biochemical, biophysical methods and statistical analysis were included. Results: Colonies of SRB were isolated from all the fecal samples, and subsequently, 35 strains were obtained. Vibrio-shaped cells stained Gram-negative were dominant in all purified studied strains. All strains had a high percentage of similarity by the 16S rRNA gene with deposited sequences in GenBank of Desulfovibrio vulgaris. Cluster analysis of sulfate reduction parameters allowed the grouping of SRB strains. Significant (p < 0.05) differences were not observed between healthy individuals and patients with IBD with regard to sulfate reduction parameters (sulfate consumption, H2S and biomass accumulation). Moreover, we found that manganese and iron contents in the cell extracts are higher among healthy individuals in comparison to unhealthy individuals that have an intestinal bowel disease, especially ulcerative colitis. Conclusions: The observations obtained from studying SRB emphasize differences in the intestinal microbial processes of healthy and unhealthy people. |
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AbstractList | Inflammatory bowel diseases (IBDs) are multifactorial illnesses of the intestine, to which microorganisms are contributing. Among the contributing microorganisms, sulfate-reducing bacteria (SRB) are suggested to be involved in the process of bowel inflammation due to the production of hydrogen sulfide (H2S) by dissimilatory sulfate reduction. The aims of our research were to physiologically examine SRB in fecal samples of patients with IBD and a control group, their identification, the study of the process of dissimilatory sulfate reduction (sulfate consumption and H2S production) and biomass accumulation. Determination of biogenic elements of the SRB and evaluation of obtained parameters by using statistical methods were also included in the research. The material for the research consisted of 14 fecal samples, which was obtained from patients and control subjects.BACKGROUNDInflammatory bowel diseases (IBDs) are multifactorial illnesses of the intestine, to which microorganisms are contributing. Among the contributing microorganisms, sulfate-reducing bacteria (SRB) are suggested to be involved in the process of bowel inflammation due to the production of hydrogen sulfide (H2S) by dissimilatory sulfate reduction. The aims of our research were to physiologically examine SRB in fecal samples of patients with IBD and a control group, their identification, the study of the process of dissimilatory sulfate reduction (sulfate consumption and H2S production) and biomass accumulation. Determination of biogenic elements of the SRB and evaluation of obtained parameters by using statistical methods were also included in the research. The material for the research consisted of 14 fecal samples, which was obtained from patients and control subjects.Microscopic techniques, microbiological, biochemical, biophysical methods and statistical analysis were included.METHODSMicroscopic techniques, microbiological, biochemical, biophysical methods and statistical analysis were included.Colonies of SRB were isolated from all the fecal samples, and subsequently, 35 strains were obtained. Vibrio-shaped cells stained Gram-negative were dominant in all purified studied strains. All strains had a high percentage of similarity by the 16S rRNA gene with deposited sequences in GenBank of Desulfovibrio vulgaris. Cluster analysis of sulfate reduction parameters allowed the grouping of SRB strains. Significant (p < 0.05) differences were not observed between healthy individuals and patients with IBD with regard to sulfate reduction parameters (sulfate consumption, H2S and biomass accumulation). Moreover, we found that manganese and iron contents in the cell extracts are higher among healthy individuals in comparison to unhealthy individuals that have an intestinal bowel disease, especially ulcerative colitis.RESULTSColonies of SRB were isolated from all the fecal samples, and subsequently, 35 strains were obtained. Vibrio-shaped cells stained Gram-negative were dominant in all purified studied strains. All strains had a high percentage of similarity by the 16S rRNA gene with deposited sequences in GenBank of Desulfovibrio vulgaris. Cluster analysis of sulfate reduction parameters allowed the grouping of SRB strains. Significant (p < 0.05) differences were not observed between healthy individuals and patients with IBD with regard to sulfate reduction parameters (sulfate consumption, H2S and biomass accumulation). Moreover, we found that manganese and iron contents in the cell extracts are higher among healthy individuals in comparison to unhealthy individuals that have an intestinal bowel disease, especially ulcerative colitis.The observations obtained from studying SRB emphasize differences in the intestinal microbial processes of healthy and unhealthy people.CONCLUSIONSThe observations obtained from studying SRB emphasize differences in the intestinal microbial processes of healthy and unhealthy people. Background: Inflammatory bowel diseases (IBDs) are multifactorial illnesses of the intestine, to which microorganisms are contributing. Among the contributing microorganisms, sulfate-reducing bacteria (SRB) are suggested to be involved in the process of bowel inflammation due to the production of hydrogen sulfide (H2S) by dissimilatory sulfate reduction. The aims of our research were to physiologically examine SRB in fecal samples of patients with IBD and a control group, their identification, the study of the process of dissimilatory sulfate reduction (sulfate consumption and H2S production) and biomass accumulation. Determination of biogenic elements of the SRB and evaluation of obtained parameters by using statistical methods were also included in the research. The material for the research consisted of 14 fecal samples, which was obtained from patients and control subjects. Methods: Microscopic techniques, microbiological, biochemical, biophysical methods and statistical analysis were included. Results: Colonies of SRB were isolated from all the fecal samples, and subsequently, 35 strains were obtained. Vibrio-shaped cells stained Gram-negative were dominant in all purified studied strains. All strains had a high percentage of similarity by the 16S rRNA gene with deposited sequences in GenBank of Desulfovibrio vulgaris. Cluster analysis of sulfate reduction parameters allowed the grouping of SRB strains. Significant (p < 0.05) differences were not observed between healthy individuals and patients with IBD with regard to sulfate reduction parameters (sulfate consumption, H2S and biomass accumulation). Moreover, we found that manganese and iron contents in the cell extracts are higher among healthy individuals in comparison to unhealthy individuals that have an intestinal bowel disease, especially ulcerative colitis. Conclusions: The observations obtained from studying SRB emphasize differences in the intestinal microbial processes of healthy and unhealthy people. Background: Inflammatory bowel diseases (IBDs) are multifactorial illnesses of the intestine, to which microorganisms are contributing. Among the contributing microorganisms, sulfate-reducing bacteria (SRB) are suggested to be involved in the process of bowel inflammation due to the production of hydrogen sulfide (H 2 S) by dissimilatory sulfate reduction. The aims of our research were to physiologically examine SRB in fecal samples of patients with IBD and a control group, their identification, the study of the process of dissimilatory sulfate reduction (sulfate consumption and H 2 S production) and biomass accumulation. Determination of biogenic elements of the SRB and evaluation of obtained parameters by using statistical methods were also included in the research. The material for the research consisted of 14 fecal samples, which was obtained from patients and control subjects. Methods: Microscopic techniques, microbiological, biochemical, biophysical methods and statistical analysis were included. Results: Colonies of SRB were isolated from all the fecal samples, and subsequently, 35 strains were obtained. Vibrio-shaped cells stained Gram-negative were dominant in all purified studied strains. All strains had a high percentage of similarity by the 16S rRNA gene with deposited sequences in GenBank of Desulfovibrio vulgaris . Cluster analysis of sulfate reduction parameters allowed the grouping of SRB strains. Significant ( p < 0.05) differences were not observed between healthy individuals and patients with IBD with regard to sulfate reduction parameters (sulfate consumption, H 2 S and biomass accumulation). Moreover, we found that manganese and iron contents in the cell extracts are higher among healthy individuals in comparison to unhealthy individuals that have an intestinal bowel disease, especially ulcerative colitis. Conclusions: The observations obtained from studying SRB emphasize differences in the intestinal microbial processes of healthy and unhealthy people. Inflammatory bowel diseases (IBDs) are multifactorial illnesses of the intestine, to which microorganisms are contributing. Among the contributing microorganisms, sulfate-reducing bacteria (SRB) are suggested to be involved in the process of bowel inflammation due to the production of hydrogen sulfide (H S) by dissimilatory sulfate reduction. The aims of our research were to physiologically examine SRB in fecal samples of patients with IBD and a control group, their identification, the study of the process of dissimilatory sulfate reduction (sulfate consumption and H S production) and biomass accumulation. Determination of biogenic elements of the SRB and evaluation of obtained parameters by using statistical methods were also included in the research. The material for the research consisted of 14 fecal samples, which was obtained from patients and control subjects. Microscopic techniques, microbiological, biochemical, biophysical methods and statistical analysis were included. Colonies of SRB were isolated from all the fecal samples, and subsequently, 35 strains were obtained. Vibrio-shaped cells stained Gram-negative were dominant in all purified studied strains. All strains had a high percentage of similarity by the 16S rRNA gene with deposited sequences in GenBank of . Cluster analysis of sulfate reduction parameters allowed the grouping of SRB strains. Significant ( < 0.05) differences were not observed between healthy individuals and patients with IBD with regard to sulfate reduction parameters (sulfate consumption, H S and biomass accumulation). Moreover, we found that manganese and iron contents in the cell extracts are higher among healthy individuals in comparison to unhealthy individuals that have an intestinal bowel disease, especially ulcerative colitis. The observations obtained from studying SRB emphasize differences in the intestinal microbial processes of healthy and unhealthy people. |
Author | Castro Sangrador, Jorge Dordević, Dani Černý, Martin Fafula, Roman Kushkevych, Ivan Rozehnalová, Monika Vítězová, Monika Rittmann, Simon K.-M. R. |
AuthorAffiliation | 4 Centre of Region Hana for Biotechnological an Agricultural Research, Central Laboratories and Research Support, Faculty of Science, Palacky University Olomouc, 77900 Olomouc, Czech Republic; Jarosova.Monika@email.cz 3 Department of Plant Origin Foodstuffs Hygiene and Technology, Faculty of Veterinary Hygiene and Ecology, University of Veterinary and Pharmaceutical Sciences, 61242 Brno, Czech Republic; dani_dordevic@yahoo.com 2 Faculty of Biology, University of Salamanca, Campus Miguel de Unamuno C/Donantes de sangre, s/n 37007 Salamanca, Spain 5 Department of Medical Biophysics, Danylo Halytsky Lviv National Medical University, 69 Pekarska St., 79010 Lviv, Ukraine; roman_fafula@ukr.net 1 Department of Experimental Biology, Faculty of Science, Masaryk University, Kamenice 753/5, 62500 Brno, Czech Republic; jorgecas@usal.es (J.C.S.); cernyarchaea@mail.muni.cz (M.C.); vitezova@sci.muni.cz (M.V.) 6 Archaea Physiology & Biotechnology Group, Department of Functional and Evolutionary Ecology, Un |
AuthorAffiliation_xml | – name: 6 Archaea Physiology & Biotechnology Group, Department of Functional and Evolutionary Ecology, Universität Wien, Althanstraße 14, 1090 Vienna, Austria – name: 2 Faculty of Biology, University of Salamanca, Campus Miguel de Unamuno C/Donantes de sangre, s/n 37007 Salamanca, Spain – name: 1 Department of Experimental Biology, Faculty of Science, Masaryk University, Kamenice 753/5, 62500 Brno, Czech Republic; jorgecas@usal.es (J.C.S.); cernyarchaea@mail.muni.cz (M.C.); vitezova@sci.muni.cz (M.V.) – name: 4 Centre of Region Hana for Biotechnological an Agricultural Research, Central Laboratories and Research Support, Faculty of Science, Palacky University Olomouc, 77900 Olomouc, Czech Republic; Jarosova.Monika@email.cz – name: 3 Department of Plant Origin Foodstuffs Hygiene and Technology, Faculty of Veterinary Hygiene and Ecology, University of Veterinary and Pharmaceutical Sciences, 61242 Brno, Czech Republic; dani_dordevic@yahoo.com – name: 5 Department of Medical Biophysics, Danylo Halytsky Lviv National Medical University, 69 Pekarska St., 79010 Lviv, Ukraine; roman_fafula@ukr.net |
Author_xml | – sequence: 1 givenname: Ivan orcidid: 0000-0002-8450-7137 surname: Kushkevych fullname: Kushkevych, Ivan – sequence: 2 givenname: Jorge surname: Castro Sangrador fullname: Castro Sangrador, Jorge – sequence: 3 givenname: Dani orcidid: 0000-0002-2435-9726 surname: Dordević fullname: Dordević, Dani – sequence: 4 givenname: Monika surname: Rozehnalová fullname: Rozehnalová, Monika – sequence: 5 givenname: Martin orcidid: 0000-0002-8231-9634 surname: Černý fullname: Černý, Martin – sequence: 6 givenname: Roman surname: Fafula fullname: Fafula, Roman – sequence: 7 givenname: Monika surname: Vítězová fullname: Vítězová, Monika – sequence: 8 givenname: Simon K.-M. R. orcidid: 0000-0002-9746-3284 surname: Rittmann fullname: Rittmann, Simon K.-M. R. |
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Cites_doi | 10.2754/avb201585010003 10.1128/9781555816834 10.1016/S0167-7012(00)00154-8 10.1017/CBO9781139170840 10.1128/jb.173.2.697-703.1991 10.3390/en11123270 10.1007/0-387-29298-5 10.1016/j.micpath.2017.09.054 10.3390/cells9030698 10.1007/s00203-018-1510-6 10.3390/jcm8101656 10.1016/S0016-5085(98)70381-6 10.1007/s00726-009-0445-2 10.33263/BRIAC94.066069 10.1097/00001574-199907000-00003 10.1098/rstb.1982.0091 10.1111/j.1751-2980.2007.00310.x 10.1515/med-2019-0010 10.33073/pjm-2015-016 10.2478/s11756-018-0118-2 10.1016/j.jab.2016.01.005 10.3748/wjg.v12.i30.4807 10.1007/s00203-019-01625-z 10.1016/j.jab.2018.01.004 10.3109/10408448409029321 10.1515/biol-2017-0009 10.3390/jcm8071054 10.1111/j.1572-0241.2004.04129.x 10.2754/avb201786040405 10.1136/gut.39.1.1 10.1007/s00044-017-2067-7 10.1111/j.1574-6968.1991.tb04799.x 10.1111/j.1574-6941.2002.tb00942.x 10.1099/00207713-26-2-238 10.3390/biom9120752 10.1002/bjs.6454 10.1515/biol-2018-0057 10.1515/med-2018-0052 10.1158/1541-7786.MCR-05-0126 10.3390/molecules21111558 10.1111/j.1365-2672.1988.tb01498.x 10.1515/biol-2018-0017 10.1006/jfca.1993.1016 |
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Keywords | toxicity bowel disease intestinal microbiota ulcerative colitis hydrogen sulfide sulfate reduction |
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References | Rowan (ref_7) 2009; 96 ref_10 Kushkevych (ref_27) 2017; 86 Scaldaferri (ref_4) 2007; 8 Kushkevych (ref_22) 2015; 62 ref_51 Kushkevych (ref_50) 2018; 200 Kushkevych (ref_21) 2015; 84 ref_17 Kushkevych (ref_8) 2019; 201 Loubinoux (ref_6) 2002; 40 Kushkevych (ref_37) 2016; 14 Gibson (ref_12) 1991; 86 ref_25 ref_20 Kushkevych (ref_18) 2019; 9 ref_29 Kushkevych (ref_39) 2020; 25 Danese (ref_2) 2004; 99 Pitcher (ref_19) 1996; 39 Abdulina (ref_36) 2020; 10 Beauchamp (ref_52) 1984; 13 Kushkevych (ref_38) 2018; 27 Kushkevych (ref_26) 2018; 13 Kolmert (ref_46) 2000; 41 Wagner (ref_54) 2006; 4 Blachier (ref_53) 2010; 39 ref_35 Weisburg (ref_44) 1991; 173 Kushkevych (ref_16) 2015; 64 Kushkevych (ref_30) 2017; 12 Florin (ref_49) 1993; 6 Kushkevych (ref_33) 2018; 13 Kushkevych (ref_14) 2018; 16 Loubinoux (ref_34) 2002; 52 Kushkevych (ref_23) 2018; 73 Peck (ref_32) 1982; 298 Kushkevych (ref_40) 2020; 25 Kushkevych (ref_15) 2015; 36 ref_47 Fiocchi (ref_5) 1998; 115 ref_45 ref_43 ref_42 Gibson (ref_28) 1988; 65 Kushkevych (ref_31) 2018; 13 Cummings (ref_11) 2003; 4 Coutinho (ref_13) 2017; 112 ref_48 ref_9 Katz (ref_1) 1999; 15 Danese (ref_3) 2006; 12 Moore (ref_41) 1976; 26 Kushkevych (ref_24) 2019; 14 |
References_xml | – volume: 84 start-page: 3 year: 2015 ident: ref_21 article-title: Activity of Na+/K+-activated Mg2+-dependent ATP hydrolase in the cell-free extracts of the sulfate-reducing bacteria Desulfovibrio piger Vib-7 and Desulfomicrobium sp. Rod-9 publication-title: Acta Vet. Brno doi: 10.2754/avb201585010003 – ident: ref_45 doi: 10.1128/9781555816834 – volume: 41 start-page: 179 year: 2000 ident: ref_46 article-title: A fast and simple turbidimetric method for the determination of sulfate in sulfate-reducing bacterial cultures publication-title: J. Microbiol. Methods doi: 10.1016/S0167-7012(00)00154-8 – ident: ref_48 doi: 10.1017/CBO9781139170840 – volume: 173 start-page: 697 year: 1991 ident: ref_44 article-title: 16S ribosomal DNA amplification for phylogenetic study publication-title: J. Bacteriol. doi: 10.1128/jb.173.2.697-703.1991 – volume: 52 start-page: 1305 year: 2002 ident: ref_34 article-title: Reclassification of the only species of the genus Desulfomonas, Desulfomonas pigra, as Desulfovibrio piger comb. nov publication-title: Int. J. Syst. Evol. Microbiol. – ident: ref_29 doi: 10.3390/en11123270 – ident: ref_42 doi: 10.1007/0-387-29298-5 – volume: 112 start-page: 126 year: 2017 ident: ref_13 article-title: Sulphate-reducing bacteria from ulcerative colitis patients induce apoptosis of gastrointestinal epithelial cells publication-title: Microb. Pathog. doi: 10.1016/j.micpath.2017.09.054 – ident: ref_51 doi: 10.3390/cells9030698 – ident: ref_35 – volume: 200 start-page: 945 year: 2018 ident: ref_50 article-title: The diversity of sulfate-reducing bacteria in the seven bioreactors publication-title: Arch. Microbiol. doi: 10.1007/s00203-018-1510-6 – ident: ref_20 doi: 10.3390/jcm8101656 – volume: 10 start-page: 55 year: 2020 ident: ref_36 article-title: ATP sulfurylase activity of sulfate-reducing bacteria from various ecotopes publication-title: 3Biotech – volume: 115 start-page: 182 year: 1998 ident: ref_5 article-title: Inflammatory bowel disease: Etiology and pathogenesis publication-title: Gastroenterology doi: 10.1016/S0016-5085(98)70381-6 – volume: 39 start-page: 335 year: 2010 ident: ref_53 article-title: Luminal sulfide and large intestine mucosa: Friend or foe? publication-title: Amino Acids doi: 10.1007/s00726-009-0445-2 – volume: 25 start-page: 1 year: 2020 ident: ref_40 article-title: Possible synergy effect of hydrogen sulfide and acetate produced by sulfate-reducing bacteria on inflammatory bowel disease development publication-title: J. Adv. Res. – volume: 9 start-page: 4066 year: 2019 ident: ref_18 article-title: Possible methods for evaluation of hydrogen sulfide toxicity against lactic acid bacteria publication-title: Biointerface Res. Appl. Chem. doi: 10.33263/BRIAC94.066069 – volume: 15 start-page: 291 year: 1999 ident: ref_1 article-title: Pathogenesis of inflammatory bowel disease publication-title: Curr. Opin. Gastroenterol. doi: 10.1097/00001574-199907000-00003 – ident: ref_17 – volume: 298 start-page: 443 year: 1982 ident: ref_32 article-title: Biochemistry of dissimilatory sulfate reduction publication-title: Philos. Trans. R. Soc. Lond. B Biol. Sci. doi: 10.1098/rstb.1982.0091 – volume: 8 start-page: 171 year: 2007 ident: ref_4 article-title: Inflammatory bowel disease: Progress and current concepts of etiopathogenesis publication-title: J. Dig. Dis. doi: 10.1111/j.1751-2980.2007.00310.x – volume: 14 start-page: 66 year: 2019 ident: ref_24 article-title: Analysis of pH dose-dependent growth of sulfate-reducing bacteria publication-title: Open Med. doi: 10.1515/med-2019-0010 – volume: 64 start-page: 107 year: 2015 ident: ref_16 article-title: Kinetic properties of pyruvate ferredoxin oxidoreductase of intestinal sulfate-reducing bacteria Desulfovibrio piger Vib-7 and Desulfomicrobium sp. Rod-9 publication-title: Pol. J. Microbiol. doi: 10.33073/pjm-2015-016 – volume: 73 start-page: 1137 year: 2018 ident: ref_23 article-title: Cross-correlation analysis of the Desulfovibrio growth parameters of intestinal species isolated from people with colitis publication-title: Biologia doi: 10.2478/s11756-018-0118-2 – ident: ref_47 – volume: 14 start-page: 125 year: 2016 ident: ref_37 article-title: Antimicrobial effect of salicylamide derivatives against intestinal sulfate-reducing bacteria publication-title: J. Appl. Biomed. doi: 10.1016/j.jab.2016.01.005 – volume: 25 start-page: 1 year: 2020 ident: ref_39 article-title: Hydrogen sulfide toxicity in the gut environment: Meta-analysis of sulfate-reducing and lactic acid bacteria in inflammatory processes publication-title: J. Adv. Res. – volume: 12 start-page: 4807 year: 2006 ident: ref_3 article-title: Etiopathogenesis of inflammatory bowel diseases publication-title: World J. Gastroenterol. doi: 10.3748/wjg.v12.i30.4807 – volume: 201 start-page: 389 year: 2019 ident: ref_8 article-title: Toxicity of hydrogen sulfide toward sulfate-reducing bacteria Desulfovibrio piger Vib-7 publication-title: Arch. Microbiol. doi: 10.1007/s00203-019-01625-z – volume: 16 start-page: 241 year: 2018 ident: ref_14 article-title: Effect of selected 8-hydroxyquinoline-2-carboxanilides on viability and sulfate metabolism of Desulfovibrio piger publication-title: J. Appl. Biomed. doi: 10.1016/j.jab.2018.01.004 – volume: 13 start-page: 25 year: 1984 ident: ref_52 article-title: A critical review of the literature on hydrogen sulfide toxicity publication-title: CRC Crit. Rev. Toxicol. doi: 10.3109/10408448409029321 – volume: 12 start-page: 82 year: 2017 ident: ref_30 article-title: Production of biogas: Relationship between methanogenic and sulfate-reducing microorganisms publication-title: Open Life Sci. doi: 10.1515/biol-2017-0009 – ident: ref_9 doi: 10.3390/jcm8071054 – volume: 99 start-page: 938 year: 2004 ident: ref_2 article-title: Platelets in inflammatory bowel disease: Clinical, pathogenic, and therapeutic implications publication-title: Am. J. Gastroenterol. doi: 10.1111/j.1572-0241.2004.04129.x – volume: 86 start-page: 405 year: 2017 ident: ref_27 article-title: Kinetic properties of growth of intestinal sulphate-reducing bacteria isolated from healthy mice and mice with ulcerative colitis publication-title: Acta Vet. Brno doi: 10.2754/avb201786040405 – volume: 4 start-page: 9 year: 2003 ident: ref_11 article-title: Intestinal Bacteria and Ulcerative Colitis publication-title: Curr. Issues Intest. Microbiol. – volume: 62 start-page: 1037 year: 2015 ident: ref_22 article-title: Activity and kinetic properties of phosphotransacetylase from intestinal sulfate-reducing bacteria publication-title: Acta Biochem. Pol. – volume: 39 start-page: 1 year: 1996 ident: ref_19 article-title: Hydrogen sulphide: A bacterial toxin in ulcerative colitis? publication-title: Gut doi: 10.1136/gut.39.1.1 – volume: 36 start-page: 106 year: 2015 ident: ref_15 article-title: Activity of selected salicylamides against intestinal sulfate-reducing bacteria publication-title: Neuro Endocrinol. Lett. – volume: 27 start-page: 278 year: 2018 ident: ref_38 article-title: Activity of ring-substituted 8-hydroxyquinoline-2-carboxanilides against intestinal sulfate-reducing bacteria Desulfovibrio piger publication-title: Med. Chem. Res. doi: 10.1007/s00044-017-2067-7 – volume: 86 start-page: 103 year: 1991 ident: ref_12 article-title: Growth and activities of sulphate-reducing bacteria in gut contents of health subjects and patients with ulcerative colitis publication-title: FEMS Microbiol. Ecol. doi: 10.1111/j.1574-6968.1991.tb04799.x – volume: 40 start-page: 107 year: 2002 ident: ref_6 article-title: Sulphate-reducing bacteria in human feces and their association with inflammatory diseases publication-title: FEMS Microbiol. Ecol. doi: 10.1111/j.1574-6941.2002.tb00942.x – volume: 26 start-page: 238 year: 1976 ident: ref_41 article-title: Emendation of Bacteroidaceae and Butyrivibrio and descriptions of Desulfomonas gen. nov. and ten new species of the genera Desulfomonas, Butyrivibrio, Eubacterium, Clostridium and Ruminococcus publication-title: Int. J. Syst. Bact. doi: 10.1099/00207713-26-2-238 – ident: ref_10 doi: 10.3390/biom9120752 – volume: 96 start-page: 151 year: 2009 ident: ref_7 article-title: Sulphate-reducing bacteria and hydrogen sulphide in the aetiology of ulcerative colitis publication-title: Br. J. Surg. doi: 10.1002/bjs.6454 – volume: 13 start-page: 481 year: 2018 ident: ref_33 article-title: Analysis of physiological parameters of Desulfovibrio strains from individuals with colitis publication-title: Open Life Sci. doi: 10.1515/biol-2018-0057 – volume: 13 start-page: 344 year: 2018 ident: ref_26 article-title: Metabolic activity of sulfate-reducing bacteria from rodents with colitis publication-title: Open Med. doi: 10.1515/med-2018-0052 – volume: 4 start-page: 9 year: 2006 ident: ref_54 article-title: Evidence that hydrogen sulfide is a genotoxic agent publication-title: Mol. Cancer Res. doi: 10.1158/1541-7786.MCR-05-0126 – ident: ref_25 doi: 10.3390/molecules21111558 – volume: 65 start-page: 103 year: 1988 ident: ref_28 article-title: Occurrence of sulphate-reducing bacteria in human faeces and the relationship of dissimilatory sulphate reduction to methanogenesis in the large gut publication-title: J. Appl. Bacteriol. doi: 10.1111/j.1365-2672.1988.tb01498.x – ident: ref_43 – volume: 13 start-page: 119 year: 2018 ident: ref_31 article-title: A new combination of substrates: Biogas production and diversity of the methanogenic microorganisms publication-title: Open Life Sci. doi: 10.1515/biol-2018-0017 – volume: 6 start-page: 140 year: 1993 ident: ref_49 article-title: Sulfate in food and beverages publication-title: J. Food Compos. Anal. doi: 10.1006/jfca.1993.1016 |
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SubjectTerms | Bacteria Bowel disease Clinical medicine Feces Inflammatory bowel disease Metabolism Microbiota Microorganisms |
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Title | Evaluation of Physiological Parameters of Intestinal Sulfate-Reducing Bacteria Isolated from Patients Suffering from IBD and Healthy People |
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