Multilocus Sequence Typing Reveals Intrafamilial Transmission and Microevolutions of Candida albicans Isolates from the Human Digestive Tract
Candida albicans is a human commensal that is also responsible for superficial and systemic infections. Little is known about the carriage of C. albicans in the digestive tract and the genome dynamics that occur during commensalisms of this diploid species. The aim of this study was to evaluate the...
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Published in | Journal of Clinical Microbiology Vol. 44; no. 5; pp. 1810 - 1820 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Washington, DC
American Society for Microbiology
01.05.2006
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Abstract | Candida albicans is a human commensal that is also responsible for superficial and systemic infections. Little is known about the carriage of C. albicans in the digestive tract and the genome dynamics that occur during commensalisms of this diploid species. The aim of this study was to evaluate the prevalence, diversity, and genetic relationships among C. albicans isolates recovered during natural colonization of the digestive tract of humans, with emphasis on Crohn's disease patients who produce anti-yeast antibodies and may have altered Candida sp. carriage. Candida sp. isolates were recovered from 234 subjects within 25 families with multiple cases of Crohn's disease and 10 control families, sampled at the oral and fecal sites. Prevalences of Candida sp. and C. albicans carriage were 53.4% and 46.5%, respectively, indicating frequent commensal carriage. No differences in prevalence of carriage could be observed between Crohn's disease patients and healthy subjects. Multilocus sequence typing (MLST) of C. albicans isolates revealed frequent colonization of a subject or several members of the same family by genetically indistinguishable or genetically close isolates. These latter isolates differed by loss-of-heterozygosity events at one or several of the MLST loci. These loss-of-heterozygosity events could be due to either chromosome loss followed by duplication or large mitotic recombination events between complementary chromosomes. This study was the first to jointly assess commensal carriage of C. albicans, intrafamilial transmission, and microevolution. The high frequency of each of these events suggests that the digestive tract provides an important and natural niche for microevolutions of diploid C. albicans through the loss of heterozygosity. |
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AbstractList | Candida albicans is a human commensal that is also responsible for superficial and systemic infections. Little is known about the carriage of C. albicans in the digestive tract and the genome dynamics that occur during commensalisms of this diploid species. The aim of this study was to evaluate the prevalence, diversity, and genetic relationships among C. albicans isolates recovered during natural colonization of the digestive tract of humans, with emphasis on Crohn's disease patients who produce anti-yeast antibodies and may have altered Candida sp. carriage. Candida sp. isolates were recovered from 234 subjects within 25 families with multiple cases of Crohn's disease and 10 control families, sampled at the oral and fecal sites. Prevalences of Candida sp. and C. albicans carriage were 53.4% and 46.5%, respectively, indicating frequent commensal carriage. No differences in prevalence of carriage could be observed between Crohn's disease patients and healthy subjects. Multilocus sequence typing (MLST) of C. albicans isolates revealed frequent colonization of a subject or several members of the same family by genetically indistinguishable or genetically close isolates. These latter isolates differed by loss-of-heterozygosity events at one or several of the MLST loci. These loss-of-heterozygosity events could be due to either chromosome loss followed by duplication or large mitotic recombination events between complementary chromosomes. This study was the first to jointly assess commensal carriage of C. albicans, intrafamilial transmission, and microevolution. The high frequency of each of these events suggests that the digestive tract provides an important and natural niche for microevolutions of diploid C. albicans through the loss of heterozygosity. Candida albicans is a human commensal that is also responsible for superficial and systemic infections. Little is known about the carriage of C. albicans in the digestive tract and the genome dynamics that occur during commensalisms of this diploid species. The aim of this study was to evaluate the prevalence, diversity, and genetic relationships among C. albicans isolates recovered during natural colonization of the digestive tract of humans, with emphasis on Crohn's disease patients who produce anti-yeast antibodies and may have altered Candida sp. carriage. Candida sp. isolates were recovered from 234 subjects within 25 families with multiple cases of Crohn's disease and 10 control families, sampled at the oral and fecal sites. Prevalences of Candida sp. and C. albicans carriage were 53.4% and 46.5%, respectively, indicating frequent commensal carriage. No differences in prevalence of carriage could be observed between Crohn's disease patients and healthy subjects. Multilocus sequence typing (MLST) of C. albicans isolates revealed frequent colonization of a subject or several members of the same family by genetically indistinguishable or genetically close isolates. These latter isolates differed by loss-of-heterozygosity events at one or several of the MLST loci. These loss-of-heterozygosity events could be due to either chromosome loss followed by duplication or large mitotic recombination events between complementary chromosomes. This study was the first to jointly assess commensal carriage of C. albicans , intrafamilial transmission, and microevolution. The high frequency of each of these events suggests that the digestive tract provides an important and natural niche for microevolutions of diploid C. albicans through the loss of heterozygosity. Article Usage Stats Services JCM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue JCM About JCM Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy JCM RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0095-1137 Online ISSN: 1098-660X Copyright © 2014 by the American Society for Microbiology. For an alternate route to JCM .asm.org, visit: JCM Candida albicans is a human commensal that is also responsible for superficial and systemic infections. Little is known about the carriage of C. albicans in the digestive tract and the genome dynamics that occur during commensalisms of this diploid species. The aim of this study was to evaluate the prevalence, diversity, and genetic relationships among C. albicans isolates recovered during natural colonization of the digestive tract of humans, with emphasis on Crohn's disease patients who produce anti-yeast antibodies and may have altered Candida sp. carriage. Candida sp. isolates were recovered from 234 subjects within 25 families with multiple cases of Crohn's disease and 10 control families, sampled at the oral and fecal sites. Prevalences of Candida sp. and C. albicans carriage were 53.4% and 46.5%, respectively, indicating frequent commensal carriage. No differences in prevalence of carriage could be observed between Crohn's disease patients and healthy subjects. Multilocus sequence typing (MLST) of C. albicans isolates revealed frequent colonization of a subject or several members of the same family by genetically indistinguishable or genetically close isolates. These latter isolates differed by loss-of-heterozygosity events at one or several of the MLST loci. These loss-of-heterozygosity events could be due to either chromosome loss followed by duplication or large mitotic recombination events between complementary chromosomes. This study was the first to jointly assess commensal carriage of C. albicans, intrafamilial transmission, and microevolution. The high frequency of each of these events suggests that the digestive tract provides an important and natural niche for microevolutions of diploid C. albicans through the loss of heterozygosity.Candida albicans is a human commensal that is also responsible for superficial and systemic infections. Little is known about the carriage of C. albicans in the digestive tract and the genome dynamics that occur during commensalisms of this diploid species. The aim of this study was to evaluate the prevalence, diversity, and genetic relationships among C. albicans isolates recovered during natural colonization of the digestive tract of humans, with emphasis on Crohn's disease patients who produce anti-yeast antibodies and may have altered Candida sp. carriage. Candida sp. isolates were recovered from 234 subjects within 25 families with multiple cases of Crohn's disease and 10 control families, sampled at the oral and fecal sites. Prevalences of Candida sp. and C. albicans carriage were 53.4% and 46.5%, respectively, indicating frequent commensal carriage. No differences in prevalence of carriage could be observed between Crohn's disease patients and healthy subjects. Multilocus sequence typing (MLST) of C. albicans isolates revealed frequent colonization of a subject or several members of the same family by genetically indistinguishable or genetically close isolates. These latter isolates differed by loss-of-heterozygosity events at one or several of the MLST loci. These loss-of-heterozygosity events could be due to either chromosome loss followed by duplication or large mitotic recombination events between complementary chromosomes. This study was the first to jointly assess commensal carriage of C. albicans, intrafamilial transmission, and microevolution. The high frequency of each of these events suggests that the digestive tract provides an important and natural niche for microevolutions of diploid C. albicans through the loss of heterozygosity. |
Author | Van Kruiningen, H Colombel, J.F Sendid, B Bouchier, C Diogo, D d'Enfert, C Poulain, D Veirmeire, S François, N Bougnoux, M.-E |
AuthorAffiliation | Unité Postulante Biologie et Pathogénicité Fongiques, INRA USC 2019, 1 Pasteur Genopole-Ile-de-France PF1, Institut Pasteur, Paris, France, 6 Laboratoire de Parasitologie-Mycologie, Service de Microbiologie, Hôpital Necker-Enfants Malades, Université Paris 5-René Descartes, Faculté de Médecine, Paris, France, 2 Unité INSERM 799, Laboratoire de Parasitologie-Mycologie, CHRU de Lille, Lille, France, 3 Gastroenterology Unit, University Hospital Gasthuisberg, Leuven, Belgium, 4 Département d'hépatogastroentérologie, Hôpital Huriez, CHRU de Lille, Lille, France, 5 Department of Pathobiology, University of Connecticut, U-3089, 61 North Eagleville Road, Storrs, Connecticut 06269-3089 7 |
AuthorAffiliation_xml | – name: Unité Postulante Biologie et Pathogénicité Fongiques, INRA USC 2019, 1 Pasteur Genopole-Ile-de-France PF1, Institut Pasteur, Paris, France, 6 Laboratoire de Parasitologie-Mycologie, Service de Microbiologie, Hôpital Necker-Enfants Malades, Université Paris 5-René Descartes, Faculté de Médecine, Paris, France, 2 Unité INSERM 799, Laboratoire de Parasitologie-Mycologie, CHRU de Lille, Lille, France, 3 Gastroenterology Unit, University Hospital Gasthuisberg, Leuven, Belgium, 4 Département d'hépatogastroentérologie, Hôpital Huriez, CHRU de Lille, Lille, France, 5 Department of Pathobiology, University of Connecticut, U-3089, 61 North Eagleville Road, Storrs, Connecticut 06269-3089 7 |
Author_xml | – sequence: 1 fullname: Bougnoux, M.-E – sequence: 2 fullname: Diogo, D – sequence: 3 fullname: François, N – sequence: 4 fullname: Sendid, B – sequence: 5 fullname: Veirmeire, S – sequence: 6 fullname: Colombel, J.F – sequence: 7 fullname: Bouchier, C – sequence: 8 fullname: Van Kruiningen, H – sequence: 9 fullname: d'Enfert, C – sequence: 10 fullname: Poulain, D |
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Cites_doi | 10.1128/JCM.40.4.1290-1297.2002 10.1128/JCM.37.9.2817-2828.1999 10.1128/JCM.37.12.3835-3843.1999 10.1056/NEJMra020831 10.1093/emboj/cdg235 10.1016/S1473-3099(03)00801-6 10.1136/gut.47.6.870 10.1099/00221287-145-10-2635 10.1128/jcm.33.6.1501-1509.1995 10.1128/jcm.34.4.767-777.1996 10.1128/JCM.36.6.1518-1529.1998 10.1099/mic.0.26495-0 10.1016/S0732-8893(98)00100-X 10.1128/IAI.70.9.5274-5278.2002 10.1099/00221287-148-4-1061 10.1093/bioinformatics/17.12.1230 10.1128/EC.3.3.705-714.2004 10.1128/jcm.35.9.2348-2358.1997 10.1053/j.gastro.2003.11.015 10.1136/gut.42.6.788 10.1073/pnas.061628798 10.1186/1471-2334-2-1 10.1097/01.MIB.0000158536.31557.90 10.1038/nrg948 10.1128/JCM.40.3.826-836.2002 10.1128/EC.4.1.156-165.2005 10.1128/jcm.33.9.2366-2371.1995 10.1016/j.fgb.2003.12.008 10.1016/S1567-1348(02)00058-8 10.1126/science.289.5477.307 10.1128/AAC.45.7.2129-2133.2001 10.1128/jcm.33.5.1223-1230.1995 10.1111/j.1572-0241.1998.00415.x 10.1128/JCM.40.8.2729-2740.2002 10.1136/gut.47.4.487 10.1016/S0732-8893(02)00364-4 10.1086/375746 10.1128/JCM.43.11.5601-5613.2005 10.1097/00054725-200108000-00003 10.1126/science.289.5477.310 10.1136/gut.2005.066860 10.1128/JCM.41.11.5265-5266.2003 10.1016/S0928-8244(03)00242-6 10.1016/j.meegid.2004.06.002 10.1016/j.jhin.2004.01.017 |
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Keywords | Fungi Candida albicans Human Yeast Microbiology Transmission Genotype Isolate Fungi Imperfecti Digestive tract Thallophyta MULTILOCUS SEQUENCE TYPING TRANSMISSION EVOLUTION MLST CROHN DISEASE HUMAN DIGESTIVE TRACT CARRIER STATE FAMILY |
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References | e_1_3_2_26_2 e_1_3_2_27_2 e_1_3_2_48_2 e_1_3_2_28_2 e_1_3_2_29_2 e_1_3_2_41_2 e_1_3_2_40_2 e_1_3_2_20_2 e_1_3_2_43_2 e_1_3_2_21_2 e_1_3_2_42_2 e_1_3_2_22_2 e_1_3_2_45_2 e_1_3_2_23_2 e_1_3_2_44_2 e_1_3_2_24_2 e_1_3_2_47_2 e_1_3_2_25_2 e_1_3_2_46_2 (e_1_3_2_8_2) 2002 e_1_3_2_9_2 e_1_3_2_15_2 e_1_3_2_38_2 e_1_3_2_16_2 e_1_3_2_37_2 e_1_3_2_7_2 e_1_3_2_17_2 e_1_3_2_6_2 e_1_3_2_18_2 e_1_3_2_39_2 e_1_3_2_19_2 e_1_3_2_30_2 e_1_3_2_32_2 e_1_3_2_10_2 e_1_3_2_31_2 e_1_3_2_5_2 e_1_3_2_11_2 e_1_3_2_34_2 e_1_3_2_4_2 e_1_3_2_12_2 e_1_3_2_33_2 e_1_3_2_3_2 e_1_3_2_13_2 e_1_3_2_36_2 e_1_3_2_2_2 e_1_3_2_14_2 e_1_3_2_35_2 12825180 - J Infect Dis. 2003 Jul 1;188(1):118-27 9620370 - J Clin Microbiol. 1998 Jun;36(6):1518-29 15142710 - J Hosp Infect. 2004 May;57(1):8-13 12743044 - EMBO J. 2003 May 15;22(10):2505-15 12459722 - Nat Rev Genet. 2002 Dec;3(12):918-30 11515844 - Inflamm Bowel Dis. 2001 Aug;7(3):192-201 10565893 - J Clin Microbiol. 1999 Dec;37(12):3835-43 10986208 - Gut. 2000 Oct;47(4):487-96 11408236 - Antimicrob Agents Chemother. 2001 Jul;45(7):2129-33 9707056 - Am J Gastroenterol. 1998 Aug;93(8):1306-10 12052625 - Diagn Microbiol Infect Dis. 2002 May;43(1):19-28 7615732 - J Clin Microbiol. 1995 May;33(5):1223-30 15050544 - Fungal Genet Biol. 2004 May;41(5):553-62 14523127 - Microbiology. 2003 Oct;149(Pt 10):2947-60 14556989 - FEMS Immunol Med Microbiol. 2003 Oct 24;39(1):1-7 15863472 - Gut. 2005 Sep;54(9):1237-43 7494029 - J Clin Microbiol. 1995 Sep;33(9):2366-71 12149321 - J Clin Microbiol. 2002 Aug;40(8):2729-40 12183581 - Infect Immun. 2002 Sep;70(9):5274-8 15643071 - Eukaryot Cell. 2005 Jan;4(1):156-65 10449459 - J Clin Microbiol. 1999 Sep;37(9):2817-28 11248064 - Proc Natl Acad Sci U S A. 2001 Mar 13;98(6):3249-53 15189991 - Eukaryot Cell. 2004 Jun;3(3):705-14 11880401 - J Clin Microbiol. 2002 Mar;40(3):826-36 10342103 - Diagn Microbiol Infect Dis. 1999 May;34(1):19-25 8815082 - J Clin Microbiol. 1996 Apr;34(4):767-77 14592598 - Lancet Infect Dis. 2003 Nov;3(11):685-702 11835694 - BMC Infect Dis. 2002;2:1 9691915 - Gut. 1998 Jun;42(6):788-91 14605179 - J Clin Microbiol. 2003 Nov;41(11):5265-6 14762777 - Gastroenterology. 2004 Feb;126(2):414-24 9276415 - J Clin Microbiol. 1997 Sep;35(9):2348-58 16272493 - J Clin Microbiol. 2005 Nov;43(11):5601-13 10894781 - Science. 2000 Jul 14;289(5477):310-3 11186432 - Gut. 2000 Dec;47(6):870-1 15450203 - Infect Genet Evol. 2004 Sep;4(3):243-52 15803025 - Inflamm Bowel Dis. 2005 Apr;11(4):360-5 11751234 - Bioinformatics. 2001 Dec;17(12):1230-1 12797998 - Infect Genet Evol. 2002 Oct;2(1):19-37 11923347 - J Clin Microbiol. 2002 Apr;40(4):1290-7 12167685 - N Engl J Med. 2002 Aug 8;347(6):417-29 10894780 - Science. 2000 Jul 14;289(5477):307-10 11932451 - Microbiology. 2002 Apr;148(Pt 4):1061-72 10537185 - Microbiology. 1999 Oct;145 ( Pt 10):2635-46 7650175 - J Clin Microbiol. 1995 Jun;33(6):1501-9 |
References_xml | – ident: e_1_3_2_6_2 doi: 10.1128/JCM.40.4.1290-1297.2002 – ident: e_1_3_2_21_2 doi: 10.1128/JCM.37.9.2817-2828.1999 – ident: e_1_3_2_47_2 doi: 10.1128/JCM.37.12.3835-3843.1999 – ident: e_1_3_2_27_2 doi: 10.1056/NEJMra020831 – ident: e_1_3_2_2_2 doi: 10.1093/emboj/cdg235 – ident: e_1_3_2_10_2 doi: 10.1016/S1473-3099(03)00801-6 – ident: e_1_3_2_28_2 doi: 10.1136/gut.47.6.870 – ident: e_1_3_2_30_2 doi: 10.1099/00221287-145-10-2635 – ident: e_1_3_2_18_2 doi: 10.1128/jcm.33.6.1501-1509.1995 – ident: e_1_3_2_19_2 doi: 10.1128/jcm.34.4.767-777.1996 – ident: e_1_3_2_26_2 doi: 10.1128/JCM.36.6.1518-1529.1998 – ident: e_1_3_2_48_2 doi: 10.1099/mic.0.26495-0 – ident: e_1_3_2_22_2 doi: 10.1016/S0732-8893(98)00100-X – ident: e_1_3_2_43_2 doi: 10.1128/IAI.70.9.5274-5278.2002 – ident: e_1_3_2_34_2 doi: 10.1099/00221287-148-4-1061 – start-page: 15 year: 2002 ident: e_1_3_2_8_2 publication-title: Candida and candidiasis – ident: e_1_3_2_15_2 doi: 10.1093/bioinformatics/17.12.1230 – ident: e_1_3_2_11_2 doi: 10.1128/EC.3.3.705-714.2004 – ident: e_1_3_2_29_2 doi: 10.1128/jcm.35.9.2348-2358.1997 – ident: e_1_3_2_23_2 doi: 10.1053/j.gastro.2003.11.015 – ident: e_1_3_2_32_2 doi: 10.1136/gut.42.6.788 – ident: e_1_3_2_44_2 doi: 10.1073/pnas.061628798 – ident: e_1_3_2_9_2 doi: 10.1186/1471-2334-2-1 – ident: e_1_3_2_45_2 doi: 10.1097/01.MIB.0000158536.31557.90 – ident: e_1_3_2_3_2 doi: 10.1038/nrg948 – ident: e_1_3_2_4_2 doi: 10.1128/JCM.40.3.826-836.2002 – ident: e_1_3_2_12_2 doi: 10.1128/EC.4.1.156-165.2005 – ident: e_1_3_2_33_2 doi: 10.1128/jcm.33.9.2366-2371.1995 – ident: e_1_3_2_41_2 doi: 10.1016/j.fgb.2003.12.008 – ident: e_1_3_2_16_2 doi: 10.1016/S1567-1348(02)00058-8 – ident: e_1_3_2_14_2 doi: 10.1126/science.289.5477.307 – ident: e_1_3_2_35_2 doi: 10.1128/AAC.45.7.2129-2133.2001 – ident: e_1_3_2_37_2 doi: 10.1128/jcm.33.5.1223-1230.1995 – ident: e_1_3_2_38_2 doi: 10.1111/j.1572-0241.1998.00415.x – ident: e_1_3_2_31_2 doi: 10.1128/JCM.40.8.2729-2740.2002 – ident: e_1_3_2_46_2 doi: 10.1136/gut.47.4.487 – ident: e_1_3_2_17_2 doi: 10.1016/S0732-8893(02)00364-4 – ident: e_1_3_2_24_2 – ident: e_1_3_2_25_2 doi: 10.1086/375746 – ident: e_1_3_2_40_2 doi: 10.1128/JCM.43.11.5601-5613.2005 – ident: e_1_3_2_36_2 doi: 10.1097/00054725-200108000-00003 – ident: e_1_3_2_20_2 doi: 10.1126/science.289.5477.310 – ident: e_1_3_2_13_2 doi: 10.1136/gut.2005.066860 – ident: e_1_3_2_7_2 doi: 10.1128/JCM.41.11.5265-5266.2003 – ident: e_1_3_2_39_2 doi: 10.1016/S0928-8244(03)00242-6 – ident: e_1_3_2_5_2 doi: 10.1016/j.meegid.2004.06.002 – ident: e_1_3_2_42_2 doi: 10.1016/j.jhin.2004.01.017 – reference: 10342103 - Diagn Microbiol Infect Dis. 1999 May;34(1):19-25 – reference: 15189991 - Eukaryot Cell. 2004 Jun;3(3):705-14 – reference: 15863472 - Gut. 2005 Sep;54(9):1237-43 – reference: 12183581 - Infect Immun. 2002 Sep;70(9):5274-8 – reference: 15803025 - Inflamm Bowel Dis. 2005 Apr;11(4):360-5 – reference: 14523127 - Microbiology. 2003 Oct;149(Pt 10):2947-60 – reference: 10565893 - J Clin Microbiol. 1999 Dec;37(12):3835-43 – reference: 15142710 - J Hosp Infect. 2004 May;57(1):8-13 – reference: 7494029 - J Clin Microbiol. 1995 Sep;33(9):2366-71 – reference: 14605179 - J Clin Microbiol. 2003 Nov;41(11):5265-6 – reference: 10986208 - Gut. 2000 Oct;47(4):487-96 – reference: 7615732 - J Clin Microbiol. 1995 May;33(5):1223-30 – reference: 14592598 - Lancet Infect Dis. 2003 Nov;3(11):685-702 – reference: 11408236 - Antimicrob Agents Chemother. 2001 Jul;45(7):2129-33 – reference: 14556989 - FEMS Immunol Med Microbiol. 2003 Oct 24;39(1):1-7 – reference: 12459722 - Nat Rev Genet. 2002 Dec;3(12):918-30 – reference: 15050544 - Fungal Genet Biol. 2004 May;41(5):553-62 – reference: 11248064 - Proc Natl Acad Sci U S A. 2001 Mar 13;98(6):3249-53 – reference: 12167685 - N Engl J Med. 2002 Aug 8;347(6):417-29 – reference: 11923347 - J Clin Microbiol. 2002 Apr;40(4):1290-7 – reference: 7650175 - J Clin Microbiol. 1995 Jun;33(6):1501-9 – reference: 16272493 - J Clin Microbiol. 2005 Nov;43(11):5601-13 – reference: 12743044 - EMBO J. 2003 May 15;22(10):2505-15 – reference: 9276415 - J Clin Microbiol. 1997 Sep;35(9):2348-58 – reference: 10894781 - Science. 2000 Jul 14;289(5477):310-3 – reference: 15643071 - Eukaryot Cell. 2005 Jan;4(1):156-65 – reference: 12052625 - Diagn Microbiol Infect Dis. 2002 May;43(1):19-28 – reference: 11515844 - Inflamm Bowel Dis. 2001 Aug;7(3):192-201 – reference: 9691915 - Gut. 1998 Jun;42(6):788-91 – reference: 11751234 - Bioinformatics. 2001 Dec;17(12):1230-1 – reference: 14762777 - Gastroenterology. 2004 Feb;126(2):414-24 – reference: 12149321 - J Clin Microbiol. 2002 Aug;40(8):2729-40 – reference: 11880401 - J Clin Microbiol. 2002 Mar;40(3):826-36 – reference: 15450203 - Infect Genet Evol. 2004 Sep;4(3):243-52 – reference: 9620370 - J Clin Microbiol. 1998 Jun;36(6):1518-29 – reference: 11186432 - Gut. 2000 Dec;47(6):870-1 – reference: 12825180 - J Infect Dis. 2003 Jul 1;188(1):118-27 – reference: 8815082 - J Clin Microbiol. 1996 Apr;34(4):767-77 – reference: 10449459 - J Clin Microbiol. 1999 Sep;37(9):2817-28 – reference: 12797998 - Infect Genet Evol. 2002 Oct;2(1):19-37 – reference: 10537185 - Microbiology. 1999 Oct;145 ( Pt 10):2635-46 – reference: 10894780 - Science. 2000 Jul 14;289(5477):307-10 – reference: 11835694 - BMC Infect Dis. 2002;2:1 – reference: 11932451 - Microbiology. 2002 Apr;148(Pt 4):1061-72 – reference: 9707056 - Am J Gastroenterol. 1998 Aug;93(8):1306-10 |
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Snippet | Candida albicans is a human commensal that is also responsible for superficial and systemic infections. Little is known about the carriage of C. albicans in... Article Usage Stats Services JCM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley... Candida albicans is a human commensal that is also responsible for superficial and systemic infections. Little is known about the carriage of C. albicans in... |
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SubjectTerms | Bacterial Typing Techniques Biological and medical sciences Candida albicans Candida albicans - classification Candida albicans - genetics Candida albicans - isolation & purification Candidiasis - complications Candidiasis - microbiology Candidiasis - transmission Carrier State - microbiology Carrier State - transmission Case-Control Studies Crohn Disease - complications Crohn Disease - microbiology DNA, Fungal - genetics DNA, Fungal - isolation & purification Evolution, Molecular Family Feces - microbiology Fundamental and applied biological sciences. Psychology Gastrointestinal Tract - microbiology Humans Infectious diseases Life Sciences Medical sciences Microbiology Microbiology and Parasitology Miscellaneous Mouth - microbiology Mycology Phylogeny |
Title | Multilocus Sequence Typing Reveals Intrafamilial Transmission and Microevolutions of Candida albicans Isolates from the Human Digestive Tract |
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