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 inJournal of Clinical Microbiology Vol. 44; no. 5; pp. 1810 - 1820
Main Authors Bougnoux, M.-E, Diogo, D, François, N, Sendid, B, Veirmeire, S, Colombel, J.F, Bouchier, C, Van Kruiningen, H, d'Enfert, C, Poulain, D
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LanguageEnglish
Published 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.
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.
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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
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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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Issue 5
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
Language English
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Corresponding author. Mailing address: Unité Postulante Biologie et Pathogénicité Fongiques, Institut Pasteur, 25 rue du Docteur Roux, 75724 Paris Cedex 15, France. Phone: 33 1 40 61 32 57. Fax: 33 1 45 68 89 38. E-mail: bougnoux@pasteur.fr.
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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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StartPage 1810
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
URI http://jcm.asm.org/content/44/5/1810.abstract
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Volume 44
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