TY - JOUR
T1 - Chaperone-usher pili loci of colonization factor-negative human enterotoxigenic Escherichia coli
AU - Del Canto, Felipe
AU - O'Ryan, Miguel
AU - Pardo, Mirka
AU - Torres, Alexia
AU - Gutiérrez, Daniela
AU - Cádiz, Leandro
AU - Valdés, Raul
AU - Mansilla, Aquiles
AU - Martínez, Rodrigo
AU - Hernández, Daniela
AU - Caro, Benjamin
AU - Levine, Myron M.
AU - Rasko, David A.
AU - Hill, Christopher M.
AU - Pop, Mihai
AU - Stine, O. Colin
AU - Vidal, Roberto
N1 - Publisher Copyright:
© 2017 Del Canto, O'Ryan, Pardo, Torres, Gutiérrez, Cádiz, Valdés, Mansilla, Martínez, Hernández, Caro, Levine, Rasko, Hill, Pop, Stine and Vidal.
PY - 2017/1/6
Y1 - 2017/1/6
N2 - Enterotoxigenic Escherichia coli (ETEC) is one of the most common causes of diarrhea worldwide. Among the 25 different ETEC adhesins, 22 are known as "colonization factors" (CFs), of which 17 are assembled by the chaperone-usher (CU) mechanism. Currently, there is no preventive therapy against ETEC, and CFs have been proposed as components for vaccine development. However, studies of diarrhea-causing ETEC strains worldwide indicate that between 15 and 50% of these are negative for known CFs, hindering the selection of the most widespread structures and suggesting that unknown adhesins remain to be identified. Here, we report the result of a comprehensive analysis of 35 draft genomes of ETEC strains which do not carry known adhesin genes; our goal was to find new CU pili loci. The phylogenetic profiles and serogroups of these strains were highly diverse, a majority of which produced only the heat-labile toxin. We identified 10 pili loci belonging to CU families β (1 locus), γ2 (7 loci), γ (1 locus), and p (1 locus), all of which contained the required number of open reading frames (ORFs) to encode functional structures. Three loci were variants of previously-known clusters, three had been only-partially described, and four are novel loci. Intra-loci genetic variability identified would allow the synthesis of up to 14 different structures. Clusters of putative γ2-CU pili were most common (23 strains), followed by putative β-CU pili (12 strains), which have not yet been fully characterized. Overall, our findings significantly increase the number of ETEC adhesion genes associated with human infections.
AB - Enterotoxigenic Escherichia coli (ETEC) is one of the most common causes of diarrhea worldwide. Among the 25 different ETEC adhesins, 22 are known as "colonization factors" (CFs), of which 17 are assembled by the chaperone-usher (CU) mechanism. Currently, there is no preventive therapy against ETEC, and CFs have been proposed as components for vaccine development. However, studies of diarrhea-causing ETEC strains worldwide indicate that between 15 and 50% of these are negative for known CFs, hindering the selection of the most widespread structures and suggesting that unknown adhesins remain to be identified. Here, we report the result of a comprehensive analysis of 35 draft genomes of ETEC strains which do not carry known adhesin genes; our goal was to find new CU pili loci. The phylogenetic profiles and serogroups of these strains were highly diverse, a majority of which produced only the heat-labile toxin. We identified 10 pili loci belonging to CU families β (1 locus), γ2 (7 loci), γ (1 locus), and p (1 locus), all of which contained the required number of open reading frames (ORFs) to encode functional structures. Three loci were variants of previously-known clusters, three had been only-partially described, and four are novel loci. Intra-loci genetic variability identified would allow the synthesis of up to 14 different structures. Clusters of putative γ2-CU pili were most common (23 strains), followed by putative β-CU pili (12 strains), which have not yet been fully characterized. Overall, our findings significantly increase the number of ETEC adhesion genes associated with human infections.
KW - Adhesin
KW - Adhesin negative-ETEC
KW - Chaperone-usher pili
KW - Colonization factors
KW - ETEC
KW - Genome analysis
UR - http://www.scopus.com/inward/record.url?scp=85012141223&partnerID=8YFLogxK
U2 - 10.3389/fcimb.2016.00200
DO - 10.3389/fcimb.2016.00200
M3 - Article
C2 - 28111618
AN - SCOPUS:85012141223
SN - 2235-2988
VL - 6
JO - Frontiers in Cellular and Infection Microbiology
JF - Frontiers in Cellular and Infection Microbiology
IS - JAN
M1 - 200
ER -