TY - JOUR
T1 - Multilocus sequence typing detects new Piscirickettsia salmonis hybrid genogroup in Chilean fish farms
T2 - Evidence for genetic diversity and population structure
AU - Isla, Adolfo
AU - Saldarriaga-Córdoba, Mónica
AU - Fuentes, Derie E.
AU - Albornoz, Romina
AU - Haussmann, Denise
AU - Mancilla-Schulz, Jorge
AU - Martínez, Alexis
AU - Figueroa, Jaime
AU - Avendaño-Herrera, Ruben
AU - Yáñez, Alejandro
N1 - Funding Information:
This work was supported by the National Commission for Scientific and Technological Research (Comisión Nacional de Investigación Científica y Tecnológica [CONICYT], Chile) through the Interdisciplinary Center for Aquaculture Research (INCAR) Fund for Research Centers in Prioritary Areas (Fondo de Financiamiento de Centros de Investigación en CZreasPrioritarias [FON?AP], Grant No. 15110027). R.A.‐H. acknowledges partial financial support from CONICYT (Grant No. FON?ECYT 1190283). A.Y., RA‐H and J.F. ac‐ knowledge partial financial support from Proyecto FIE‐2015‐V014 Grant Nº 122929.
PY - 2019/5/1
Y1 - 2019/5/1
N2 -
Piscirickettsia salmonisis the causative bacterial pathogen of piscirickettsiosis, a salmonid disease that causes notable mortalities in the worldwide aquaculture industry. Published research describes the phenotypic traits, virulence factors, pathogenicity and antibiotic-resistance potential for various P. salmonisstrains. However, evolutionary and genetic information is scarce for P. salmonis. The present study used multilocus sequence typing (MLST) to gain insight into the population structure and evolution of P. salmonis. Forty-two Chilean P. salmonisisolates, as well as the type strain LF-89
T
, were recovered from diseased Salmo salar, Oncorhynchus kisutchand Oncorhynchus mykissfrom two Chilean Regions. MLST assessed the loci sequences of dnaK, efp, fumC, glyA, murG, rpoD and trpB. Bioinformatics analyses established the genetic diversity among P. salmonis isolates (H = 0.5810). A total of 23 sequence types (ST) were identified, 53.48% of which were represented by ST1, ST5 and ST2. Population structure analysis through polymorphism patterns showed few polymorphic sites (218 nucleotides from 4,010 bp), while dN/dS ratio analysis indicated purifying selection for dnaK, epf, fumC, murG, and rpoD but neutral selection for the trpB loci. The standardized index of association indicated strong linkage disequilibrium, suggesting clonal population structure. However, recombination events were detected in a group of seven isolates. Findings included genogroups homologous to the LF-89
T
and EM-90 strains, as well as a seven-isolate hybrid genogroup recovered from both assessed regions (three O. mykiss and four S. salar isolates). The presented MLST scheme has comparative potential, with promising applications in studying distinct P. salmonis isolates (e.g., from different hosts, farms, geographical areas) and in understanding the epidemiology of this pathogen.
AB -
Piscirickettsia salmonisis the causative bacterial pathogen of piscirickettsiosis, a salmonid disease that causes notable mortalities in the worldwide aquaculture industry. Published research describes the phenotypic traits, virulence factors, pathogenicity and antibiotic-resistance potential for various P. salmonisstrains. However, evolutionary and genetic information is scarce for P. salmonis. The present study used multilocus sequence typing (MLST) to gain insight into the population structure and evolution of P. salmonis. Forty-two Chilean P. salmonisisolates, as well as the type strain LF-89
T
, were recovered from diseased Salmo salar, Oncorhynchus kisutchand Oncorhynchus mykissfrom two Chilean Regions. MLST assessed the loci sequences of dnaK, efp, fumC, glyA, murG, rpoD and trpB. Bioinformatics analyses established the genetic diversity among P. salmonis isolates (H = 0.5810). A total of 23 sequence types (ST) were identified, 53.48% of which were represented by ST1, ST5 and ST2. Population structure analysis through polymorphism patterns showed few polymorphic sites (218 nucleotides from 4,010 bp), while dN/dS ratio analysis indicated purifying selection for dnaK, epf, fumC, murG, and rpoD but neutral selection for the trpB loci. The standardized index of association indicated strong linkage disequilibrium, suggesting clonal population structure. However, recombination events were detected in a group of seven isolates. Findings included genogroups homologous to the LF-89
T
and EM-90 strains, as well as a seven-isolate hybrid genogroup recovered from both assessed regions (three O. mykiss and four S. salar isolates). The presented MLST scheme has comparative potential, with promising applications in studying distinct P. salmonis isolates (e.g., from different hosts, farms, geographical areas) and in understanding the epidemiology of this pathogen.
KW - genetic evolution
KW - hybrid genogroup
KW - MLST scheme
KW - Piscirickettsia salmonis
KW - salmonid pathogen
UR - http://www.scopus.com/inward/record.url?scp=85062781108&partnerID=8YFLogxK
U2 - 10.1111/jfd.12976
DO - 10.1111/jfd.12976
M3 - Article
C2 - 30851000
AN - SCOPUS:85062781108
SN - 0140-7775
VL - 42
SP - 721
EP - 737
JO - Journal of Fish Diseases
JF - Journal of Fish Diseases
IS - 5
ER -