TY - JOUR
T1 - Improved understanding of biofilm development by Piscirickettsia salmonis reveals potential risks for the persistence and dissemination of piscirickettsiosis
AU - Levipan, Héctor A.
AU - Irgang, Rute
AU - Yáñez, Alejandro
AU - Avendaño-Herrera, Ruben
N1 - Funding Information:
This research was supported by the "Program for Health Management Aquaculture" which is publically and privately financed by the Ministry of Economy, Development, and Tourism and the Association of the Chilean Salmon Industry AG (Salmon Chile), implemented by the National Fisheries and Aquaculture Service (SER-NAPESCA) FIE‐2015‐V014 Grant Nº 122929. Further financial support for this study was received through FONDECYT Grant 1190283 (CONICYT, Chile) and the FONDAP-INCAR Center Grant Nº 15110027 (CONI-CYT, Chile). The Cytation-5 device was funded by a CONICYT-FONDEQUIP EQM160131 instrumentation grant (Universidad de Playa Ancha). H. Levipan thanks CONICYT-PAI/Convocatoria Nacional Subvención a la Instalación en la Academia, Convocatoria 2018-Folio 77180039. The authors thank Diana Tapia-Cammas for technical assistance with skin-mucus samples.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - Piscirickettsia salmonis is the causative agent of piscirickettsiosis, a disease with high socio-economic impacts for Chilean salmonid aquaculture. The identification of major environmental reservoirs for P. salmonis has long been ignored. Most microbial life occurs in biofilms, with possible implications in disease outbreaks as pathogen seed banks. Herein, we report on an in vitro analysis of biofilm formation by P. salmonis Psal-103 (LF-89-like genotype) and Psal-104 (EM-90-like genotype), the aim of which was to gain new insights into the ecological role of biofilms using multiple approaches. The cytotoxic response of the salmon head kidney cell line to P. salmonis showed interisolate differences, depending on the source of the bacterial inoculum (biofilm or planktonic). Biofilm formation showed a variable-length lag-phase, which was associated with wider fluctuations in biofilm viability. Interisolate differences in the lag phase emerged regardless of the nutritional content of the medium, but both isolates formed mature biofilms from 288 h onwards. Psal-103 biofilms were sensitive to Atlantic salmon skin mucus during early formation, whereas Psal-104 biofilms were more tolerant. The ability of P. salmonis to form viable and mucus-tolerant biofilms on plastic surfaces in seawater represents a potentially important environmental risk for the persistence and dissemination of piscirickettsiosis.
AB - Piscirickettsia salmonis is the causative agent of piscirickettsiosis, a disease with high socio-economic impacts for Chilean salmonid aquaculture. The identification of major environmental reservoirs for P. salmonis has long been ignored. Most microbial life occurs in biofilms, with possible implications in disease outbreaks as pathogen seed banks. Herein, we report on an in vitro analysis of biofilm formation by P. salmonis Psal-103 (LF-89-like genotype) and Psal-104 (EM-90-like genotype), the aim of which was to gain new insights into the ecological role of biofilms using multiple approaches. The cytotoxic response of the salmon head kidney cell line to P. salmonis showed interisolate differences, depending on the source of the bacterial inoculum (biofilm or planktonic). Biofilm formation showed a variable-length lag-phase, which was associated with wider fluctuations in biofilm viability. Interisolate differences in the lag phase emerged regardless of the nutritional content of the medium, but both isolates formed mature biofilms from 288 h onwards. Psal-103 biofilms were sensitive to Atlantic salmon skin mucus during early formation, whereas Psal-104 biofilms were more tolerant. The ability of P. salmonis to form viable and mucus-tolerant biofilms on plastic surfaces in seawater represents a potentially important environmental risk for the persistence and dissemination of piscirickettsiosis.
UR - http://www.scopus.com/inward/record.url?scp=85088382629&partnerID=8YFLogxK
U2 - 10.1038/s41598-020-68990-4
DO - 10.1038/s41598-020-68990-4
M3 - Article
C2 - 32699383
AN - SCOPUS:85088382629
SN - 2045-2322
VL - 10
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 12224
ER -