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Inapparent Streptococcus agalactiae infection in adult/commercial tilapia
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AbstractWe report on inapparent infections in adult/commercial tilapia in major tilapia fish farms in Guangdong. A total of 146 suspected isolates were confirmed to be S. agalactiae using an API 20 Strep system and specific PCR amplification. All isolates were identified as serotype Ia using multiplex serotyping PCR. An MLST assay showed single alleles of adhP (10), atr (2), glcK (2), glnA (1), pheS (1), sdhA (3) and tkt (2) and this profile was designated ‘unique ST 7’. The analysis of virulence genes resulted in 10 clusters, of which dltr-bca-sodA-spb1-cfb-bac (62, 42.47%) was the predominant virulence gene profile. The PFGE analysis of S. agalactiae yielded 6 distinct PFGE types (A, B, C, D, F and G), of which Pattern C (103) was the predominant type, accounting for approximately 70.55% (103/146) of the total S. agalactiae strains. Therefore, unlike what has been found in juvenile tilapia, in which PFGE pattern D/F is the major prevalent pattern, we found that pattern C was the major prevalent pattern in inapparent infected adult/commercial tilapia in Guangdong, China. In conclusion, we close a gap in the current understanding of S. agalactiae epidemiology and propose that researchers should be alert for inapparent S. agalactiae infections in adult/commercial tilapia to prevent a potential threat to food safety.
Springer Science and Business Media LLC
Title: Inapparent Streptococcus agalactiae infection in adult/commercial tilapia
Description:
AbstractWe report on inapparent infections in adult/commercial tilapia in major tilapia fish farms in Guangdong.
A total of 146 suspected isolates were confirmed to be S.
agalactiae using an API 20 Strep system and specific PCR amplification.
All isolates were identified as serotype Ia using multiplex serotyping PCR.
An MLST assay showed single alleles of adhP (10), atr (2), glcK (2), glnA (1), pheS (1), sdhA (3) and tkt (2) and this profile was designated ‘unique ST 7’.
The analysis of virulence genes resulted in 10 clusters, of which dltr-bca-sodA-spb1-cfb-bac (62, 42.
47%) was the predominant virulence gene profile.
The PFGE analysis of S.
agalactiae yielded 6 distinct PFGE types (A, B, C, D, F and G), of which Pattern C (103) was the predominant type, accounting for approximately 70.
55% (103/146) of the total S.
agalactiae strains.
Therefore, unlike what has been found in juvenile tilapia, in which PFGE pattern D/F is the major prevalent pattern, we found that pattern C was the major prevalent pattern in inapparent infected adult/commercial tilapia in Guangdong, China.
In conclusion, we close a gap in the current understanding of S.
agalactiae epidemiology and propose that researchers should be alert for inapparent S.
agalactiae infections in adult/commercial tilapia to prevent a potential threat to food safety.
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