2013
DOI: 10.1016/j.jcpa.2012.10.003
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Establishment of a Model of Streptococcus iniae Meningoencephalitis in Nile Tilapia (Oreochromis niloticus)

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Cited by 40 publications
(23 citation statements)
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“…Finally, eye tissue presented severe granulomatous endophthalmitis (Figure e), choroiditis and corneal oedema, as well as severe haemorrhagic and necrotic granulomatous myositis (Figure f). These findings are consistent with the development process of bacterial septicaemia, with similar histological descriptions existing for Streptococcus bacteria in tilapia (Baums et al., ; Chen et al., ; Zamri‐Saad et al., ).…”
Section: Resultssupporting
confidence: 90%
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“…Finally, eye tissue presented severe granulomatous endophthalmitis (Figure e), choroiditis and corneal oedema, as well as severe haemorrhagic and necrotic granulomatous myositis (Figure f). These findings are consistent with the development process of bacterial septicaemia, with similar histological descriptions existing for Streptococcus bacteria in tilapia (Baums et al., ; Chen et al., ; Zamri‐Saad et al., ).…”
Section: Resultssupporting
confidence: 90%
“…Furthermore, the hearts of five San Luis Potosí fish were surrounded by white‐greyish, purulent‐mass membranes (Figure f). The pathological picture for San Luis Potosí and Querétaro fish, for both internal and external wounds, clearly corresponded to the description of a typical streptococcosis process in tilapia (Baums et al., ; Chen et al., ; Ramesh et al., ; Zamri‐Saad et al., ), which was apparently more chronic at the San Luis Potosí farm.…”
Section: Resultssupporting
confidence: 77%
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“…), showing amplification 822 bp for scpI , 994 bp for simA , 713 bp for pgm , 534 bp for cpsD , 381 bp for pdi and 190 bp for sagA , which were identical to that produced in the strain S. iniae K288 (Baums et al . ).…”
Section: Resultsmentioning
confidence: 97%
“…In the study, two strains were investigated for six main virulence genes ( simA , scpI , pdi , pgm , cpsD and sagA , Table ) of S. iniae by a multiplex PCR (Baums, Hermeyer, Leimbach, Adamek, Czerny, Hörstgen Schwark, Valentin Weigand, Baumgärtner & Steinhagen ). The amplification was performed using a reaction mixture which contained PCR buffer 10×, 1.5 mM MgCl 2 , 0.2 mM each of the four deoxynucleotide triphosphates, 2.0 U TaqDNA polymerase (Takara, Dalian, China), 116 nM of each primer for simA , 58 nM of each primer for scpI, pgm and cpsD , 93 nM of each primer for pdi , 116 nM of each primer for sagA and 5 μg of template DNA in a final volume of 50 μL in a thermal cycler (C1000; Bio‐Rad, Hercules, CA, USA).…”
Section: Methodsmentioning
confidence: 99%