2021
DOI: 10.1186/s12917-021-02820-1
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Establishment and evaluation of an indirect ELISA for detection of antibodies to goat Klebsiella pneumonia

Abstract: Background Klebsiella pneumonia, a Gram-negative bacterium belonging to the genus Enterobacter, causes many human and livestock diseases. Notably, infected goats may develop pneumonia, septicemia, which can lead to occasional death, resulting in great economic losses in goat-farming industry. However, there are little systematic methods for detection of goat Klebsiella pneumoniae in livestock production. Results In this study, we developed a Klebsi… Show more

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Cited by 13 publications
(8 citation statements)
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“…The ratio (OD value of the tested sample/control sample, P/N) ≥ 2.1 was regarded as the positive sample. [ 25 ] Glycan microarrays are an efficient means to investigate the antigenicity of oligosaccharides with different lengths and frameshifts. [ 5,26 ] The synthetic oligosaccharides and O2 LPS were printed on glycan microarrays for antigenicity evaluation with O2 LPS immunized positive rabbit sera (anti‐O2 LPS antisera) (Figure 2A).…”
Section: Resultsmentioning
confidence: 99%
“…The ratio (OD value of the tested sample/control sample, P/N) ≥ 2.1 was regarded as the positive sample. [ 25 ] Glycan microarrays are an efficient means to investigate the antigenicity of oligosaccharides with different lengths and frameshifts. [ 5,26 ] The synthetic oligosaccharides and O2 LPS were printed on glycan microarrays for antigenicity evaluation with O2 LPS immunized positive rabbit sera (anti‐O2 LPS antisera) (Figure 2A).…”
Section: Resultsmentioning
confidence: 99%
“…Indirect ELISA for the detection of antibody titer was established [ 57 ]. A volume of 100 µL sodium carbonate–bicarbonate buffer (1.59 g/L Na 2 CO 3 , 2.93 g/L NaHCO 3 , 0.05 M, pH 9.6) supplied with 2 μg of recombinant protein was used to coat each well of 96-well polystyrene microtiter ELISA plates overnight at 4 °C.…”
Section: Methodsmentioning
confidence: 99%
“…The wells were incubated with a 1:8,000 dilution of affinity-purified, peroxidase-labeled goat anti-chicken IgG (H+L) (KPL Inc., MD, USA) for 1 h. OD 450 was measured with a microplate reader VICTORTM X4 (PerkinElmer Inc., Waltham, MA, USA) after the reaction was stopped with 4.5 N H 2 SO 4 . The OD 450 average value of negative serum samples plus the standard deviation (SD) of three times was used as the cut-off value ( 27 ).…”
Section: Methodsmentioning
confidence: 99%