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Comparative evaluation of RBPT, I-ELISA, and CFT for the diagnosis of brucellosis and PCR detection of Brucella species from Ethiopian sheep, goats, and cattle sera
by
Getachew, Belayneh
, Mekuriaw, Aregitu
, Birhanu, Kenaw
, Gelaye, Esayas
, Weldemedhin, Wubet
, Abayneh, Takele
, Tesgera, Takele
, Deresse, Getaw
, Legesse, Abinet
in
Animal diseases
/ Animal health
/ Animals
/ Antibodies
/ Antigens
/ Assaying
/ Bacteria
/ Biological Microscopy
/ Biomedical and Life Sciences
/ Blood
/ Brucella
/ Brucella species
/ Brucellosis
/ Cattle
/ CFT
/ Comparative analysis
/ Complement fixation
/ Cross-sectional studies
/ Diagnosis
/ Diseases
/ Enzyme-linked immunosorbent assay
/ Enzymes
/ Epidemiology
/ Evaluation
/ Goats
/ I-ELISA
/ Infections
/ Life Sciences
/ Medical research
/ Microbiology
/ Mycology
/ Parasitology
/ PCR
/ Polymerase chain reaction
/ Public health
/ RBPT
/ Risk factors
/ Sensitivity analysis
/ Serology
/ Sheep
/ Tabulation
/ Vaccination
/ Virology
2023
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Comparative evaluation of RBPT, I-ELISA, and CFT for the diagnosis of brucellosis and PCR detection of Brucella species from Ethiopian sheep, goats, and cattle sera
by
Getachew, Belayneh
, Mekuriaw, Aregitu
, Birhanu, Kenaw
, Gelaye, Esayas
, Weldemedhin, Wubet
, Abayneh, Takele
, Tesgera, Takele
, Deresse, Getaw
, Legesse, Abinet
in
Animal diseases
/ Animal health
/ Animals
/ Antibodies
/ Antigens
/ Assaying
/ Bacteria
/ Biological Microscopy
/ Biomedical and Life Sciences
/ Blood
/ Brucella
/ Brucella species
/ Brucellosis
/ Cattle
/ CFT
/ Comparative analysis
/ Complement fixation
/ Cross-sectional studies
/ Diagnosis
/ Diseases
/ Enzyme-linked immunosorbent assay
/ Enzymes
/ Epidemiology
/ Evaluation
/ Goats
/ I-ELISA
/ Infections
/ Life Sciences
/ Medical research
/ Microbiology
/ Mycology
/ Parasitology
/ PCR
/ Polymerase chain reaction
/ Public health
/ RBPT
/ Risk factors
/ Sensitivity analysis
/ Serology
/ Sheep
/ Tabulation
/ Vaccination
/ Virology
2023
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Comparative evaluation of RBPT, I-ELISA, and CFT for the diagnosis of brucellosis and PCR detection of Brucella species from Ethiopian sheep, goats, and cattle sera
by
Getachew, Belayneh
, Mekuriaw, Aregitu
, Birhanu, Kenaw
, Gelaye, Esayas
, Weldemedhin, Wubet
, Abayneh, Takele
, Tesgera, Takele
, Deresse, Getaw
, Legesse, Abinet
in
Animal diseases
/ Animal health
/ Animals
/ Antibodies
/ Antigens
/ Assaying
/ Bacteria
/ Biological Microscopy
/ Biomedical and Life Sciences
/ Blood
/ Brucella
/ Brucella species
/ Brucellosis
/ Cattle
/ CFT
/ Comparative analysis
/ Complement fixation
/ Cross-sectional studies
/ Diagnosis
/ Diseases
/ Enzyme-linked immunosorbent assay
/ Enzymes
/ Epidemiology
/ Evaluation
/ Goats
/ I-ELISA
/ Infections
/ Life Sciences
/ Medical research
/ Microbiology
/ Mycology
/ Parasitology
/ PCR
/ Polymerase chain reaction
/ Public health
/ RBPT
/ Risk factors
/ Sensitivity analysis
/ Serology
/ Sheep
/ Tabulation
/ Vaccination
/ Virology
2023
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Comparative evaluation of RBPT, I-ELISA, and CFT for the diagnosis of brucellosis and PCR detection of Brucella species from Ethiopian sheep, goats, and cattle sera
Journal Article
Comparative evaluation of RBPT, I-ELISA, and CFT for the diagnosis of brucellosis and PCR detection of Brucella species from Ethiopian sheep, goats, and cattle sera
2023
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Overview
Background
Brucellosis is an economically devastating animal disease and has public health concern. Serological methods such as Rose Bengal Plate Test (RBPT), Complement Fixation Test (CFT), and Indirect-Enzyme-Linked Immunosorbent Assay (I-ELISA) have been used to detect brucellosis. However, there is limited comparative evaluation studies and lack of molecular confirmation of the causative agents in the study areas. The study was aimed to compare RBPT, I-ELISA, CFT, and confirmation using Polymerase Chain Reaction (PCR). A total of 2317 sera samples were collected from brucellosis-affected areas of Ethiopia with no vaccination history. All sera were subjected to comparative serological assays. Post-cross tabulation, sensitivity, and specificity were determined using Receiver Operating Characteristics (ROC) curve analysis software. PCR was performed on 54 seropositive samples using genus- and species-specific primers.
Results
Among the 2317 sera tested for comparative serological assays, 189 (8.16%) were positive for RBPT, 191 (8.24%) for I-ELISA, and 48 (2.07%) for CFT. Sensitivity to RBPT was 100% (95%) in shoats and 74% (95%) in cattle. Specificity on RBPT was 98.69% (95%), 99.28% (95%), 100% (95%) in sheep, goats, and cattle, respectively. CFT sensitivity was 4 (95%) in sheep, 9.65 (95%) goats, and 72 (95%) cattle. Specificity on CFT was 100% (95%) for sheep, goats, and cattle. A 223bp Brucella genus-specific and 156bp
B. abortus
species-specific detected. However,
B. melitensis
not detected.
Conclusion
In this study, I-ELISA was the most sensitive and specific test. RBPT detected all Brucellosis-infected sheep and goats; nevertheless, it showed false positive in sheep and goats and false negative in cattle. The presence of
B. abortus
in small and large ruminants was confirmed by PCR. This is the first report of
B. abortus
detection in small ruminant in Ethiopia.
B.abortus
detected in non-preferred hosts. The findings suggest further study on molecular epidemiology of Brucella species.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
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