scholarly journals Diagnosis of animal rabies: comparison of direct fluorescent antibody test (DFAT), reverse transcriptase -PCR and real-time PCR

2016 ◽  
Vol 4 (Spl-3-ADPCIAD) ◽  
pp. S69-S74 ◽  
Author(s):  
Manjunathareddy GB ◽  
◽  
Sumana K ◽  
Yogisharadhya R ◽  
Susan Cherian ◽  
...  
2020 ◽  
Vol 7 (2) ◽  
pp. 66 ◽  
Author(s):  
Jarlath E. Nally ◽  
Ahmed A. A. Ahmed ◽  
Ellie J. Putz ◽  
Debra E. Palmquist ◽  
Marga G. A. Goris

Cattle are susceptible to infection with multiple serovars of pathogenic leptospires, resulting in abortion, stillbirth, premature birth, reproductive failure and milk drop syndrome. Cattle also act as a reservoir host for L. borgpetersenii serovar Hardjo which is excreted from renal tubules via urine into the environment where it persists in suitable moist conditions. Our previous work demonstrated that 7% of urine samples from beef cattle were positive for L. borgpetersenii serovar Hardjo by culture and/or the fluorescent antibody test (FAT). In this study, a real-time PCR (rtPCR) assay was applied to determine the relative performance of rtPCR based detection of L. borgpetersenii serovar Hardjo compared to previously reported culture and FAT techniques. Of 42 bovine urine samples positive for leptospires by culture and/or FAT, 60% (25/42) were positive by rtPCR. Of 22 culture-positive samples, 91% (20/22) were rtPCR-positive. Of 32 FAT-positive samples, 50% (16/32) were rtPCR-positive. For 10 samples that were culture-positive but FAT-negative, 90% (9/10) were rtPCR-positive. For 20 samples that were FAT-positive but culture-negative, 25% (5/20) were rtPCR-positive. Collectively, these results indicate that no single assay is optimal, and the use of more than one assay to detect leptospires in urine from naturally infected cattle is recommended.


2004 ◽  
Vol 26 (2) ◽  
pp. 107-114 ◽  
Author(s):  
M. Takenokuchi ◽  
C. Yasuda ◽  
K. Takeuchi ◽  
Y. Nakamachi ◽  
M. Mukai ◽  
...  

2019 ◽  
Vol 3 (1) ◽  
pp. 80-85
Author(s):  
Thangaraj Sekar ◽  
Ananda Arone Premkumar ◽  
Ganesan Chandra Mohan ◽  
Balaraman Sekar ◽  
Bheeman Sundaran ◽  
...  

2018 ◽  
Vol 134 (1) ◽  
pp. 57-62 ◽  
Author(s):  
Kim Appler ◽  
Scott Brunt ◽  
Jodie A. Jarvis ◽  
April D. Davis

Objectives: Each year, rabies virus infection results in the death of more than 50 000 persons worldwide. In the United States, the Centers for Disease Control and Prevention (CDC) reported 23 human rabies cases from May 1, 2008, through October 1, 2017. Although rabies testing in the United States is highly reliable, some specimens submitted to rabies laboratories do not have adequate tissues or may be substantially decomposed. In these instances, the specimen may be considered unsatisfactory for testing or produce indeterminate results using the gold standard direct fluorescent antibody test. The objective of this study was to evaluate the number of unsatisfactory samples or samples with indeterminate results that were positive for rabies virus after additional testing using real-time reverse transcriptase polymerase chain reaction (RT-PCR). Methods: In 2016, we retested all unsatisfactory specimens or specimens with indeterminate results using real-time RT-PCR. We further typed any sample that was real-time RT-PCR positive to identify the infecting rabies virus variant. Results: Of 210 retested unsatisfactory specimens or specimens with indeterminate results, 9 (4.3%) were positive for rabies. In each case, the animal was infected with a homologous rabies virus variant. Conclusion: These results confirm the recommendation by CDC and state public health laboratories that indeterminate results should be considered positive and justify the prompt treatment of exposed persons through an animal that is suspected to have rabies.


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