Development of TaqMan-based qPCR method for detection of caprine arthritis–encephalitis virus (CAEV) infection
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A specific and sensitive two-step TaqMan real-time PCR has been developed for rapid diagnosis of caprine arthritis-encephalitis virus (CAEV) infection by using a set of specific primers and a TaqMan probe targeting a highly conserved region within the gene encoding the viral capsid protein (CA). The assay successfully detected CAEV proviral DNA in total DNA extracts originating from cell culture, whole blood samples and isolated PBMCs, with a lower detection limit of 102 copies and a linear dynamic range of 105 to 1010 copies/ml. There was no cross-reaction with other animal viruses (e.g., goat pox virus, bovine leukemia virus, bovine mucosal disease virus, swine influenza virus and Nipah virus). When applied in parallel with serological AGID and conventional PCR for detection of CAEV in field samples, this assay exhibited a higher sensitivity than these traditional methods, and 7.8 % of the 308 specimens collected in the Shanxi and Tianjin regions of China from 1993 to 2011 were found to be positive. Thus, the TaqMan qPCR assay provides a fast, specific and sensitive means for detecting CAEV proviral DNA in goat specimens and should be useful for large-scale detection in eradication programs and epidemiological studies.
Caprine arthritis-encephalitis virus (CAEV) is a member of the genus Lentivirus, family Retroviridae  and induces persistent and progressive degenerative inflammatory disease in infected goats . Although most infected goats remain asymptomatic, they are lifelong carriers and keep shedding the virus to the environment, leading to infection of naïve goats. Nevertheless, after prolonged incubation, a substantial population of CAEV-infected goats develop clinical signs primarily characterized by leukoencephalomyelitis in kids  and chronic polyarthritis and indurative mastitis in adults . CAEV is mainly macrophage-tropic; expression of the viral genome depends on the maturation state of the cells, and viral transcripts are produced only when the cells mature into macrophages [9, 21]. Epidemiological evidence indicates that the virus is transmitted from infected does to their offspring through the consumption of virus-infected colostrum and milk  or through prolonged close contact with infected adult animals .
CAEV infection is one of the most destructive and economically important viral diseases of the goat industry and is spread throughout many countries of the world, including the United States (31 %) , Norway (86 %) , Great Britain (54.5 %) , Switzerland (26.9 %) , Spain (20.6 %) , Poland (12.1 %) , Italy (6.58 %) , Japan (63.3 %) , Mexico (56.8 %) , Brazil (35 %) , Jordan (23.2 %) , Korea (2.73 %)  and China (0.2 %–30 %) . Overall, the live-animal trade and exportation of goats play a major role in CAEV dissemination across large geographical regions . Economic losses attributed to CAEV infection are considerably adverse in countries with intensive animal husbandry, with 5 %–10 % goats reported to be culled annually due to arthritis, and the decrease in milk production in infected does was estimated to be 10 %–15 % in Switzerland . The differences in the content of protein (3.35 % vs. 3.40 %), fat (3.54 % vs. 3.69 %), and lactose (4.25 % vs. 4.30 %) between seropositive and seronegative milk are significant . In udder halves with intramammary infection, milk SCC (somatic cell count) was significantly increased .
Currently, there are no effective drugs or vaccines available for treatment or prevention of CAEV infection. Therefore, immediate and accurate diagnosis is of particular importance for identifying and culling CAEV-positive animals from the rest of the herd to reduce economic losses . Routine laboratory diagnosis of CAEV infection is mainly based on serological assays . An agar gel immunodiffusion (AGID) test, an assay that is based on the CAEV serology, is recommended by the Office International des Epizooties (OIE). Enzyme-linked immunosorbent assay (ELISA), which uses recombinant capsid (CA) or TM envelope protein subunits as antigen [6, 27, 35], has proven more sensitive than AGID; however, the antigenic heterogeneity of CA and TM  may result in a lack of sensitivity, if the animal was infected with a lentivirus genotype different from that employed in the assay . Additionally, preparation of antigen is expensive, time-consuming and unpractical for routine diagnosis .
During our routine surveillance, we found that 4 out of 34 AGID-seronegative animals were PCR positive, suggesting that the classical management practice (AGID) recommended for CAEV control is insufficient . PCR-based diagnostic techniques vary according to their targets, such as reverse transcription PCR for the detection of viral RNA , semi-nested PCR  or loop-mediated isothermal amplification (LAMP) of proviral DNA , and real-time PCR detection of the CAEV env gene. The real-time PCR gave earlier positive detection results (15 days postinfection) than serological methods(ELISA and AGID, about 40-60 days postinfection) . An early/fast laboratory diagnosis for CAEV infection can be very useful for effective prophylactic action, and PCR is a useful tool for decreasing the risk of breeding AGID-false-negative animals . The aim of this study was to develop a TaqMan-based qPCR method to detect and quantify CAEV DNA in infected goat tissues by targeting a highly conserved region encoding the viral capsid protein (CA).
Materials and methods
Cells and viruses
GSM (goat synovial membrane) cells were maintained in DMEM supplemented with 10 % FBS at 37 °C with 5 % CO2. The cells were infected with the CAEV-Shanxi strain and monitored daily for cytopathic effect (CPE), as indicated by multinucleated cells and refractile stellate cells. When CPE reached to 50 to 80 %, cells were harvested and stored at −80 °C until used for nucleic acid extraction. DNA extracts of goat pox virus and bovine leukemia virus from cell culture and cDNA of swine influenza virus, bovine mucosal disease virus and Nipah virus were provided by the Tianjin Entry-Exit Inspection and Quarantine Bureau.
Nucleic acid extraction
Total DNA from PBMCs and infected cell cultures was extracted using a TIANamp Genomic DNA Kit (Tiangen Biotech Inc., Beijing, China), following the manufacturer’s instructions. The DNA was quantified by spectrophotometry (Nano Drop 1000 Spectrophotometer, Thermo Fisher Scientific Inc.) and stored at −20 °C until TaqMan qPCR was performed. CAEV RNA from a 250-μL sample containing 105 TCID50 of CAEV Shannxi strain culture was extracted using a QIAamp Viral RNA Mini Kit, and cDNA synthesis was performed using reverse transcriptase (QIAGEN, Beijing, China).
Conditions for TaqMan PCR and PCR
TaqMan qPCR primers and probe
Target gene (bp)
Amplicon size (bp)
Number of positive and negative samples detected by TaqMan qPCR, PCR assay and AGID
No. of Samples
No. of positive samples (%)
The primers CAF and CAR for TaqMan qPCR were also used for regular PCR. The PCR reaction mixture included 1 μL of plasmid DNA (approximately 0.038 μg), 0.25 μM CAF and 0.25 μM CAR, 0.2 μM dNTP mixture, 5 μL 10 × PCR buffer, 2.5 U of Platinum® Taq DNA polymerase (Invitrogen Beijing, China), and DNase-free water in a final volume of 50 μL. The PCR amplification parameters included an activation step at 95 °C for 10 min, 35 cycles of amplification (94 °C for 30 s, 55 °C for 30 s, and 72 °C for 30 s) and a final extension at 72 °C for 5 min. PCR products were electrophoresed in a 1.5 % agarose gel, stained with ethidium bromide, and visualised under UV light.
Sensitivity and specificity of the TaqMan qPCR and PCR
To generate a DNA standard curve, the gene encoding the CA capsid protein was cloned into the pGEM-T vector to generate the recombinant plasmid pGEM-T-CA. The concentration of the plasmid was determined by measuring OD absorbance at 260 nm, and the copy number was calculated by the following formula: plasmid copy (copies/μL) = [plasmid DNA concentration (g/μL) × 6.02 × 1023]/[length of DNA (bp) × 660]. The recombinant plasmid pGEM-T-CA was then serially diluted in tenfold steps, ranging from 1010 to 105 copies/ml, and used to generate a standard curve for quantification.
CAEV mRNA was extracted from GSM cells infected with the CAEV Shanxi strain, using an RNeasy Mini Kit, QIAGEN) and then reverse transcribed with primer CAR. The sensitivity of TaqMan qPCR and regular PCR was subsequently determined using a series of tenfold-diluted cDNA as template. The specificity of the TaqMan qPCR and PCR assay was evaluated by cross-reaction tests using DNA or cDNA templates extracted from some other animal viruses, including swine influenza virus, goat pox virus, bovine leukemia virus, bovine mucosal disease virus and Nipah virus. All of those virus specimens were provided by the Tianjin Entry-Exit Inspection and Quarantine Bureau.
Detection of CAEV in field samples
A total of 308 field samples were used to evaluate the sensitivity and specificity of the TaqMan qPCR in comparison to other traditional methods (Table 2). Since these samples were collected from three different herds with a history of CAEV infection in 1993, 2001 and 2010-2011, they therefore were divided into three groups (A, B and C). Group A consisted of 48 goats that originated from 8 flocks in Shanxi Province with a history of CAEV infection, group B samples were collected in 2001 from 20 goats from a mixed flock where sheep and goats were kept together in Tianjin City, and group C consisted of 240 goats that came from two flocks in Tianjin.
All blood samples were collected by jugular vein puncture. To isolate PBMCs, 10 ml of whole blood were collected in vacutainer tubes with EDTA, layered on an equal volume of Histopaque-1077 (Sigma-Aldrich, Germany), and then spun at 400×g for 30 min. The PBMC-containing layer was collected and washed twice, first with 10 ml and then with 5 ml isotonic phosphate-buffered saline solution, and used for extraction of genomic DNA. Twenty nanograms of total DNA was used for TaqMan qPCR and PCR detection.
Sensitivity of the TaqMan qPCR and PCR assay
Specificity of TaqMan qPCR
TaqMan qPCR detection of CAEV in field samples
CAEV control has remained a big challenge for the goat industry, as prophylactic vaccinations do not induce antibodies that result in efficient viral clearance and provide protection against arthritis . The control measures therefore rely heavily on accurate and reasonable laboratory diagnosis to identify and cull the CAEV-infected subjects so as to reduce economic losses .
PCR-based methods are now routinely used for laboratory diagnosis of pathogens, with acceptably high specificity. Based on regular PCR, we have developed a TaqMan qPCR assay for rapid CAEV diagnosis. This assay was simple to carry out and sensitive enough to detect viral DNA directly from PBMCs. Our results showed that the detection rate of TaqMan qPCR is higher than that of conventional PCR. Due to strain variation and the low viral load in vivo, the choice of the target region of the primers and probes can affect the efficiency of a PCR assay, and we therefore chose the region coding for viral capsid protein. This region is conserved in the CAEV genome, and it is obviously more suitable than other regions for the purpose of viral detection. Furthermore, the primers recognizing this region have high specificity and did not cross-amplify the sequences from swine influenza virus, goat poxvirus, bovine leukemia virus, bovine mucosal disease virus and Nipah virus.
As reported previously , real-time PCR can identify an infection much earlier (15 days postinfection) than serological methods (ELISA and AGID, 40-60 days postinfection). When applied to clinical diagnosis of CAEV, this method serves as a feasible and attractive method for large-scale screening, particularly at times of CAEV outbreaks. Rapid laboratory diagnosis of CAEV infections at an early stage of the disease can yield information relevant to goat industry management and help facilitate biosecurity protocols.
In Tianjin, the prevalence of CAEV-positive animals decreased during the years 2001 to 2010-2011. This is largely attributed to the measures for CAEV eradication that were taken in most farms of Tianjin, including serum antibody detection by AGID and viral DNA detection by PCR. Following diagnosis, all positive goats were slaughtered and removed, newborn kids were disinfected and separated from their does, and the kids were fed with milk or milk replacer rather than colostrum from CAEV-infected does. Other biosecurity practices were also implemented. In conclusion, the emphasis on identification CAEV infection is clearly evident, and the TaqMan qPCR method will be a sensitive, specific, and effective tool in CAEV control and eradication programs.
This work was supported by the National Natural Science Foundation of China (No. 30771613) and the Science and Technology Project of State Quality Inspection Administration (TJCIQ-2011 IK241) in China.
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