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Brazilian Journal of Microbiology

Print version ISSN 1517-8382

Braz. J. Microbiol. vol.42 no.3 São Paulo July/Sept. 2011

http://dx.doi.org/10.1590/S1517-83822011000300039 

VETERINARY MICROBIOLOGY

 

Retrospective study on Porcine circovirus-2 by nested pcr and real time pcr in archived tissues from 1978 in Brazil

 

 

Fernanda Miquelitto Figueira da SilvaI; Abelardo Silva JúniorII; Ethel Fernandes de Oliveira PeternelliI; Vinícius Winter VianaII; Orlando Chiarelli NetoI; Juliana Lopes Rangel FiettoI; Marlene Izabel VargasII; Luís Augusto NeroII; Márcia Rogéria de AlmeidaI,*

IDepartamento de Bioquímica e Biologia Molecular, Universidade Federal de Viçosa, Viçosa, MG, Brasil
IIDepartamento de Veterinária, Universidade Federal de Viçosa, Viçosa, MG, Brasil

 

 


ABSTRACT

Porcine circovirus-2 (PCV-2) infection is currently considered an important disease of swine. The pathogenic agent was first described in Brazil in 2000. This study detected the PCV-2 DNA in four Brazilian pig tissues collected between 1978 and 1979. This observation is the oldest description of this virus in Brazil.

Key words: PCV-2, retrospective study, Brazil.


 

 

Porcine circovirus (PCV) is a member of Circoviridae family along with other animal circoviruses, such as psittacine beak and feather disease virus and chicken anemia virus (4). PCV is one of the smallest viruses that replicates autonomously in mammalian cells and it is characterized as an icosahedral non-enveloped virus with 17 nm containing a single-stranded circular DNA genome with about 1.76 kb (9, 22). Currently, two species of PCV are recognized, PCV-1 and PCV-2. PCV-1 was originally identified in the porcine kidney cell line (PK15) (22) and is being considered a nonpathogenic virus. PCV-2 is associated with postweaning multisystemic wasting syndrome (PMWS) (3, 8, 10).

PCV-2 is usually associated to porcine dermatitis and nephropathy syndrome (PDNS), abortions, reproductive failure in sows, respiratory porcine disease complex and PMWS (13, 17, 21, 23). The association of PCV-2 with any of these diseases is currently named as PCV-2 associated diseases (PCVAD). PCVAD are considered as important swine diseases causing significant economic losses in swine worldwide industry (2, 11, 18).

PCV-2 infection was first described in Canada in 1991 associated to PMWS (7). This agent has a worldwide distribution (1), including Brazil, where it was first described in 2000 (5). Since the first record, retrospective studies with stored tissues have been conducted in several countries and used techniques such as in situ hybridization (ISH), immunohistochemistry using monoclonal antibody or nested-PCR. Considering these studies, PCV-2 was detected in Spain in lung and lymph node stored tissues from 1986 (19), in Thailand in tonsil lymph nodes and spleen from 1993 (12), even in Brazil, in the kidney, liver and lymph nodes from 1988 (6).

The aim of this study was to conduct a retrospective research of PCV-2 DNA in Brazilian sample tissues collected in 1978 and 1979, stored in blocks of paraffin for histological analyses.

We used the quantitative real time polymerase chain reaction (qPCR), which is an extremely useful tool to clarify the pathogenic action of viral agents in animal infectious diseases. This technique, qPCR, when compared to other methodologies, such as, conventional PCR and in situ hybridization allowing an increase in the detection frequency of viral agents and becoming an interesting technique for pathogen diagnosis (15).

Twelve histological sections of lung, renal, liver and lymphoid tissues stored in paraffin blocks from 1978 and 1979 were selected considering the presence of suspected lesions caused by PCV-2. Information about clinical signs, macroscopic and microscopic animal lesions were collected from the log file of the protocols in the tissue collections from the Histopathology Laboratory from Veterinary Department from the Federal University of Viçosa, located in Viçosa, Minas Gerais, Brazil.

The 10 µm selected histological sections were treated with xylol to remove the paraffin, and then centrifuged and washed with ethanol (100%). After the supernatants were discarded, the DNA from tissue was extracted using the WIZARD SV Genomic Purification System kit (Promega, Madison, USA). The DNAs were quantified by spectrophotometric assays.

A full length PCV-2 genome (GenBank access number: DQ364560) cloned into pGEM vector (Promega, Madison, USA) and propagated in DH5α Escherichia coli cells was used as internal standard for PCV-2 DNA quantification assays. The plasmid was purified using the commercial kit Wizard Plus SV Minipreps DNA Purification System (PROMEGA, Madison, USA), and quantified by spectrophotometry. The primers and probe used for qPCR were described by Olvera et al. (16). The optimized reactions contained 200nM of each primers, 200nM probe, 12.5µL TaqMan® universal master mix (Applied Biosystems, Foster City, USA) and 300ng DNA template. Autoclaved ultra purified water was added to achieve the final volume of 25µL. Amplifications were carried out under universal cycling conditions (10 min at 95ºC, 2 min at 50ºC, 40 cycles of 15 sec at 95ºC, and 1 min at 60ºC). The ABI Prism 7.500 detection software generated a standard curve with the threshold cycle (Ct) values of the 10-fold dilutions of PCV-2 plasmid (from 109 to 101 copies of the viral genome). Positive and negative reference samples were tested along with the unknown samples in each run. The detection software calculated the correlation PCV-2 copy number of the samples considering the standard curve.

Alternatively, the samples was tested using the nested PCR previously described by Lyoo et al. (14). The nested PCR products were purified and sequenced by the commercial Macrogen facility (Macrogen, Seoul, Korea). The ORF2 partial sequences were compared to sequences of PCV-2 in GenBank through the Basic Local Alignment Search Tool (BLAST) (http://www.ncbi.nlm.nih.gov/).

Four of the tested sample tissues showed positive results for PCV-2 DNA by the qPCR technique (Table 1). Positive samples were from the 1978 stored tissues, and presented numbers of genome copies between 1.08 and 2.00 (log10 values) in 300ng of DNA (Figure 1). The sensitivity can be attributed to the degree of conservation of the samples because they were stored in paraffin for nearly 20 years and the quality of DNA obtained was not satisfactory. It was not possible to perform immunohistochemical tests because of the degree of deterioration of the samples.

The same samples that presented positive results for PCV-2 DNA by qPCR and nested PCR showed typical lesions of viral infection (Table 1). The observed lesions were compatible with PCV-2 infection, and were characterized by the presence of interstitial pneumonia with mixed inflammatory cell infiltrate. These characteristic lesions associated with the detection of the PCV-2 DNA diagnosis support the hypothesis of PCV-2 respiratory infection. The nucleotide analysis showed that the sequences obtained in this study have 99-100% identity with other sequences of PCV-2 in GenBank (Table 1).

These results indicate the presence of PCV-2 in Brazil since 1978, despite the fact that this viral agent became significant for world swine production only in 1997 when the clinical signs were experimentally reproduced by Clark (7). The detection of PCV-2 in stored tissues from years before 1997 was also observed in other countries (12, 19), even in Brazil (6). According to Segalés et al. (20) several tissue samples could be associated to PCV-2 after the description of PMWS, indicating the presence of this pathogen since 1969. However, these works have not classified the genotype of PCV-2.

The detection of PCV-2 in stored tissues from 1978 by qPCR and nested PCR shows the presence of this viral agent in porcine production before its first record in Brazil, which occurred in 2000. This result indicates that the evolution of PCV-2 in Brazil may have occurred since this period. Furthermore, the utilization of qPCR in a retrospective study opened a new way to investigate the evolution of PCV-2 in a worldwide perspective.

 

ACKNOWLEDGEMENTS

This research was supported by grants from FAPEMIG and CNPq.

 

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Submitted: September 19, 2010; Returned to authors for corrections: October 21, 2010; Approved: March 14, 2011.

 

 

* Corresponding Author. Mailing address: Laboratório de Infectologia Molecular Animal - Instituto de Biotecnologia Aplicada à Agropecuária - Universidade Federal de Viçosa - Viçosa - Minas Gerais - 36570-000.; Tel.: + 55 31 3899 2911 Fax: + 55 31 3899 2864.; E-mail: marcia@ufv.br

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