1.Epidemiological characteristics of pulmonary pneumocystosis and concurrent infections in pigs in Jeju Island, Korea.
Ki Seung KIM ; Ji Youl JUNG ; Jae Hoon KIM ; Sang Chul KANG ; Eui Kyung HWANG ; Bong Kyun PARK ; Dae Yong KIM ; Jae Hoon KIM
Journal of Veterinary Science 2011;12(1):15-19
Epidemiological characteristics of swine pulmonary Pneumocystis (P.) carinii and concurrent infections were surveyed on Jeju Island, Korea, within a designated period in 172 pigs submitted from 54 farms to the Department of Veterinary Medicine, Jeju National University. The submitted cases were evaluated by histopathology, immunohistochemistry, PCR/RT-PCR, and bacteriology. P. carinii infection was confirmed in 39 (22.7%) of the 172 pigs. Histopathologically, the lungs had moderate to severe lymphohistioctyic interstitial pneumonia with variable numbers of fungal organisms within lesions. Furthermore, porcine reproductive and respiratory syndrome virus (PRRSV) and porcine circovirus type 2 (PCV-2) co-infection was a common phenomenon (12.8%, 20.5%, and 48.7% were positive for PRRS, PCV-2, or both, respectively, as determined by PCR/RT-PCR). Infection was much more concentrated during winter (December to March) and 53.8% of the infected pigs were 7- to 8-weeks old. In addition, three pigs showed co-infection with bacteria such as Pasteurella multocida and Streptococcus suis. The results of the present study suggest that the secondary P. carinii infection is common following primary viral infection in swine in Korea. They further suggest that co-infection of P. carinii might be enhanced by the virulence of primary pathogens or might have synergistic effects in the pigs with chronic wasting diseases.
Aging
;
Animals
;
*Circovirus/pathogenicity
;
Incidence
;
Pasteurella Infections/complications/epidemiology/veterinary
;
Pasteurella multocida/i
;
*Pneumocystis carinii/immunology/pathogenicity
;
Pneumonia, Pneumocystis/complications/epidemiology/physiopathology/*veterinary
;
Porcine Postweaning Multisystemic Wasting Syndrome/complications/*epidemiology
;
Porcine Reproductive and Respiratory Syndrome/*epidemiology
;
*Porcine respiratory and reproductive syndrome virus/pathogenicity
;
Prevalence
;
Republic of Korea/epidemiology
;
Reverse Transcriptase Polymerase Chain Reaction
;
Sea
;
Streptococcal Infections/complications/epidemiology/veterinary
;
Streptococcus suis/i
;
Sus scrofa
;
Swine Diseases/epidemiology/virology
2.A new recombined porcine reproductive and respiratory syndrome virus virulent strain in China
Jian guo DONG ; Lin yang YU ; Pei pei WANG ; Le yi ZHANG ; Yan ling LIU ; Peng shuai LIANG ; Chang xu SONG
Journal of Veterinary Science 2018;19(1):89-98
Porcine reproductive and respiratory syndrome (PRRS) is one of the most important swine diseases worldwide. In the present study, a new virulent strain of PRRS virus (PRRSV), GDsg, was isolated in Guangdong province, China, and caused high fever, high morbidity, and high mortality in sows and piglets. The genome of this new strain was 15,413 nucleotides (nt) long, and comparative analysis revealed that GDsg shared 82.4% to 94% identity with type 2 PRRSV strains, but only 61.5% identity with type 1 PRRSV Lelystad virus strain. Phylogenetic analysis indicated that type 2 PRRSV isolates include five subgenotypes (I, II, III, IV, and V), which are represented by NADC30, VR-2332, GM2, CH-1a, and HuN4, respectively. Moreover, GDsg belongs to a newly emerging type 2 PRRSV subgenotype III. More interestingly, the newly isolated GDsg strain has multiple discontinuous nt deletions, 131 (19 + 18 + 94) at position 1404–1540 and a 107 nt insertion in the NSP2 region. Most importantly, the GDsg strain was identified as a virus recombined between low pathogenic field strain QYYZ and vaccine strain JXA1-P80. In conclusion, a new independent subgenotype and recombinant PRRSV strain has emerged in China and could be a new threat to the swine industry of China.
China
;
Fever
;
Genome
;
Mortality
;
Nucleotides
;
Porcine Reproductive and Respiratory Syndrome
;
Porcine respiratory and reproductive syndrome virus
;
Swine
;
Swine Diseases
3.Assessing PCV2 antibodies in field pigs vaccinated with different porcine circovirus 2 vaccines using two commercial ELISA systems.
Min Kyoung SHIN ; Seung Hyun YOON ; Myung Hwui KIM ; Young Soo LYOO ; Seung Won SUH ; Han Sang YOO
Journal of Veterinary Science 2015;16(1):25-29
Porcine circovirus type 2 (PCV2) is the primary causative agent for post-weaning, multisystemic, wasting syndrome. Consequently, serologic detection of and vaccination against PCV2 are important for the swine industry. Among several serological tests, the enzyme-linked immunosorbent assay (ELISA) is commonly used to measure anti-PCV2 antibody levels. In the present study, we used two commercial ELISA systems to comparatively evaluate anti-PCV2 antibodies in field pigs treated with three different PCV2 vaccines. Among a total of 517 serum samples, the results of the two ELISAs were fully concordant for 365 positive and 42 negative samples, indicating 78.7% agreement. In addition, the Pearson coefficient (0.636) indicated a moderate correlation between data from the two ELISAs. Results from the farms with pigs vaccinated with the three different PCV2 vaccines demonstrated that most of the vaccinated animals underwent seroconversion. However, the increase and duration of antibody titers varied depending on the vaccine, the presence of maternal antibodies, and the vaccination program. PCV2 serologic status and anti-PCV2 antibody levels of herds from this study could be utilized to determine the best timing for vaccination and assessing vaccination compliance.
Aging
;
Animals
;
Antibodies, Viral/*blood
;
Circovirus/*classification/immunology
;
Enzyme-Linked Immunosorbent Assay/methods/*veterinary
;
Female
;
Porcine Postweaning Multisystemic Wasting Syndrome/blood/immunology/*prevention & control
;
Republic of Korea/epidemiology
;
Swine
;
Swine Diseases/*prevention & control/virology
;
Viral Vaccines/*immunology
4.An enhanced immunochromatographic strip test using colloidal gold nanoparticle-labeled dual-type N proteins for detection of antibodies to PRRS virus
Ji Eun YU ; In Ohk OUH ; Hyeonjeong KANG ; Hye young LEE ; Kwang Myun CHEONG ; In Soo CHO ; Sang Ho CHA
Journal of Veterinary Science 2018;19(4):519-527
Porcine reproductive and respiratory syndrome (PRRS) is recognized as one of the most important infectious diseases causing serious economic loss in the swine industry worldwide. Due to its increasing genetic diversity, a rapid and accurate diagnosis is critical for PRRS control. The immunochromatographic strip test (ICST) is a rapid and convenient type of immunoassay. In this study, an on-site immunochromatographic assay-based diagnostic method was developed for detection of PRRS virus (PRRSV)-specific antibodies. The method utilized colloidal gold nanoparticle-labeled dual-type nucleocapsid proteins encoded by open reading frame 7. We evaluated 991 field samples from pig farms and 66 serum samples from experimentally PRRSV-inoculated pigs. Based on true PRRSV-specific antibody-positive or
Agriculture
;
Antibodies
;
Colloids
;
Communicable Diseases
;
Diagnosis
;
Enzyme-Linked Immunosorbent Assay
;
Fluorescent Antibody Technique
;
Genetic Variation
;
Gold Colloid
;
Immunoassay
;
Immunochromatography
;
Immunoglobulin M
;
Methods
;
Nucleocapsid Proteins
;
Open Reading Frames
;
Porcine Reproductive and Respiratory Syndrome
;
Porcine respiratory and reproductive syndrome virus
;
Sensitivity and Specificity
;
Swine
5.Generation, characterization, and application in serodiagnosis of recombinant swine vesicular disease virus-like particles.
Wanhong XU ; Melissa GOOLIA ; Tim SALO ; Zhidong ZHANG ; Ming YANG
Journal of Veterinary Science 2017;18(S1):361-370
Swine vesicular disease (SVD) is a highly contagious viral disease that causes vesicular disease in pigs. The importance of the disease is due to its indistinguishable clinical signs from those of foot-and-mouth disease, which prevents international trade of swine and related products. SVD-specific antibody detection via an enzyme-linked immunosorbent assay (ELISA) is the most versatile and commonly used method for SVD surveillance and export certification. Inactivated SVD virus is the commonly used antigen in SVD-related ELISA. A recombinant SVD virus-like particle (VLP) was generated by using a Bac-to-Bac baculovirus expression system. Results of SVD-VLP analyses from electron microscopy, western blotting, immunofluorescent assay, and mass spectrometry showed that the recombinant SVD-VLP morphologically resemble authentic SVD viruses. The SVD-VLP was evaluated as a replacement for inactivated whole SVD virus in competitive and isotype-specific ELISAs for the detection of antibodies against SVD virus. The recombinant SVD-VLP assay produced results similar to those from inactivated whole virus antigen ELISA. The VLP-based ELISA results were comparable to those from the virus neutralization test for antibody detection in pigs experimentally inoculated with SVD virus. Use of the recombinant SVD-VLP is a safe and valuable alternative to using SVD virus antigen in diagnostic assays.
Animals
;
Antibodies
;
Baculoviridae
;
Blotting, Western
;
Certification
;
Enterovirus B, Human
;
Enzyme-Linked Immunosorbent Assay
;
Foot-and-Mouth Disease
;
Mass Spectrometry
;
Methods
;
Microscopy, Electron
;
Neutralization Tests
;
Serologic Tests*
;
Swine Vesicular Disease*
;
Swine*
;
Virus Diseases
6.Construction and identification of a recombinant PRRSV expressing ORF2 of porcine circovirus type 2.
Tingjie ZHANG ; Xing LIU ; Tao SUN ; Xuejiao ZHU ; Baochao FAN ; Juan BAI ; Ping JIANG
Chinese Journal of Virology 2015;31(1):65-73
Porcine reproductive and respiratory syndrome virus (PRRSV) and porcine circovirus type 2 (PCV2) are very two important pathogens that have coursed huge economic losses in swine production in worldwide. In this study,a vector pCMV-TJM containing the full-length cDNA clone of PRRSV attenuated strain TJM-F92 was firstly constructed by PCR method. Then a gene sequence containing Afl II/Mlu I e restriction enzyme sites and a transcription regulatory sequence for ORF6 (TRS6) was inserted be- tween ORF7 and 3'UTR, yielding a expression vector pCMV-TJM-TRS. Subsequently, a plasmid pCMV-TJM-Cap was constructed by cloning of PCV2 ORF2 gene into the unique sites Afl II /Mlu I of pCMV- TJM-TRS plasmid DNA. Then three recombinant PRRSV, rTJM, rTJM/TRS and rTJM/Cap, were rescued by transfection of pCMV-TJM, pCMV-TJM-TRS and pCMV-TJM-Cap into Marc-145 cells, respectively,and confirmed by the genome sequence, restriction enzyme digestion, Western Blot and IFA. They all had the molecular markers which was different from the parent virus. The growth characteristics of the rescued viruses were similar to that of parent virus. rTJM/Cap could also express efficiently PCV2 Cap protein in Marc-145 cells. At passage 8, it still had PCV2 ORF2 gene which examined by RT-PCR. It indicated that the full-length cDNA clone of PRRSV attenuated strain TJM-F92 and recombinant PRRSV rTJM/Cap expressing PCV2 Cap protein were successfully constructed. It made an important foundation for studying on the pathogenic mechanisms of PRRSV and PRRSV-PCV2 vaccine in the future.
Animals
;
Capsid Proteins
;
genetics
;
immunology
;
Cell Line
;
Circoviridae Infections
;
veterinary
;
virology
;
Circovirus
;
classification
;
genetics
;
metabolism
;
Gene Expression
;
Open Reading Frames
;
Porcine Reproductive and Respiratory Syndrome
;
virology
;
Porcine respiratory and reproductive syndrome virus
;
genetics
;
metabolism
;
Recombination, Genetic
;
Swine
;
Swine Diseases
;
virology
;
Viral Vaccines
;
genetics
;
immunology
7.Prevalence of porcine reproductive and respiratory syndrome virus, porcine circovirus type 2 and porcine parvovirus from aborted fetuses and pigs with respiratory problems in Korea.
Kwang Soo LYOO ; Yong Ho PARK ; Bong Kyun PARK
Journal of Veterinary Science 2001;2(3):201-207
Porcine reproductive and respiratory syndrome virus(PRRSV)0, porcine circovirus type 2(PCV-2) and porcine parvovirus (PPV)0 infections were investigated as possible causes of the postweaning multisystemic wasting syndrome(PMWS). Specific primers for RT-PCR and PCR were designed for the differential detection of PRRSV, PCV-2 and PPV. Using PCR, these viruses were detected in homogenized tissue samples from pigs that had respiratory of reproductive problems in the time period between 1998 and 2000; the overall prevalences were: PRRSV 31.4%, PCV-2 46.5%, and PPV 8.1%. PCV-2 was also detected in aborted fetal tissues.
Aborted Fetus/virology
;
Animals
;
Base Sequence
;
Circoviridae Infections/diagnosis/epidemiology/*veterinary
;
Circovirus/genetics/isolation&purification
;
DNA Primers
;
Diagnosis, Differential
;
Korea/epidemiology
;
Parvoviridae Infections/diagnosis/epidemiology/*veterinary
;
Parvovirus, Porcine/genetics/isolation&purification
;
Polymerase Chain Reaction/methods/veterinary
;
Porcine Reproductive and Respiratory Syndrome/diagnosis/*epidemiology
;
Porcine respiratory and reproductive syndrome virus/genetics/isolation & purification
;
Prevalence
;
Respiratory Tract Infections/veterinary/virology
;
Reverse Transcriptase Polymerase Chain Reaction/methods/veterinary
;
Sequence Homology
;
Swine
;
Swine Diseases/diagnosis/*epidemiology
;
Wasting Syndrome/*veterinary/virology
8.Localization of Porcine Reproductive and Respiratory Syndrome Virus Infection in Boars by In Situ Riboprobe Hybridization.
Jin Ho SHIN ; Thomas W MOLITOR
Journal of Veterinary Science 2002;3(2):87-95
The capability of porcine reproductive and respiratory syndrome virus (PRRSV) to be shed in semen for extended periods of time has been suggested to be a principal factor for viral transmission via insemination. In attempts to gain insights into the mechanism of PRRSV persistence in boars, tissue distribution and sites of viral infection were investigated by in situ hybridization (ISH) using digoxigenin-labeled RNA probe and the ISH results were compared with those of reverse transcription-nested polymerase chain reaction (RT-nested PCR). Animals were intranasally inoculated with 104 median tissue culture infectious dose of PRRSV VR-2332 and tissues collected at different times were examined. At day 7 postinfection, limited number of hybridization positive signals was observed in cells within or between seminiferous tubules in the testis sections while relatively abundant hybridization positive signals were observed in the brain stem and tracheobronchial lymph node. At later days of infection, hybridization positive signals were observed in cells within seminiferous tubules with much reduced frequency. Lack of agreement with the RT-nested PCR assay results in testis tissues obtained at days 14, 28, and 59 postinfection suggested that PRRSV infection in the testis may be extremely restricted, and may not necessarily constitute a major viral source in semen during extended periods of seminal shedding.
Animals
;
Brain Stem/virology
;
Endopeptidase K/metabolism
;
*In Situ Hybridization
;
Lymph Nodes/virology
;
Male
;
Microwaves
;
Porcine Reproductive and Respiratory Syndrome/transmission/*virology
;
Porcine respiratory and reproductive syndrome virus/*genetics/*isolation & purification
;
RNA Probes
;
Reverse Transcriptase Polymerase Chain Reaction
;
Semen/virology
;
Seminiferous Tubules/virology
;
Sensitivity and Specificity
;
Sexually Transmitted Diseases, Viral/transmission/veterinary/virology
;
Swine/*virology
;
Testis/virology
9.How far can African swine fever spread?
Journal of Veterinary Science 2019;20(4):e41-
African Swine Fever (ASF) is a highly contagious and deadly viral disease affecting both domestic pig and wild boar populations. Once introduced, it is a terrible disease that can devastate the swine industry in many countries. ASF has spread most recently beyond China to Southeast Asia, and parts of the Korean Peninsula. The majority of Asian countries consume pork as the primary source of meat compared to all other meat products. Particular emphasis is on the spread of ASF within North Korea and on future perspectives including protective guidelines. Thus far, the Korean peninsula has endured an extensive history of diseases, most notably from foot and mouth disease. For this reason, the Korean swine industries are familiar with the detrimental impacts of such a disease. On the other hand, exposure to a disease like ASF will decimate the swine industry even further. Therefore, it is crucial to bring urgent awareness to the spread of ASF.
African Swine Fever
;
Animals
;
Asia, Southeastern
;
Asian Continental Ancestry Group
;
China
;
Democratic People's Republic of Korea
;
Epidemiology
;
Foot-and-Mouth Disease
;
Hand
;
Humans
;
Meat
;
Meat Products
;
Red Meat
;
Sus scrofa
;
Swine
;
Virus Diseases
10.Porcine deltacoronavirus induces mitochondrial apoptosis in ST cells.
Shaoyong JIAO ; Cui LIN ; Liuyang DU ; Junli LIU ; Jinyan GU ; Jiyong ZHOU
Chinese Journal of Biotechnology 2019;35(6):1050-1058
Porcine deltacoronavirus (PDCoV) is a newly emerging enteropathogenic swine coronavirus causing acute diarrhea and vomiting in pigs. The apoptosis of ST cells induced by PDCoV infection was studied in this research. In ST cells, caspase activity assay showed that the activity of caspase 3, caspase 8 and caspase 9 increased significantly with the infection of PDCoV, but not observed in UV irradiated PDCoV-infected cells, indicating that PDCoV infection activated both endogenous and exogenous apoptotic pathways in ST cells, and the induction of apoptosis depended on viral replication. To further investigate the endogenous apoptosis induced by PDCoV, cytochrome C and apoptosis-inducing factors in cytoplasm and mitochondria were detected. Compared with normal cells, the amount of cytochrome C released from mitochondria to cytoplasm increased significantly in PDCoV-infected cells, and the release increased with the prolongation of infection, while the apoptosis-inducing factor was always localized to mitochondria, suggesting that PDCoV induced apoptosis was initiated through caspase-dependent mitochondrial apoptosis pathway by promoting cytochrome C in the mitochondrial membrane gap into the cytosol. In conclusion, this study reveals the mechanism of PDCoV inducing apoptosis.
Animals
;
Apoptosis
;
Coronavirus
;
Coronavirus Infections
;
Mitochondria
;
Swine
;
Swine Diseases