1.An overview of swine influenza virus infection in humans.
Chinese Journal of Virology 2013;29(5):559-565
Since the first report of a swine influenza virus (SIV) infection in humans in 1958, cases have occurred continuously and increased significantly after the 2009 H1N1 pandemic. Although exposure to swine is thought to be a risk factor for human SIVs infections, approximately half of the reported cases had no known exposure to pigs. Besides, epidemiological investigation showed that several cases had limited human-to-human transmission. Based on the analyses of data on swine influenza virus infection in humans in this review, both the improved SIVs surveillance in humans and swine population and wider vaccination coverage among occupational workers are critical strategies in pandemic preparedness and response.
Animals
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Humans
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Influenza A virus
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genetics
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isolation & purification
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physiology
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Influenza, Human
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diagnosis
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epidemiology
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transmission
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virology
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Orthomyxoviridae Infections
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diagnosis
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epidemiology
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veterinary
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virology
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Swine
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Swine Diseases
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diagnosis
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epidemiology
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transmission
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virology
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Zoonoses
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diagnosis
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epidemiology
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transmission
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virology
2.Sample type is vital for diagnosing infection with peste des petits ruminants virus by reverse transcription PCR.
Pam Dachung LUKA ; Chrisostom AYEBAZIBWE ; David SHAMAKI ; Frank Norbert MWIINE ; Joseph ERUME
Journal of Veterinary Science 2012;13(3):323-325
Peste des petits ruminants (PPR) diagnosis from suspected samples from sheep and goats was carried out. Buffy coat, tissues, and oculo-nasal swabs were analyzed using nucleoprotein (NP3/NP4) and fusion protein (F1/F2) gene primers, respectively. Analysis of the sample types and primer set revealed that buffy coat are the best type of samples for PPR diagnosis and the use of two set of primers will increase the number of positives.
Animals
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DNA Primers/analysis
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Eye/virology
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Goat Diseases/blood/*diagnosis/epidemiology/virology
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Goats
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Hair/virology
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Nose/virology
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Nucleoproteins/analysis
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Peste-des-Petits-Ruminants/blood/*diagnosis/epidemiology/virology
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Peste-des-petits-ruminants virus/genetics/*isolation & purification
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Pigmentation
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RNA, Viral/genetics/*isolation & purification
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Reverse Transcriptase Polymerase Chain Reaction/*methods/standards/veterinary
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Sheep
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Sheep Diseases/blood/*diagnosis/epidemiology/virology
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Uganda/epidemiology
3.Detection of 12 Respiratory Viruses with Two-set Multiplex Reverse Transcriptase-PCR Assay Using a Dual Priming Oligonucleotide System.
Soo Jin YOO ; Eun Young KUAK ; Bo Moon SHIN
The Korean Journal of Laboratory Medicine 2007;27(6):420-427
BACKGROUND: We intended to evaluate the diagnostic usefulness of a multiplex reverse transcriptase- PCR (mRT-PCR) assay kit under dual priming oligonucleotide system (DPO) for the childhood acute respiratory tract infections. METHODS: Two hundred nasopharyngeal aspirates were taken from children < or = 5 yr old admitted due to acute respiratory infections in 2004. Direct fluorescent antibody (FA) assays were performed with fresh specimens; then, mRT-PCRs for the detection of 12 respiratory viruses (Seeplex RV detection kit, SeeGene, Seoul, Korea) were tested with frozen specimens. RESULTS: FA assays for five common respiratory viruses showed positive results in 66 patients (33.0%), while mRT-PCR detected causative viruses in 112 patients (56.0%), including 16 co-infected cases (8.0%). A total of 129 viruses were identified: respiratory syncytial virus A/B (38.0%/7.8%), influenza virus A/B (10.1%/5.4%), parainfluenza virus 1/2/3 (7.0%/3.1%/7.8%), coronavirus 229E or NL63 (6.2%), human metapneumovirus (4.7%), adenovirus (4.7%), rhinovirus (3.9%), and coronavirus OC43 (1.6%). CONCLUSIONS: DPO-based mRT-PCR was found as a sensitive tool for the detection of the viruses that cause childhood respiratory infections. Clinical significances of the agents detected by mRTPCR need further evaluations.
Child, Preschool
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DNA, Viral/analysis
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Fluorescent Antibody Technique, Direct
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Humans
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Infant
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Infant, Newborn
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Oligonucleotide Probes
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Reproducibility of Results
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Respiratory Tract Infections/*diagnosis/epidemiology/virology
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Reverse Transcriptase Polymerase Chain Reaction/*methods
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Virus Diseases/*diagnosis/epidemiology/virology
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Viruses/genetics/*isolation & purification
4.Cloning and sequence analysis of the DHBV genome of the brown ducks in Guilin region and establishment of the quantitative method for detecting DHBV.
He-Ling SU ; Ri-Dong HUANG ; Song-Qing HE ; Qing XU ; Hua ZHU ; Zhi-Jing MO ; Qing-Bo LIU ; Yong-Ming LIU
Chinese Journal of Virology 2013;29(2):180-184
Brown ducks carrying DHBV were widely used as hepatitis B animal model in the research of the activity and toxicity of anti-HBV dugs. Studies showed that the ratio of DHBV carriers in the brown ducks in Guilin region was relatively high. Nevertheless, the characters of the DHBV genome of Guilin brown duck remain unknown. Here we report the cloning of the genome of Guilin brown duck DHBV and the sequence analysis of the genome. The full length of the DHBV genome of Guilin brown duck was 3 027bp. Analysis using ORF finder found that there was an ORF for an unknown peptide other than S-ORF, PORF and C-ORF in the genome of the DHBV. Vector NTI 8. 0 analysis revealed that the unknown peptide contained a motif which binded to HLA * 0201. Aligning with the DHBV sequences from different countries and regions indicated that there were no obvious differences of regional distribution among the sequences. A fluorescence quantitative PCR for detecting DHBV was establishment based on the recombinant plasmid pGEM-DHBV-S constructed. This study laid the groundwork for using Guilin brown duck as a hepatitis B animal model.
Animals
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Base Sequence
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China
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epidemiology
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Cloning, Molecular
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Ducks
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Genome, Viral
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Hepadnaviridae Infections
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diagnosis
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veterinary
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virology
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Hepatitis B Virus, Duck
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classification
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genetics
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isolation & purification
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Molecular Sequence Data
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Phylogeny
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Polymerase Chain Reaction
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methods
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Poultry Diseases
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diagnosis
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virology
5.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
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Animals
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Base Sequence
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Circoviridae Infections/diagnosis/epidemiology/*veterinary
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Circovirus/genetics/isolation&purification
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DNA Primers
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Diagnosis, Differential
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Korea/epidemiology
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Parvoviridae Infections/diagnosis/epidemiology/*veterinary
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Parvovirus, Porcine/genetics/isolation&purification
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Polymerase Chain Reaction/methods/veterinary
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Porcine Reproductive and Respiratory Syndrome/diagnosis/*epidemiology
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Porcine respiratory and reproductive syndrome virus/genetics/isolation & purification
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Prevalence
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Respiratory Tract Infections/veterinary/virology
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Reverse Transcriptase Polymerase Chain Reaction/methods/veterinary
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Sequence Homology
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Swine
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Swine Diseases/diagnosis/*epidemiology
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Wasting Syndrome/*veterinary/virology
6.Infections after lung transplantation: time of occurrence, sites, and microbiologic etiologies.
Ji Hyun YUN ; Sang Oh LEE ; Kyung Wook JO ; Se Hoon CHOI ; Jina LEE ; Eun Jin CHAE ; Kyung Hyun DO ; Dae Kee CHOI ; In Cheol CHOI ; Sang Bum HONG ; Tae Sun SHIM ; Hyeong Ryul KIM ; Dong Kwan KIM ; Seung Il PARK
The Korean Journal of Internal Medicine 2015;30(4):506-514
BACKGROUND/AIMS: Infections are major causes of both early and late death after lung transplantation (LT). The development of prophylaxis strategies has altered the epidemiology of post-LT infections; however, recent epidemiological data are limited. We evaluated infections after LT at our institution by time of occurrence, site of infections, and microbiologic etiologies. METHODS: All consecutive patients undergoing lung or heart-lung transplantation between October 2008 and August 2014 at our institution were enrolled. Cases of infections after LT were initially identified from the prospective registry database, which was followed by a detailed review of the patients' medical records. RESULTS: A total of 108 episodes of post-LT infections (56 bacterial, 43 viral, and nine fungal infections) were observed in 34 LT recipients. Within 1 month after LT, the most common bacterial infections were catheter-related bloodstream infections (42%). Pneumonia was the most common site of bacterial infection in the 2- to 6-month period (28%) and after 6 months (47%). Cytomegalovirus was the most common viral infection within 1 month (75%) and in the 2- to 6-month period (80%). Respiratory viruses were the most common viruses after 6 months (48%). Catheter-related candidemia was the most common fungal infection. Invasive pulmonary aspergillosis developed after 6 months. Survival rates at the first and third years were 79% and 73%, respectively. CONCLUSIONS: Although this study was performed in a single center, we provide valuable and recent detailed epidemiology data for post-LT infections. A further multicenter study is required to properly evaluate the epidemiology of post-LT infections in Korea.
Adult
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Bacterial Infections/diagnosis/*microbiology/mortality
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Catheter-Related Infections/microbiology/virology
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Cytomegalovirus Infections/virology
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Female
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Heart-Lung Transplantation/*adverse effects/mortality
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Humans
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Kaplan-Meier Estimate
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Lung Transplantation/*adverse effects/mortality
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Male
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Medical Records
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Middle Aged
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Mycoses/diagnosis/*microbiology/mortality
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Pneumonia, Bacterial/microbiology
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Registries
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Republic of Korea/epidemiology
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Risk Factors
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Time Factors
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Treatment Outcome
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Virus Diseases/diagnosis/mortality/*virology
7.The first confirmed pediatric case with H7N9 avian influenza virus infection in China.
Mei ZENG ; Yan-feng ZHU ; Yan-ling GE ; Ai-mei XIA ; Dong-bo PU ; Hui YU ; Xiao-hong WANG ; Qi-rong ZHU
Chinese Journal of Pediatrics 2013;51(9):665-669
OBJECTIVETo understand the clinical and epidemiological aspects of avian influenza A (H7N9) virus infection in children.
METHODThe clinical data of the first confirmed pediatric case of avian influenza A(H7N9) virus infection were collected, and the epidemiological information, presenting symptoms, laboratory investigation, management and outcome were analyzed. The data of the pediatric cases were also compared with those of the adults cases.
RESULTThe case reported in this paper was a previously healthy 3.6-year-old boy residing in rural area of Shanghai. He had onset of fever and mild rhinorrhea on 31 March 2013 and he was afebrile and well since April 3. Influenza A (H7N9) virus was detected in his nasopharyngeal sample collected on 1 April through national Influenza-like Illness surveillance using real-time reverse transcriptase PCR and virus culture.His family raised domestic poultry with no apparent disease and there was no virological evidence of H7N9 infection. Monitoring and testing of 16 contacts had not found any secondary infection.
CONCLUSIONThe clinical course of H7N9 avian influenza virus infection in children was relatively mild as compared to adult cases. The source of infection and detail of exposure for children have not been known yet. Continued surveillance studies of mild and severe respiratory disease and subclinical infection are essential to further characterize the epidemiology and clinical spectrum of this emerging H7N9 virus infection in children.
Animals ; Child, Preschool ; China ; epidemiology ; Communicable Diseases, Emerging ; Humans ; Influenza A Virus, H7N9 Subtype ; genetics ; isolation & purification ; Influenza in Birds ; Influenza, Human ; diagnosis ; drug therapy ; virology ; Male ; Oseltamivir ; therapeutic use ; Poultry ; Real-Time Polymerase Chain Reaction ; Retrospective Studies ; Reverse Transcriptase Polymerase Chain Reaction