28 results match your criteria: "Korea Centers for Diseases Control and Prevention[Affiliation]"

The aim of this study was to compare the virulence of type 1 and type 2 porcine reproductive and respiratory syndrome virus (PRRSV) as assessed by the level of viral replication, viral distribution and apoptosis in stillborn fetuses and live-born piglets from infected pregnant gilts. Type 1 or type 2 PRRSV was given intranasally to pregnant gilts at 3 weeks before the expected date of parturition. Regardless of virus genotype, PRRSV-infected gilts farrowed between 102 and 109 days of gestation, while control uninfected gilts carried the pregnancy to term and farrowed at 114-115 days of gestation.

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Hospital-based HIV/HSV-2 seroprevalence among male patients with anal disease in Korea: cross sectional study.

BMC Infect Dis

January 2014

Division of AIDS, Center for Immunology and Pathology, Korea Centers for Diseases Control and Prevention, Osong Health Technology Adminstration Complex, 187 Osongsaengmyeong2(i)-ro, Cheongwon-gun, Chungcheongbukdo 363-951, Korea.

Background: This study aimed to identify the characteristics of HIV and herpes simplex virus (HSV)-2 seroprevalence in male patients with anal disease.

Methods: HIV seroprevalence was estimated for different age groups of male patients with anal disease who were treated at Songdo colorectal hospital in Korea between 2001 and 2011. HIV seroprevalence of patients with anal disease was compared with that of patients with nonanal disease for each year from 2007 to 2011.

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The first outbreak of giardiasis with drinking water in Korea.

Osong Public Health Res Perspect

April 2013

Division of Malaria and Parasitic Diseases, Korea National Institute of Health, Osong, Korea. ; Division of Epidemic Intelligence Service, Korea Centers for Diseases Control and Prevention, Osong, Korea.

Objectives: To identify the pathogen of the diarrhea outbreak in a village in Jeollabuk province in Korea in April 2010.

Methods: DNA extraction was performed from the 120 L of collected water, which was centrifuged at 10,000 x g for 30 min. PCR reactions were conducted in a total of 25 ul, which included PCR premix (GenDEPOT, Barker, TX, USA), 2 ul (∼100 ng) of extracted DNA, and 10 pmol of each primer.

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