1.An Outbreak of Yersinia pseudotuberculosis Infection.
Hong Jong JOO ; Keun Hee CHUNG ; Yoo Mee KIM ; Soon Gi KIM ; Moon Soo PARK ; Jin Keun CHANG ; Sung Woo SHIN
Journal of the Korean Pediatric Society 1990;33(3):342-350
No abstract available.
Yersinia pseudotuberculosis*
;
Yersinia*
2.A Case of Acute Interstitial Nephritis Associated with Yersinia Pseudotuberculosis Infection.
Keun Hee CHUNG ; Yoo Mee KIM ; Mee Won KIM ; Soon Gi KIM ; Moon Soo PARK ; Jin Keun CHANG
Journal of the Korean Pediatric Society 1990;33(8):1122-1127
No abstract available.
Nephritis, Interstitial*
;
Yersinia pseudotuberculosis*
;
Yersinia*
3.Serotype of yersinia pseudotuberculosis isolated from animals in korea.
Chul Soon CHOI ; Jeong Seon KIM ; Sang In CHUNG ; Yong Tae YANG
Journal of the Korean Society for Microbiology 1993;28(1):7-12
No abstract available.
Animals*
;
Korea*
;
Yersinia pseudotuberculosis*
;
Yersinia*
4.Mesenteric lymphadenitis due to Yersinia pseudotuberculosis 5b.
Myung Sook KOO ; Seung Ik AHN ; Byung Wook YOO
Korean Journal of Infectious Diseases 1993;25(3):253-258
No abstract available.
Mesenteric Lymphadenitis*
;
Yersinia pseudotuberculosis*
;
Yersinia*
5.Mesenteric lymphadenitis due to Yersinia pseudotuberculosis 5b.
Myung Sook KOO ; Seung Ik AHN ; Byung Wook YOO
Korean Journal of Infectious Diseases 1993;25(3):253-258
No abstract available.
Mesenteric Lymphadenitis*
;
Yersinia pseudotuberculosis*
;
Yersinia*
6.Study on the Development of a Rapid Detection Method for Pathogenic Yersinia enterocolitica and Yersinia pseudotuberculosis by Nested Polymerase Chain Reaction.
Ho Jung OH ; Hong Ki MIN ; Yeo Won SOHN ; Seung Hwa HONG
Journal of the Korean Society for Microbiology 1999;34(2):175-187
A nested polymerase chain reaction (PCR) was applied to detect and identify pathogenic Yersinia enterocolitica and Y. pseudotuberculosis. We used photochemical postamplification procedure with 8-methoxypsoralen to control carryover contamination. Using the ail and inv gene, the sensitivity and specificity of DNA amplification by nested PCR was considerably improved. The amplified fragment sizes were 298 bp for the ail gene and 295 bp for the inv gene. Amplification was successful when the template was derived from three sources: purified DNA, aliquots of boiled bacterial suspension and aliquots of lysed bacterial suspension. The detection limits were 10 fg of DNA and 2 * 10 colony forming units (CFU) for Y. enterocolitica and 10 fg DNA and 2 CFU for Y. pseudotuberculosis.
DNA
;
Limit of Detection
;
Methoxsalen
;
Polymerase Chain Reaction*
;
Sensitivity and Specificity
;
Stem Cells
;
Yersinia enterocolitica*
;
Yersinia pseudotuberculosis*
;
Yersinia*
8.A case of Erythema Nodosum due to Yersinia Pseudotuberculosis.
Keun Hee CHUNG ; Hong Jong JOO ; Yoo Mi KIM ; Soon Ki KIM ; Moon Soo PARK ; Jin Keun CHANG ; Sung Woo SHIN
Journal of the Korean Pediatric Society 1990;33(4):528-533
No abstract available.
Erythema Nodosum*
;
Erythema*
;
Yersinia pseudotuberculosis*
;
Yersinia*
9.Molecular identification of the Vietnamese yersinia pestis isolated in Vietnam using pla sequence of plasmid pPCP1 as genetic marker
Journal of Vietnamese Medicine 2003;283(4):1-11
Pla sequence composes of 480 nucleodides of pPCP1 plasmide originated from Yersinia pestis isolated from Viet Nam and collected by the technique of PCR of chemical line into TA vector and demonstrated in turn. PCR reaction gave specific result from 3 diversified sources for mould: total extracted ADN, ADN extracted from plasmide isolated from bacterium complete cell. A fast and accurate method of diagnosis was created basing on this operation. By BLAST programme for accessing Gene Bank, the pla-gene sequence of Yersinia pestis in Viet Nam is analogue to other strains worldwide
Yersinia pestis
;
Genetic Markers
;
Biochemistry
10.Characteristics of plague focus at Eawy commune, Dak Lak province
Journal of Preventive Medicine 2002;12(2):36-39
Plague cases were reported at Eawy commune, Eah'leo district of Dak lak province in March 1997. Y. pestis was isolated from 1.42% of rat samples. 2.89% of rat serum samples and 20% of human serum samples contained anti-plague antibody. The reproductive season of X.cheopis has been coincided with plague season, peaking in the dry season. The plague and vector development seasons in Eawy have all typical characteristics of plague in the High-Plateau region
Plague
;
Yersinia pestis
;
Rats
;
Humans
Result Analysis
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