• 한국미생물·생명공학회지
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• 제31권1호
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• pp.13-17
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• 2003

우리나라 연안해역의 해수나 어패류에서 V. cholerae non-O1의 분포를 밝힘과 동시에 1996년 4월부터 동년 11월까지 분리된 환경분리주와 1984년부터 1996년까지 서울 및 부산소재 각 대학병원에서 환자로부터 분리된 총 55균주를 대상으로 생화학적 특성과 혈청형을 분석하였다. V. cholerae non-O1은 한국의 연안에서 206거체중 21검체(10%)에서 분리되었으나 V. cholerae O1 및 O139는 검출되지 않았다. 지역별로는 군산에서 16%로 검출률이 제일 높았다. 환경이나 환자에서 분리된 V. cholerae non-O1 55 균주에 대한 혈청형 분석결과 15종류의 혈청형이 검출되었는데 환경분리주 12종류, 환자분리주에서는 6종류이였다. 그런데 환경분리주에서는 O14가 68.3%(28/41)이였고, 환자분리주에서는 O8이 약 36%(5/14)로 많았고 그다음으로 O2와 O10등의 순이었다. 그리고 O2, O10와 O39는 환경 및 환자분리주에서 동시에 검출되었다.

• 미생물학회지
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• 제35권3호
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• pp.248-252
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• 1999

한국의 환경에서 분리된 47주와 환자 혈액에서 분리된 18주의 Vibrio cholerae serovar non-O1 및 non-O139를 대상으로 하여 콜레라 독소, 콜레라 독소 유전자, 용혈소, 그리고 혈구응집소 등이 병독인자 분포를 알아보았다. 시험된 65균주 중 용혈소만 생산하는 균은 29균주였고, 용혈소와 혈구 응집소를 생산하는 것은 65균주 중 36 균주였다. 용혈소, 콜레라 독소 및 유전자, 그리고 혈구응집소 모두를 가지고 있는 것은 환경에서 분리된 O37형 한 균주이었다. 한편 첨가한 당농도에 따른 혈구응집소 억제시험에서, 1% 이하의 mannose 와 galactose에서 응짐이 억제된 것은 환경분리균주 47 균주 중에서 26균주로 내혈구응집소나 외혈구응집소가 비슷한 비율로 분포하였고, 반면 환자분리균주는 18균주 중에서 5균주가 외혈구응집소의 비율이 훨씬 높았다. 따라서 V.cholerae non-1 및 non-O139의 용혈소가 주독소로 병독인자 분포는 다양하게 나타났다. 콜레라 독소가 유일한 병독이자라고 인식하기는 어려웠고 여러 가지 인자들이 복합적으로 작용될 것으로 생각되었다. 특히 환경분리주 O37 형에서 콜레라 독소 생성윤이 발견된 것을 향후 역학적인 측면에서 많은 연구가 되어야 할 것으로 사료되었다.

• Journal of Microbiology and Biotechnology
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• 제23권4호
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• pp.555-559
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• 2013

Vibrio cholerae O1 and O139 are the major serotypes associated with illness, and some V. cholera non-O1 and non-O139 isolates produce cholera toxin. The present study describes a quantitative polymerase chain reaction (qPCR) assay for the species-specific detection and quantitation of V. cholera using a primer pair based on an outer membrane lipoprotein lolB gene for the amplification of a 195 bp DNA fragment. The qPCR primer set for the accurate diagnosis of V. cholera was developed from publically available genome sequences. This quantitative PCR-based method will potentially simplify and facilitate the diagnosis of this pathogen and guide disease management.

• 한국수산과학회지
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• 제56권5호
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• pp.626-633
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• 2023

Vibrio spp. are aquatic bacteria that are ubiquitous in warm estuarine and marine environments. Especially, V. vulnificus and V. cholerae are currently known to cause potentially fatal infections in humans. This study investigated the distribution and antibiotic resistance of V. vulnificus and V. cholerae isolated from coastal areas of Gyeongsangnam-do in 2022. A total of 252 samples of water, shellfish and coastal sediment were collected from 7 locations along the coast, and 124 samples of fishery products were collected from markets. Among the 252 samples, forty-four V. vulnificus (11.7%) and fourteen V. cholerae non-O1/non-O139 (3.7%), none of which carried the ctx gene, were isolated. Out of the 124 samples, 6 (4.8%) tested positive for V. vulnificus and V. cholerae was not detected. The isolation rates of V. vulnificus and V. cholerae showed a significant correlation with environmental factors such as seawater temperature and salinity. In an antibiotic resistance test, V. vulnificus was susceptible to amikacin, gentamicin, imipenem trimethoprim/sulfamethoxazole, and ciprofloxacin, but resistant to cefoxitin (100.0%), followed by tetracycline (9.1%). Multidrug resistance was also observed. Continuous monitoring of Vibrio pathogens with water temperature and salinity is expected to help reduce the outbreaks, and rational use of antibiotic agents is needed to prevent the accession of antibiotic-resistant microorganisms in aquatic ecosystems.

• 한국환경보건학회지
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• 제44권2호
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• pp.133-142
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• 2018

Objectives: The pathogenic Vibrios genus denotes halophilic bacteria that are distributed in aquatic environments, including both sea and freshwater. Vibrio cholerae, Vibrio vulnificus, and Vibrio parahaemolyticus are the most important species since they can be potent human pathogens and leading causes of septicemia, wound infections, and seafood borne gastroenteritis. The recent emergence of a potential pandemic clone, V. cholera serotype O1 and the cholera outbreak in South Korea in 2016 indicates the importance of consistent surveillance of pathogenic Vibrio genus within coastal areas. Methods: The present study was undertaken to determine where and how vibrios live in the aquatic environment adjacent to coastal areas of South Korea. For this survey, a total of 838 samples were obtained at 35 different sites in South Korean coastal areas during the period from January 2016 to December 2016. Pathogenic vibrios was determined using the real-time PCR method, and its clones were isolated using three selective plating media. We also monitored changes in seawater and atmospheric temperature, salinity, turbidity, and hydrogen ion concentration at the collection points. Results: The total isolation rates of V. vulnificus, V. cholera (non-pathogenic, non-O1, non-O139 serogroups), and V. parahaemolyticus from seawater specimens in 2016 were 14.2, 13.48, and 67.06%, respectively. Conclusions: The isolation rates of pathogenic vibrios genus showed a positive correlation with temperature of seawater and atmosphere but were negatively correlated with salinity and turbidity.

• Journal of Microbiology and Biotechnology
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• 제26권8호
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• pp.1473-1480
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• 2016

This study focused on the variations in the non-coding sequences between ctxB and rstR of various CTX phages. The non-coding sequences of CTX-1 and CTX-cla are phage type-specific. The length of the non-coding region of CTX-1 and CTX-cla is 601 and 730 nucleotides, respectively. The non-coding sequence of CTX phage could be divided into three regions. There is a phage type-specific Variable region between two homologous Common regions (Common regions 1 and 2). The non-coding sequence of RS1 element is similar to CTX-1 except that Common region 1 is replaced by a short RS1-specific sequence. The non-coding sequences of CTX-2 and CTX-cla are homologous, indicating the non-coding sequence of CTX-2 is derived from CTX-cla. The non-coding region of CTX-O139 is similar to CTX-cla and CTX-2; however, it contains an extra phage type-specific sequence between Common region 2 and rstR. The variations in the non-coding sequences of CTX phages might be associated with the difference in the replication efficiency and the directionality in the integration into the V. cholerae chromosome.