• 한국수산과학회지
• /
• 제54권5호
• /
• pp.644-651
• /
• 2021

Viral hemorrhagic septicemia virus (VHSV) is a fish pathogen responsible for causing enormous economic loss to the aquaculture industry not only in Korea but worldwide. Thus, it is necessary to identify natural compounds that can be used to control the spread of VHSV. In this study, the anti-VHSV activities of five catechol derivatives, i.e., catechol, pyrogallol, 3-methyl catechol, veratrole, and 3-methyl veratrole-extracted from green tea-were assessed. The antiviral activities of these derivatives were found to be dependent on their structure, i.e., the hydroxyl or methoxyl group and their substituent groups-on the benzene ring. Catechol, pyrogallol, and 3-methyl catechol exhibited relatively high 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activities than veratrole, and 3-methyl veratrole. Moreover, 3-methyl catechol harboring a methyl substituent group increased the viability of the virus-infected cells and resulted in a 2.86 log reduction in the gene copies of VHSV N (per mL) in real-time PCR analysis. In conclusion, the catechol derivatives harboring hydroxyl groups in their benzene ring exhibited higher antioxidant activities than those harboring the methoxyl groups. However, catechol derivatives with a methyl group at the 3'-position of the benzene ring exhibited higher antiviral activity than those harboring a hydroxyl group. To our knowledge, this is the first study to evaluate the relationship between the structure and the anti-VHSV activity of catechol derivatives.

• Parasites, Hosts and Diseases
• /
• 제61권1호
• /
• pp.15-23
• /
• 2023

Concerns about foodborne illnesses caused by Kudoa septempunctata are steadily growing, but reports of K. septempunctata in clinical and food specimens related to food poisoning in Korea are limited. This study aimed to genetically identify K. septempunctata in patients with acute diarrhea and in clinical and food samples related to food poisoning caused by sashimi consumption. Both real-time and nested polymerase chain reaction assays were performed to detect K. septempunctata 18S and 28S rDNA genes in the stools of 348 patients with acute diarrhea, 11 samples (6 stool and 5 rectal swab samples) from patients with food poisoning, and 2 raw Paralichthys olivaceus samples collected from a restaurant where a food poisoning incident occurred. K. septempunctata was identified in 5 clinical specimens (4 stools and 1 rectal swab) and 1 P. olivaceus sashimi sample. All detected K. septempunctata were of genotype ST3. This is the first study to identify K. septempunctata in both patients and food samples with epidemiological relevance in Korea, providing evidence that it is a pathogen that causes food poisoning. Also, this is the first study to confirm the presence of K. septempunctata genes in rectal swabs. Despite continuing suspected occurrences of Kudoa foodborne outbreaks, the rate of identification of K. septempunctata is very low. One reason for this is the limitation in obtaining stool and vomit samples for the diagnosis of Kudoa infection. We strongly suggest the inclusion of rectal swabs among the diagnostic specimens for Kudoa food poisoning.

• 한국식품위생안전성학회지
• /
• 제28권3호
• /
• pp.227-233
• /
• 2013

신선편의 샐러드와 유기농 채소에 오염되어 있는 식중독균인 B. cereus, S. aureus 그리고 E. coli를 대상으로 살균소독제와 유기산에 대한 감수성을 평가하여 신선편의 식품의 미생물학적 안전성의 확보를 위한 올바른 세척제와 사용량을 제시하고자 하였다. S. aureus는 2% acetic acid, malic acid, tartaric acid와 1% CaO에 대하여 고농도의 염소계, 과산화수소계 보다 높은 살균 효과를 보였고 E. coli의 경우에는 1% acetic acid와 CaO처리에 의해 80%의 분리주가 감소하여 50% 에탄올과 400 ppm 차아염소산나트륨과 대등한 감소율을 보였다. B. cereus 분리주에 대한 1% CaO, 0.5% acetic acid, 2% malic acid와 tartaric acid 처리는 200 ppm의 차아염소산나트륨보다 높은 감소율을 나타내었고, 1%의 과산화수소와 대등한 감소율을 나타내었다. 본 연구에 따라 천연 물질 유래 살균 소독제인 CaO와 유기산은 기존의 화학적 살균제를 대체할 수 있는 천연 살균 소독제로 활용될 수 있을 것이고 특히 환경 친화적이고 안전한 유기산은 고품질의 신선편의 채소를 안전성으로 공급하는데 효과적인 것으로 판단되었다.

• Journal of Microbiology and Biotechnology
• /
• 제24권3호
• /
• pp.363-370
• /
• 2014

Campylobacter jejuni is a prevalent foodborne pathogen worldwide. Human infection by C. jejuni primarily arises from contaminated poultry meats. Genes expressed in vivo may play an important role in the pathogenicity of C. jejuni. We applied an immunoscreening method, in vivo-induced antigen technology (IVIAT), to identify in vivo-induced genes during human infection by C. jejuni. An inducible expression library of genomic proteins was constructed from sequenced C. jejuni NCTC 11168 and was then screened using adsorbed, pooled human sera obtained from clinical patients. We successfully identified 24 unique genes expressed in vivo. These genes were implicated in metabolism, molecular biosynthesis, genetic information processing, transport, and other processes. We selected six genes with different functions to compare their expression levels in vivo and in vitro using real-time RT-PCR. The results showed that the selected six genes were significantly upregulated in vivo but not in vitro. In short, these identified in vivo-induced genes may contribute to human infection of C. jejuni, some of which may be meaningful vaccine candidate antigens or diagnosis serologic markers for campylobacteriosis. IVIAT may present a significant and efficient method for understanding the pathogenicity mechanism of Campylobacter and for finding targets for its prevention and control.

• 농촌의학ㆍ지역보건
• /
• 제43권4호
• /
• pp.258-269
• /
• 2018

2018년 6월 12일 충청북도 옥천군 소재 A고등학교에서 노로바이러스의 유행을 지연신고하는 사례가 발생하였고, 이에 대한 원인과 전파양식 등을 규명하고 예방 및 관리대책을 마련 하기 위하여 역학조사를 수행하였다. A고등학교 학생 183명을 대상으로 설문조사, 환례자 60명, 조리종사자 10명을 대상으로 세균 10종 및 바이러스 5종에 대한 검체검사를 실시하였다. 설문조사는 최초환자 발생일 6월 5일을 기준으로 3일 전인 6월 2일부터 12일까지의 식단을 이용하여 환자-대조군 조사를 시행하였다. 학생, 교직원, 조리종사자 785명 중 환례는 61명으로 노로바이러스의 발병률은 7.8% 이었다. 위험요인 분석에서 정수기 음용수가 유의한 변수이었다. 검체검사에서 학생 2명, 정수기 음용수, 환경검체에서 동일 유형의Norovirus GI-8이 검출되었다. 이번 유행의 원인으로 본관, 기숙사, 급식실 정수기 음용수가 오염되고 그로 인해 원인병원체 노로바이러스의 전파가 이루어졌다고 판단하였다. 이번 연구는 6월 5일 첫 환례자가 발생했음에도 신고가 7일이 경과한 6월 12일 지연신고 되어 장관감염증 확산 조기차단이 이루어지지 않아 환례자가 더 많이 발생한 것으로 추정된다. 향후 학교급식 시 발생하는 수인성 및 식품매개성질병으로부터 학생을 보호하고 집단발생을 예방하기 위하여 학생의 증상을 가장 우선적으로 파악이 가능한 담임선생님과 보건교사의 공조체제 개선, 보건교사 부재 시 대응방안, 보건교사의 학교 감염병 집단발생에 대한 인식제고를 위한 시스템 보완이 이루어져야 할 것이다. 또한 질병관리본부의 기본 역학조사서 서식에 지연신고에 대한 사유를 기록하는 항목을 추가하여 지연신고에 대한 원인에 대한 규명과 그에 따른 대책을 마련해야 할 것이다.

• 한국식품위생안전성학회지
• /
• 제29권4호
• /
• pp.305-311
• /
• 2014

본 연구는 정량적 미생물 위해평가(Quantitative microbial risk assessment: QMRA)에 절대적으로 필요한 9종의 식중독 세균, 2종의 바이러스, 1종의 원생동물에 대한 최소 감염량(minimum infective dose)을 선정한 연구이다. 주요 식중독 미생물들의 최소 감염량을 선정하기 위하여, 1980년부터 2012년까지 PubMed, ScienceDirect database 등에서 주요 식중독 미생물들의 최소 감염량 및 위해평가 자료 82종을 수집하였다. 수집된 자료는 메타분석(mata-analysis)에서 사용되고 있는 relative frequency(fi, 상대빈도 값)를 계산하여 가장 적정한 최소 감염량을 추정 및 선정하였다. 주요 식중독 미생물들의 최소 감염량은, B. cereus $10^5cells/g$ (fi = 0.32), C. jejuni 500 cells/g (fi = 0.57), Cl. perfringens $10^7cells/g$ (fi = 0.56), Pathogenic E. coli 중 EHEC 10 cells/g (fi = 0.47), ETEC $10^8cells/g$ (fi = 0.71), EPEC $10^6cells/g$ (fi = 0.70), EIEC $10^6cells/g$ (fi = 0.60), L. monocytogenes $10^2{\sim}10^3cells/g$ (fi = 0.23), Salmonella spp. 10 cells/g (fi = 0.30), Shigella spp. 100 cells/g (fi = 0.32), S. aureus $10^5cells/g$ (fi = 0.45), V. parahaemolyticus $10^6cells/g$ (fi = 0.64), Hepatitis A virus $10{\sim}10^2particles/g$ (fi = 0.33), Noro virus 10 particles/g (fi = 0.71), C. pavum $10{\sim}10^2oocyst/g$ (fi = 0.33)으로 나타났다. 본 연구결과는 향후 국내 QMRA를 통한 위해수준 추정결과의 정확성을 향상시키는데 기여할 수 있을 것으로 기대된다.

• 한국식품과학회지
• /
• 제48권5호
• /
• pp.437-444
• /
• 2016

최근 건강과 위생에 대한 소비자의 의식 향상으로 인해 농수축산 분야를 비롯한 식품의 가공 유통 분야에서도 식품의 안전성 확보를 위한 시험 검사가 실시되고 있고, HACCP과 같은 식품안전관리 프로그램의 조기 도입을 유도하고 있어 식품중독균에 대한 검사량이 증가하고 있다. 이에 따른 신속, 정확하고 대량의 시료를 처리할 수 있는 식품중독균 검사의 필요성이 증가되고 있다. 국내 식품 미생물의 확인시험방법은 전통적인 미생물 동정법인 그램 염색 등과 같은 형태학적 특성과 생화학적 분석에 의해서 주로 확인되는데, 확인 과정이 복잡하고 장시간이 소요된다. 이를 극복하기 위한 새로운 미생물 동정법인 MALDI-TOF 질량분석기반 미생물 동정법을 식품의 식품중독균 검사에 적용하기 위해 식품공전에서 주로 검사하는 식품중독균 10종에 대한 질량 패턴 데이터를 국내 질량분석 데이터베이스인 MicroID에 적용하였다. 표준 균주와 식품중독균이 검출된 시료에서 분리한 균으로 비교했을 때 질량분석기반 미생물 동정은 현재 사용되고 있는 생화학적 분석결과와 일치한 결과를 보여주었다. 또한, 식품중독균을 포함한 국내 미생물 균주를 이용해서 구축한 데이터베이스, MicroID는 기존의 상용화된 해외 MALDI-TOF 질량분석 데이터베이스 Biotyper와 동등 이상의 정확도를 나타내었다. 국내 식품관련 미생물에 대한 질량스펙트럼을 추가하여 데이터베이스를 지속적으로 확장시키면 신속 정확한 미생물 동정법으로 자리매김할 수 있을 것이다.

• 한국가금학회지
• /
• 제45권1호
• /
• pp.1-15
• /
• 2018

Salmonella infections in livestock industry cause various problems such as worsening animal welfare and productivity, damaging consumer confidence in the food safety of animal products. Chicken meat and eggs are known as major source of pathogen causing human foodborne infections. Therefore food safety concerns have prompted the poultry producers and governments to introduce the strategy and regulation to control these pathogens. Salmonella can persist for long periods of time in a wide range of spaces including feed bin, feed processing facilities, poultry farm, slaughterhouse, processing plants, etc. For the effective and constant Salmonella control, combination of pre-harvest, harvest and post-harvest measures should be considered comprehensively. The control measures would be most effective at farm level where the contamination initiates. Transmission of pathogen from feed origin to the live poultry and finally to the products was proven already. To control bacteria in the feed ingredients and formula feed, thermal processing, irradiation or chemical treatment may be applied. Chemical treatments to inhibit Salmonella in the feed involve the use of products containing organic acids, formaldehyde, or a combination of such compounds. However, recontamination which might occur during storage and transport process and/or by other various factors should always be under control and eliminated. Feed additives used to control Salmonella in birds' gastrointestinal track can be of various types, including prebiotics, probiotics, organic acids and bacteriophages. Although their mode of action varies, they ultimately inhibit the colonization of Salmonella in the gut and improve the performance of birds. This review describes the strategies that could be adapted to the management of feedstuffs and the use of feed additives in pre-harvest stage to control Salmonella contamination in poultry farming.

• Journal of Microbiology and Biotechnology
• /
• 제24권2호
• /
• pp.217-224
• /
• 2014

Chicken are considered as the most important source of human infection by Campylobacter jejuni, which primarily arises from contaminated poultry meats. However, the genes expressed in vivo of the interaction between chicken and C. jejuni have not been screened. In this regard, in vivo-induced antigen technology (IVIAT) was applied to identify expressed genes in vivo during interaction between chicken and C. jejuni, a prevalent foodborne pathogen worldwide. Chicken sera were obtained by inoculating C. jejuni NCTC 11168 into Leghorn chickens through oral and intramuscular administration. Pooled chicken sera, adsorbed against in vitro-grown cultures of C. jejuni, were used to screen the inducible expression library of genomic proteins from sequenced C. jejuni NCTC 11168. Finally, 28 unique genes expressed in vivo were successfully identified after secondary and tertiary screenings with IVIAT. The genes were implicated in metabolism, molecular biosynthesis, genetic information processing, transport, regulation and other processes, in addition to Cj0092, with unknown function. Several potential virulence-associated genes were found to be expressed in vivo, including chuA, flgS, cheA, rplA, and Cj0190c. We selected four genes with different functions to compare their expression levels in vivo and in vitro using real-time RT-PCR. The results indicated that these selected genes were significantly upregulated in vivo but not in vitro. In short, the expressed genes in vivo may act as potential virulence-associated genes, the protein encoded by which may be meaningful vaccine candidate antigens for campylobacteriosis. IVIAT provides an important and efficient strategy for understanding the interaction mechanisms between Campylobacter and hosts.

• Journal of Microbiology and Biotechnology
• /
• 제33권3호
• /
• pp.329-338
• /
• 2023

Enterohemorrhagic Escherichia coli (EHEC) is a foodborne pathogen that produces attaching and effacing lesions on the large intestine and causes hemorrhagic colitis. It is primarily transmitted through the consumption of contaminated meat or fresh produce. Similar to other bacterial pathogens, antibiotic resistance is of concern for EHEC. Furthermore, since the production of Shiga toxin by this pathogen is enhanced after antibiotic treatment, alternative agents that control EHEC are necessary. This study aimed to discover alternative treatments that target virulence factors and reduce EHEC toxicity. The locus of enterocyte effacement (LEE) is essential for EHEC attachment to host cells and virulence, and most of the LEE genes are positively regulated by the transcriptional regulator, Ler. GrlA protein, a transcriptional activator of ler, is thus a potential target for virulence inhibitors of EHEC. To identify the GrlA inhibitors, an in vivo high-throughput screening (HTS) system consisting of a GrlA-expressing plasmid and a reporter plasmid was constructed. Since the reporter luminescence gene was fused to the ler promoter, the bioluminescence would decrease if inhibitors affected the GrlA. By screening 8,201 compounds from the Korea Chemical Bank, we identified a novel GrlA inhibitor named Grlactin [3-[(2,4-dichlorophenoxy)methyl]-4-(3-methylbut-2-en-1-yl)-4,5-dihydro-1,2,4-oxadiazol-5-one], which suppresses the expression of LEE genes. Grlactin significantly diminished the adhesion of EHEC strain EDL933 to human epithelial cells without inhibiting bacterial growth. These findings suggest that the developed screening system was effective at identifying GrlA inhibitors, and Grlactin has potential for use as a novel anti-adhesion agent for EHEC while reducing the incidence of resistance.