• 제목/요약/키워드: Intestine bacteria

검색결과 209건 처리시간 0.021초

유산간균 Lactobacilli 경구투여에 의한 자돈의 장내균총형성 및 증체에 미치는 영향 (Studies of the effect of dietary lactobacilli on the intestinal flora and body weight gains in suckling piglets)

  • 윤성식
    • 한국식품영양학회지
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    • 제1권1호
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    • pp.33-40
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    • 1988
  • A Study was conducted to investigate the effect of feeding Lactobacillus casei YS on the growing performance and gastrointestinal flora of the suckling piglets, which were delivered from 2 heads of three-way crossbred(Landrace$\times$Large White$\times$Duroc) pigs, for 4 weeks. The results from the present study was summarized as follows. Average body weight gains of feeding group was slightly better than that of control group and diarrhea was prevented by successive 7 days feeding. Population levels of lactic acid bacteria were maintained about 107 colony forming unit(cfu) per gram of the contents in both feeding and control group at upper parts of small intestine. In this part, coliform count was greatly reduced in (ceding group but not in control group. pH values of the intestinal contents were gradually decreased especially at the upper part of alimentary track of feeding group. Among lactic acid bacteria, L. salivarius, L. cases and L. fermentum were found most predominant strains in feeding group, Wheareas L. salivarius, L. acidophilus and L. cunts in control group. In the other hand, Escherichia coli recovered from scouring pigs were resistant to the drug such as streptomycin, ampicillin and sensitive to gentamycin and neomycin in vitro test.

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넙치(Paralichthys olivaceus) 장관의 배양 및 비배양 방법에 의한 세균의 다양성 (Diversity of Cultured and Uncultured Bacteria in the Gut of Olive Flounder Paralichthys olivaceus)

  • 김아란;김도형
    • 한국수산과학회지
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    • 제48권4호
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    • pp.447-453
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    • 2015
  • We determined the optimal culture conditions for obtaining the maximum number of intestinal bacteria from the olive flounder Paralichthys olivaceus, and studied bacterial diversity using both culture-dependent and culture-independent methods. Using six culture conditions, mean bacterial numbers were greater than $10^6$ per gram of gut mucus, regardless of the medium. However, the bacterial diversity, based on colony morphology, appeared much higher on Marine agar (MA) and Zobell 2216 agar than on other media. We found eight and 17 cultured bacterial phylotypes with 99% minimum similarity in gut mucus grown on MA and tryptic soy agar, respectively. Furthermore, we used genomic DNA extracted from gut mucus to generate 78 random clones, which were grouped into 25 phylotypes. Of these, six were affiliated with Firmicutes, Actinobacteria, and Verrucomicrobia, and were not found using our culture-dependent methods. Consequently, we believe that Marine agar and Zobell 2216 agar are optimal media for culturing diverse intestinal microbes; we also discovered several novel sequences not previously recognized as part of the gut microbiota of olive flounder.

A Mixed Formulation of Lactic Acid Bacteria Inhibits Trinitrobenzene-Sulfonic-Acid-Induced Inflammatory Changes of the Colon Tissue in Mice

  • Cha, Yeon Suk;Seo, Jae-Gu;Chung, Myung-Jun;Cho, Chung Won;Youn, Hyun Joo
    • Journal of Microbiology and Biotechnology
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    • 제24권10호
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    • pp.1438-1444
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    • 2014
  • Lactic acid bacteria (LAB) are probiotics that provide numerous beneficial effects on the host body, especially on the intestine. Combining several strains of LAB, we prepared a formulation containing four different LAB and studied its anti-inflammatory activity both in vitro and in vivo. The formulation significantly reduced NO production from RAW 264.7 cells treated with bacterial lipopolysaccharide, indicating that the formulation might include anti-inflammatory activity. The formulation also suppressed inflammatory change induced by trinitrobenzene sulfonic acid (TNBS) in mice, where oral or rectal administration of the formulation protected the colon tissue from the damage by TNBS. Expressions of the IL-6 and FasL genes appeared to be down-regulated by the formulation in TNBS-treated colon tissues, suggesting that the suppression of those genes may be involved in the anti-inflammatory activity of the formulation.

Lactobacillus plantarumCLP-1이 돼지바이러스에 미치는 효과 (The Effect of Lactobacillus plantarumCLP-1 on the Swine Viruses)

  • 이건희;김영희;조현아;강성기;김동건
    • KSBB Journal
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    • 제26권1호
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    • pp.62-68
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    • 2011
  • To isolate Lactic acid bacteria for animals, we have screened from Kim-chi, swine intestine, swine feces, and dairy products by random selection and anti-viral, antipathogenic bacteria test. Among them, CLP-1 shown that inhibitory effect against rotavirus, porcine epidemic diarrhea (PED) virus, Salmonella sp, and E.coli. By examining biological property, API-ZYM and identified Lactobacillus plantarum by 16S rDNAgene sequence. CLP-1 determined resistance to low pH and bile salt. Futhermore, the cell body of CLP-1 adhered to the intestinal epithelium tissue of swine and Caco-2 cell. CLP-1 was examined on cell immune system modulating activity in vitro. The whole cell and cell culture supernatant was increasing of interferon-${\beta}$ activity. And then, CLP-1 increased prevention effect by Salmonella enteritidis infection in SPF chickens. And we determined similar result in pigs.

An integrated DNA barcode assay microdevice for rapid, highly sensitive and multiplex pathogen detection at the single-cell level

  • Jung, Jae Hwan;Cho, Min Kyung;Chung, So Yi;Seo, Tae Seok
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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    • pp.276-276
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    • 2013
  • Here we report an integrated microdevice consisting of an efficient passive mixer, a magnetic separation chamber, and a capillary electrophoretic microchannel in which DNA barcode assay, target pathogen separation, and barcode DNA capillary electrophoretic analysis were performed sequentially within 30 min for multiplex pathogen detection at the single-cell level. The intestine-shaped serpentine 3D micromixer provides a high mixing rate to generate magnetic particle-pathogenic bacteria-DNA barcode labelled AuNP complexes quantitatively. After magnetic separation and purification of those complexes, the barcode DNA strands were released and analyzed by the microfluidic capillary electrophoresis within 5 min. The size of the barcode DNA strand was controlled depending on the target bacteria (Staphylococcus aureus, Escherichia coli O157:H7, and Salmonella typhimurium), and the different elution time of the barcode DNA peak in the electropherogram allows us to recognize the target pathogen with ease in the monoplex as well as in the multiplex analysis. In addition, the quantity of the DNA barcode strand (~104) per AuNP is enough to be observed in the laser-induced confocal fluorescence detector, thereby making single-cell analysis possible. This novel integrated microdevice enables us to perform rapid, sensitive, and multiplex pathogen detection with sample-in-answer-out capability to be applied for biosafety testing, environmental screening, and clinical trials.

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Intestinal Bacterial ${\beta}-Glucuronidase$ Activity of Patients with Colon Cancer

  • Kim, Dong-Hyun;Jin, Young-Ho
    • Archives of Pharmacal Research
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    • 제24권6호
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    • pp.564-567
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    • 2001
  • The fecal ${\beta}-glucuronidase$ activity of patients with colon cancer and healthy controls were measured to determine the relationship between the fluctuation of intestinal bacterial ${\beta}-glucuronidase$ and colon cancer. The fecal ${\beta}-glucuronidase$ activity of patients with colon cancer was 1.7 times higher than that of the healthy controls. However, when these fecal specimens were sonicated, the enzyme activity of patients with colon cancer was 12.1 times higher than that of the healthy controls. The fecal ${\beta}-glucuronidase$ activity of human Intestinal bacteria was drastically induced by its substrate or the bile secreted after a subcutaneous injection of 1,2-dimethylhydrazine (DMH) and benzo[a]pyrene into rats. DMH-and benzo[a]pyrene-treated biles induced ${\beta}-glucuronidase$ activity in the human intestinal microflora by approximately 1.5- and 2.3-fold, respectively. They also induced ${\beta}-glucuronidase$ in E. coli HGU-3, which is a ${\beta}-glucuronidase$-producing bacterium from the human intestine. D-saccharic acid 1,4-lactone similarly inhibited fecal ${\beta}-glucuronidase$ in several patients with colon cancer in addition to the healthy controls. This suggests that potent ${\beta}-glucuronidase$ activity is a prime factor in the etiology of colon cancer.

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Fatal Peritonitis associated with Pasteurella multocida in an Asian Small-Clawed Otter (Aonyx cinereus)

  • Kyung-Seok Na;Hyoung-Seok Yang;Won-Hee Hong;Jae-Hoon Kim
    • 한국임상수의학회지
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    • 제41권1호
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    • pp.54-59
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    • 2024
  • A 12-year-old female small-clawed Asian otter (Anoyx cinereus) with a one-week history of anorexia, chills, and abdominal distension was found dead. Grossly, yellowish-brown turbid fluids accumulated in abdominal cavity of the otter, and yellowish thread-like fibrinous materials were found on the surface of abdominal organs. Several variable sized yellowish-white crystalloids were scattered on the medullary space of kidneys. Histologically, diffuse serositis (peritonitis) characterized by the fibrinous exudates, thickened serosal capsule and the swelling of mesothelial cells were observed in the serosa of liver, spleen, stomach, and intestine. Multifocal necrosis, hemorrhage, infiltration of macrophage, and brown pigments were presented in the liver. Isolated bacteria from ascites and fibrinous materials in abdominal visceral surface were white, smooth and convex with characteristic mousy odor on blood agar plate. These bacteria were confirmed as Pasteurella (P.) multocida type A by polymerase chain reaction analysis. Based on the gross examination, histopathologic findings and bacterial experiments, this otter was diagnosed as severe peritonitis associated with P. multocida and necrotic hepatitis.

16S rDNA 염기서열 분석을 통한 제주연안 소라(Turbo cornutus) 장내세균 다양성 조사 (Analysis of Intestinal Microbial Communities of Topshell (Turbo cornutus) fromCoast of Jeju Island, Korea by 16S rDNA Sequence Analysis)

  • 김민선;한송헌;최정화;허문수;고준철
    • 생명과학회지
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    • 제32권9호
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    • pp.721-728
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    • 2022
  • 본 논문은 제주연안에서 채집한 소라(Turbo cornutus)의 장내세균을 분리하고 군집의 다양성을 조사하였다. 표준배지를 사용하여 순수 정체 배양 결과 MA agar에서 가장 많은 군집을 나타났다. 일반 배양 CFU값은 평균 1.8×105, 혐기 배양 CFU값은 평균 0.4×10으로 보다 적게 나타났다. 기존 표준균주와 16S rDNA sequence 유사도 비교 분석 결과 크게 4문 12과 26속 67종으로 분류되었다. 표준균주와의 상동성 범위는 93-100%로 나타났다. 소라장내세균 군집은 크게 Proteobacteria 39% (α-proteobacteria; Phyllobacteriaceae (1), Rhodobacteraceae (8) / γ-proteobacteria; Alteromonadaecae (1), Shewanellaceae (4), Vibrionaceae(12))로 가장 우점하였고, Firmicutes 34% (Bacillaceae (21), Paenibacillaceae (2)), Actinobacteria 21% (Cellulomonadaceae (1), Mycobacteriaceae (6), Nocardiaceae (4), Streptomycetacea (3)), Bacteroidetes 6% (Flavobacteriaceae (4))로 각각 나타났다. Bacillus sp., Vibrio sp.이 가장 우점 하였으며, 그 외 대부분의 분리 균주는 해양 유래 관련 균주로 나타났다. 이전 보고된 제주 연안에 서식하는 해양동물 장내세균군과 비슷한 양상을 보였다. 분리된 일부 균주가 단당류(Cellulose), 다당류(alginate, agar)분해능을 갖고 있는 것으로 나타났는데, 대부분이 해조류 유래 세균으로 소라의 섭이가 장내세균군과 관련됨을 알 수 있었다. 동시에 probiotics 기능을 갖고 있는 일부 균주도 분리되었다.

알긴산 나트륨을 이용한 유산균 캡슐화의 상업화 공정 개발 (Development of a Commercial Process for Micro-Encapsulation of Lactic Acid Bacteria Using Sodium Alginate)

  • 김지연;유성식
    • Korean Chemical Engineering Research
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    • 제55권3호
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    • pp.313-321
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    • 2017
  • 바이오 고분자인 알긴산 나트륨(Sodium Alginate)을 이용하여 기존의 방법에 비해 생산성이 우수한 캡슐화의 상업화 공정을 개발하고자 하였다. 또한, 동일 공정으로 키토산을 알긴산과 함께 캡슐화하여 알긴산 나트륨으로 캡슐화 된 유산균과 비교하였다. 유산균 캡슐화의 상업화 공정의 주요 공정은 캡슐화 후 기존의 동결건조 대신에 본 연구진이 개발한 생산성이 우수한 유동화 건조 방법에 의하여 건조시간을 15~24이상 단축할 수 있었지만, 생균수는 동결건조와 유동층 건조의 비율이 1:0.75로 동결건조 방법이 좋았다. 하지만 건조에 드는 비용과 시간을 고려 해 볼 때 유동층 건조 방법으로 상업화 공정이 가능함을 확인할 수 있었다. Chitosan-alginate 캡슐은 알긴산 칼슘캡슐과 생균수를 비교하였을 때, 알긴산을 이용한 캡슐은 희석배수 $10^{-9}$, 즉 약 $1{\times}10^9$ 마리 이상의 균이 존재하고, 키토산을 이용한 캡슐은 희석배수 $10^{-3}$, 즉 약 $1{\times}10^3$ 마리의 균이 존재함을 확인 할 수 있었다. 본 연구의 기술로 제조된 유산균 캡슐은 pH 4.65, 6.01에서 96시간 이상 동안 안정하였지만, pH 7.07, 8.35에서는 1시간 이내에 모두 붕해되었다. 이는 유산균 캡슐이 위산에서 안정성을 보이고 pH 7이상을 띠는 소화기관인 소장과 대장에서는 쉽게 붕해가 일어날 수 있음을 알 수 있었다.

Bacterial Diversity at Different Sites of the Digestive Tract of Weaned Piglets Fed Liquid Diets

  • Hong, Tran Thi Thu;Passoth, Volkmar;Lindberg, Jan Erik
    • Asian-Australasian Journal of Animal Sciences
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    • 제24권6호
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    • pp.834-843
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    • 2011
  • Bacterial diversity was studied using PCR-DGGE, cloning and sequencing. DNA was isolated from digesta samples from stomach, ileum and colon of 28 weaned piglets (Large White${\times}$Mong Cai) fed dry control feed, naturally fermented liquid feed (FE) and a liquid diet with inclusion of rice distiller's residue feed. General bacterial diversity was described using DGGE analysis of the V3 region of 16S rDNA. The microbial populations in the stomach and the ileum were considerably influenced by the diet, while only marginal effects were observed in the colon. There was a large variation of the microbial flora in the stomach between individuals fed non-fermented diets. In contrast, animals fed diet FE had a more uniform microbial flora in the stomach and the ileum compared to the other diets. In total 47 bands from the DGGE profiles were cloned. In stomach, most frequently lactic acid bacteria were found. Feeding diet FE resulted in the occurrence of Pediococcus species in stomach and ileum. In pigs fed the other diets, Lactobacillus gallinarum, Lactobacillus johnsonii and Lactobacillus fermentum were found in stomach and ileum. Most of the sequences of bands isolated from colon samples and several from ileum matched to unknown bacteria, which often grouped within Prevotellaceae, Enterobacteriaceae, Bacteroidaceae and Erysipelotrichaceae. This study demonstrates that fermented liquid feed affects bacterial diversity and the specific microflora in stomach and ileum, which provides a potential to modulate the gut microflora with dietary means to increase the abundance of beneficial bacteria and improve piglets' health.