3.Two Cases of Campylobacter fetus Septicemia.
Yunsop CHONG ; Yoon Chung KIM ; Samuel Y LEE ; Young Myoung MOON
Yonsei Medical Journal 1979;20(1):56-60
Campylobacter fetus subsp. intestinalis was isolated from the blood of two different patients. One patient was a 46-year-old male with liver cirrhosis and the other a 44-year-old male with co1on carcinoma. These are the second and third documented infections of this kind in Korea. Difficulties of their isolation were well illustrated. For instance, the growth was detected after a long incubation of 4 to 6 days. All of the 3 blood cultures from the carcinoma patient, but on1y 2 of 3 specimens from the other patient, yielded the organism.
Adult
;
Campylobacter/isolation & purification*
;
Campylobacter Infections/microbiology
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Campylobacter fetus/isolation & purification*
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Colonic Neoplasms/microbiology
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Culture Media
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Human
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Liver Cirrhosis/microbiology
;
Male
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Middle Age
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Septicemia/microbiology*
4.Multi-PCR identification and virulence genes detection of Campylobacter jejuni isolated from China.
Mao-jun ZHANG ; Yi-xin GU ; Lu RAN ; Jian-zhong ZHANG
Chinese Journal of Epidemiology 2007;28(4):377-380
OBJECTIVEThis study was to simultaneously identify Campylobacter jejuni and Campylobacter coli isolates in China by Multi-PCR assay and to study the prevalence of six virulence and toxin genes on them.
METHODSA multi-PCR method with three sets of primers specifically designed for application of a 16S rRNA as a universal control, mapA, ceuE based on the specific sequence of C. jejuni and C. coli, was applied to detect 65 Campylobacter isolates from China. Another two separately PCR Primers were directed towards the hippuricase gene (hipO) characteristic of C.jejuni and glyA gene characteristic of C. coli were performed for further confirmation. The presence of the cadF, virB11, flaA, cdtA, cdtB, cdtC genes among these 65 strains were investigated by PCR.
RESULTSFrom multi-PCR detection, 42 isolates belonged to C. jejuni, other 23 isolates belong to C. coli. Data showing the identification were 100% in concordance with the separated PCR for hipO and glyA amplification. The efficiency (100%) of identification by these three primers multi-PCR method was higher than the biochemical test (83.1%). The cadF and flaA genes were detected from 100% (65/65) of the isolates and the PCR product of each gene were identical with each isolate. Only 10.8% (7/65) of the isolates were positive for virB11. The cdtA gene was found in 92% (60/65) of the isolates. 97.6% (41/42) of C. jejuni had cdtB gene, whereas no PCR product with this primers for all the C. coli isolates. cdtC was presented in all the isolates but the lengths of PCR products were different. For C. jejuni, it was 555 bp, for C. coli, it was about 465 bp.
CONCLUSIONThis three primers simultaneous multi-PCR method seemed to be useful for the identification of C. jejuni and C. coli isolates from China since cadF and flaA genes were widely spread in Campylobacter isolates in this country. The present report on virB11 was similar to previous reports from other countries, but the distribution of cdt gene cluster in Campylobacter species isolated from China might be different.
Campylobacter coli ; genetics ; isolation & purification ; pathogenicity ; Campylobacter jejuni ; genetics ; isolation & purification ; pathogenicity ; China ; DNA Primers ; Genes, Bacterial ; Polymerase Chain Reaction ; Virulence ; genetics
5.Establishment of immunomagnetic capture-fluorescent PCR detection method for Campylobacter jejuni.
Guang-Ming LIU ; Wen-Jin SU ; Hui-Nong CAI ; Ming-Xing XIE ; Tang LIU ; Xiao-Li PENG
Chinese Journal of Biotechnology 2005;21(2):336-340
In order to develop a rapid method which can check Campylobacter jejuni in animal and poultry foods nicely, an immunomagnetic capture-fluorescent PCR (IMC-FPCR) method was established in this paper. The reported method involves isolation of the target pathogen by immunocapture prior to the fluorescent PCR step, therefore the immunomagnetic-beads for Campylobacter were developed, and two groups of primer/probe, which targeted for the species special sequence of flaA gene and hipO gene for Campylobacter jejuni were designed. The immunomagnetic capture-fluorescent PCR assay amplification of the hipO gene and flaA gene for detection of Campylobacter jejuni was firstly reported in this paper. Result indicated that IMC-FPCR method permits direct detection of the pathogen without an enrichment step and can be performed in approximately 24 h. The assay results are positive for all of the isolates of Campylobacter jejuni (3 isolates, including type strain ATCC 33560 and ATCC8341) with a detection limit of approximately 10 cfu/mL, are negative for Campylobacter coli and several other bacteria. IMC-FPCR assay provide not only a rapid, sensitive method for quantitative detection of Campylobacter jejuni, but also an important method for detecting of Campylobacter jejuni of viable but non-culturerable (VNC) state.
Campylobacter jejuni
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genetics
;
isolation & purification
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Fluorescence
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Immunomagnetic Separation
;
methods
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Polymerase Chain Reaction
;
methods
;
Sensitivity and Specificity
6.Pyogenic arthritis of the hip due to Campylobacter fetus: a case report.
Chan Dong HAN ; Jin Woo LEE ; Yunsop CHONG
Yonsei Medical Journal 1992;33(1):87-90
Septic arthritis of the hip caused by Campylobacter fetus subsp. fetusis very rare. The authoris isolated C. fetus subsp. fetus from a specimen of the left hip. The patient was a 53-year old man with a history of heavy drinking, diabetes, and chronic hepatitis, and had been suffering from avascular necrosis of both femoral heads. It was considered that the organism invaded already damaged tissue of the joint. The patient was treated with intravenous antibiotics and later received successful total hip replacement.
Arthritis, Infectious/*etiology
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*Campylobacter Infections
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Campylobacter fetus/*isolation & purification
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Case Report
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Femur Head Necrosis/etiology
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Hip/*microbiology
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Human
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Male
;
Middle Age
7.Investigation of campylobacter jejuni infection in children with diarrhea in Guangzhou.
Yong-Qiang XIE ; Zhen-Wen ZHOU ; Yan GUO ; Qiu-Lian DENG ; Yong HUANG
Chinese Journal of Contemporary Pediatrics 2009;11(6):422-424
OBJECTIVETo investigate the incidence of campylobacter jejuni (CJ) infection and the drug resistance of CJ in children with diarrhea in Guangzhou.
METHODSThe fecal samples of 3,351 children with diarrhea between July 2005 and June 2008 were collected for CJ culture. The species of CJ strains were identified by Lior methods. The drug susceptibility tests were performed by the Kirby-Bauer method.
RESULTSTwo hundred and sixty-seven CJ strains (8.0%) were isolated from 3,351 samples. The children at age of 1 month to 1 year were susceptible to CJ, accounting for 91.0%. A higher incidence of CJ infection (76.8%) was found in summer and autumn. The CJ strains were susceptible to imipenem, amikacin, cefoperazone/sulbactam, chloramphenicol, macrolides and lincomycins. Parts of CJ strains (20%-40%) were resistant to ampicillin, quinolones and ambramycin. All CJ strains were resistant to sulfamethoxazole/trimethoprim and cefditoren. Two hundred and one strains (75.3%) were CJ biotype I.
CONCLUSIONSCJ is an important pathogen of diarrhea in children from Guangzhou. CJ is resistant to some antibiotics used often in clinical practice, and so it is thus important to use antibiotics based on the results of drug susceptibility tests in children with CJ infection.
Campylobacter Infections ; microbiology ; Campylobacter jejuni ; classification ; drug effects ; isolation & purification ; Child, Preschool ; Diarrhea ; microbiology ; Female ; Humans ; Infant ; Male ; Microbial Sensitivity Tests
8.A case of chronic inflammatory demyelination polyradiculopathy related to Campylobacter jejuni infection in human and animals.
Chao LIU ; Fang-cheng CAI ; Qin LI ; Li LI ; Ping YIN
Chinese Journal of Pediatrics 2004;42(4):308-309
Animals
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Antibodies, Bacterial
;
blood
;
Campylobacter Infections
;
complications
;
microbiology
;
Campylobacter jejuni
;
isolation & purification
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Child, Preschool
;
Enzyme-Linked Immunosorbent Assay
;
Fatal Outcome
;
Humans
;
Male
;
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
;
etiology
;
Swine
9.Evaluation of the Impact of Automated Specimen Inoculation, Using Previ Isola, on the Quality of and Technical Time for Stool Cultures.
Alexander MISCHNIK ; Marlies TRAMPE ; Stefan ZIMMERMANN
Annals of Laboratory Medicine 2015;35(1):82-88
BACKGROUND: This study was designed as a quasi-experiment to evaluate automatic inoculation of fecal specimens, using the automated specimen inoculator Previ Isola (bioMerieux, France). METHODS: We evaluated the quality of cultures, recovery rates of enteropathogenic bacteria (Salmonella, Shigella, Campylobacter, and Yersinia species), and cost-effectiveness in terms of technical time. The Previ Isola recovery rates for the two-year period from August 2009 to July 2011 were compared with historical manual inoculation data of the previous two years (August 2007 to July 2009). The regional (Baden-Wurttemberg) and nationwide (Germany) trends of recovery rates for this four-year period were referred. RESULTS: A total of 5,884 fecal specimens were collected over the study period. Most positive cultures were for Salmonella, followed by Campylobacter. Compared with the historical data, the numbers of Campylobacter-positive specimens for a year between August and July were increased significantly, from 19 in 2007-2008 and 10 in 2008-2009 to 32 in 2009-2010 (P=0.002) and 32 in 2010-2011 (P=0.003), respectively. During the study period, the official data for our region and nationwide did not show this increase in the recovery rate of Campylobacter. For Salmonella, Shigella, and Yersinia, no significant changes were observed. Compared with manual inoculation, the mean hands-on time with Previ Isola inoculation was significantly shortened, from 37:30 min to 8:42 min per 15 fecal specimens. CONCLUSIONS: Inoculation by Previ Isola improves the quality of routine culture of fecal specimens, with better sensitivity for Campylobacter and less hands-on time.
Automation
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Bacteria/*isolation & purification
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Bacteriological Techniques/*methods/standards
;
Campylobacter/isolation & purification
;
Feces/*microbiology
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Humans
;
Quality Control
;
Salmonella/isolation & purification
;
Shigella/isolation & purification
;
Yersinia/isolation & purification
10.Antimicrobial susceptibility of Campylobacter fetus subsp. fetus isolated from blood and synovial fluid.
So Yong KWON ; Dong Hee CHO ; Samuel Y LEE ; Kyungwon LEE ; Yunsop CHONG
Yonsei Medical Journal 1994;35(3):314-319
Campylobacter fetus subsp. fetus is a rare human pathogen, but can cause serious extraintestinal infections. Effective antimicrobial agent is required for the therapy, but we have very limited knowledge on the susceptibility of the organism. In this study, the susceptibility of 25 isolates of the organism to 14 antimicrobial agents was tested by an agar dilution method. Antimicrobial agents with low MIC ranges, in micrograms/ml, were: meropenem Y or = 0.25, dirithromycin < or = 0.5, gentamicin > or = 1, amikacin, ofloxacin, tetracycline and erythromycin < or = 2. The MIC range of cefepime was 0.5-8 micrograms/ml, but those of other beta-lactams were relatively high. All of the isolates were interpreted to be susceptible to cefepime, meropenem, amikacin, gentamicin, ofloxacin, tetracycline and dirithromycin. A significant proportion of the isolates were either intermediate or resistant to ampicillin, cephalothin, cefotaxime, aztreonam, loracarbef and erythromycin. In conclusion, the organism remains susceptible to aminoglycosides and tetracycline. Greater in vitro activity of meropenem, ofloxacin and dirithromycin require clinical evaluation.
Antibiotics/*pharmacology
;
Blood/*microbiology
;
Campylobacter fetus/*drug effects/isolation & purification
;
Human
;
Microbial Sensitivity Tests
;
Synovial Fluid/*microbiology