Literature DB >> 27965724

Enterogenous infection of Candida albicans in immunocompromised rats under severe acute pancreatitis.

Xiang-Wang Zhao1, Lei Yan2, Dan Xu3, Yu-Hui Cui3, Chun-Hui Yang3, Yan-Jun Zhou4, Jian-Guo Tang3.   

Abstract

BACKGROUND: Opportunistic infection of Candida albicans (C. albicans) has become a serious problem in immunocompromised patients. The study aimed to explore the mechanism of enterogenous infection of C. albicans in immunocompromised rats under severe acute pancreatitis (SAP).
METHODS: Sprague Dawley (SD) rats (n=100) were randomly assigned into 5 groups as the following: blank group, cyclophosphamide+ceftriaxone+SAP group, cyclophosphamide+ceftriaxone group, cyclophosphamide+SAP group, and cyclophosphamide group. The rats were sacrificed at 5 and 10 days, and their jejunum, colon, mesenteric lymph nodes, pancreas, intestinal content, and blood were quickly collected to detect C. albicans. A region of the 25S rRNA gene was chosen and amplified by polymerase chain reaction (PCR) to differentiate C. albicans genotypes. The amplified products were further sequenced and compared to judge their homology.
RESULTS: Compared with the Cyclophosphamide group, the combination of immunosuppressants and broad-spectrum antibiotics significantly increased the colonization of C. albicans in intestine in 5 and 10 days. Pure SAP stress did not increase the opportunistic infection of C. albicans. The PCR products of C. albicans isolates all belonged to the genotype A family, and sequence alignment showed that the amplified fragments were homologous.
CONCLUSION: The damage of immune system and broad-spectrum antimicrobial agents are important risk factors for opportunistic fungal infection. Intestinal tract is an important source for genotype-A C. albicans to translocate and invade into bloodstream.

Entities:  

Keywords:  Candida albicans; Genotype; Immunosuppression; Severe acute pancreatitis

Year:  2016        PMID: 27965724      PMCID: PMC5153366          DOI: 10.5847/wjem.j.1920-8642.2016.04.010

Source DB:  PubMed          Journal:  World J Emerg Med        ISSN: 1920-8642


  22 in total

1.  Early gut barrier dysfunction in patients with severe acute pancreatitis: attenuated by continuous blood purification treatment.

Authors:  Jianbin Zhang; Chen Yuan; Gan Hua; Ruyan Tong; Xiangfeng Luo; Zhou Ying
Journal:  Int J Artif Organs       Date:  2010-10       Impact factor: 1.595

Review 2.  Disruption of the intestinal mucosal barrier in Candida albicans infections.

Authors:  Lei Yan; Chunhui Yang; Jianguo Tang
Journal:  Microbiol Res       Date:  2013-03-30       Impact factor: 5.415

3.  Genotype distribution of Candida albicans isolates by 25S intron analysis with regard to invasiveness.

Authors:  Z C Karahan; H Güriz; H Ağirbaşli; N Balaban; J S Göçmen; D Aysev; N Akar
Journal:  Mycoses       Date:  2004-12       Impact factor: 4.377

4.  Candida albicans versus non-albicans bloodstream infections: the comparison of risk factors and outcome.

Authors:  Hung-Wei Chi; Ya-Sung Yang; Shi-Ta Shang; Ke-Hung Chen; Kuo-Ming Yeh; Feng-Yee Chang; Jung-Chung Lin
Journal:  J Microbiol Immunol Infect       Date:  2011-01-20       Impact factor: 4.399

5.  Molecular and phenotypic characterization of genotypic Candida albicans subgroups and comparison with Candida dubliniensis and Candida stellatoidea.

Authors:  M J McCullough; K V Clemons; D A Stevens
Journal:  J Clin Microbiol       Date:  1999-02       Impact factor: 5.948

6.  Mortality, length of hospitalization, and costs associated with invasive fungal infections in high-risk patients.

Authors:  Joseph Menzin; Juliana L Meyers; Mark Friedman; John R Perfect; Amelia A Langston; Robert P Danna; George Papadopoulos
Journal:  Am J Health Syst Pharm       Date:  2009-10-01       Impact factor: 2.637

Review 7.  Yeasts in the gut: from commensals to infectious agents.

Authors:  Jürgen Schulze; Ulrich Sonnenborn
Journal:  Dtsch Arztebl Int       Date:  2009-12-18       Impact factor: 5.594

8.  The intestinal mucus layer is a critical component of the gut barrier that is damaged during acute pancreatitis.

Authors:  Jordan E Fishman; Gal Levy; Vamsi Alli; Xiaozhong Zheng; Damian J Mole; Edwin A Deitch
Journal:  Shock       Date:  2014-09       Impact factor: 3.454

9.  Melatonin reduces bacterial translocation by preventing damage to the intestinal mucosa in an experimental severe acute pancreatitis rat model.

Authors:  Xuecheng Sun; Yingying Shao; Yin Jin; Jiaping Huai; Qiong Zhou; Zhiming Huang; Jiansheng Wu
Journal:  Exp Ther Med       Date:  2013-10-10       Impact factor: 2.447

Review 10.  Epidemiology and risk factors for invasive candidiasis.

Authors:  Nur Yapar
Journal:  Ther Clin Risk Manag       Date:  2014-02-13       Impact factor: 2.423

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