TY - JOUR
T1 - Altered Profiles of Gut Microbiota in Klebsiella pneumoniae-Induced Pyogenic Liver Abscess
AU - Chen, Nan
AU - Ling, Zong Xin
AU - Jin, Tong Tong
AU - Li, Ming
AU - Zhao, Sheng
AU - Zheng, Li Shuang
AU - Xi, Xin
AU - Wang, Lin Lin
AU - Chen, Ying Ying
AU - Shen, Yue Liang
AU - Zhang, Li Ping
AU - Sun, Shao cong
N1 - Funding Information:
Funding This study was sported by Natural Science Foundation of Hebei Province (No. H2015201076), National Natural Science Foundation of China (No. 81000760), Medical Construction Special Project of Hebei University (No. 2014A2003).
Funding Information:
We thank the support from Affiliated Hospital of Hebei University Postdoctoral workstation and Hebei University Biology Postdoctoral research station. We also thank the support from Key Bioengineering Discipline of Hebei Province. Nan Chen and Zong-Xin Ling have contributed equally to this work.
Funding Information:
Biology Postdoctoral research station. We also thank the support from Key Bioengineering Discipline of Hebei Province.
Funding Information:
Acknowledgements We thank the support from Affiliated Hospital of Hebei University Postdoctoral workstation and Hebei University
Publisher Copyright:
© 2018, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2018/7/1
Y1 - 2018/7/1
N2 - Intestinal microbiota plays a crucial role in preventing the colonization and invasion by pathogens, and disruption of microbiota may cause opportunistic infections and diseases. Pathogens often have strategies to escape from the colonization resistance mediated by microbiota, but whether they also modulate the microbiota composition is still a topic of investigation. In the present study, we addressed this question using an opportunistic pathogen, Klebsiella pneumoniae serotype K1, which is known to cause pyogenic liver abscess (KLA) in about 30% of mice. We examined the effect of K. pneumoniae infection on cecal microbiota composition by performing high-throughput 454 pyrosequencing of the hypervariable V3–V4 regions of bacterial 16S rRNA gene. Our data revealed that K. pneumoniae inoculation substantially changed the cecal microbiota composition when analyzed at the phylum, order, and family levels. Most strikingly, the KLA-infected mice had significantly increased abundance of Bacteroidales and Enterobacteriales and decreased abundance of Lactobacillales and Eggerthellales. Furthermore, by comparing the infected mice with or without KLA disease symptoms, we identified specific microbiota changes associated with the KLA disease induction. Especially, the KLA group had dramatically decreased sequence identical to Lactobacillus compared with non-KLA mice. These findings suggest that the pathogenic process of KLA infection may involve alteration of microbiota compositions, particularly reduction in Lactobacillus.
AB - Intestinal microbiota plays a crucial role in preventing the colonization and invasion by pathogens, and disruption of microbiota may cause opportunistic infections and diseases. Pathogens often have strategies to escape from the colonization resistance mediated by microbiota, but whether they also modulate the microbiota composition is still a topic of investigation. In the present study, we addressed this question using an opportunistic pathogen, Klebsiella pneumoniae serotype K1, which is known to cause pyogenic liver abscess (KLA) in about 30% of mice. We examined the effect of K. pneumoniae infection on cecal microbiota composition by performing high-throughput 454 pyrosequencing of the hypervariable V3–V4 regions of bacterial 16S rRNA gene. Our data revealed that K. pneumoniae inoculation substantially changed the cecal microbiota composition when analyzed at the phylum, order, and family levels. Most strikingly, the KLA-infected mice had significantly increased abundance of Bacteroidales and Enterobacteriales and decreased abundance of Lactobacillales and Eggerthellales. Furthermore, by comparing the infected mice with or without KLA disease symptoms, we identified specific microbiota changes associated with the KLA disease induction. Especially, the KLA group had dramatically decreased sequence identical to Lactobacillus compared with non-KLA mice. These findings suggest that the pathogenic process of KLA infection may involve alteration of microbiota compositions, particularly reduction in Lactobacillus.
UR - https://www.scopus.com/pages/publications/85045142784
UR - https://www.scopus.com/pages/publications/85045142784#tab=citedBy
U2 - 10.1007/s00284-018-1471-7
DO - 10.1007/s00284-018-1471-7
M3 - Article
C2 - 29637226
AN - SCOPUS:85045142784
SN - 0343-8651
VL - 75
SP - 952
EP - 959
JO - Current Microbiology
JF - Current Microbiology
IS - 7
ER -