The antibiotic resistance and pathogenicity of a multidrug‐resistant Elizabethkingia anophelis isolate
Abstract Elizabethkingia anophelis 12012‐2 PRCM was isolated from a patient with multiple organ dysfunction syndrome and lower respiratory tract infection in China. Minimum inhibitory concentration (MIC) analysis demonstrated that it was resistant to 20 antibiotics including trimethoprim/sulfamethox...
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doaj-497688e90b2441f8957e78fe126e15c92020-11-24T21:45:55ZengWileyMicrobiologyOpen2045-88272019-11-01811n/an/a10.1002/mbo3.804The antibiotic resistance and pathogenicity of a multidrug‐resistant Elizabethkingia anophelis isolateMingxi Wang0Hongzhi Gao1Nanfei Lin2Yaping Zhang3Nan Huang4Edward D. Walker5Desong Ming6Shicheng Chen7Shaohua Hu8Yun Leung Laboratory for Molecular Diagnostics, School of Medicine Huaqiao University Xiamen, Fujian ChinaClinical Center for Molecular Diagnosis and Therapy Fujian Medical University 2nd Affiliated Hospital Quanzhou, Fujian ChinaClinical Center for Molecular Diagnosis and Therapy Fujian Medical University 2nd Affiliated Hospital Quanzhou, Fujian ChinaDepartment of Pulmonary and Critical Care Medicine Fujian Medical University 2nd Affiliated Hospital Quanzhou, Fujian ChinaQuanzhou Medical College Quanzhou, Fujian ChinaDepartment of Microbiology and Molecular Genetics Michigan State University East Lansing MichiganDepartment of Clinical Laboratory Quanzhou First Hospital Affiliated to Fujian Medical University Fujian ChinaDepartment of Microbiology and Molecular Genetics Michigan State University East Lansing MichiganState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases The First Affiliated Hospital of Medical College, Zhejiang University Hangzhou, Zhejiang ChinaAbstract Elizabethkingia anophelis 12012‐2 PRCM was isolated from a patient with multiple organ dysfunction syndrome and lower respiratory tract infection in China. Minimum inhibitory concentration (MIC) analysis demonstrated that it was resistant to 20 antibiotics including trimethoprim/sulfamethoxazole and ciprofloxacin, which were effective for the elimination of other Elizabethkingia infections. To investigate multidrug resistance and pathogenicity mechanisms, we analyzed genome features of 12012‐2 PRCM and compared them to the other Elizabethkingia species. The draft genome size was 4.02 Mb with a GC content of 32%, comparable to that of other E. anophelis strains. Phylogenetic analysis showed that E. anophelis 12012‐2 PRCM formed a sister group with E. anophelis 502, distinct from clades formed by other clinical and environmental E. anophelis isolates. E. anophelis 12012‐2 PRCM contained multiple copies of β‐lactamase genes as well as genes predicted to function in antimicrobial efflux. It also contained 92 genes that were potentially involved in virulence, disease, and defense, and were associated with resistance and pathogenicity. Comparative genomic analysis showed high homology among three clinical and two environmental E. anophelis strains having a variety of similar antibiotic resistance and virulence factor genes, and similar genomic structure. Applications of this analysis will contribute to understanding the antibiotic resistance and pathogenic mechanisms of E. anophelis infections, which will assist in the management of infections as it increases in prevalence.https://doi.org/10.1002/mbo3.804antibiotic resistance mechanismscomparative genomic analysisElizabethkingia anophelisgenome sequencingpathogenicity mechanisms |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mingxi Wang Hongzhi Gao Nanfei Lin Yaping Zhang Nan Huang Edward D. Walker Desong Ming Shicheng Chen Shaohua Hu |
spellingShingle |
Mingxi Wang Hongzhi Gao Nanfei Lin Yaping Zhang Nan Huang Edward D. Walker Desong Ming Shicheng Chen Shaohua Hu The antibiotic resistance and pathogenicity of a multidrug‐resistant Elizabethkingia anophelis isolate MicrobiologyOpen antibiotic resistance mechanisms comparative genomic analysis Elizabethkingia anophelis genome sequencing pathogenicity mechanisms |
author_facet |
Mingxi Wang Hongzhi Gao Nanfei Lin Yaping Zhang Nan Huang Edward D. Walker Desong Ming Shicheng Chen Shaohua Hu |
author_sort |
Mingxi Wang |
title |
The antibiotic resistance and pathogenicity of a multidrug‐resistant Elizabethkingia anophelis isolate |
title_short |
The antibiotic resistance and pathogenicity of a multidrug‐resistant Elizabethkingia anophelis isolate |
title_full |
The antibiotic resistance and pathogenicity of a multidrug‐resistant Elizabethkingia anophelis isolate |
title_fullStr |
The antibiotic resistance and pathogenicity of a multidrug‐resistant Elizabethkingia anophelis isolate |
title_full_unstemmed |
The antibiotic resistance and pathogenicity of a multidrug‐resistant Elizabethkingia anophelis isolate |
title_sort |
antibiotic resistance and pathogenicity of a multidrug‐resistant elizabethkingia anophelis isolate |
publisher |
Wiley |
series |
MicrobiologyOpen |
issn |
2045-8827 |
publishDate |
2019-11-01 |
description |
Abstract Elizabethkingia anophelis 12012‐2 PRCM was isolated from a patient with multiple organ dysfunction syndrome and lower respiratory tract infection in China. Minimum inhibitory concentration (MIC) analysis demonstrated that it was resistant to 20 antibiotics including trimethoprim/sulfamethoxazole and ciprofloxacin, which were effective for the elimination of other Elizabethkingia infections. To investigate multidrug resistance and pathogenicity mechanisms, we analyzed genome features of 12012‐2 PRCM and compared them to the other Elizabethkingia species. The draft genome size was 4.02 Mb with a GC content of 32%, comparable to that of other E. anophelis strains. Phylogenetic analysis showed that E. anophelis 12012‐2 PRCM formed a sister group with E. anophelis 502, distinct from clades formed by other clinical and environmental E. anophelis isolates. E. anophelis 12012‐2 PRCM contained multiple copies of β‐lactamase genes as well as genes predicted to function in antimicrobial efflux. It also contained 92 genes that were potentially involved in virulence, disease, and defense, and were associated with resistance and pathogenicity. Comparative genomic analysis showed high homology among three clinical and two environmental E. anophelis strains having a variety of similar antibiotic resistance and virulence factor genes, and similar genomic structure. Applications of this analysis will contribute to understanding the antibiotic resistance and pathogenic mechanisms of E. anophelis infections, which will assist in the management of infections as it increases in prevalence. |
topic |
antibiotic resistance mechanisms comparative genomic analysis Elizabethkingia anophelis genome sequencing pathogenicity mechanisms |
url |
https://doi.org/10.1002/mbo3.804 |
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