Genetic Study of Capsular Switching between Neisseria meningitidis Sequence Type 7 Serogroup A and C Strains

Author:

Wang Quan123,Shao Zhujun4,Wang Xiaoting123,Gao Yuan4,Li Machao4,Xu Li4,Xu Jianguo14,Wang Lei12356

Affiliation:

1. TEDA School of Biological Sciences and Biotechnology, Nankai University, TEDA, Tianjin, China

2. Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, Tianjin, China

3. The Engineering and Research Center for Microbial Functional Genomics and Detection Technology, Ministry of Education, Tianjin, China

4. National Institute for Communicable Disease Control and Prevention and State Key Laboratory for Infectious Disease Prevention and Control, Chinese Center for Disease Control and Prevention, Beijing, China

5. Tianjin Key Laboratory of Microbial Functional Genomics, Tianjin, China

6. Tianjin Research Center for Functional Genomics and Biochip, Tianjin, China

Abstract

ABSTRACT Neisseria meningitidis is a leading cause of septicemia and meningitis worldwide. N. meningitidis capsular polysaccharides have been classified into 13 distinct serogroups which are defined by antibody reactivity and structural analysis, and the capsule plays an important role in virulence. Serogroups A, B, C, W135, and Y have been reported to be clinically important. Several newly identified serogroup C isolates belonging to the unique sequence type 7 (ST-7) were identified in China. Since most ST-7 isolates from China belonged to serogroup A, the newly identified ST-7 serogroup C strains were proposed to have arisen from those belonging to ST-7 serogroup A. In this study, six ST-7 serogroup C and three ST-7 serogroup A isolates were analyzed by pulsed-field gel electrophoresis to confirm their sequence type. In order to clarify the genetic basis of capsular switching between ST-7 serogroup A and C strains, the whole capsular gene clusters and surrounding genes of the two representative ST-7 strains belonging to serogroups A and C, respectively, were sequenced and compared. Potential recombination sites were analyzed using the RDP3 beta software, and recombination-related regions in two other ST-7 serogroup A and five ST-7 serogroup C strains were also sequenced and compared to the representative ST-7 serogroup A and C strain sequences.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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