Journal
ARCHIVES OF MICROBIOLOGY
Volume 204, Issue 8, Pages -Publisher
SPRINGER
DOI: 10.1007/s00203-022-02987-7
Keywords
Human leptospirosis vaccine; Icterohaemorrhagiae serogroup; Proteomics; Epidemic isolate; China
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Funding
- National Key R&D Program of China [2018YFC1603900]
- National Natural Science Funds, China [81471968]
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This study analyzed the proteomic differences between the vaccine strain and circulating isolate of Leptospira interrogans serogroup Icterohaemorrhagiae in China. Many proteins showed differential expression between the two strains, including immunogenic and virulence-related proteins. Differences in carbohydrate, amino acid, and energy metabolism and transport were also observed, indicating potential metabolic diversity and adaptation of the pathogens to different environments.
Leptospira interrogans serogroup Icterohaemorrhagiae is the predominant pathogen causing leptospirosis in China and is still used as the vaccine strain for the current human inactivated vaccine. Unlike the clade ST17, which is distributed worldwide, ST1 is the most prevalent in serogroup Icterohaemorrhagiae in China. To further characterize leptospiral pathogens, isobaric tags for relative and absolute quantitation and parallel reaction monitoring were used to analyze differences at the proteomic level between serogroup Icterohaemorrhagiae vaccine strain 56001 (ST1) and circulating isolate 200502 (ST17) from different periods. Two hundred and eighty-one proteins were differentially expressed between the circulating isolate and vaccine strain, of which 166 were upregulated (> 1.2-fold change, P < 0.05) and 115 (< 0.8-fold change, P < 0.05) were downregulated. Function prediction revealed that nine upregulated proteins were outer membrane proteins, including several known immunogenic and/or virulence-related proteins, such as ompL1, LipL71, and LipL41. Furthermore, important expression differences in carbohydrate, amino acid, and energy metabolism and transport proteins were identified between both strains from different clusters, suggesting that these differences may reflect metabolic diversity and the potential of the pathogens to adapt to different environments. In summary, our findings provide insights into a better understanding of the component strains of the Chinese human leptospirosis vaccine at the proteomic level. Additionally, these data facilitate evaluating the mechanisms by which pathogenic Leptospira species adapt to the host environment.
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