Protective Immunity against Infection with Mycoplasma haemofelis

被引:10
|
作者
Hicks, Chelsea A. E. [1 ,4 ]
Willi, Barbara [2 ,3 ]
Riond, Barbara [2 ]
Novacco, Marilisa [2 ,4 ]
Meli, Marina L. [2 ,4 ]
Stokes, Christopher R. [1 ]
Helps, Christopher R. [1 ]
Hofmann-Lehmann, Regina [2 ,4 ]
Tasker, Severine [1 ]
机构
[1] Univ Bristol, Sch Vet Sci, Bristol BS18 7DU, Avon, England
[2] Univ Zurich, Clin Lab, Vetsuisse Facil, Zurich, Switzerland
[3] Univ Zurich, Clin Small Anim Internal Med, Vetsuisse Facil, Zurich, Switzerland
[4] Univ Zurich, Vetsuisse Facil, Ctr Clin Studies, Zurich, Switzerland
基金
英国生物技术与生命科学研究理事会;
关键词
REGULATORY T-CELLS; MARBOFLOXACIN TREATMENT; HAEMOBARTONELLA-FELIS; BARTONELLA-HENSELAE; CATS; HEMOPLASMA; DISEASE; INTERLEUKIN-12; COINFECTION; PREVALENCE;
D O I
10.1128/CVI.00581-14
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hemoplasmas are potentially zoonotic mycoplasmal pathogens, which are not consistently cleared by antibiotic therapy. Mycoplasma haemofelis is the most pathogenic feline hemoplasma species. The aim of this study was to determine how cats previously infected with M. haemofelis that had recovered reacted when rechallenged with M. haemofelis and to characterize the immune response following de novo M. haemofelis infection and rechallenge. Five specific-pathogen-free (SPF)-derived naive cats (group A) and five cats that had recovered from M. haemofelis infection (group B) were inoculated subcutaneously with M. haemofelis. Blood M. haemofelis loads were measured by quantitative PCR (qPCR), antibody response to heat shock protein 70 (DnaK) by enzyme-linked immunosorbent assay (ELISA), blood lymphocyte cell subtypes by flow cytometry, and cytokine mRNA levels by quantitative reverse transcriptase PCR. Group A cats all became infected with high bacterial loads and seroconverted, while group B cats were protected from reinfection, thus providing the unique opportunity to study the immunological parameters associated with this protective immune response against M. haemofelis. First, a strong humoral response to DnaK was only observed in group A, demonstrating that an antibody response to DnaK is not important for protective immunity. Second, proinflammatory cytokine interleukin-6 (IL-6) mRNA levels appeared to increase rapidly postinoculation in group B, indicating a possible role in protective immunity. Third, an increase in IL-12p35 and -p40 mRNA and decrease in the Th2/Th1 ratio observed in group A suggest that a Th1-type response is important in primary infection. This is the first study to demonstrate protective immunity against M. haemofelis reinfection, and it provides important information for potential future hemoplasma vaccine design.
引用
收藏
页码:108 / 118
页数:11
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