Unbiased Proteomics Analysis Demonstrates Significant Variability in Mucosal Immune Factor Expression Depending on the Site and Method of Collection

被引:26
作者
Birse, Kenzie M. [1 ,2 ]
Burgener, Adam [1 ,2 ,6 ]
Westmacott, Garrett R. [3 ]
McCorrister, Stuart [3 ]
Novak, Richard M. [4 ]
Ball, T. Blake [1 ,2 ,5 ,6 ]
机构
[1] Univ Manitoba, Dept Med Microbiol, Winnipeg, MB, Canada
[2] Publ Hlth Agcy Canada, Natl Lab HIV Immunol, Prote Grp, Winnipeg, MB, Canada
[3] Publ Hlth Agcy Canada, Natl Microbiol Lab, Mass Spectrometry Core Facil, Winnipeg, MB, Canada
[4] Univ Illinois, Infect Dis Sect, Chicago, IL USA
[5] Univ Nairobi, Dept Med Microbiol, Nairobi, Kenya
[6] Publ Hlth Agcy Canada, Natl Lab HIV Immunol, Winnipeg, MB, Canada
基金
美国国家卫生研究院;
关键词
FEMALE GENITAL-TRACT; ANTI-HIV-1; ACTIVITY; HIV-1; INFECTION; MICROBICIDE; IDENTIFICATION; INFLAMMATION; PROTECTION; INHIBITOR; S100A8/A9; CYTOKINE;
D O I
10.1371/journal.pone.0079505
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Female genital tract secretions are commonly sampled by lavage of the ectocervix and vaginal vault or via a sponge inserted into the endocervix for evaluating inflammation status and immune factors critical for HIV microbicide and vaccine studies. This study uses a proteomics approach to comprehensively compare the efficacy of these methods, which sample from different compartments of the female genital tract, for the collection of immune factors. Matching sponge and lavage samples were collected from 10 healthy women and were analyzed by tandem mass spectrometry. Data was analyzed by a combination of differential protein expression analysis, hierarchical clustering and pathway analysis. Of the 385 proteins identified, endocervical sponge samples collected nearly twice as many unique proteins as cervicovaginal lavage (111 vs. 61) with 55% of proteins common to both (213). Each method/site identified 73 unique proteins that have roles in host immunity according to their gene ontology. Sponge samples enriched for specific inflammation pathways including acute phase response proteins (p = 3.37x10(-24)) and LXR/RXR immune activation pathways (p = 8.82x10(-22)) while the role IL-17A in psoriasis pathway (p = 5.98x10(-24)) and the complement system pathway (p = 3.91x10(-3)) were enriched in lavage samples. Many host defense factors were differentially enriched (p<0.05) between sites including known/potential antimicrobial factors (n = 21), S100 proteins (n = 9), and immune regulatory factors such as serpins (n = 7). Immunoglobulins (n = 6) were collected at comparable levels in abundance in each site although 25% of those identified were unique to sponge samples. This study demonstrates significant differences in types and quantities of immune factors and inflammation pathways collected by each sampling technique. Therefore, clinical studies that measure mucosal immune activation or factors assessing HIV transmission should utilize both collection methods to obtain the greatest representation of immune factors secreted into the female genital tract.
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页数:11
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