» Articles » PMID: 16495519

Profiling of Human Antibody Responses to Chlamydia Trachomatis Urogenital Tract Infection Using Microplates Arrayed with 156 Chlamydial Fusion Proteins

Overview
Journal Infect Immun
Date 2006 Feb 24
PMID 16495519
Citations 60
Authors
Affiliations
Soon will be listed here.
Abstract

The available chlamydial genome sequences have made it possible to comprehensively analyze host responses to all chlamydial proteins, which is essential for further understanding of chlamydial pathogenesis and development of effective chlamydial vaccines. Microplates arrayed with 156 Chlamydia trachomatis fusion proteins were used to evaluate antibody responses in women urogenitally infected with C. trachomatis. Based on both the antibody recognition frequency and titer, seven chlamydial antigens encoded by open reading frames (ORFs) CT089, CT147, CT226, CT681, CT694, CT795, and CT858, respectively, were identified as relatively immunodominant; six of these are encoded by hypothetical ORFs. Antibody binding to these chlamydial fusion proteins was blocked by C. trachomatis-infected but not by normal HeLa cell lysates or irrelevant bacterial lysates. These results have revealed novel immune-reactive chlamydial antigens, not only indicating that the hypothetical ORF-encoded proteins are expressed during chlamydial infection in humans but also providing the proof of principle that the fusion protein-based approach can be used to profile human immune responses to chlamydial infection at the whole-genome scale.

Citing Articles

Preclinical screen for protection efficacy of chlamydial antigens that are immunogenic in humans.

Lu C, Wang J, Zhong G Infect Immun. 2023; 91(11):e0034923.

PMID: 37889004 PMC: 10652899. DOI: 10.1128/iai.00349-23.


The emerging complexity of Chlamydia trachomatis interactions with host cells as revealed by molecular genetic approaches.

Bastidas R, Valdivia R Curr Opin Microbiol. 2023; 74:102330.

PMID: 37247566 PMC: 10988583. DOI: 10.1016/j.mib.2023.102330.


The Polymorphic Membrane Protein G Has a Neutral Effect and the Plasmid Glycoprotein 3 an Antagonistic Effect on the Ability of the Major Outer Membrane Protein to Elicit Protective Immune Responses against a Respiratory Challenge.

Slepenkin A, Pal S, Hoang-Phou S, Abisoye-Ogunniyan A, Rasley A, Dhaeseleer P Vaccines (Basel). 2023; 11(3).

PMID: 36992088 PMC: 10051784. DOI: 10.3390/vaccines11030504.


Chlamydia trachomatis plasmid-encoding Pgp3 protein induces secretion of distinct inflammatory signatures from HeLa cervical epithelial cells.

Cheong H, Cheok Y, Chan Y, Tang T, Sulaiman S, Looi C BMC Microbiol. 2023; 23(1):58.

PMID: 36870960 PMC: 9985209. DOI: 10.1186/s12866-023-02802-3.


The inclusion membrane protein IncS is critical for initiation of the Chlamydia intracellular developmental cycle.

Cortina M, Bishop R, DeVasure B, Coppens I, Derre I PLoS Pathog. 2022; 18(9):e1010818.

PMID: 36084160 PMC: 9491573. DOI: 10.1371/journal.ppat.1010818.


References
1.
Fan T, Lu H, Hu H, Shi L, McClarty G, Nance D . Inhibition of apoptosis in chlamydia-infected cells: blockade of mitochondrial cytochrome c release and caspase activation. J Exp Med. 1998; 187(4):487-96. PMC: 2212145. DOI: 10.1084/jem.187.4.487. View

2.
Brunham R, Peeling R . Chlamydia trachomatis antigens: role in immunity and pathogenesis. Infect Agents Dis. 1994; 3(5):218-33. View

3.
LaVerda D, Albanese L, Ruther P, Morrison S, Morrison R, Ault K . Seroreactivity to Chlamydia trachomatis Hsp10 correlates with severity of human genital tract disease. Infect Immun. 1999; 68(1):303-9. PMC: 97135. DOI: 10.1128/IAI.68.1.303-309.2000. View

4.
Read T, Brunham R, Shen C, Gill S, Heidelberg J, White O . Genome sequences of Chlamydia trachomatis MoPn and Chlamydia pneumoniae AR39. Nucleic Acids Res. 2000; 28(6):1397-406. PMC: 111046. DOI: 10.1093/nar/28.6.1397. View

5.
Stephens R . Chlamydial genomics and vaccine antigen discovery. J Infect Dis. 2000; 181 Suppl 3:S521-3. DOI: 10.1086/315631. View