Identification and differential expression of serotransferrin and apolipoprotein A-I in the plasma of HIV-1 patients treated with first-line antiretroviral therapy

被引:4
作者
Barik, Sushanta Kumar [1 ]
Mohanty, Keshar Kunja [1 ]
Mohanty, Ashok Kumar [2 ]
Rawat, Preeti [2 ]
Gopal, G. [3 ]
Bisht, Deepa [1 ]
Patil, Shripad A. [1 ]
Singh, Rananjay [1 ]
Sharma, Devesh [1 ]
Tripathy, Srikanth Prasad [4 ]
Tandon, Rekha [5 ]
Singh, Tej Pal [5 ]
Jena, Srikanta [6 ]
机构
[1] Natl JALMA Inst Leprosy & Other Mycobacterial Dis, ICMR, Agra 282004, Uttar Pradesh, India
[2] Natl Dairy Res Inst, ICAR, Karnal 132001, India
[3] Canc Inst, Chennai 600020, Tamil Nadu, India
[4] Natl Inst Res TB, ICMR, Chennai 600031, Tamil Nadu, India
[5] Sarojini Naidu Med Coll, Agra 282002, Uttar Pradesh, India
[6] Ravenshaw Univ, Cuttack 753003, Odisha, India
关键词
HIV; AIDS; First line ART; Drug resistant; Drug respondent; PROTEIN-BINDING; DISCOVERY; IMMUNODEFICIENCY;
D O I
10.1186/s12879-020-05610-6
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Plasma proteins are known to interfere the drug metabolism during therapy. As limited information is available regarding the role of plasma proteins in HIV drug resistance during ART in HIV/AIDS patients, the present study aimed to identify and characterize the differentially expressed plasma proteins in the drug resistant and drug respondent groups of HIV-1 infected patients with > 6 years of first line ART. Methods Four-drug resistant (treatment failure) and four-drug respondent (treatment responder) patients were selected for plasma proteomic analysis based on viral load and drug resistance associated mutations from a cohort study designed on the first line ART patients who were enrolled in the antiretroviral therapy center, Sarojini Naidu Medical College, Agra, India from December 2009 to November 2016. After depleting high abundant proteins, plasma proteins were resolved using two-dimensional gel electrophoresis on IPG strips, pH range of 3-10. Spots were selected in the gel based on the density of staining which was common in the drug resistant and drug respondent groups separately. The fold change of each spot was calculated using image-J. Each protein spot was identified using the matrix assisted laser desorption/ionization-time of flight/time of flight (MALDI-TOF/TOF) after tryptic digestion. Peptide peaks were identified through flex analysis version 3.3, and a search against a protein data base using the internal Mascot. Gene ontology study was completed through STRING v.11 and Panther15.0. Results Out of eight spots from 2D gel samples analyzed by MALDITOF/TOF, two proteins were found to have significant score (> 56) after Flex analysis. These two proteins were identified to be apolipoprotein A1 and serotransferrin. The fold change expression of these two proteins were analyzed in drug resistant and drug respondent group. Apolipoprotein-A1 and serotransferrin were observed to be expressed 1.76 and 1.13-fold more respectively in drug respondent group compared to drug resistant group. The gene ontology analysis revealed the involvement of these two proteins in various important physiological processes. Conclusion Apolipoprotein A-I and serotransferrin were found to be expressed more in drug respondent group compared to drug resistant group.
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