Although gut microbiota alteration and related blood microbe profiles in human immunodeficiency virus (HIV)-infected individuals are associated with the disease progression, how abnormal blood microbe profiles influence the inflammation and immune restoration are not fully understood. To address these issues, this study enrolled 24 healthy controls (HCs) and 91 HIV-infected individuals, including 30 treatment-naïve individuals (TNs), 31 immunological non-responders (INRs), and 30 immunological responders (IRs); subsequently, we analyzed blood microbe profiles using metagenomic sequencing and Olink proteomics technology, and identify inflammation-related proteins in peripheral blood samples of these individuals. The results showed increased translocation of microbes in the blood of TNs. This translocation did not return to normal level in either IRs or INRs who received antiretroviral therapy. In addition,
Porphyromonas gingivalis
significantly increased in TNs, IRs, and INRs compared to HCs.
P. gingivalis
was inversely associated with CD4
+
T-cell counts, CD4/CD8 ratio, latency-associated peptide transforming growth factor-β1, and tumor necrosis factor-related activation-induced cytokine (TRANCE) and positively associated with HIV reservoirs.
Burkholderia multivorans
and
Bacillus thuringiensis
significantly decreased in TNs, IRs, and INRs compared to HCs and were positively associated with CD4
+
T-cell counts and the CD4/CD8 ratio and negatively associated with HIV reservoir size and pro-inflammatory factors. We identified several species of microbes that were associated with CD4
+
T-cell restoration on antiretroviral therapy,
Prevotella
sp
. CAG:5226, Eubacterium
sp
. CAG:251, Phascolarctobacterium succinatutens, Anaerobutyricum hallii, Prevotella
sp
. AM34-19LB,
and
Phocaeicola plebeius
were positively associated with HIV reservoir size and pro-inflammatory proteins. Another group of bacteria,
B. multivorans, B. thuringiensis, Vibrio vulnificus,
and
Acinetobacter baumannii
, which were negatively associated and pro-inflammatory proteins. In conclusion, different microbes within blood of HIV-infected individuals were found to be closely associated with persistent inflammation and immune restoration, suggesting the blood microbe profiles of HIV-infected individuals also influence disease progression.
IMPORTANCE
The characteristics of blood microbiota in HIV-infected individuals and their relevance to disease progression are still unknown, despite alterations in gut microbiota diversity and composition in HIV-infected individuals. Here, we present evidence of increased blood microbiota diversity in HIV-infected individuals, which may result from gut microbiota translocation. Also, we identify a group of microbes,
Porphyromonas gingivalis
,
Prevotella
sp.
CAG:5226
,
Eubacterium
sp.
CAG:251
,
Phascolarctobacterium succinatutens
,
Anaerobutyricum hallii
,
Prevotella
sp.
AM34-19LB
, and
Phocaeicola plebeius
, which are linked to poor immunological recovery. This work provides a scientific foundation toward therapeutic strategies targeting blood microbiota for immune recovery of HIV infection.