# Identification of Chlamydia pneumoniae and NLRP3 inflammasome activation in Alzheimer’s disease retina

## TL;DR

This study finds that Chlamydia pneumoniae infection and NLRP3 inflammasome activation are linked to Alzheimer’s disease in the retina and brain, suggesting potential new diagnostic markers and treatment approaches.

## Contribution

The study is the first to identify Chlamydia pneumoniae inclusions and NLRP3 activation in Alzheimer’s retinas and brains, linking them to neurodegeneration and cognitive decline.

## Key findings

- Chlamydia pneumoniae inclusions increased 2.9–4.1-fold in AD retinas and brains compared to controls.
- Retinal Cp was strongly associated with Aβ42, caspase-1, and pyroptotic cell death markers.
- Machine learning models using retinal Cp or NLRP3 with Aβ42 effectively predicted AD diagnosis and cognitive decline.

## Abstract

Emerging evidence implicates bacterial infections, including Chlamydia pneumoniae (Cp), a gram-negative obligate intracellular bacterium responsible for community-acquired pneumonia, in Alzheimer’s disease (AD) pathogenesis. However, the involvement of Cp in early and advanced AD in the retina is unknown. Here, we identified the existence and distribution of intracellular Cp inclusions and related NLRP3 inflammasome activation and neurodegeneration in postmortem retinas and brains from 95 human donors. Histological analysis in neuropathologically-confirmed MCI and AD patients compared with cognitively normal individuals (n=70), revealed 2.9–4.1-fold increases of Cp inclusions in AD retinas and brains, respectively, with no significant increases in MCI retinas or brains. Mass spectrometry-based proteomics in additional cohorts (n=30), revealed dysregulated brain and retinal bacterial infection-related proteins and inflammasome-associated pathways. Retinal Cp was strongly linked to Aβ42, caspase-1 and NLRP3-inflammasome activation components, as well as cleaved caspase-3+ apoptosis and cleaved gasdermin D pyroptotic cell death. Despite increased IBA1+ microgliosis in the AD retina, the Cp-associated microglial population was reduced by 62%, suggesting impaired microglial phagocytosis. Higher retinal Cp burden correlated with APOEε4 status, advanced Braak stage, and cognitive decline. Machine learning models revealed that retinal Cp or NLRP3, in combination with retinal Aβ42, effectively predicted AD diagnosis, Braak stage, and cognition. These findings suggest that Cp infection contributes to AD dementia but is unlikely to initiate AD pathological changes, whereas elevated retinal NLRP3 may serve as an early AD marker. These results underscore the need for future studies investigating Cp’s role in AD dementia and testing early antibiotic or inflammasome-targeting therapies.