The gut microbiome following acute HIV-1 infection

To our knowledge, this is the most comprehensive prospective study investigating the longitudinal impact of acute HIV-1 infection in an HIV-1 hyperendemic area such as the Manhiça district in Mozambique. This unique study confirms and extends previous findings in non-human primate models and provides critical insights into the impact of infections in the gut microbiome as well as into the pathogenesis of HIV-1 infection.

Published in Microbiology

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The gut associated lymphoid tissue (GALT) is rapidly and severely damaged upon HIV-1 infection. The extreme damage to the GALT leads the leaky gut phenomenon, where bacterial cells and products usually contained within the gut lumen can now translocate the gut epithelia and enter the lamina propria, thus initiating immune activation and inflammation.

Hence, it is crucial to understand the changes occurring in the gut mucosa as well as in the gut microbiota following first stages of HIV-1 infection. Once we are able to identify them and understand the host-microbiota interplay, we may be able to design new therapeutic approaches to help ameliorate the immune deterioration linked to HIV-1 infection by modulating the gut microbiome.

A major strength in our work is prospectively following-up people from Mozambique after acute HIV-1 infection for up to one year and a half. This longitudinal studies in the developed countries are basically restricted to non-human primate models since acute infections are very difficult to diagnose. First fecal sample from our recently HIV-1 infected individuals (RHI) was collected within the first 1-2 months after viral infection and subsequent fecal and blood samples were periodically collected. Remarkably, we were also able to compare changes in the gut microbiota occurring within the first 18 months to two groups of chronically HIV-1 infected subjects, either on active antiretroviral treatment (ART) or ART-naïve, and HIV-1 negative individuals, thus conforming a huge and clinically relevant cohort. 

Surprisingly, longitudinal analysis reported significant increases in microbial richness and diversity in RHI subjects. Deeper analyses including clinical data showed significant decreases in HIV-1 viral load and in CD8+ T-cell counts for the first 6 months of follow-up. Interestingly, this observation led us to hypothesize whether the gut microbiota experiences some transient recovery after an initial negative impact (i.e. implying reduction in ecological markers) that mirror the partial recovery of CD4+T cells after initial peak of viremia (see figure below). If true, this would suggest that to understand the acute effect of HIV-1 infection on the gut microbiota, it is crucial to test the first days, at most the first weeks, after viral entry, and that collecting samples at month 1 might be already too late to see the negative impact on the gut microbiota following HIV-1 infection.

 Interestingly we also saw a potential role of eukaryotic viruses related to HIV-1 pathogenesis with significant increased fecal shedding of Adenovirus, Enterovirus and Cytomegalovirus in HIV-1 infected groups. Remarkably, Adenovirus shedding was already increased in RHI and maintained in chronically HIV-1 infected groups regardless of ART, compared to HIV-1 negative controls. These observations reinforce the idea that analyses of the gut microbiome should expand beyond bacteria and understanding the inter and intra-dynamics within the gut microbiota during the first month after HIV-1 infection is strongly needed.

More information: https://rdcu.be/bCk58 

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Harnessing plant microbiomes to improve performance and mechanistic understanding

This is a Cross-Journal Collection with Microbiome, Environmental Microbiome, npj Science of Plants, and npj Biofilms and Microbiomes. Please click here to see the collection page for npj Science of Plants and npj Biofilms and Microbiomes.

Modern agriculture needs to sustainably increase crop productivity while preserving ecosystem health. As soil degradation, climate variability, and diminishing input efficiency continue to threaten agricultural outputs, there is a pressing need to enhance plant performance through ecologically-sound strategies. In this context, plant-associated microbiomes represent a powerful, yet underexploited, resource to improve plant vigor, nutrient acquisition, stress resilience, and overall productivity.

The plant microbiome—comprising bacteria, fungi, and other microorganisms inhabiting the rhizosphere, endosphere, and phyllosphere—plays a fundamental role in shaping plant physiology and development. Increasing evidence demonstrates that beneficial microbes mediate key processes such as nutrient solubilization and uptake, hormonal regulation, photosynthetic efficiency, and systemic resistance to (a)biotic stresses. However, to fully harness these capabilities, a mechanistic understanding of the molecular dialogues and functional traits underpinning plant-microbe interactions is essential.

Recent advances in multi-omics technologies, synthetic biology, and high-throughput functional screening have accelerated our ability to dissect these interactions at molecular, cellular, and system levels. Yet, significant challenges remain in translating these mechanistic insights into robust microbiome-based applications for agriculture. Core knowledge gaps include identifying microbial functions that are conserved across environments and hosts, understanding the signaling networks and metabolic exchanges between partners, and predicting microbiome assembly and stability under field conditions.

This Research Topic welcomes Original Research, Reviews, Perspectives, and Meta-analyses that delve into the functional and mechanistic basis of plant-microbiome interactions. We are particularly interested in contributions that integrate molecular microbiology, systems biology, plant physiology, and computational modeling to unravel the mechanisms by which microbial communities enhance plant performance and/or mechanisms employed by plant hosts to assemble beneficial microbiomes. Studies ranging from controlled experimental systems to applied field trials are encouraged, especially those aiming to bridge the gap between fundamental understanding and translational outcomes such as microbial consortia, engineered strains, or microbiome-informed management practices.

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Our understanding of the intricate relationship between the microbiome and reproductive health holds profound translational implications for fertility, pregnancy, and reproductive disorders. To truly advance this field, it is essential to move beyond descriptive and associative studies and focus on mechanistic research that uncovers the functional underpinnings of the host–microbiome interface. Such studies can reveal how microbial communities influence reproductive physiology, including hormonal regulation, immune responses, and overall reproductive health.

Recent advances have highlighted the role of specific bacterial populations in both male and female fertility, as well as their impact on pregnancy outcomes. For example, the vaginal microbiome has been linked to preterm birth, while emerging evidence suggests that gut microbiota may modulate reproductive hormone levels. These insights underscore the need for research that explores how and why these microbial influences occur.

Looking ahead, the potential for breakthroughs is immense. Mechanistic studies have the power to drive the development of microbiome-based therapies that address infertility, improve pregnancy outcomes, and reduce the risk of reproductive diseases. Incorporating microbiome analysis into reproductive health assessments could transform clinical practice and, by deepening our understanding of host–microbiome mechanisms, lay the groundwork for personalized medicine in gynecology and obstetrics.

We invite researchers to contribute to this Special Collection on Microbiome and Reproductive Health. Submissions should emphasize functional and mechanistic insights into the host–microbiome relationship. Topics of interest include, but are not limited to:

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