Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.09.24.678402

Bee Microbiomes Harbor Diverse Antimicrobial Resistance Genes on Plasmids

Abstract

Antimicrobial resistance (AMR) is an emerging public health threat. In North America, tetracycline and macrolide antibiotics are often used to prevent or treat bacterial infections in honey bees. Previous research has shown that this practice has led to widespread drug resistance in honey bee gut microbiomes. However, where bee-associated bacteria encode AMR, genomically or on mobile genetic elements, is less well understood. Moreover, how the abundance, diversity, and mechanism of AMR differs between managed honey bees and other bees remains largely unexplored. Here we use existing metagenomic data from two previous studies to profile the AMR genes associated with managed honey bees, commercially produced bumble bees, and wild bumble bees. Our results suggest that honey bee associated bacteria house a greater diversity of AMR genes, specifically on plasmids, compared to bumble bees. In addition, we show that honey and bumble bee bacteria likely develop resistance to tetracyclines via different mechanisms. Overall, this study showcases how agricultural management has shaped the AMR genes associated with bees, and offers insights into the ecological context of differential AMR evolution within host-associated systems.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Sbardellati, D. L., Vannette, R. L.. 2025-09-24. Bee Microbiomes Harbor Diverse Antimicrobial Resistance Genes on Plasmids. https://doi.org/10.1101/2025.09.24.678402

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Understanding malaria transmission in Angola: first detection of Plasmodium malariae in Anopheles spp. and the role of secondary vectors in the Balombo region, Benguela Province

Background: Angola is one of the most affected countries in sub-Saharan Africa and was off-track to meet the WHO Global Technical Strategy targeting of a 75% reduction in malaria incidence and mortality by 2025. Recent studies highlighted major knowledge gaps regarding malaria vectors in Angola, particularly secondary vectors. A malaria control project initiated in 2007 in Balombo (Benguela Province, central Angola) has monitored malaria dynamics for 18 years, revealing increased Plasmodium prevalence and more frequent detection of non-falciparum species, mainly Plasmodium malariae (in co-infection with P. falciparum) in villagers of the Balombo region. This study aimed to characterize Anopheles populations in this region by assessing species composition, behavioural patterns, and infection rate. And to a less extent, to compare the performance of two indoor and outdoor mosquito trapping methods. Methods: Surveys were conducted during the rainy (December 2023 and 2024) and dry seasons (July 2024) in villages around the town of Balombo. Adult mosquitoes were collected indoors and outdoors using CDC Light Traps and BG-Pro traps in randomly selected houses. Female Anopheles were morphologically and molecularly identified. Primary and secondary vectors were screened for Plasmodium spp. using qPCR-high resolution melting, and positive samples were sequenced. Results: A strong seasonal effect was observed in Anopheles populations, with higher abundance, diversity, and Plasmodium- infection rates during the rainy season. An. funestus remained the main vector, but Plasmodium spp. was also detected in five other species: An. arabiensis, An. gambiae, An. marshallii, An. rufipes, and An. maculipalpis. This is the first report of P. malariae in Anopheles mosquitoes and the first mention of the role of secondary vectors in malaria transmission in Benguela Province. Conclusion: This study provides a thorough and updated inventory of Anopheles species in the Balombo region. Molecular biology confirmed the presence of P. falciparum and P. malariae in several species of Anopheles underscoring the existence of a complex transmission system in villages of Balombo. Infected exophagic and exophilic Anopheles species, exhibiting opportunistic behaviour, likely contribute, as secondary vectors, to the increase of Plasmodiumspp. transmission in the study sites. Therefore, confirming the need to implement complementary interventions targeting outdoor malaria transmission.

microbiology↗

Set202 is a histone lysine methyltransferase that enables Cryptococcus neoformans to adapt to the host environment

All pathogens rely on dynamic gene expression for host adaptation and disease causation. This is especially important for pathogens that normally are found in the environment, like Cryptococcus neoformans, given that environmental and host conditions are dramatically different. Epigenetic modifications, like those carried out by SET-domain histone lysine methyltransferases (HKMTs), are essential for this genome expression flexibility. While transcription factors and signaling cascades have been well-studied in C. neoformanss host adaptation, the role of HKMTs in this process has not been explored. Here, we characterize the gene SET202, previously reported as a putative HKMT important for growth in host lungs. We show that set202{Delta} mutants have 50% less phagosomal permeabilization than the wild-type fungi, have phagosomal maturation defects, and poor intracellular survival. Additionally, they are defective in traits promoting virulence, including significantly smaller capsules, less melanin, and poor growth under host-like conditions. These phenotypes contributed to reduced virulence in a murine model of infection but, notably, this defect was host-temperature-dependent. In order to explain mechanistically how SET202 deletion could affect such a wide range of processes, we assessed and demonstrated, for the first time, that Set202 is a true histone-3-lysine 36 methyltransferase, supporting its role in epigenetically modifying the fungal genome to enable adaptation to the hostile host conditions. Consequently, our findings support the study of the biological function of Set202, as it can serve as a potential future therapeutic target for the treatment of infections caused by C. neoformans, and possibly other pathogenic fungi.

microbiology↗

Pichinde virus models intrauterine infection by hemorrhagic fever-causing arenaviruses

Arenavirus infection during pregnancy can cause severe maternal disease, congenital infection, and fetal demise. Many arenaviruses are endemic in economically disadvantaged areas and must be studied in high containment laboratories, which has limited our understanding of arenavirus pathogenesis in the placenta. Pichinde virus (PICV) is a nonpathogenic arenavirus that recapitulates many aspects of viral hemorrhagic fever in guinea pigs. Using a combination of experiments in human placental cells and guinea pigs, we characterized the tropism and impact of PICV infection during pregnancy. PICV replicated in human trophoblast stem cells (TSCs), TSC-derived trophoblasts, and explanted term placenta. When guinea pigs were infected at mid-gestation, PICV caused fetal demise. High infectious titers were recovered from placenta and decidua, but PICV was infrequently detected in fetal tissues or amniotic fluid. In situ hybridization confirmed that the placenta, decidua, and fetal membranes were all infected by the virus. Transcriptional profiling of PICV-infected human trophoblasts and guinea pig tissues revealed that infection upregulated canonical antiviral responses, which could contribute to placental dysfunction and pregnancy loss. Thus, PICV is safe and tractable model of zoonotic arenavirus infection during pregnancy with utility for preclinical therapeutic and vaccine development.

microbiology↗