Data from: Drivers of host-pathogen community assemblies in European forests and urban green spaces (Part II to II)

ABSTRACT: Major advances in the understanding of infectious diseases have been achieved in the last decades. However, the persistence and re-emergence of pathogens continues to raise public and veterinary health concerns, of which the recent COVID-19 pandemic may be one of the most dramatic examples. Understanding the impact of habitat alterations and concomitant biodiversity loss on pathogen transmission and emergence from wildlife remains challenging. Here, we aim to elucidate the interlinkages between biodiversity and rodent-borne diseases at local and European scales. We present recently collected host-pathogen data from 21 temperate forest sites and eight urban green spaces throughout five European countries, environments where rodents are abundant and human/domestic animals – wildlife interactions are likely to occur. 3766 specimens were analyzed during the period from 2020 to 2022 comprising 15 different small mammal species. Different organ tissues of each specimen were screened for bacteria by either 16S rRNA amplicon sequencing or specific PCR. The presence of antibodies to different families of viruses were screened using immunofluorescent assays. A multitude of pathogens of zoonotic potential from several genera including Bartonella, Borrelia, Mycoplasma, Anaplasma, Neoehrlichia, Leptospira, Orthohantavirus and Orthopoxvirus were detected at non-negligible prevalence in 11 different terrestrial mammal species. A shift in host community composition was observed along the anthropization gradient with more urban adapters in more anthropized sites. Parasite richness increased with an increase in host species diversity, following the “host-diversity begets parasite-diversity” hypothesis. The absence of some vector-transmitted parasites in urban areas suggest a shift in parasite community along the anthropization gradient. Host species and host intrinsic factors were dominant explanatory variables for endoparasitic Mycoplasma species and Sarcocystidae, while extrinsic environmental and climatic factors where influential in explaining variations in occurrences of several vector-transmitted pathogens. Apodemus sylvaticus and Clethrionomys glareolus were important connector host species in respectively urban green spaces and temperate forests. Increased host diversity, but not anthropization, correlated with a richer pathogen community. These results ultimately lead to an increased understanding of the complex host-pathogen system at the local landscape that can aid future management decisions and support the public health sector. FILE DESCRIPTION: Information concerning the small mammal colon samples and the positive and negative controls multiplexed in the 16Sv4 MiSeq sequencing runs This CSV file contains the Sequencing_run_ID, PCR_ID, PCR_replicate, Sequence file name (read 1 fastq file), Sequence file name (read 2 fastq file), Rodent_ID, Sample_ID, Sample_type, and Extraction Kit for the 7735 PCR products multiplexed in 10 different Illumina MiSeq runs, corresponding to 3766 individuals performed in two technical replicates and 203 negative and positive controls. File name: Sequencing_informations_colon_samples.csv MiSeq raw sequences of the 16Sv4 rRNA gene from colons of small mammal samples These GZ files contain the FASTQ files of the paired-end reads (R1: reads 1; R2: reads 2) produced for each colon rodent sample using the MiSeq platform. The 7735 multiplexed PCR products were indexed using both forward and reverse indices on 10 sequencing MiSeq runs. Information of the multiplexed samples (n=3766 in replicate) and positive (n= 44) & negative controls (n= 159) is provided in the following CSV file titled: Sequencing_informations_colon_samples.csv File names: MiSeq_Reads_16S_Colon_Run01.gzMiSeq_Reads_16S_Colon_Run03.gzMiSeq_Reads_16S_Colon_Run05.gzMiSeq_Reads_16S_Colon_Run07.gzMiSeq_Reads_16S_Colon_Run09.gzMiSeq_Reads_16S_Colon_Run11.gzMiSeq_Reads_16S_Colon_Run13.gzMiSeq_Reads_16S_Colon_Run15.gzMiSeq_Reads_16S_Colon_Run17.gzMiSeq_Reads_16S_Colon_Run19.gz

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-06-24
DOI
https://doi.org/10.5281/zenodo.12527196
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00
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article

Data from: Drivers of host-pathogen community assemblies in European forests and urban green spaces (Part II to II)

Zenodo (CERN European Organization for Nuclear Research)
Single-cell and spatial transcriptomics
article

Data from: Drivers of host-pathogen community assemblies in European forests and urban green spaces (Part II to II)

article en

Abstract

ABSTRACT: Major advances in the understanding of infectious diseases have been achieved in the last decades. However, the persistence and re-emergence of pathogens continues to raise public and veterinary health concerns, of which the recent COVID-19 pandemic may be one of the most dramatic examples. Understanding the impact of habitat alterations and concomitant biodiversity loss on pathogen transmission and emergence from wildlife remains challenging. Here, we aim to elucidate the interlinkages between biodiversity and rodent-borne diseases at local and European scales. We present recently collected host-pathogen data from 21 temperate forest sites and eight urban green spaces throughout five European countries, environments where rodents are abundant and human/domestic animals – wildlife interactions are likely to occur. 3766 specimens were analyzed during the period from 2020 to 2022 comprising 15 different small mammal species. Different organ tissues of each specimen were screened for bacteria by either 16S rRNA amplicon sequencing or specific PCR. The presence of antibodies to different families of viruses were screened using immunofluorescent assays. A multitude of pathogens of zoonotic potential from several genera including Bartonella, Borrelia, Mycoplasma, Anaplasma, Neoehrlichia, Leptospira, Orthohantavirus and Orthopoxvirus were detected at non-negligible prevalence in 11 different terrestrial mammal species. A shift in host community composition was observed along the anthropization gradient with more urban adapters in more anthropized sites. Parasite richness increased with an increase in host species diversity, following the “host-diversity begets parasite-diversity” hypothesis. The absence of some vector-transmitted parasites in urban areas suggest a shift in parasite community along the anthropization gradient. Host species and host intrinsic factors were dominant explanatory variables for endoparasitic Mycoplasma species and Sarcocystidae, while extrinsic environmental and climatic factors where influential in explaining variations in occurrences of several vector-transmitted pathogens. Apodemus sylvaticus and Clethrionomys glareolus were important connector host species in respectively urban green spaces and temperate forests. Increased host diversity, but not anthropization, correlated with a richer pathogen community. These results ultimately lead to an increased understanding of the complex host-pathogen system at the local landscape that can aid future management decisions and support the public health sector. FILE DESCRIPTION: Information concerning the small mammal colon samples and the positive and negative controls multiplexed in the 16Sv4 MiSeq sequencing runs This CSV file contains the Sequencing_run_ID, PCR_ID, PCR_replicate, Sequence file name (read 1 fastq file), Sequence file name (read 2 fastq file), Rodent_ID, Sample_ID, Sample_type, and Extraction Kit for the 7735 PCR products multiplexed in 10 different Illumina MiSeq runs, corresponding to 3766 individuals performed in two technical replicates and 203 negative and positive controls. File name: Sequencing_informations_colon_samples.csv MiSeq raw sequences of the 16Sv4 rRNA gene from colons of small mammal samples These GZ files contain the FASTQ files of the paired-end reads (R1: reads 1; R2: reads 2) produced for each colon rodent sample using the MiSeq platform. The 7735 multiplexed PCR products were indexed using both forward and reverse indices on 10 sequencing MiSeq runs. Information of the multiplexed samples (n=3766 in replicate) and positive (n= 44) & negative controls (n= 159) is provided in the following CSV file titled: Sequencing_informations_colon_samples.csv File names: MiSeq_Reads_16S_Colon_Run01.gzMiSeq_Reads_16S_Colon_Run03.gzMiSeq_Reads_16S_Colon_Run05.gzMiSeq_Reads_16S_Colon_Run07.gzMiSeq_Reads_16S_Colon_Run09.gzMiSeq_Reads_16S_Colon_Run11.gzMiSeq_Reads_16S_Colon_Run13.gzMiSeq_Reads_16S_Colon_Run15.gzMiSeq_Reads_16S_Colon_Run17.gzMiSeq_Reads_16S_Colon_Run19.gz

Zenodo (CERN European Organization for Nuclear Research)
University of Helsinki (FI), University of Antwerp (BE), University of Potsdam (DE), Natural Resources Institute Finland (FI), Maladies Infectieuses et Vecteurs: Écologie, Génétique, Évolution et Contrôle (FR), Munster Technological University (IE), Centre de Biologie pour la Gestion des Populations (FR), Gdańsk Medical University (PL)
Sustainable cities and communities
Openalex Percentile: Top 54%
Single-cell and spatial transcriptomics
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