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Insect-derived environmental surveillance of lumpy skin disease virus using synanthropic flies

Abstract

Lumpy skin disease (LSD) is a transboundary viral disease of cattle with substantial economic impact. Conventional surveillance strategies rely primarily on host-based sampling and clinical observation, which may be logistically constrained or insufficient during early or post-clinical phases of outbreaks. In this study, we used synanthropic flies as environmental micro-samplers to investigate temporal dynamics of LSDV under real-world outbreak conditions. Systematic fly collections were conducted at a confirmed LSDV-positive cattle farm during an active outbreak, followed by molecular screening and targeted sequencing. Both non-blood-feeding and opportunistic blood-feeding fly species, including Musca domestica and Hydrotaea spp., were analyzed to assess the presence of LSDV nucleic acids across multiple sampling periods. LSDV nucleic acids were detected in synanthropic flies, with temporal variation corresponding to the implementation of outbreak control measures. Viral signals declined over successive sampling rounds, indicating that insect-derived sampling reflects changes in environmental viral loads following intervention. Phylogenetic analysis of partial GPCR gene sequences revealed close genetic relationships between viruses detected in insect and cattle specimens, while also capturing minor sequence variation within a single outbreak setting. These findings support the concept that synanthropic flies can serve as environmental sentinels for monitoring pathogen persistence and diversity without direct animal sampling. Overall, insect-derived environmental sampling using synanthropic flies provides a non-invasive approach for capturing temporal patterns of LSDV under outbreak conditions.

Abbreviations

LSD:

Lumpy skin disease

LSDV:

Lumpy skin disease virus

WOAH:

The World Organization for Animal Health

OIE:

The Office International des Epizooties

VRI:

Veterinary Research Institute

PCR:

Polymerase chain reaction

GPCR:

The G-protein coupled chemokine receptor

RPO30:

An RNA polymerase subunit

qPCR:

Quantitative real-time polymerase chain reaction

Acknowledgements

The authors are grateful to Dr. Yan-Chang Tu from VRI for his assistance, and Kinmen Country Animal and Plant Disease Control Center for collecting clinical specimens from cattle. We also appreciate the support of Dr. Lu-Jen Ting for the early work relating to insect specimen analysis in the present study.

Funding

This paper was supported by grants given to W. T. Liu by Animal and Plant Health Inspection Agency, Ministry of Agriculture, Taiwan (113AS-5.5.2-VP-01).

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Wei-Ting Liu.

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Chuang, YC., Hu, SC., Tu, WC. et al. Insect-derived environmental surveillance of lumpy skin disease virus using synanthropic flies.
Sci Rep (2026). https://doi.org/10.1038/s41598-026-68488-5

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  • DOI: https://doi.org/10.1038/s41598-026-68488-5

Keywords

  • Xenodiagnosis
  • Insect-based environmental surveillance
  • Lumpy skin disease
  • Synanthropic fly

  • Musca domestica

  • Hydrotaea


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