Share

Export Citation

APA
MLA
Chicago
Harvard
Vancouver
BIBTEX
RIS
Universitas Hasanuddin
Research output:Contribution to journalArticlepeer-review

Molecular Detection of Clostridium-Related DNA in Bats from Soppeng, Indonesia

Arifin M.E.

Media Publikasi Promosi Kesehatan Indonesia

Q4
Published: 2026

Abstract

Introduction: Clostridium spp. are anaerobic, spore-forming bacteria widely distributed in soil, water, and the gastrointestinal tracts of humans and animals. Several species are associated with important human and veterinary diseases. Information regarding Clostridium-related bacteria in bats remains limited in Indonesia. This study aimed to generate preliminary molecular evidence of Clostridium-related bacterial DNA in bats from Soppeng Regency, South Sulawesi, Indonesia. Methods: Bat samples were collected in Soppeng Regency, South Sulawesi, Indonesia. Ten fruit bats (Cynopterus brachyotis) were captured near roosting and foraging sites, and three intestinal tissue samples were selected for molecular analysis based on sample integrity and DNA preservation quality. Genomic DNA was extracted using a commercial extraction kit following aseptic sample processing. Molecular detection was performed using PCR targeting the bacterial 16S rRNA gene, followed by agarose gel electrophoresis. PCR-positive amplicons were subjected to Sanger sequencing and analyzed using BLAST against the NCBI/GenBank database based on sequence identity, query coverage, and E-value. Results: All three analyzed samples produced positive amplification bands at the expected amplicon size of approximately 1,465 bp. BLAST analysis showed the closest sequence matches to Clostridium septicum (K1; 94% query cover; 97.57% identity; E=0.0), Paraclostridium sordellii (K3; 97% query cover; 96.64% identity; E=0.0), and Clostridium haemolyticum (K5; 95% query cover; 98.06% identity; E=0.0). Conclusion: This study provides preliminary molecular evidence of Clostridium-related bacterial DNA in fruit bats from Soppeng Regency. However, DNA detection alone does not confirm bacterial viability, pathogenicity, transmission potential, or reservoir status. Further studies involving culture confirmation, toxin gene characterization, environmental sampling, and broader wildlife surveillance are needed to clarify the ecological and public health significance of these findings.

Access to Document

10.56338/mppki.v9i7.11276

Other files and links

Fingerprint

BiologySciences
AmpliconSciences
genomic DNASciences
Polymerase chain reactionSciences
16S ribosomal RNASciences
ClostridiaSciences
BacteriaSciences
DNASciences
MicrobiologySciences
DNA sequencingSciences
Agarose gel electrophoresisSciences
DNA extractionSciences
ClostridiumSciences
MetagenomicsSciences
Ribosomal RNASciences
Sanger sequencingSciences
Sequence analysisSciences
Computational biologySciences
GeneSciences
Ribosomal DNASciences
Multiplex polymerase chain reactionSciences
Clostridium perfringensSciences
GeneticsSciences
Gel electrophoresisSciences