Ants, common in urban ecosystems, often infiltrate hospital environments, where they can interfere with infection control measures. This study examined their ecological role in 15 hospitals across Nigeria, focusing on high-risk areas such as kitchens, waste disposal zones, and patient wards. Over 500 ant specimens were aseptically collected and analyzed using molecular and microbiological techniques, revealing contamination with pathogenic microorganisms like Listeria monocytogenes and Staphylococcus aureus. Ants were identified using morphological keys, and bacteria were isolated from the specimens using selective agars. The presence of antimicrobial-resistant bacteria carried by ants highlights the need for heightened awareness and stricter infection control measures in healthcare settings. While ants may act as mechanical vectors, facilitating the transmission of infectious agents, within healthcare settings, particularly in areas with suboptimal sanitation and inadequate pest control this study emphasizes the importance of addressing this issue in infection control protocols. This study recommends integrated pest management, routine sanitation, and structural modifications to reduce ant infestations. It also suggests adopting DNA-based microbial monitoring for early detection of contaminants. Hospitals should prioritize simple yet effective measures, such as proper hand hygiene, judicious use of antimicrobials, and robust pest control programs. By addressing ant-mediated pathogen spread, this research offers valuable insights to improve infection control strategies and enhance patient safety in modern healthcare environments.
Published in | International Journal of Ecotoxicology and Ecobiology (Volume 10, Issue 2) |
DOI | 10.11648/j.ijee.20251002.12 |
Page(s) | 31-39 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2025. Published by Science Publishing Group |
Ants, Pathogenic Microorganisms, Hospital Environments, Infection, Ecology, Mechanical Vector
S/N | Ward | Ant species | Colony morphology | |||||||
---|---|---|---|---|---|---|---|---|---|---|
External culture | Internal culture | |||||||||
N A | SSA | EMB | MSA | NA | SSA | EMB | MSA | |||
1 | Accident and emergency | Pheidole species | Tiny flat milky growth | Translucent flat colony | Pink creamy growth | Large creamy colony | Translucent flat colony | Flat greenish metallic sheen | ||
2 | Accident and emergency | Camponotus vesicus | Round creamy colonies | Translucent flat colony | Pink creamy growth | Tiny creamy colony | Translucent flat colony | Pink creamy growth | ||
3 | General outpatient clinic | Pheidole species | Round Creamy colony | Translucent flat colony | Pink-purple colony | Red round cocci growth | Translucent flat colony | Pink-purple creamy growth | Yellow or colourless colonies | |
4 | Pediatric | Cremastogaster | Round Creamy colony | Blackish creamy colonies with colourless edge | Pink creamy growth | Flat pinkish colonies | Creamy cocci colonies | Blackish creamy colonies with colourless edge | Purple mucoid growth | Pink flat colonies |
5 | Pediatric | Pheidole species1 | Round Creamy colony | Translucent flat colony | Flat pink-purple colonies | Yellow or colourless colonies | Tiny creamy colonies | Blackish creamy colonies with colourless edge | Large mucoid pink-purple colony | Yellow or colourless colonies |
6 | Pediatric | Pheidole species2 | Round Creamy colony | No growth observed | Pink creamy growth | Yellow or colourless colonies | Tiny creamy colonies | Blackish creamy colonies with colourless edge | Flat purple growth | Yellow or colourless colonies |
External culture | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
Ant species | Media | Gram reaction | Cat | Cit | Oxi | Ure | Ind | VP | MR | Organism |
Pheidole sp. | NA | - | + | - | - | - | + | - | + | Escherichia coli |
SSA | - | + | - | - | - | - | - | + | Shigella spp. | |
EMB | - | - | + | - | - | - | - | + | Salmonella spp. | |
Componotus vesicus | NA | + | + | + | - | + | - | + | + | Staphylococcus spp. |
SSA | - | + | - | - | - | - | - | + | Shigella spp. | |
EMB | - | + | + | - | - | - | + | - | Enterobacter aerogenes | |
Internal culture | ||||||||||
Pheidole sp. | NA | + | + | + | - | + | - | + | + | Staphylococcus spp. |
SSA | - | + | - | - | - | - | - | + | Shigella spp. | |
EMB | - | + | - | - | - | + | - | + | Escherichia coli | |
Componotus vesicus | NA | - | + | - | - | - | + | - | + | Escherichia coli |
SSA | - | + | - | - | - | - | - | + | Shigella spp. | |
EMB | - | + | + | - | - | - | + | - | Enterobacter aerogenes |
External culture | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
Ant species | Media | Gram reaction | Cat | Cit | Oxi | Ure | Ind | VP | MR | Organism |
Pheidole sp. | NA | + | + | + | - | + | - | + | + | Staphylococcus spp. |
SSA | - | + | - | - | - | - | - | + | Shigella spp. | |
EMB | - | + | + | - | - | - | + | - | Enterobacter aerogenes | |
Internal culture | ||||||||||
Pheidole sp. | NA | - | + | + | - | + | - | - | + | Proteus spp. |
SSA | - | + | - | - | - | - | - | + | Shigella spp. | |
EMB | - | + | - | - | - | + | - | + | Escherichia coli | |
MSA | + | + | + | - | + | - | + | + | Staphylococcus spp. |
External culture | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
Ant species | Media | Gram reaction | Cat | Cit | Oxi | Ure | Ind | VP | MR | Organism |
Crematogaster species | NA | + | + | + | - | + | - | + | + | Staphylococcus spp. |
SSA | - | - | - | - | - | - | - | + | Salmonella spp. | |
EMB | - | + | + | - | - | - | + | - | Enterobacter aerogenes | |
MSA | + | + | - | - | + | + | - | Staphylococcus spp. | ||
Pheidole sp1. | NA | + | + | + | - | + | - | + | + | Staphylococcus spp. |
SSA | - | - | - | - | - | - | - | + | Salmonella spp. | |
EMB | - | + | + | - | - | - | + | - | Enterobacter aerogenes | |
MSA | + | + | + | - | + | - | + | + | Staphylococcus spp. | |
Pheidole sp2. | NA | + | + | + | - | + | - | + | + | Staphylococcus spp. |
SSA | ____ | ____ | ____ | ____ | ____ | ____ | ____ | ____ | ________________ | |
EMB | - | + | + | - | - | - | + | - | Enterobacter aerogenes | |
MSA | + | + | + | - | + | - | + | + | Staphylococcus spp. | |
Internal culture | ||||||||||
Crematogaster species | NA | - | + | - | - | - | + | - | + | Escherichia coli |
SSA | - | - | - | - | - | - | - | + | Salmonella spp. | |
EMB | - | + | + | - | + | - | + | - | Klebsiella spp. | |
MSA | + | + | + | - | + | - | + | + | Staphylococcus spp. | |
Pheidole sp1. | NA | - | + | - | - | - | + | - | + | Escherichia coli |
SSA | - | - | - | - | - | - | - | + | Salmonella spp. | |
EMB | - | + | + | - | + | - | + | - | Klebsiella spp. | |
MSA | + | + | + | - | + | - | + | + | Staphylococcus spp. | |
Pheidole sp2. | NA | - | + | - | - | - | + | - | + | Escherichia coli |
SSA | - | - | - | - | - | - | - | + | Salmonella spp. | |
EMB | - | + | + | - | - | - | + | - | Enterobacter aerogenes | |
MSA | + | + | + | - | + | - | + | + | Staphylococcus spp. |
HAI | Hospital Acquired Infection |
EMB | Eosin Methylen Blus |
SSA | Salmonela Shigella Agar |
NA | Nutrient Agar |
MSA | Mannitol Salt Agar |
[1] | Abdul-Mutalib, N. A., Nordin, S. A., Osman, M., Roslan, A. M., Ishida, N., Sakai, K., Tashiro, Y., Tashiro, K., Maeda, T., & Shirai, Y. (2016). The prevalence of foodborne pathogenic bacteria on cutting boards and their ecological correlation with background biota. AIMS Microbiology, 2(2), 138-151. |
[2] | Adamu, A. I., Pam, V. A., Ashigar, M. A., Ombugadu, A., Maikenti, J. I., Ahmed, H. O., Sangari, J. S., Osehgele, P. A., Karenegbe, P., & Haruna, S. (2024). Nest biota and composition of household ants in Lafia Local Government Area, Nasarawa State. Asian Journal of Biological and Medical Research, 7(1), 21. |
[3] | Akinwande, K. L., Atunwa, O. B., & Adewale, P. O. (2024). Anthropization drives indoor establishment, dispersal, and foodborne pathogens’ carrying capacity of ants (Hymenoptera: Formicidae). Tropical Zoology. |
[4] | Alruwaili, R. F., Alsadaan, N., Alruwaili, A. N., & Alrumayh, A. G. (2024). Unveiling the symbiosis of environmental sustainability and infection control in health care settings: A systematic review. Sustainability. |
[5] | Anicetus, A., Nguvumali, D. T., & Mbise, G. W. (2022). Assessment of environmental cleaning practices and their impacts on infection prevention and control in selected hospitals in Tanzania. Journal of Hospital Infection. |
[6] | Ashigar, M. A., & Majid, A. H. A. (2021). 16S rDNA metabarcoding of the bacterial community associated with workers of Pheidole rugaticeps Emery (Hymenoptera: Formicidae). Asian Pacific Journal of Tropical Biomedicine, 24(1), 176. |
[7] | Chi, N. T. Q., Lan, N. T. H., Toyama, K., & Mukai, Y. (2020). Microbial inspection of a Vietnamese hospital kitchen with reference to a Japanese hospital kitchen. Journal of Food Safety, 40(5), e12827. |
[8] | Gaucher, M. L., Thibodeau, A., Fravalo, P., Archambault, M., Arsenault, J., Fournaise, S., Letellier, A., & Quessy, S. (2018). Broiler chicken carcasses and their associated abattoirs as a source of enterotoxigenic Clostridium perfringens: Prevalence and critical steps for contamination. AIMS Microbiology, 4(3), 439-454. |
[9] | Lima, W. R. dos S., Marques, S. G., Rodrigues, F. S., & Rebêlo, J. M. M. (2013). Ants in a hospital environment and their potential as mechanical bacterial vectors. Revista da Sociedade Brasileira de Medicina Tropical, 46(6), 637-640. |
[10] | Leistner, R., et al. (2023). Environmental cleaning to prevent hospital-acquired infections on non-intensive care units: A pragmatic, single-center, cluster-randomized controlled, crossover trial comparing soap-based, disinfection, and probiotic cleaning. Infection Control & Hospital Epidemiology. |
[11] | MacFaddin, J. F. (1980). Biochemical tests for identification of medical bacteria. Williams & Wilkins Co. |
[12] | Muratore, M., Prather, C., Sun, Y., & Ishaq, S. L. (2020). The gut bacterial communities across six grasshopper species from a coastal tallgrass prairie. PLOS ONE, 15(1), e0228406. |
[13] | Nascimento, L. E., Amaral, R. R., Ferreira, R. M. A., Trindade, D. V. S., Nascimento, R. E., Costa, T. S., Souto, R. N. P., & Rust, M. (2020). Ants (Hymenoptera: Formicidae) as potential mechanical vectors of pathogenic bacteria in a public hospital in the Eastern Amazon, Brazil. Journal of Medical Entomology, 57(5), 1619. |
[14] | Nguyen, V. T., Bian, L., Tamaoki, J., Otsubo, S., Muratani, M., Kawahara, A., & Kobayashi, M. (2020). Generation and characterization of keap1a- and keap1b-knockout zebrafish. Redox Biology, 36, 101667. |
[15] | Oliveira, B. R. M., Sousa, L. F., Soares, R. C., Nascimento, T. C., Madureira, M. S., & Fortuna, J. L. (2017). Ants as vectors of bacteria in hospital environments. Journal of Microbiology Research, 7(1), 1-7. |
[16] | Papatheodorou, S. A., Halvatsiotis, P., & Houhoula, D. (2021). A comparison of different DNA extraction methods and molecular techniques for the detection and identification of foodborne pathogens. AIMS Microbiology, 7(3), 304-319. |
[17] | Pramitasuri, T. I., Susilawathi, N. M., Tarini, N. M. A., Sudewi, A. A. R., & Evans, M. C. (2023). Cholesterol-dependent cytolysins and the brain: Revealing a potential therapeutic avenue for bacterial meningitis. AIMS Microbiology, 9(4), 647-667. |
[18] | Raheem, D. (2016). Outbreaks of listeriosis associated with deli meats and cheese: An overview. AIMS Microbiology, 2(3), 230-250. |
[19] | Saadeh, D., et al. (2022). Water, sanitation, and hygiene and infection prevention and control in Jordanian hospitals in the context of COVID-19: A national assessment. BMC Health Services Research. |
[20] | Schroeder, A. R., Dahlen, A., Purington, N., Alvarez, F., Brooks, R., Destino, L., Madduri, G., Wang, M., & Coon, E. R. (2022). Healthcare utilization in children across the care continuum during the COVID-19 pandemic. PLOS ONE, 17(10), e0276461. |
[21] | Tiritelli, R., Giannetti, D., Schifani, E., Grasso, D. A., & Cilia, G. (2024). Neighbors sharing pathogens: The intricate relationship between Apis mellifera and ants (Hymenoptera: Formicidae) nesting in hives. Journal of Applied Entomology. |
[22] | Xu, Y., Nagy, A., Bauchan, G. R., Xia, X., & Nou, X. (2017). Enhanced biofilm formation in dual-species culture of Listeria monocytogenes and Ralstonia insidiosa. AIMS Microbiology, 3(4), 774-783. |
APA Style
Ifeoma, K. P. (2025). The Ecological Role of Ants in Hospital Environments and Implications for Infection Control. International Journal of Ecotoxicology and Ecobiology, 10(2), 31-39. https://doi.org/10.11648/j.ijee.20251002.12
ACS Style
Ifeoma, K. P. The Ecological Role of Ants in Hospital Environments and Implications for Infection Control. Int. J. Ecotoxicol. Ecobiol. 2025, 10(2), 31-39. doi: 10.11648/j.ijee.20251002.12
@article{10.11648/j.ijee.20251002.12, author = {Kingsley Peace Ifeoma}, title = {The Ecological Role of Ants in Hospital Environments and Implications for Infection Control }, journal = {International Journal of Ecotoxicology and Ecobiology}, volume = {10}, number = {2}, pages = {31-39}, doi = {10.11648/j.ijee.20251002.12}, url = {https://doi.org/10.11648/j.ijee.20251002.12}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijee.20251002.12}, abstract = {Ants, common in urban ecosystems, often infiltrate hospital environments, where they can interfere with infection control measures. This study examined their ecological role in 15 hospitals across Nigeria, focusing on high-risk areas such as kitchens, waste disposal zones, and patient wards. Over 500 ant specimens were aseptically collected and analyzed using molecular and microbiological techniques, revealing contamination with pathogenic microorganisms like Listeria monocytogenes and Staphylococcus aureus. Ants were identified using morphological keys, and bacteria were isolated from the specimens using selective agars. The presence of antimicrobial-resistant bacteria carried by ants highlights the need for heightened awareness and stricter infection control measures in healthcare settings. While ants may act as mechanical vectors, facilitating the transmission of infectious agents, within healthcare settings, particularly in areas with suboptimal sanitation and inadequate pest control this study emphasizes the importance of addressing this issue in infection control protocols. This study recommends integrated pest management, routine sanitation, and structural modifications to reduce ant infestations. It also suggests adopting DNA-based microbial monitoring for early detection of contaminants. Hospitals should prioritize simple yet effective measures, such as proper hand hygiene, judicious use of antimicrobials, and robust pest control programs. By addressing ant-mediated pathogen spread, this research offers valuable insights to improve infection control strategies and enhance patient safety in modern healthcare environments. }, year = {2025} }
TY - JOUR T1 - The Ecological Role of Ants in Hospital Environments and Implications for Infection Control AU - Kingsley Peace Ifeoma Y1 - 2025/09/02 PY - 2025 N1 - https://doi.org/10.11648/j.ijee.20251002.12 DO - 10.11648/j.ijee.20251002.12 T2 - International Journal of Ecotoxicology and Ecobiology JF - International Journal of Ecotoxicology and Ecobiology JO - International Journal of Ecotoxicology and Ecobiology SP - 31 EP - 39 PB - Science Publishing Group SN - 2575-1735 UR - https://doi.org/10.11648/j.ijee.20251002.12 AB - Ants, common in urban ecosystems, often infiltrate hospital environments, where they can interfere with infection control measures. This study examined their ecological role in 15 hospitals across Nigeria, focusing on high-risk areas such as kitchens, waste disposal zones, and patient wards. Over 500 ant specimens were aseptically collected and analyzed using molecular and microbiological techniques, revealing contamination with pathogenic microorganisms like Listeria monocytogenes and Staphylococcus aureus. Ants were identified using morphological keys, and bacteria were isolated from the specimens using selective agars. The presence of antimicrobial-resistant bacteria carried by ants highlights the need for heightened awareness and stricter infection control measures in healthcare settings. While ants may act as mechanical vectors, facilitating the transmission of infectious agents, within healthcare settings, particularly in areas with suboptimal sanitation and inadequate pest control this study emphasizes the importance of addressing this issue in infection control protocols. This study recommends integrated pest management, routine sanitation, and structural modifications to reduce ant infestations. It also suggests adopting DNA-based microbial monitoring for early detection of contaminants. Hospitals should prioritize simple yet effective measures, such as proper hand hygiene, judicious use of antimicrobials, and robust pest control programs. By addressing ant-mediated pathogen spread, this research offers valuable insights to improve infection control strategies and enhance patient safety in modern healthcare environments. VL - 10 IS - 2 ER -