Costa, F. et al. Global morbidity and mortality of leptospirosis: A systematic review. PLoS Negl. Trop. Dis. 9, e0003898. https://doi.org/10.1371/journal.pntd.0003898 (2015).
Google Scholar
Cosson, J.-F. et al. Epidemiology of Leptospira transmitted by rodents in southeast Asia. PLoS Negl. Trop. Dis. 8, e2902. https://doi.org/10.1371/journal.pntd.0002902 (2014).
Google Scholar
Jonsson, C. B., Figueiredo, L. T. M. & Vapalahti, O. A global perspective on Hantavirus ecology, epidemiology, and disease. Clin. Microbiol. Rev. 23, 412–441. https://doi.org/10.1128/CMR.00062-09 (2010).
Google Scholar
Vaheri, A. et al. Uncovering the mysteries of Hantavirus infections. Nat. Rev. Microbiol. 11, 539–550. https://doi.org/10.1038/nrmicro3066 (2013).
Google Scholar
Peniche Lara, G., Dzul-Rosado, K. R., Zavala Velázquez, J. E. & Zavala-Castro, J. Murine typhus: Clinical and epidemiological aspects. Colomb. Med. (Cali) 43, 175–180 (2012).
Google Scholar
Pimentel, D., Lach, L., Zuniga, R. & Morrison, D. Environmental and economic costs of nonindigenous species in the United States. Bioscience 50, 53–65. https://doi.org/10.1641/0006-3568(2000)050[0053:EAECON]2.3.CO;2 (2000).
Google Scholar
Smith, R. & Meyer, A. Rodent control methods: Non-chemical and non-lethal chemical, with special reference to food stores. in Rodent Pests and Their Control (Buckle, A.P., Smith, R. eds.). 2nd edn. 101–122. (CAB International, 2015).
Himsworth, C. G., Jardine, C. M., Parsons, K. L., Feng, A. Y. T. & Patrick, D. M. The characteristics of wild rat (Rattus spp.) populations from an inner-city neighborhood with a focus on factors critical to the understanding of rat-associated zoonoses. PLoS ONE 9, e91654. https://doi.org/10.1371/journal.pone.0091654 (2014).
Google Scholar
Mari Saez, A. et al. Rodent control to fight Lassa fever: Evaluation and lessons learned from a 4-year study in Upper Guinea. PLoS Negl. Trop. Dis. 12, e0006829–e0006829. https://doi.org/10.1371/journal.pntd.0006829 (2018).
Google Scholar
Baldwin, R., Quinn, N., Davis, D. & Engeman, R. Effectiveness of rodenticides for managing invasive roof rats and native deer mice in orchards. Environ. Sci. Pollut. Res. 21, 5795–5802. https://doi.org/10.1007/s11356-014-2525-4 (2014).
Google Scholar
Hadler, M. R. & Buckle, A. P. Forty five years of anticoagulant rodenticides—Past, present and future trends. Proc. Vertebr. Pest Conf. 15, 149–155 (1992).
Rost, S. et al. Novel mutations in the VKORC1 gene of wild rats and mice – A response to 50 years of selection pressure by warfarin?. BMC Genet. 10, 4. https://doi.org/10.1186/1471-2156-10-4 (2009).
Google Scholar
Buckle, A., Prescott, C. & Ward, K. J. Resistance to the first and second generation anticoagulant rodenticides – A new perspective. Proc. Verebr. Pest Conf. 16, 138–144 (1994).
Goulois, J., Lambert, V., Legros, L., Benoit, E. & Lattard, V. Adaptative evolution of the Vkorc1 gene in Mus musculus domesticus is influenced by the selective pressure of anticoagulant rodenticides. Ecol. Evol. 7, 2767–2776. https://doi.org/10.1002/ece3.2829 (2017).
Google Scholar
Meerburg, B. G., van Gent-Pelzer, M. P. E., Schoelitsz, B. & van der Lee, T. A. J. Distribution of anticoagulant rodenticide resistance in Rattus norvegicus in the Netherlands according to Vkorc1 mutations. Pest Manag. Sci. 70, 1761–1766. https://doi.org/10.1002/ps.3809 (2014).
Google Scholar
Lund, M. Rodent resistance to the anticoagulant rodenticides, with particular reference to Denmark. Bull. World Health Organ. 47, 611–618 (1972).
Google Scholar
Lee, M. J. et al. Effects of culling on Leptospira interrogans carriage by rats. Emerg. Infect. Dis. 24, 356–360. https://doi.org/10.3201/eid2402.171371 (2018).
Google Scholar
Greaves, J. H. Resistance to anticoagulant rodenticides. in Rodent Pests and Their Control (Buckle, A.P., Smith, R. eds.). 2nd edn. 187–208. (CAB International, 2015).
Lefebvre, S. B., Benoit, E. & Lattard, V. Comparative biology of the resistance to vitamin K antagonists: An overview of the resistance mechanisms in Anticoagulation Therapy (Basaran, O., Biteker, M. eds.). 20–45. (Intech Open, 2016).
Grandemange, A. et al. Consequences of the Y139F Vkorc1 mutation on resistance to AVKs: In-vivo investigation in a 7th generation of congenic Y139F strain of rats. Pharmacogenet. Genomics. 19, 742–750. https://doi.org/10.1097/FPC.0b013e32832ee55b (2009).
Google Scholar
Sadowski, J. A., Esmon, C. T. & Suttie, J. W. Vitamin K-dependent carboxylase. Requirements of the rat liver microsomal enzyme system. J. Biol. Chem. 251, 2770–2776 (1976).
Google Scholar
Mooney, J. et al. VKORC1 sequence variants associated with resistance to anticoagulant rodenticides in Irish populations of Rattus norvegicus and Mus musculus domesticus. Sci. Rep. 8, 4535. https://doi.org/10.1038/s41598-018-22815-7 (2018).
Google Scholar
Thijssen, H. H. W. Warfarin-based rodenticides: Mode of action and mechanism of resistance. Pestic. Sci. 43, 73–78. https://doi.org/10.1002/ps.2780430112 (1995).
Google Scholar
Bell, R. G. & Caldwell, P. T. Mechanism of warfarin resistance. Warfarin and the metabolism of vitamin K1. Biochemistry 12, 1759–1762. https://doi.org/10.1021/bi00733a015 (1973).
Google Scholar
Pelz, H.-J. et al. The genetic basis of resistance to anticoagulants in rodents. Genetics 170, 1839–1847. https://doi.org/10.1534/genetics.104.040360 (2005).
Google Scholar
Baert, K., Stuyck, J., Breyne, P., Maes, D. & Casaer, J. Distribution of anticoagulant resistance in the brown rat in Belgium. Belg. J. Zool. 142, 39–48 (2012).
Prescott, C. V., Buckle, A. P., Gibbings, J. G., Allan, E. N. W. & Stuart, A. M. Anticoagulant resistance in Norway rats (Rattus norvegicus Berk.) in Kent – A VKORC1 single nucleotide polymorphism, tyrosine139phenylalanine, new to the UK. Int. J. Pest Manag. 57, 61–65. https://doi.org/10.1080/09670874.2010.523124 (2010).
Google Scholar
Grandemange, A., Lasseur, R., Longin-Sauvageon, C., Benoit, E. & Berny, P. Distribution of VKORC1 single nucleotide polymorphism in wild Rattus norvegicus in France. Pest Manag. Sci. 66, 270–276. https://doi.org/10.1002/ps.1869 (2009).
Google Scholar
Goulois, J. et al. Evidence of a target resistance to antivitamin K rodenticides in the roof rat Rattus rattus: Identification and characterisation of a novel Y25F mutation in the Vkorc1 gene. Pest Manag. Sci. 72, 544–550. https://doi.org/10.1002/ps.4020 (2015).
Google Scholar
Endepols, S., Klemann, N., Jacob, J. & Buckle, A. P. Resistance tests and field trials with bromadiolone for the control of Norway rats (Rattus norvegicus) on farms in Westphalia, Germany. Pest Manag. Sci. 68, 348–354. https://doi.org/10.1002/ps.2268 (2011).
Google Scholar
Andru, J., Cosson, J.-F., Caliman, J.-P. & Benoit, E. Coumatetralyl resistance of Rattus tanezumi infesting oil palm plantations in Indonesia. Ecotoxicology 22, 377–386. https://doi.org/10.1007/s10646-012-1032-y (2012).
Google Scholar
Department of Statistics Singapore. Population and Population Structure. https://www.singstat.gov.sg/find-data/search-by-theme/population/population-and-population-structure/latest-data (2020).
Department of Statistics Singapore. Environment. https://www.singstat.gov.sg/find-data/search-by-theme/society/environment/latest-data (2020).
Department of Statistics Singapore. M890531—Licensed Food Establishments (End of Period), Annual. https://www.tablebuilder.singstat.gov.sg/publicfacing/createDataTable.action?refId=14624 (2021).
QGIS Development Team. QGIS Geographic Information System. QGIS Association. https://www.qgis.org/en/site/ (2021).
Ivanova, N. V., Clare, E. L. & Borisenko, A. V. in DNA Barcodes: Methods and Protocols (John Kress, W. & Erickson, D.L. eds.) 153–182 (Humana Press, 2012).
Pagès, M. et al. Revisiting the taxonomy of the Rattini tribe: A phylogeny-based delimitation of species boundaries. BMC Evol. Biol. 10, 184. https://doi.org/10.1186/1471-2148-10-184 (2010).
Google Scholar
Pagès, M. et al. Cytonuclear discordance among Southeast Asian black rats (Rattus rattus complex). Mol. Ecol. 22, 1019–1034. https://doi.org/10.1111/mec.12149 (2013).
Google Scholar
Rungrojn, A. et al. Prevalence and molecular characterization of Rickettsia spp. from wild small mammals in public parks and urban areas of Bangkok metropolitan, Thailand. Trop. Med. Infect. Dis. https://doi.org/10.3390/tropicalmed6040199 (2021).
Google Scholar
Wulandhari, S. A. et al. High prevalence and low diversity of chigger infestation in small mammals found in Bangkok metropolitan parks. Med. Vet. Entomol. 35, 534–546. https://doi.org/10.1111/mve.12531 (2021).
Google Scholar
Cowan, P. E. et al. Vkorc1 sequencing suggests anticoagulant resistance in rats in New Zealand. Pest Manag. Sci. 73, 262–266. https://doi.org/10.1002/ps.4304 (2016).
Google Scholar
Rost, S. et al. Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2. Nature 427, 537–541. https://doi.org/10.1038/nature02214 (2004).
Google Scholar
Wong, T. W. et al. Hantavirus infections in humans and commensal rodents in Singapore. Trans. R. Soc. Trop. Med. Hyg. 83, 248–251. https://doi.org/10.1016/0035-9203(89)90666-4 (1989).
Google Scholar
Dubock, A. Pulsed baiting – A new technique for high potency, slow acting rodenticides. Proc. Vertebr. Pest Conf. 10, 123–136 (1982).
Garg, N., Singla, N., Jindal, V. & Babbar, B. Studies on bromadiolone resistance in Rattus rattus populations from Punjab, India. Pestic. Biochem. Physiol. 139, 24–31 (2017).
Google Scholar
Song, Y., Lan, Z. & Kohn, M. H. Mitochondrial DNA phylogeography of the Norway rat. PLoS ONE 9, e88425. https://doi.org/10.1371/journal.pone.0088425 (2014).
Google Scholar
Aplin, K. P. et al. Multiple geographic origins of commensalism and complex dispersal history of black rats. PLoS ONE 6, e26357. https://doi.org/10.1371/journal.pone.0026357 (2011).
Google Scholar
Boyle, C. M. Case of apparent resistance of Rattus norvegicus Berkenhout to anticoagulant poisons. Nature 188, 517. https://doi.org/10.1038/188517a0 (1960).
Google Scholar
Jackson, W. B. & Kaukeinen, D. Resistance of wild Norway rats in North Carolina to warfarin rodenticide. Science 176, 1343 (1972).
Google Scholar
Ma, X. et al. Low warfarin resistance frequency in Norway rats in two cities in China after 30 years of usage of anticoagulant rodenticides. Pest Manag. Sci. 74, 2555–2560. https://doi.org/10.1002/ps.5040 (2018).
Google Scholar
Markussen, M. D. K., Heiberg, A.-C., Fredholm, M. & Kristensen, M. Differential expression of cytochrome P450 genes between bromadiolone-resistant and anticoagulant-susceptible Norway rats: A possible role for pharmacokinetics in bromadiolone resistance. Pest Manag. Sci. 64, 239–248. https://doi.org/10.1002/ps.1506 (2008).
Google Scholar
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