Determining Factors for Acquiring Human Leptospirosis from Dogs along Morogoro Municipality, Tanzania
John B Tsaxra1*, Bakari I Ngecha3, Madoshi, PB4, Godfrey Katusi2 and Abdul AS Katakweba2
1Livestock Training Agency (LITA), Mabuki Campus, Mwanza, Tanzania
2Institute of Pest Management, Sokoine University of Agriculture, Morogoro, Tanzania
3Livestock Training Agency (LITA), Morogoro Campus, Morogoro, Tanzania
4ST. Francis University College of Health and Allied Sciences, Department of Public Health, Ifakara, Tanzania
*Corresponding Author: John B Tsaxra, Livestock Training Agency (LITA), Mabuki Campus, Mwanza, Tanzania.
Received:
October 25, 2024; Published: November 21, 2024
Abstract
Introduction: Leptospirosis is a global zoonotic disease of which natural reservoirs are rodents. However, diverse mammals, including pets, serve as transient maintenance hosts and often pass the disease to humans. Due to their mutualistic association with humans, infected dogs may serve as important vectors of leptospirosis. Human get infected after coming in contact with an environment contaminated with the urine of infected dogs. A serological study was conducted in free roaming and confined dogs in Morogoro, Tanzania, to determine the prevalence of leptospirosis in the canines.
Methodology: Blood samples were collected from 155 and 110 free roaming and confined dogs, respectively. Serum was separated by centrifugation at 3500 rpm for five minutes in the laboratory at the Institute of Pest Management and examined using the Microscopic Agglutination Test (MAT). Tested Leptospira spp antigens included serovars Sokoine, Pomona, Hebdomadis, Grippotyphosa and Kenya.
Results: The overall seroprevalence of leptospirosis in the dogs was 163 (61.5%), of which 88 (54.0%) and 75 (46.0%) had single and multiple leptospira serovars respectively. Furthermore, seroprevalence of 67.3% and 35.78% for free 1roaming and confined dogs respectively were recorded. The serovars in infected dogs were: Sokoine (54.6%), Pomona (41.1%), Grippotyphosa (23.9%), Hebdomadis (22.7%), and Kenya (19.6%). The seroprevalence for free roaming dogs was; serovar Sokoine (45.2%), Pomona (22.6%), Hebdomadis (18.7%), Grippotyphosa (16.8%) and Kenya (15.5%). In the confined dogs the serovar prevalence were Sokoine (14.7%), Grippotyphosa (7.3%), Kenya (3.7%), Pomona (22.0%) and Hebdomadis (4.6%). Of the positive dogs, 82 were males and 81 were females of which 133 and 30 were adults and puppies, respectively.
Conclusion: Higher prevalence of leptospirosis was found in free roaming than in confined dogs and serovars Pomona and Sokoine were the most frequent in the two groups of animals. Free roaming dogs have a bigger chance to be exposed to Leptospira spp due to broader interactions in diverse environments. Confinement and vaccination of dogs should be encouraged in Morogoro to reduce leptospirosis transmission in the animals and incidentally humans.
Keywords: Leptospirosis; Confined; Free Roaming; Dogs; Serovars; Morogoro
References
- Sykes JE., et al. “2010 ACVIM small animal consensus statement on leptospirosis: diagnosis, epidemiology, treatment, and prevention”. Journal of Veterinary Internal Medicine 25.1 (2011): 1-13.
- Chomel Bruno B. "Emerging and Re-Emerging Zoonoses of Dogs and Cats". Animals 4.3 (2014): 434-445.
- Allan KJ., et al. “Epidemiology of Leptospirosis in Africa: A Systematic Review of a Neglected Zoonosis and a Paradigm for ‘One Health’ in Africa”. PLOS Neglected Tropical Diseases 9.9 (2014): e0003899.
- Costa F., et al. “Global Morbidity and Mortality of Leptospirosis: A Systematic Review”. PLOS Neglected Tropical Diseases 9.9 (2015): e0003898.
- Lau CL., et al. “Climate change, flooding, urbanisation and leptospirosis: fuelling the fire?" Transactions of the Royal Society of Tropical Medicine and Hygiene 104 (2010b): 631-638.
- Hartskeerl RA., et al. “Emergence, control and re-emerging leptospirosis: dynamics of infection in the changing world”. Clinical Microbiology and Infection 17 (2011): 494-501.
- Wasinski B and Dutkiewicz J. “Leptospirosis-current risk factors connected with human activity and the environment”. Annals of Agricultural and Environmental Medicine 20.2 (2013).
- Bharti BR., et al. “Leptospirosis: a zoonotic disease of global importance”. The Lancet Infectious Diseases 3 (2003): 757-771.
- Mwachui MA., et al. “Environmental and behavioural determinants of leptospirosis transmission: a systematic review”. PLoS Neglected Tropical Diseases 9.9 (2015): e0003843.
- Adler B and Moctezuma AP. “Leptospira and leptospirosis”. Veterinary Microbiology 140 (2010): 287-296.
- Vijayachari P., et al. “Leptospirosis: an emerging global public health problem”. Journal of Biosciences 33 (2008): 557-569.
- Picardeau M. “Diagnosis and epidemiology of leptospirosis”. Medecine et Maladies Infectieuses 43 (2013): 1-9.
- Picardeau M. “Virulence of the zoonotic agent of leptospirosis: still terra incognita?” Nature Reviews Microbiology 15.5 (2017): 297-307.
- Shukla J., et al. “DNA probes for identification of leptospires and disease diagnosis”. Southeast Asian Journal of Tropical Medicine and Public Health 35 (2004): 346-352.
- Birnbaum N., et al. “Naturally acquired leptospirosis in 36 dogs: Serologic and clinicopathological features”. Journal of Small Animal Practice 39 (1998): 231.
- Perret PC., et al. “Risk factors and frequency of positive antibodies for leptospirosis in a sub urban population near Santiago”. Revista Medica de Chile 133 (2005): 426-431.
- Faine S., et al. “Leptospira and Leptospirosis. Medisci Melbourne, Australia” (1999).
- Levett PN. “Leptospirosis”. Clinical Microbiology 14.2 (2001): 296-326.
- Machang'u RS., et al. “Characterization of Leptospira isolates from captive giant pouched rats, Cricetomys gambianus. In Rats, Mice and People, Rodent Biology and Management pp 40-42. Edited by Singleton G. R., Hinds L. A., Krebs C. J., Spratt M. D. Canberra: Australian Centre for International Agricultural Research (2003).
- Weekes CC., et al. “Sero-epidemiology of canine leptospirosis on the island of Barbados”. Veterinary Microbiology 51 (1997): 215-222.
- Adesiyun AA., et al. “Sero-epidemiology of canine leptospirosis in Trinidad: serovars, implications for vaccination and public health”. Journal of Veterinary Medicine. B, Infectious Diseases and Veterinary Public Health 53 (2006): 91-99.
- Jimenez-Coello M., et al. “Stray dogs as reservoirs of the zoonotic agents Leptospira interrogans, Trypanosoma cruzi, and Aspergillus spp. in an urban area of Chiapas in southern Mexico”. Vector-Borne and Zoonotic Diseases (2010): 135-141.
- Bulach DM., et al. “Genome reduction in Leptospira borgpetersenii reflects limited transmission potential”. Proceedings of the National Academy of Sciences of the United States of America 103.39 (2006): 14560-14565.
- Cullen PA., et al. “Outer membrane proteins of pathogenic Spirochetes”. FEMS Microbiology Reviews 28.3 (2004): 291-318.
- Grooms DL. “Reproductive losses caused by bovine viral diarrhea virus and leptospirosis”. Theriogenology 66 (2006): 624-628.
- Said K., et al. “Seroprevalence of canine leptospirosis, in Urban and Periurban, Morogoro, Tanzania”. African Journal of Microbiology Research21 (2018): 481-487.
- Faine S. “Guidelines for the control of leptospirosis. Offset publication no. 67. World Health Organization, Geneva (1982).
- World Health Organization (2003): Human leptospirosis: Guidance for diagnosis, surveillance and control (2003).
- Assenga JA., et al. “Predominant leptospiral serogroups circulating among humans, livestock and wildlife in Katavi-Rukwa ecosystem, Tanzania”. PLOS Neglected Tropical Diseases 3 (2015): 1-14.
- Korver H. “Microscopic agglutination test (MAT) for the diagnosis of leptospirosis and serotyping of leptospires. In: Leptospirosis on the African continent. Proceedings of a CEC/STD 3 Research Meeting”. Harare, Zimbabwe (1992): 148-155.
- Abdul AS., et al. “Prevalence of haemoparasites, leptospires and coccobacilli with potential for human infection in the blood of rodents and shrews from selected localities in Tanzania, Namibia and Swaziland” (2012).
- Machang'u RS., et al. “Serological and molecular characterization of Leptospira serovar Kenya from captive African giant pouched rats (Cricetomys gambianus) from Morogoro Tanzania”. FEMS Immunology and Medical Microbiology 41 (2004): 117- 121.
- Mgode GF., et al. “New Leptospira serovar Sokoine of serogroup Icterohaemorrhagiae from cattle in Tanzania”. International Journal of Systematic and Evolutionary Microbiology 56 (2006): 593-597.
- Mgode GF., et al. “LeptospiraSerovars for Diagnosis of Leptospirosis in Humans and Animals in Africa: Common Leptospira Isolates and Reservoir Hosts”. PLOS Neglected Tropical Diseases 12 (2015): e0004251.
- Ahmed N., et al. “Multilocus sequence typing method for identification and genotypic classification of pathogenic Leptospira species”. Annals of Clinical Microbiology and Antimicrobials1 (2006): 1-10.
- Machang’u RS., et al. “Leptospirosis in animals and humans in selected areas of Tanzania”. Belgian Journal of Zoology 127 (1997): 97-104.
- Georgies F Mgode., et al. “Leptospira infections in freshwater fish in Morogoro Tanzania: a hidden public health Threat”. Tanzania Journal of Health Research 16 (2014).
Citation
Copyright