The first recorded epidemic of leptospirosis in sheep in Egypt

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Rev. sci. tech. Off. int. Epiz., 2014, 33 (3),... -... The first recorded epidemic of leptospirosis in sheep in Egypt This paper (No. 27022014-00027-EN) has been peer-reviewed, accepted, edited, and corrected by authors. It has no yet been formatted for printing. It will be published in December 2014 in issue 33-3 of the Scientific and Technical Review. M.E. Hatem & A. Samir * Department of Microbiology, Faculty of Veterinary Medicine, Cairo University, P.O. Box 12211, Cairo, Egypt *Corresponding author: ahmed.samir@cu.edu.eg; ahmedsamir121@hotmail.com This work was carried out at the Department of Microbiology, Faculty of Veterinary Medicine, Cairo University Summary An outbreak of leptospirosis in sheep is recorded as the first epidemic of ovine leptospirosis in Egypt. The sick animals showed typical symptoms such as fever, jaundice, red urine and abortion, with a fatal course. Acute and convalescent sera were tested for demonstration of seroconversion using the microscopic agglutination test to confirm infection. Long-acting tetracycline was successfully used for treatment. Keywords Egypt Epidemic Leptospirosis Ovine Record Sheep. Introduction Leptospirosis is a re-emerging zoonosis caused by Leptospira spp. The natural reservoirs and carriers of leptospires are domestic and wild animals (1). The disease is serious, with public health significance, and is considered a hazard for occupations that imply close contact with animals, such as agricultural and dairy farmers, sewer workers, veterinarians and fishing industry workers (2). Serological evidence of leptospirosis in sheep has been reported by No. 27022014-00027-EN 1/6

many authors in India (3); in Brazil the epidemiology of leptospirosis in sheep is complex and the bacterium can infect a large number of animals in the herd (4). The disease may become endemic for a small number of serovars more adapted to sheep. In Egypt, several recent studies have confirmed the re-emergence of leptospirosis in humans (2, 5, 6) but few (1, 7, 8) have reported on the surveillance of leptospirosis in animals. One report in farm animals over 20 years ago found that 4.2% of sheep were seropositive for Leptospira spp. (8), whereas in a recent study (1) none of the collected ovine sera was seroreactive. In this paper, a recent outbreak of leptospirosis is documented on a sheep farm in Northern Egypt, on the Cairo Alexandria road, near Alexandria. Materials and methods In December 2012 (wet season), a sheep farm in Northern Egypt on the Cairo Alexandria road, with 1,500 ewes and 500 suckling lambs, had 45 cases (2.3%) of leptospiral infection. The animals suffered from fever, were off their feed, and showed icteric symptoms and red urine. Blood samples were collected from the 45 cases during the first week of clinical signs (acute phase), and sera were used in the microscopic agglutination test (MAT). Some of the sick animals had received medication before the blood samples were collected. A further 20 blood samples were taken as controls from animals in the same flock that showed no clinical signs. Veterinarians at the farm started treatment at the onset of clinical signs with a full dose of Pen & Strep (Norbrook, Ireland), a combination of procaine penicillin (dose: 8 mg/kg bodyweight) and dihydrostreptomycin sulphate (dose: 10 mg/kg bodyweight), and then changed the medication to the longacting tetracycline Alamycin 300 (Norbrook, Ireland), dose: 20 mg/kg bodyweight. The MAT was performed according to Cole et al. (9), using 12 serovars of the genus Leptospira previously isolated in Egypt as antigens (1, 2, 5, 10). The serovars used were Alexi, Australis, Bataviae, Bratislava, Canicola, Grippotyphosa, Hardjo, Hebdomadis, No. 27022014-00027-EN 2/6

Icterohaemorrhagiae, Pomona, Pyrogenes and Wolfii. Briefly, live suspensions of leptospires representing the 12 serovars were added to serially diluted serum specimens in 96-well microtitre plates and incubated at an ambient temperature for 1.5 h. Agglutination was examined using dark-field microscopy at 100 magnification. Titres were calculated as the highest serum dilution that agglutinated at least 50% of the leptospires for each serovar used. Follow-up serum samples (convalescent stage) were obtained two weeks later and tested for seroconversion. Isolation of leptospires was attempted by inoculating each sample of body fluids (blood, milk, urine) and uterine discharges into three or four tubes of Ellinghausen McCullough Johnson Harris (EMJH) liquid medium. The EMJH base (BD, United States [USA]) was prepared and autoclaved, then EMJH enrichment (BD, USA) and 5-fluorouracil (200 μg/ml; Sigma Chemical Co., St. Louis, MO) were added aseptically (1). All cultures were incubated at 30 C for up to 12 weeks and examined weekly by dark-field microscopy. Results The MAT results (Table I) showed that all the sera from the acute cases were reactive with the Icterohaemorrhagiae serovar (titres 1:400 to 1:800) and some also showed reactivity with the Pomona serovar (titres 1:200 to 1:400). Sera from the convalescent cases reacted with the same two serovars: Icterohaemorrhagiae (titres 1:1,600 to 1:12,800) and Pomona (titres 1:800 to 1:6,400). The 20 control sera showed no seroreactivity. The isolation of leptospires from blood, urine, milk and uterine discharges in the affected cases was unsuccessful (12 weeks post-culture). Discussion An outbreak of leptospirosis in sheep was recorded for the first time in Northern Egypt. The animals were suffering from typical symptoms and infection was confirmed by the demonstration of seroconversion using MAT. Inspection at the affected farm identified brown rats (Rattus norvegicus) in the feed store area (silage store); these animals No. 27022014-00027-EN 3/6

are a possible source of infection, as confirmed in a recent study in the Delta region in Egypt (1), where brown rats have been captured, bled and found to be an important source transmitting leptospires to humans and other animal species. Although treatment with the full dose of Pen & Strep was initiated at the onset of clinical signs, the disease was not controlled and new clinical cases appeared (a total of 45 cases, among which four ewes aborted); in total, 26 of the 1,500 ewes died (1.7%). The medication strategy was changed to long-acting tetracycline, which helped in the recovery of the sick animals and in the prevention of new cases. Tetracycline is recommended (2) as an anti-leptospiral drug; however, it is unclear why the penicillin/streptomycin combination failed, as it is considered an effective treatment (6). Isolation of the pathogen was unsuccessful (12 weeks postinoculation), although some of the animals had started treatment before sample collection and this might have affected the isolation process. Some culture tubes showed variable rates of contamination despite the addition of a selective supplement to the media and this may be due to the nature of the samples: urine, milk and uterine discharges after abortions. Failure to recover leptospires does not eliminate the possibility that the animal is infected, it merely indicates that the animal was not excreting detectable numbers of leptospires at the time of testing (11). Although clinical leptospirosis is uncommon in sheep, both sporadic and epidemic disease can occur (12). This report is of an outbreak of leptospirosis among sheep in Egypt in which the animals showed typical clinical presentation. The diagnosis was confirmed in the laboratory using the gold standard serological test (MAT), which has been proven to detect rising titres (seroconversion) of antibodies in serum samples from clinical cases. The epidemic disappeared after appropriate treatment was initiated. Conflicts of interest Nothing to declare. No. 27022014-00027-EN 4/6

References 1. Felt S.A., Wasfy M.O., El-Tras W.F., Samir A., Adel Rahman B., Boshra M., Parker T.M., Hatem M.E., El-Bassiouny A.A., Murray C.K. & Pimentel G. (2011). Cross-species surveillance of Leptospira in domestic and peri-domestic animals in Mahalla City, Gharbeya Governorate, Egypt. Am. J. trop. Med. Hyg., 84 (3), 420 425. 2. Ismail T.F., Wasfy M.O., Adul-Rahman B., Murray C.K., Hospenthal D.R., Abdel-Fadeel M., Abdel-Maksoud M., Samir A., Hatem M.E., Klena J., Pimentel G., El-Sayed N. & Hajjeh R. (2006). Retrospective serosurvey of leptospirosis among acute febrile illness and hepatitis patients in Egypt. Am. J. trop. Med. Hyg., 75, 1085 1089. 3. Balakrishnan G., Govindarajan R., Meenambigai T.V. & Murali Manohar B. (2011). Seroprevalence of leptospirosis among sheep in Tamilnadu. J. vet. anim. Sci., 7 (6), 285 289. 4. Lucheis S.B. & Ferreira J.R. (2011). Ovine leptospirosis in Brazil. J. venom. Anim. Toxins incl. trop. Dis., 17 (4), 394 405. 5. Murray C.K., Gray M.R., Mende K., Parker T.M., Samir A., Adel Rahman B., Habashy E.E., Hospenthal D.R. & Pimentel G. (2011). Use of patient-specific Leptospira isolates in the diagnosis of leptospirosis employing microscopic agglutination testing (MAT). Trans. roy. Soc. trop. Med. Hyg., 105 (4), 209 213. 6. Murray C.K., Pimentel G., Parker T., Beckius M.L., Samir A., Abdel-Rahman B., Mende K., Galloway R.L. & Hospenthal D.R. (2008). Antimicrobial susceptibilities of clinical human isolates of Leptospira from Egypt. In 57th Annual Meeting of the American Society of Tropical Medicine and Hygiene. Am. J. trop. Med. Hyg., 79 (6), 78. 7. Hamdy A.H., Brownlow W.J. & Dedeaux J.D. (1962). Leptospirosis in bovines and their human contacts in Egypt (UAR). Am. J. trop. Med. Hyg., 11, 98 101. No. 27022014-00027-EN 5/6

8. Sebek Z., Sixl W., Valova M. & Schaffler R. (1989). Leptospirosis in man, in wild and in domestic animals at waste disposal sites in Cairo. Geogr. med. Suppl., 3, 141 150. 9. Cole J.R., Sulzer C.R. & Pursell A.R. (1973). Improved microtechnique for the leptospiral microscopic agglutination test. Appl. Microbiol., 25, 976 980. 10. Parker T.M., Murray C.K., Richards A.K, Samir A., Ismail T.F, Abdel-Fadeel M., Ju Jiang, Wasfy M.O. & Pimentel G. (2007). Concurrent infections in acute febrile illness patients in Egypt. Am. J. trop. Med. Hyg., 77 (2), 390 392. 11. World Organisation for Animal Health (OIE) (2008). Leptospirosis, Chapter 2.1.9. Terrestrial Animal Health Code, OIE, Paris, 251 264. Available at: www.oie.int/fileadmin/home/eng/health_standards/tahm/2.01.09_le PTO.pdf (accessed in January 2013). 12. Thorenton R. (1994). Leptospirosis in New Zealand sheep. Surveillance, 21 (2), 13 14. Table I Titres of two serovars of Leptospira spp. in acute and convalescent serum samples showing seroconversion (rising titres) No. of serum specimens Acute sera Convalescent sera Icterohaemorrhagiae Pomona Icterohaemorrhagiae Pomona 8 1:400 Nil 1:6,400 Nil 15 1:800 Nil 1:6,400 Nil 10 1:800 Nil 1:12,800 Nil 2 1:800 1:200 1:3,200 1:800 6 1:800 1:200 1:6,400 1:1,600 4 1:800 1:400 1:6,400 1:3,200 45 No. 27022014-00027-EN 6/6