RESEARCH PAPER
Screening for anthrax occurrence in soil of flooded rural areas in Poland after rainfalls in spring 2010
 
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National Institute of Public Health – National Institute of Hygiene, Department of Bacteriology, Warsaw, Poland
 
 
Corresponding author
Aleksandra A. Zasada   

National Institute of Public Health – National Institute of Hygiene, Department of Bacteriology, Warsaw, Poland
 
 
Ann Agric Environ Med. 2014;21(3):460-463
 
KEYWORDS
ABSTRACT
Introduction and objective:
Anthrax spores remain viable and infectious in soil for decades. Flood water can percolate towards the surface the spores buried in soil. Moreover, the flood water might transport spores to areas previously unaffected. After the water recedes the spores located on the surface of the ground can be consumed by grazing animals and cause outbreaks of anthrax.

Material and Methods:
Soil samples were collected in areas of Poland most affected by floods in 2010 (Lubelskie, Świętokrzyskie, Podkarpackie and Mazowieckie provinces). After heating with the aim to kill vegetative forms of bacteria, the samples were cultured on PLET agar and the resulted colonies were investigated in terms of motility and presence of anthrax specific chromosomal (SG-749, plcR) and plasmid markers (capB, pagA).

Results:
In total, 424 spore-forming, aerobically growing isolates were collected from the tested soil samples. Eighty-nine of them were non-motile. All the isolates were negative in PCR for anthrax specific chromosomal and plasmid markers.

Conclusions:
Spores of B. anthracis that could be related to risk of anthrax outbreaks were not detected in soil samples tested in this study. The negative results presented may not be proof that Poland is country free of anthrax. The results, however, may suggest a relatively low risk of anthrax outbreaks being triggered in the sampled areas

 
REFERENCES (21)
1.
Koehler TM. Anthrax. Springer-Verlsg Berlin Heidelberg New York, 2002.
 
2.
De Vos V. The ecology of anthrax in the Kruger National Park, South Africa. Salisbury Med Bull. 1990; 68S: 19–23.
 
3.
Turnbull PCB. Guidelines for the surveillance and control of anthrax in humans and animals. 3 rd ed. WHO/EMC/ZDI./98.6.
 
4.
Fasanella A, Galante D, Garofolo G, Jones MH. Anthrax undervalued zoonosis. Vet Micorbiol. 2010; 140: 318–331.
 
5.
Durrheim DN, Freeman P, Roth I, Hornitzky M. Epidemiologic questions from anthrax outbreaks, Hunter Valley, Australia. Emerg Infect Dis. 2009; 15: 840–842.
 
6.
Lewerin SS, Elvander M, Westermark T, Hartzell LN, Norstrom AK, Ehrs S, et al. Anthrax outbreak in a Swedish beef cattle herd – 1 st case in 27 years: case report. Acta Vet Scand. 2010; 52: 7.
 
7.
Knisely RF. Selective medium for Bacillus anthracis. J Bacteriol. 1966; 92: 784–786.
 
8.
Gierczyński R, Zasada AA, Raddadi N, Merabishvili M, Daffonchio D, Rastawicki W, et al. Specific Bacillus anthracis identification by a plcR-targeted restriction site insertion-PCR (RSI-PCR) assay. FEMS Microbiol Lett. 2007; 272: 55–59.
 
9.
Daffonchio D, Borin S, Frova G, Gallo R, Mori E, Fani R, et al. A randomly amplified polymorphic DNA marker specific for the Bacillus cereus group is diagnostic for Bacillus anthracis. Appl Environ Microbiol. 1999; 65: 1298–1303.
 
10.
Zasada AA, Gierczyński R, Kałużewski S, Jagielski M. Virulotypes of Bacillus anthracis strains isolated in Poland. Med Dośw Mikrobiol. 2005; 57: 269–275.
 
11.
Naruszewicz-Lesiuk D. Wąglik. In: Kostrzewski J. Choroby zakaźne w Polsce i ich zwalczanie w latach 1919–1962. Warszawa, PZWL, 1964. p. 380–389 (in Polish).
 
12.
Anusz Z. Wąglik. In: Kostrzewski J. Choroby zakaźne w Polsce i ich zwalczanie w latach 1961–1970. Warszawa, PZWL, 1973. p. 292–297 (in Polish).
 
13.
Anusz Z. Wąglik. In: Kostrzewski J. Choroby zakaźne w Polsce i ich zwalczanie w latach 1970–1979. Wrocław, Ossolineum, 1984. p. 292–294 (in Polish).
 
14.
PZH. Meldunki o zachorowaniach na choroby zakaźne, zakażeniach i zatruciach w Polsce. http://www.pzh.gov.pl/epimeld/... (access: 2013.02.05) (in Polish).
 
15.
Hamplson K, Lembo T, Bessell P, Auty H, Packer C, Holliday J, et al. Predictability of anthrax infection in the Serengeti, Tanzania. J Appl Ecol. 2011; 48: 1333–1344.
 
16.
Epp T, Walander C, Argue CK. Case-control study investigating an anthrax outbreak in Saskatchewan, Canada – Summer 2006. Can Vet J. 2010; 51: 973–978.
 
17.
Munang’andu HM, Banda F, Siamudaala VM, Munyeme M, Kasanga CJ, Hamududu B. The effect of seasonal variation on anthrax epidemiology in the upper Zambezi floodplain of western Zambia. J Vet Sci. 2012; 13: 293–298.
 
18.
Bielawska-Drózd A, Niemcewicz M, Bartoszcze M. The evaluation of methods for detection of Bacillus anthracis spores in artificially contaminated soil samples. Pol J Environ Stud. 2008; 17: 5–10.
 
19.
Van der Auwera GA, Timmery S, Hoton F, Mahillon J. Plasmid exchanges among members of the Bacillus cereus group in food-stuff. Int J Food Microbiol. 2007; 113: 164–172.
 
20.
Scott II E., Dyer DW. Divergence of the SigB regulon and pathogenesis of the Bacillus cereus sensu lato group. BMC Genomics. 2012; 13: 564.
 
21.
Hu X, Van der Auwera G, Timmery S, Zhu L, Mahillon J. Distribution, diversity, and potential mobility of extrachromosomal elements related to the Bacillus anthracis pXO1 and pXO2 virulence plasmids. Appl Environ Microbiol. 2009; 75: 3016–3028.
 
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ISSN:1232-1966
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