Detection of Atypical Motile Staphylococcus aureus from Rain Floods
DOI:
https://doi.org/10.3889/oamjms.2022.8686Keywords:
Colony spreading, Staphylococci, Rainwater, Oil displacement activityAbstract
Abstract:
Heavy rain floods is one of the primary risk factors for human health, and it can significantly
regulate microbial communities and enhance the transfer of infections within the affected areas. Recently, the flood crisis is becoming one of the severe natural events in Mosul / Iraq. It may continue for months during which samples of accumulated rainwater were collected.
Twelve Staphylococcus aureus were isolated by using two selective media: Mannitol Salt agar and Vogel-Johnson media in addition to Blood agar. An unusual colony spreading which resembles. "Bacillus colonies in twelve Staphylococcus aureus isolates was observed on Mannitol Salt agar and semisolid nutrient agar. Actively motile cocci in single and cluster arrangements that is not characteristic of brownian movement was shown in wet mount microscopic observation Furthermore, biosurfactant detection by oil spreading method ( oil displacement activity) showed that all isolates demonstrated various degrees of surfactant production which has beeen reported. to be responsible for stimulating "colony spreading" phenomenon in S. aureux. Motility can play a crucial role for survival bacterial species by which they get nutrients, avoid toxins and predators, and genetic information exchange by mating.
The present study highlights for the first time. Mosul city a motile opportunistic aureus obtained from harvested rainwater samples during high-rainfall periods. Utilization of untreated harvested rainwater could thus offer a significant health threat to consumers, especially children.
and immunocompromised individuals.
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References
Okaka FO, Odhiambo BD. Relationship between flooding and out break of infectious diseases in Kenya: A review of the literature. J Environ Public Health. 2018;2018:5452938. https://doi.org/10.1155/2018/5452938 PMid:30416526 DOI: https://doi.org/10.1155/2018/5452938
Paterson DL, Wright H, Harris PN. Health risks of flood disasters. Clin Infect Dis. 2018;67(9):1450-4. https://doi.org/10.1093/cid/ciy227 PMid:30986298 DOI: https://doi.org/10.1093/cid/ciy227
Rodgers K, McLellan I, Peshkur T, Williams R, Tonner R, Hursthouse AS, et al. Can the legacy of industrial pollution influence antimicrobial resistance in estuarine sediments. Environ Chem Lett. 2019;17:595-607. DOI: https://doi.org/10.1007/s10311-018-0791-y
Shokri A, Sabzevari S, Hashemi SA. Impacts of flood on health of Iranian population: Infectious diseases with an emphasis on parasitic infections. Parasite Epidemiol Control 2020;9:e00144. https://doi.org/10.1016/j.parepi.2020.e00144 PMid:32215322 DOI: https://doi.org/10.1016/j.parepi.2020.e00144
Hamilton K, Reyneke B, Waso M, Clements Y, Ndlovu T, Khan W, et al. A global review of the microbiological quality and potential health risks associated with roof-harvested rainwater tanks. NPJ Clean Water. 2019;2:7. https://doi.org/10.1038/s41545-019-0030-5 DOI: https://doi.org/10.1038/s41545-019-0030-5
Tsompanidou E, Denham EL, Sibbald MJ, Yang XM, Seinen J, Friedrich AW, et al. The Sortase A Substrates FnbpA, FnbpB, ClfA and ClfB antagonize colony spreading of Staphylococcus aureus. PLoS One. 2012;7(9):e44646. https://doi.org/10.1371/journal.pone.0044646 PMid:22970276 DOI: https://doi.org/10.1371/journal.pone.0044646
Kruse E. Varianter af Staphylococcus aureus og albus. Nord Veterinaermed. 1953;5:982-94.
Henrichsen J. Bacterial surface translocation: A survey and a classification. Bacteriol Rev. 1972;36(4):478-503. https://doi.org/10.1128/br.36.4.478-503.1972 PMid:4631369 DOI: https://doi.org/10.1128/br.36.4.478-503.1972
Kinsinger RF, Shirk MC, Fall R. Rapid surface motility in Bacillus subtilis is dependent on extracellular surfactin and potassium ion. J Bacteriol. 2003;185(18):5627-31. https://doi.org/10.1128/JB.185.18.5627-5631.2003 PMid:12949115 DOI: https://doi.org/10.1128/JB.185.18.5627-5631.2003
Kaito C, Sekimizu K. Colony spreading in Staphylococcus aureus. J Bacteriol. 2007;189(6):2553-7. https://doi.org/10.1128/JB.01635-06 PMid:17194792 DOI: https://doi.org/10.1128/JB.01635-06
Tsompanidou E, Sibbald MJ, Chlebowicz MA, Dreisbach A, Back JW, Van Dijl JM, et al. Requirement of the agr locus for colony spreading of Staphylococcus aureus. J Bacteriol. 2011;193(5):1267-72. https://doi.org/10.1128/JB.01276-10 PMid:21169484 DOI: https://doi.org/10.1128/JB.01276-10
Kaito C, Omae Y, Matsumoto Y, Nagata M, Yamaguchi H, Aoto T, et al. A novel gene, fudoh, in the SCCmec region suppresses the colony spreading ability and virulence of Staphylococcus aureus. PLoS One. 2008;3(12):e3921. https://doi.org/10.1371/journal.pone.0003921 PMid:19079549 DOI: https://doi.org/10.1371/journal.pone.0003921
Morikawa M, Hirata Y, Imanaka T. A study on the structure-function relationship of lipopeptide biosurfactants. Biochim Biophys Acta. 2000;1488(3):211-8. https://doi.org/10.1016/s1388-1981(00)00124-4 PMid:11082531 DOI: https://doi.org/10.1016/S1388-1981(00)00124-4
Ueda T, Kaito C, Omae Y, Sekimizu K. Sugar-responsive gene expression and the agr system are required for colony spreading in Staphylococcus aureus. Microb Pathog. 2011;51(3):178-85. https://doi.org/10.1016/j.micpath.2011.04.003 PMid:21514374 DOI: https://doi.org/10.1016/j.micpath.2011.04.003
Josenhans C, Suerbaum S. The role of motility as a virulence factor in bacteria. Int J Med Microbiol. 2002;291(8):605-14. https://doi.org/10.1078/1438-4221-00173 PMid:12008914 DOI: https://doi.org/10.1078/1438-4221-00173
Jarrell KF, McBride MJ. The surprisingly diverse ways that prokaryotes move. Nat Rev Microbiol. 2008;6(6):466-76. https://doi.org/10.1038/nrmicro1900 PMid:18461074 DOI: https://doi.org/10.1038/nrmicro1900
Omae Y, Sekimizu K, Kaito C. Identification of Staphylococcus aureus colony-spreading stimulatory factors from mammalian serum. PLoS One. 2014;9(5):e97670. https://doi.org/10.1371/journal.pone.0097670 PMid:24831518 DOI: https://doi.org/10.1371/journal.pone.0097670
Tsompanidou E, Denham EL, Becher D, De Jong A, Buist G, Van Oosten M, et al. Distinct roles of phenol-soluble modulins in spreading of Staphylococcus aureus on wet surfaces. Appl Environ Microbiol. 2013;79(3):886-95. https://doi.org/10.1128/AEM.03157-12 PMid:23183971 DOI: https://doi.org/10.1128/AEM.03157-12
Pollitt EJ, Crusz1 SA, Diggle SP. Staphylococcus aureus forms spreading dendrites that have characteristics of active motility. Sci Rep. 2015;5:17698. https://doi.org/10.1038/srep17698 PMid:26680153 DOI: https://doi.org/10.1038/srep17698
Lin MH, Ke WJ, Liu CC, Yang MW. Modulation of Staphylococcus aureus spreading by water. Sci Rep. 2016;6:25233. https://doi.org/10.1038/srep25233 PMid:27125382 DOI: https://doi.org/10.1038/srep25233
Otto M. Phenol-soluble modulins. Int J Med Microbiol. 2014;304(2):164-9. https://doi.org/10.1016/j.ijmm.2013.11.019 DOI: https://doi.org/10.1016/j.ijmm.2013.11.019
Chatterjee SS, Chen L, Joo HS, Cheung GY, Kreiswirth BN, Otto M. Distribution and regulation of the mobile genetic element-encodedphenol-soluble modulin PSM-mecin methicillin-resistant Staphylococcus aureus. PLoS One6. 2011;6(12):e28781. https://doi.org/10.1371/journal.pone.0028781 PMid:22174895 DOI: https://doi.org/10.1371/journal.pone.0028781
Plaza G, Zjawiony I, Banat I. Use of different methods for detection of thermophilic biosurfactant-producing bacteria from hydrocarbon-contaminated bioremediated soils. J Petro Sci Eng. 2006;50(1):71-7. https://doi.org/10.1016/j.petrol.2005.10.005 DOI: https://doi.org/10.1016/j.petrol.2005.10.005
Youssef NH, Duncan KE, Nagle DP, Savage KN, Knapp RM, McInerney MJ. Comparison of methods to detect biosurfactant production by diverse microorganisms. J Microbiol Methods. 2004;56(3):339-47. https://doi.org/10.1016/j.mimet.2003.11.001 PMid:14967225 DOI: https://doi.org/10.1016/j.mimet.2003.11.001
Laanto E, Bamford JK, Laakso J, Sundberg LR. Phage-driven loss of virulence in a fish pathogenic bacterium. PLoS One. 2012;7(12):e53157. https://doi.org/10.1371/journal.pone.0053157 PMid:23308090 DOI: https://doi.org/10.1371/journal.pone.0053157
Margarit I, Rinaudo CD, Galeotti CL, Maione D, Ghezzo C, Buttazzoni E, et al. Preventing bacterial infections with pilus-based vaccines: The group B Streptococcus paradigm. J Infect Dis. 2009;199(1):108-15. https://doi.org/10.1086/595564 PMid:19086816 DOI: https://doi.org/10.1086/595564
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Copyright (c) 2022 Yusra Agha, Ashwak Hazem Najim, Reem Ayad Talaat, Shababa Abdulatife Bahjat (Author)
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