Next Article in Journal
Investigation of the Antimicrobial Impact of Cold Atmospheric Plasma on Wet and Dry Microorganisms
Previous Article in Journal
Innovative Microorganisms in Environmental Cleanup: Effective Microorganism-Based Bioprocesses
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Proceeding Paper

Presence and Distribution of Human-Related Microsporidian Spores across Different Topsoil Areas across Alcalá de Henares (Spain) †

by
Antonio Peña-Fernández
1,2,*,
Manuel Higueras
3,
María del Carmen Lobo-Bedmar
4,
Fernando Izquierdo
5 and
Umar Anjum
2
1
Department of Surgery, Medical and Social Sciences, Faculty of Medicine and Health Sciences, University of Alcalá, Ctra. Madrid-Barcelona, Km. 33.600, 28871 Alcalá de Henares, Spain
2
Leicester School of Allied Health Sciences, De Montfort University, Leicester LE1 9BH, UK
3
Scientific Computation & Technological Innovation Center (SCoTIC), Universidad de La Rioja, 26004 Logroño, Spain
4
Departamento de Investigación Agroambiental, IMIDRA, Finca el Encín, Crta. Madrid-Barcelona Km, 38.2, 28800 Alcalá de Henares, Spain
5
Facultad de Farmacia, Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, 28660 Boadilla del Monte, Spain
*
Author to whom correspondence should be addressed.
Presented at the 2nd International Electronic Conference on Microbiology, 1–15 December 2023; Available online: https://ecm2023.sciforum.net.
Biol. Life Sci. Forum 2024, 31(1), 5; https://doi.org/10.3390/ECM2023-16461
Published: 30 November 2023
(This article belongs to the Proceedings of The 2nd International Electronic Conference on Microbiology)

Abstract

:
Humans can potentially be exposed to Enterocytozoon bieneusi and Encephalitozoon spp. from topsoils when playing or spending time in recreational areas. Two hundred and seventy-seven topsoil samples were collected across Alcalá de Henares (Spain) in July 2017: one hundred and fifty-five urban, sixty industrial and twelve from a public garden. Simultaneous detection was performed using a SYBR Green real-time PCR following the appropriate extraction of DNA with Fast-Prep for Soil®. The organic matter content (OM), pH, electrical conductivity (EC) and soil texture (percentages of sand, clay and silt) were also determined. E. bieneusi was detected in nine (five urban, four industrial); meanwhile, Encephalitozoon spp. was detected in 22 topsoil samples (sixteen urban, six industrial; ten E. intestinalis, nine E. intestinalis/E. hellem and three E. cuniculi). The presence of E. bieneusi was associated with urban soils that presented lower EC (0.50 vs. 0.71 dS/m; p-value = 0.0110), as this factor may provide a richer environment for the survival of spores. The presence of microsporidian spores was higher in those topsoils with a higher OM content for E. bieneusi (6.96% vs. 4.98%; p-value = 0.0342) and E. intestinalis/E. hellem in one of the four quadrants into which the urban area was divided (5.54% vs. 3.12%; p-value = 0.0007). E. intestinalis is present in industrial topsoils with significantly lower contents of sand (14.5% vs. 21.74; p-value = 0.00003) but higher contents of silt (78.5% vs. 64.9%; p-value = 0.0229), which might be attributed to the differences in the capacity of topsoils to retain moisture, depending on their texture. Moreover, the provision of enough oxygen might play a role in the higher presence of E. intestinalis/E. hellem in urban topsoils with lower contents of clay (11% vs. 19%; p-value = 0.0200). A better understanding of these potential associations is critical in selecting appropriate decontamination techniques and strategies to prevent and minimise human exposure.

1. Introduction

Microsporidia are a diverse group of unicellular obligate intracellular parasites that have been recently classified as fungi, either as a basal branch or as a sister group [1]. Phylogenetic studies suggest that microsporidia are closely related to a group of obligate intracellular parasites called the Cryptomycota or Rozellomycota [2]. About 1400 microsporidia species distributed within 200 genera that appear to infect all animals have been described [3]; however, to date, only nine genera have been shown to be capable of producing infections in humans [4]: Vittaforma, Anncaliia, Pleistophora, Encephalitozoon, Enterocytozoon, Trachipleistophora, Tubulinosema, Endoreticulatus and Microsporidium. Within these genera, seventeen species are related to human infection [5], the most relevant being Enterocytozoon bieneusi and Encephalitozoon species, which include E. intestinalis, E. hellem and E. cuniculi.
Human-related microsporidia species can affect both immunocompromised and immunocompetent individuals and produce oval-shaped microscopic spores that are highly resistant to harsh environmental conditions [1,4]. Although it is considered that microsporidia are ubiquitous in the environment, their diversity in soils and sand has been little explored, despite the literature suggesting that there could be a wide diversity of microsporidian species in soils and composts [3]. Thus, Ardila-Garcia et al. [3] identified 22 novel microsporidian sequences in soils, sands and composts collected from the Vancouver metropolitan area (BC, Canada) and Union Bay Natural Area in Seattle, USA.
Despite the fact that humans, especially children and immunodeficient individuals, could be potentially exposed to Enterocytozoon bieneusi and Encephalitozoon spp. from topsoils when playing or spending time in green and recreational areas in urban environments, previous studies have not detected these species in sands collected from playgrounds in parks in southern Madrid (Spain) [6]. However, these authors explored the presence of microsporidian spores using microscopic methods. As a result, we carried out a preliminary study using molecular methods and described, for the first time, spores of E. bieneusi and Encephalitozoon spp. in topsoils collected from urban parks across Alcalá de Henares (central Spain, northeast of Madrid) [7].
The main aim of this study was to study whether the physicochemical properties and/or the texture of the Alcalá’s topsoils monitored across the different urban parks in the urban city and green areas and parks from an adjacent industrial site in Alcalá de Henares would impact the presence and distribution of Enterocytozoon bieneusi and Encephalitozoon spp.

2. Material and Methods

A total of 227 topsoil samples (0–3 cm depth) were collected in July 2017 across different urban (155) and industrial (60) areas in Alcalá de Henares (Spain) and in a public garden in the city centre (12), following previous methods described by our team, Peña-Fernández et al. [8]. Briefly, topsoil samples were dried at room temperature for 2 weeks, ground and sieved with a 2 mm sieve to remove stones, coarse materials and other debris. The collected topsoil samples were further prepared and concentrated as follows. Samples were kept in 15–20 mL of PBS (1% sterile) for 24 h in agitation to obtain a homogenised supernatant. After 24 h, supernatants were collected in sterile 50 mL Falcon tubes and centrifuged at 3000 rpm for 30 min. Pellets were collected and suspended in 5 mL of sterile PBS (1%); aliquots were kept at −80 C for the molecular analysis.
DNA was extracted by disrupting the spores using Fast-Prep for Soil® following the manufacturer’s methodologies (MP Biomedicals, Solon, OH, USA), as described by Da Silva et al. [9]. PCR inhibitors were removed using a QIAquick PCR kit (QIAGEN, Chastsworth, CA, USA), followed by a SYBR Green real-time PCR according to the methods described by Polley et al. [10]. Species identification was based on the melting temperature (Tm) of the amplicons, as described by Andreu-Ballester et al. [11]. Spores of Encephalitozoon intestinalis (Cali et al.) from Hartskeerl et al. (nasal isolate from an HIV-seropositive individual; ATCC® 50507™; https://www.atcc.org/products/50507, accessed on 29 November 2023) and Encephalitozoon cuniculi from Levaditi et al. (urine from an AIDS patient; ATCC® 50602™; https://www.atcc.org/products/50602, accessed on 29 November 2023) were used as positive controls. A positive control was also used for E. bieneusi, which was kindly provided by the parasitology group at the University of San Pablo CEU (Spain).
Topsoils were also further screened for organic matter content (OM), pH, electric conductivity (EC) and texture (percentages of sand, clay and silt), according to the Spanish official methodology for soil analysis [12]. Briefly, the pH and EC were measured in suspension using a 1:2.5 (w/v) ratio of soil and deionised water; the OM content was analysed using the Walkley–Black method; and the soil texture was determined using a Bouyoucos densitometer [13].
Statistical analyses were performed using the free software R-project, version 4.1.0 [14]. Significance scores were based on Student’s t-test. Differences were considered statistically significant at p-values lower than 0.05.

3. Results and Discussion

E. bieneusi was detected in nine topsoil samples (five urban, four industrial); meanwhile, Encephalitozoon spp. was detected in twenty-two topsoil samples (sixteen urban, six industrial; ten E. intestinalis, nine E. intestinalis/E. hellem and three E. cuniculi). Our results are in line with a pilot study performed by our group in 2016, in which these species were detected in twenty-eight samples (topsoil and sand from a kid’s playground) collected from five parks across Alcalá city [15]; with a preliminary test performed in which only sixty of all these samples were processed [16]; and with our previous presentation [7]. To our knowledge, this is the first report reporting the presence of human-related microsporidian spores in topsoils from Alcalá de Henares in urban and industrial areas and the first time that these emerging human parasites have been detected and further explored in an urban area in the Madrid region. Thus, Dado et al. [6] did not observe spores of microsporidia after processing six hundred and twenty-five sand samples collected from 67 parks in southern Madrid. However, this could be attributed to the fact that these samples were only processed using microscopical methods. The type of sample, i.e., sand, might also affect the presence of these emerging species. Thus, similar reports exploring the presence of helminth eggs have reported higher frequencies in samples collected across sports fields and park playgrounds than from fenced sandpits [17].
The lower presence of E. bieneusi in Alcalá topsoils versus the presence of Encephalitozoon spp. might be explained by unknown behavioural and/or characteristics of their spores in topsoils, as E. bieneusi is known to affect a large variety of vertebrate hosts, so a higher frequency was expected, as urban animals, including mammals and birds, could act as potential reservoirs, which would facilitate the environmental contamination of cities and its continuous transmission. Thus, Galván-Díaz et al. [18] observed a higher frequency of E. bieneusi than E. intestinalis in faeces from different animal species collected in Spain, including Madrid.
The presence of E. bieneusi was associated with urban soils that presented lower EC (0.50 vs. 0.71 dS/m; p-value = 0.0110), as this factor may provide a richer environment for the survival of spores. The presence of microsporidian spores was mostly more intense in those topsoils with higher OM contents, irrespective of the area. Thus, significant differences were observed for E. bieneusi spores when considering all the topsoils monitored together (6.96% vs. 4.98%; p-value = 0.0342) and for E. intestinalis/E. hellem in one of the four quadrants into which the urban area was divided (5.54% vs. 3.12%; p-value = 0.0007). The OM content can modify the physical and chemical properties of the soil by changing its texture and preserving the soil moisture [19], which might contribute to the presence of these spores.
The presence of any of these parasitic species did not exhibit a statistical relation with the pH of the topsoils (range = 6.25–7.95) for any of the areas monitored. This could be attributed to the fact that the optimum pH range for most soil microorganisms has been described to be from 5 to 8 [20].
In relation to the topsoil textures, E. intestinalis was present in industrial topsoils with a significantly lower content of sand (14.5% vs. 21.74%; p-value = 0.00003) but a higher content of silt (78.5% vs. 64.9%; p-value = 0.0229), which might be attributed to the differences in the capacity of topsoils to retain moisture depending on their texture [19]. These authors have found lower frequencies of protozoan and helminth eggs in soils with higher percentages of sand than in those with a high presence of silt and clay, which they explain as being due to the poor retention of water in sandy soils. However, spores of E. intestinalis/E. hellem were more present in those topsoils with lower contents of clay in the main urban area (11% vs. 19%; p-value = 0.0200). Paller and De Chavez [21] have observed more eggs from soil-transmitted helminths in sandy soils than in clayey soils, which they explain as being due to an insufficient provision of oxygen in clayey soils for egg development. Thus, the provision of enough oxygen might impact the persistence of microsporidian spores in topsoils, which should be further explored. Clear information on the impact of soil physicochemical factors and texture on the presence and distribution of emerging human-related microsporidian spores is necessary to identify the appropriate public health interventions and decontamination options/techniques to protect human health and minimise potential exposures [22].

4. Conclusions

To our knowledge, this is the first report discussing the presence and distribution of spores of E. bieneusi and Encephalitozoon species (E. intestinalis, E. hellem, E. cuniculi) in topsoils across urban and industrial locations in Alcalá de Henares and the first report reporting the presence of these emerging zoonotic parasites in soils from the Madrid region. A better understanding of these potential associations is critical to selecting appropriate decontamination techniques and strategies to prevent and minimise human exposure.

Author Contributions

Conceptualization, A.P.-F.; methodology, A.P.-F., M.H., M.d.C.L.-B., F.I., U.A.; validation, A.P.-F., F.I., U.A.; formal analysis, A.P.-F., M.H., F.I., U.A.; investigation, A.P.-F., M.d.C.L.-B., F.I., U.A.; resources, A.P.-F., M.d.C.L.-B.; data curation, A.P.-F., M.H., U.A.; writing—original draft preparation, A.P.-F.; writing—review and editing, A.P.-F., M.H., M.d.C.L.-B., F.I., U.A.; visualization, A.P.-F., M.H., M.d.C.L.-B., F.I., U.A.; supervision, A.P.-F.; project administration, A.P.-F., M.d.C.L.-B.; internal funding acquisition, A.P.-F., M.d.C.L.-B. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding. It was partially supported with internal funds from the Leicester School of Allied Health Sciences, De Montfort University, England.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author. The data are not publicly available due to further processing for a future submission as a manuscript.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Han, B.; Pan, G.; Weiss, L.M. Microsporidiosis in humans. Clin. Microbiol. Rev. 2021, 34, e00010-20. [Google Scholar] [CrossRef] [PubMed]
  2. Wadi, L.; Reinke, A.W. Evolution of microsporidia: An extremely successful group of eukaryotic intracellular parasites. PLoS Pathog. 2020, 16, e1008276. [Google Scholar] [CrossRef] [PubMed]
  3. Ardila-Garcia, A.M.; Raghuram, N.; Sihota, P.; Fast, N.M. Microsporidian Diversity in Soil, Sand, and Compost of the Pacific Northwest. J. Eukaryot. Microbiol. 2013, 60, 601–608. [Google Scholar] [CrossRef] [PubMed]
  4. Moratal, S.; Magnet, A.; Izquierdo, F.; del Águila, C.; López-Ramon, J.; Dea-Ayuela, M.A. Microsporidia in Commercially Harvested Marine Fish: A Potential Health Risk for Consumers. Animals 2023, 13, 2673. [Google Scholar] [CrossRef] [PubMed]
  5. Chen, Y.; Lv, Q.; Liao, H.; Xie, Z.; Hong, L.; Qi, L.; Pan, G.; Long, M.; Zhou, Z. The microsporidian polar tube: Origin, structure, composition, function, and application. Parasites Vectors 2023, 16, 305. [Google Scholar] [CrossRef] [PubMed]
  6. Dado, D.; Izquierdo, F.; Vera, O.; Montoya, A.; Mateo, M.; Fenoy, S.; Galván, A.L.; García, S.; García, A.; Aránguez, E.; et al. Detection of zoonotic intestinal parasites in public parks of Spain. Potential epidemiological role of microsporidia. Zoonoses Public Health 2012, 59, 23–28. [Google Scholar] [CrossRef] [PubMed]
  7. Peña-Fernández, A.; Lobo-Bedmar, M.C.; Anjum, U. Biological contamination due to microsporidia in urban soils: An emerging risk? In ISEE Conference Abstracts; EHP: Durham NC, USA, 2021; Volume 2021. Available online: https://ehp.niehs.nih.gov/doi/abs/10.1289/isee.2021.P-468 (accessed on 29 November 2023).
  8. Peña-Fernández, A.; González-Muñoz, M.J.; Lobo-Bedmar, M.C. Establishing the importance of human health risk assessment for metals and metalloids in urban environments. Environ. Int. 2014, 72, 176–185. [Google Scholar] [CrossRef] [PubMed]
  9. Da Silva, A.J.; Bornay-Llinares, F.J.; Moura, I.N.; Slemenda, S.B.; Tuttle, J.L.; Pieniazek, N.J. Fast and reliable extraction of protozoan parasite DNA from fecal specimens. Mol. Diagn. 1999, 4, 57–64. [Google Scholar] [CrossRef] [PubMed]
  10. Polley, S.D.; Boadi, S.; Watson, J.; Curry, A.; Chiodini, P.L. Detection and species identification of microsporidial infections using SYBR Green real-time PCR. J. Med. Microbiol. 2011, 60, 459–466. [Google Scholar] [CrossRef] [PubMed]
  11. Andreu-Ballester, J.C.; Garcia-Ballesteros, C.; Amigo, V.; Ballester, F.; Gil-Borras, R.; Catalan-Serra, I.; Magnet, A.; Fenoy, S.; Aguila, C.D.; Ferrando-Marco, J.; et al. Microsporidia and its relation to Crohn’s disease. A retrospective study. PLoS ONE 2013, 8, e62107. [Google Scholar] [CrossRef] [PubMed]
  12. MAPA. Métodos Oficiales de Análisis; Secretaría General Técnica Ministerio de Agricultura, Pesca y Alimentación: Madrid, Spain, 1994; Volume III. [Google Scholar]
  13. Gil-Díaz, M.; Pinilla, P.; Alonso, J.; Lobo, M.C. Viability of a nanoremediation process in single or multi-metal (loid) contaminated soils. J. Hazard. Mater. 2017, 321, 812–819. [Google Scholar] [CrossRef] [PubMed]
  14. Core Team R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing: Vienna, Austria, 2021. Available online: https://www.R-project.org/ (accessed on 29 November 2023).
  15. Martinez-Fernandez, C.; Magnet, A.; Izquierdo, F.; Gomes, T.S.; Vaccaro, L.; Ollero, D.; Peña-Fernández, A.; Fenoy, S.; del Águila, C. Detection of Opportunistic Parasites in Public Parks in Alcalá de Henares (Madrid, Spain). In Proceedings of the XX Spanish Congress of Parasitology (SOCEPA), Santa Cruz de Tenerife, Spain, 19–21 July 2017; Oral presentation. [Google Scholar]
  16. Peña-Fernández, A.; Lobo-Bedmar, M.C.; Izquierdo, F.; Anjum, U. Presence and distribution of emerging human pathogens microsporidia in soils from Alcalá de Henares (Spain) according to their physicochemical properties. XXIII Spanish Congress of Toxicology and VII Ibero-American, Sevilla, 26–28 June 2019. Rev. Toxicol. 2019, 36, 81. Available online: http://rev.aetox.es/wp/index.php/vol-36-num-1-2019/ (accessed on 9 October 2023).
  17. Blaszkowska, J.; Kurnatowski, P.; Damiecka, P. Contamination of the soil by eggs of geohelminths in rural areas of Lodz district (Poland). Helminthologia 2011, 48, 67–76. [Google Scholar] [CrossRef]
  18. Galván-Díaz, A.L.; Magnet, A.; Fenoy, S.; Henriques-Gil, N.; Haro, M.; Gordo, F.P.; Miró, G.; Águila, C.D.; Izquierdo, F. Microsporidia detection and genotyping study of human pathogenic E. bieneusi in animals from Spain. PLoS ONE 2014, 9, e92289. [Google Scholar] [CrossRef] [PubMed]
  19. Etewa, S.E.; Abdel-Rahman, S.A.; Abd El-Aal, N.F.; Fathy, G.M.; El-Shafey, M.A.; Ewis, A.M.G. Geohelminths distribution as affected by soil properties, physicochemical factors and climate in Sharkyia governorate Egypt. J. Parasit. Dis. 2016, 40, 496–504. [Google Scholar] [CrossRef] [PubMed]
  20. Smith, J.L.; Doran, J.W. Measurement and use of pH and electrical conductivity for soil quality analysis. Methods Assess. Soil Qual. 1997, 49, 169–185. [Google Scholar]
  21. Paller, V.G.V.; De Chavez, E.R.C. Toxocara (Nematoda: Ascaridida) and other soil-transmitted helminth eggs contaminating soils in selected urban and rural areas in the Philippines. Sci. World J. 2014, 2014, 386232. [Google Scholar] [CrossRef] [PubMed]
  22. Peña-Fernández, A.; Guetiya Wadoum, R.E.; Koroma, S.; Acosta, L.; Anjum, U. Applicability of the UK Recovery Handbook for Biological Incidents to tackle human-virulent microsporidian spores in tap water in Makeni (Sierra Leone). VIII Training Conference in Toxicology, blended event, 25 March 2021. Rev. Toxicol. 2021, 38, 62. Available online: http://rev.aetox.es/wp/index.php/vol-38-1/ (accessed on 29 November 2023).
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Peña-Fernández, A.; Higueras, M.; Lobo-Bedmar, M.d.C.; Izquierdo, F.; Anjum, U. Presence and Distribution of Human-Related Microsporidian Spores across Different Topsoil Areas across Alcalá de Henares (Spain). Biol. Life Sci. Forum 2024, 31, 5. https://doi.org/10.3390/ECM2023-16461

AMA Style

Peña-Fernández A, Higueras M, Lobo-Bedmar MdC, Izquierdo F, Anjum U. Presence and Distribution of Human-Related Microsporidian Spores across Different Topsoil Areas across Alcalá de Henares (Spain). Biology and Life Sciences Forum. 2024; 31(1):5. https://doi.org/10.3390/ECM2023-16461

Chicago/Turabian Style

Peña-Fernández, Antonio, Manuel Higueras, María del Carmen Lobo-Bedmar, Fernando Izquierdo, and Umar Anjum. 2024. "Presence and Distribution of Human-Related Microsporidian Spores across Different Topsoil Areas across Alcalá de Henares (Spain)" Biology and Life Sciences Forum 31, no. 1: 5. https://doi.org/10.3390/ECM2023-16461

Article Metrics

Back to TopTop