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Occurrence of Cryptosporidium spp., Giardia spp. and other pathogenic intestinal parasites in the Beberibe River in the State of Pernambuco, Brazil

Abstract

INTRODUCTION:

Transmission of pathogenic protozoa and helminths by water is a serious public health problem. In this study, we analyzed the presence of these organisms in the Beberibe River in Pernambuco, Brazil.

METHODS:

Parasite analysis was performed using the Hoffman, Pons, & Janer method followed by centrifugation and preparation of slides by staining with acetic acid and Lugol's solution. Protozoan oocysts were isolated by the modified Ziehl Neelsen method.

RESULTS:

Cryptosporidium spp., Giardia spp. and other parasites were found in the Beberibe River.

CONCLUSIONS:

Sanitation companies must assess pathogenic intestinal parasites in water basins providing public water and subsequently develop improved treatment systems for removal of such parasites.

Protozoa; Beberibe River; Cryptosporidium spp


Transmission of pathogenic protozoa by water is a major public health concern(1)Franco RMB, Branco N, Leal DAG. Parasitologia Ambiental: Métodos de Concentração e Detecção de Cryptosporidium spp. e Giardia spp. em amostras de água. Rev Patol Trop 2012; 41:119-135. and therefore a challenge for producers and distributors of water systems(2)Cantusio Neto R, Santos LU, Sato MIZ,. Franco RMB Controle de qualidade analítica dos métodos utilizados para a detecção de protozoários patogênicos em amostras de água. Arq Inst Biol (São Paulo) 2011; 78:169-178.. For example, the pathogenic intestinal protozoa Giardia spp. and Cryptosporidium spp. exhibit resistance to chemical disinfectants and are long-lived in the environment; thus, these pathogenic parasites are highly problematic for sanitation companies and public health officials(3)Ives RL, Kamarainen AM, John DE, Rose JB. Use of cell culture to assess Cryptosporidium parvum survival rates in natural ground waters and surface waters. Appl Environ Microbiol 2007; 73:5968-5970.. Although conventional water treatment stations are able to remove 99% of Cryptosporidium spp. oocysts from water sources, there is still a risk of transmission(4)Keegan A, Daminato D, Sant CP, Monis PT. Effect of water treatment processes on Cryptosporidium infectivity. Water Res 2008; 42:1805-1811.. Indeed, because oocysts exhibit high compressibility during filtration, these oocysts can behave as small particles (2-4μm), allowing them to pass through commonly used filters and enter treated water provided to consumers(5)Franco RMB. Protozoários de veiculação hídrica: relevância em saúde pública. Rev Panam Infectol 2007; 9:36-43. . Therefore, improved methods for detection and removal of such pathogenic parasites is necessary.

Cryptosporidium spp. and Giardia spp. have been found in surface water in several countries, such as the United States on Lake Texoma (on the border of Texas and Oklahoma)(6)Keeley A, Faulkner BR. Influence of land use and watershed characteristics on protozoa contamination in a potential drinking water resources reservoir. Water Res2008; 42:2803-2813., in France on Seine River and its tributary Marne River(7)Mons C, Dumetre A, Gosselin S, Galliot C, Moulin L. Monitoring of Cryptosporidium and Giardia River contamination in Paris area. Water Res2009; 43:211-217., in Hungary on the Danube River(8)Plutzer J, Tako MH, Marialigeti K, Torokne A, Karanis P. First investigations into the prevalence of Cryptosporidium and Giardia spp. in Hungarian drinking water. J Water Health 2007;5:573-584., and in China in the reservoir of the Three Gorges Dam(9)Xiao G, Qiu Z, Qi J, Chen Ji-Na, Liu F, Liu W, et al. Occurrence and potential health risk of Cryptosporidium and Giardia in the Three Gorges Reservoir, China. Water Res2013; 47:2431-2445.. In Brazil, in accordance with decree number 2914 of the Health Ministry (year 2011), which describes water quality procedures for human consumption and potability patterns, sanitation companies are expected to survey water intended for human consumption for the presence of Giardia spp. and Cryptosporidium spp.(10)10 Ministério da Saúde. Portaria MS n° 2914 de 12/12/2011. Dispõe sobre os procedimentos de controle e de vigilância da qualidade da água para consumo humano e seu padrão de potabilidade. Brasília: Ministério da Saúde; 2011.. However, methods for detection of Cryptosporidium spp. are complex, and proper survey of water supplies would require specialized human resources, which are scarce. Additionally, there is little information about these pathogens in national surface water bodies(1)Franco RMB, Branco N, Leal DAG. Parasitologia Ambiental: Métodos de Concentração e Detecção de Cryptosporidium spp. e Giardia spp. em amostras de água. Rev Patol Trop 2012; 41:119-135.. Therefore, while many researchers are studying Cryptosporidium spp. and Giardia spp., more studies are needed to further characterize these pathogens(6)Keeley A, Faulkner BR. Influence of land use and watershed characteristics on protozoa contamination in a potential drinking water resources reservoir. Water Res2008; 42:2803-2813.. Indeed, in the northeast region of Brazil, few studies have characterized or identified pathogenic intestinal parasites, such as some species of helminths and protozoa. An initial report describing water supply sources showed contamination by Cryptosporidium spp. in the Capibaribe River and the Tapacura reservoir(11)11 Machado ECL, Stamford TLM, Machado EHL, Soares DS. Albuquerque MNL. Ocorrência de oocistos de Cryptosporidium spp. em águas superficiais na região metropolitana de Recife-PE. Arq Bras Med Vet Zootec 2009; 61:1459-1462. in State of Pernambuco, Northeast Brazil.

In this study, we characterized the presence of intestinal parasites in the Beberibe River in Pernambuco. The human population at the Beberibe River basin is approximately 590,000 inhabitants, with an average population density of 7,300 inhabitants/km2. Moreover, this area has many low-income settlements in the Recife metropolitan region (RMR); these settlements are scattered in risk areas, hills, and flooded areas and are characterized by poor urban infrastructure.

The Beberibe River is one of the most polluted rivers in Pernambuco due to the insufficient sanitary conditions of Olinda and Recife. Despite this, the Beberibe River is one of the water sources for the public water system, supplying about 10% of the volume of water distributed throughout the RMR. In particular, the Beberibe River contributes enough water for approximately 100,000 people in the RMR(12)12 Companhia Pernambucana de Saneamento (COMPESA). Sistemas de Abastecimento - Sistema Alto de Ceu. Recife: COMPESA; 2012. [Cited 2013 December 15]. Available at: http://www.compesa.com.br/saneamento/abastecimentodeagua
http://www.compesa.com.br/saneamento/aba...
.

Between May 2012 and May 2013, water samples were collected in duplicate from the Beberibe River at two locations where sampling was easy (i.e., convenience sampling). Samples were collected from the Beberibe River in sterile 1-L plastic bottles and transported to the Laboratory of Parasitology, Department of Tropical Medicine of the Federal University of Pernambuco [University Federal of Pernambuco (UFPE)] for analysis of intestinal parasites. Protozoa and helminths were analyzed using the Hoffman, Pons, & Janer method or spontaneous sedimentation. The time to sedimentation was between 24 and 48h for 250-mL samples. Subsequently, aliquots of the sediment were centrifuged at 900rpm for 5-10 min. During the water sampling, turbidity (portable turbidity meter, Hanna Instruments model HI93703), water temperature, and depth of the river water were also analyzed. The pH of water samples was measured using the standard method (SM 4,500-H+) and electrometric method(13)13 American Public Health Association (APHA). Standard Methods for the Examination of Water and Wastewater. 21th ed. Washington: APHA; 2005..

For each sample in duplicate, two slides were made with approximately 1mL of the centrifuged sample. Because collections were made at two points of the river, a total of eight slides were made for each collection day; samples were collected on 16 days, yielding a total of 128 slides. The slides were stained with Lugol iodine and analyzed under an optical microscope at 10× and 40× magnification for qualitative evaluation of protozoa and helminth parasite contamination.

A modified Ziehl Neelsen method was used for identification of Cryptosporidium spp. oocysts, with fuchsin-phenolated solution followed by spontaneous sedimentation. For the identification of Cryptosporidium spp. oocysts by optical microscopy, an oil-immersion 100× objective lens was used to visualize the whole smear, observing the shape, color, and size of oocysts. A micrometer was coupled to the microscope for confirmation of the morphometric identification of the parasite.

Bacteriological parameters were evaluated in water samples by determination of total coliforms and Escherichia coli between June 2012 and May 2013. Samples (250mL) were collected in sterilized polyethylene containers. Fermentation in multiple tubes was performed with chromogenic substrate(13)13 American Public Health Association (APHA). Standard Methods for the Examination of Water and Wastewater. 21th ed. Washington: APHA; 2005., with results presented as the most probable number (MPN) in 100-mL samples (MPN/100mL).

Table 1 shows parasite contamination in the Beberibe River and physicochemical parameters. Cryptosporidum spp. oocysts: 75% (12/16), Giardia ssp. cysts: 50% (8/16), complexes of Entamoeba histolytica/E. dispar: 50% (8/16), Cystoisospora belli: 6.3% (1/16), Endolimax nana: 81.3% (13/16), Entamoeba coli: 37.5% (6/16), and Iodamoeba butschlii: 6.3% (1/16) were detected in the water samples collected from the Beberibe River in this study. The sizes of Cryptosporidium spp. oocysts found in the Beberibe River ranged from 3.3 to 6.6μm, with 0-8 oocysts per slide. Endolimax nana with 81.3% (13/16) was frequently present, as shown by microscopic analysis of the water samples; these data confirmed that the Beberibe River was contaminated with human excreta.

Table 1:
Occurrence of intestinal parasites in water samples from the Beberibe River.

Helminths were also present in water samples from the Beberibe River; we identified Strongyloides ssp.: 81.3% (13/16), Ascaris spp. eggs: 68.8% (11/16), hookworm eggs: 12.5% (2/16,) and larvae: 31.3% (5/16), Hymenolepis nana: 37.5% (6/16), and Hymenolepis diminuta 6.3% (1/16). The number of total coliforms in the Beberibe River ranged from ≥ 1,600 to ≥ 160,000 NMP/100mL, while that for Escherichia coli ranged from 50,000 to ≥ 160,000 NMP/100mL.

Similar results of intestinal parasites were observed in a study performed in the catchment area of the Danube River in the Galati region of Romania, with particularly high frequency of the protozoa Cryptosporidium spp., Giardia spp., Iodamoeba butschli, Endolimax nana, Entamoeba coli, and Entamoeba histolytica and helminths such as Ascaris lumbricoides, Hymenolepis diminuta, and Strongyloides stercoralis (14)14 Ajeagah GA, Cioroi M, Praisler M, Constantin O, Palela M, Bahrim G. An Ecological Assessment of the Pollution Status of the Danube River Basin in the Galati Region-Romania. J Water Resource Prot 2013; 5:876-886.. Cryptosporidium spp., Giardia spp., Ascaris spp., Schistosoma spp.,and Acantamoeba spp. were also detected in water samples from two recreational lakes in the region of Selangor, Malaysia(15)15 Onichandran S, Kumar T, Lim YAL, Sawangjaroen N, Andiappan H, Salibay CC. et al. Waterborne parasites and physico-chemical assessment of selected lakes in Malaysia. Parasitol Res 2013; 112:4185-4191..

The Beberibe River is characterized by constant discharge of domestic wastewater; this may have influenced the pH values of the water samples, which were slightly alkaline values (Table 2).

Table 2:
Physicochemical parameters measured in the Beberibe River between May 2012 and May 2013.

Due to the detection of parasite contamination in the Beberibe river, we suggest that water production and distribution companies should assess the presence of intestinal parasites (particularly protozoa and helminths) in public water supplies and should consider improving their treatment systems to ensure removal of such pathogens, which are known to be highly resistant to chemical disinfectants and to be particularly long-lived in the environment.

We hope that the information presented in this study, i.e., the presence of pathogenic intestinal parasites in the Beberibe River in Pernambuco, Brazil, may contribute to improvements in public health. In addition, public authorities need to create documentation for informing the population of the occurrence of parasites in watersheds providing public water supplies.

  • 1
    Franco RMB, Branco N, Leal DAG. Parasitologia Ambiental: Métodos de Concentração e Detecção de Cryptosporidium spp. e Giardia spp. em amostras de água. Rev Patol Trop 2012; 41:119-135.
  • 2
    Cantusio Neto R, Santos LU, Sato MIZ,. Franco RMB Controle de qualidade analítica dos métodos utilizados para a detecção de protozoários patogênicos em amostras de água. Arq Inst Biol (São Paulo) 2011; 78:169-178.
  • 3
    Ives RL, Kamarainen AM, John DE, Rose JB. Use of cell culture to assess Cryptosporidium parvum survival rates in natural ground waters and surface waters. Appl Environ Microbiol 2007; 73:5968-5970.
  • 4
    Keegan A, Daminato D, Sant CP, Monis PT. Effect of water treatment processes on Cryptosporidium infectivity. Water Res 2008; 42:1805-1811.
  • 5
    Franco RMB. Protozoários de veiculação hídrica: relevância em saúde pública. Rev Panam Infectol 2007; 9:36-43.
  • 6
    Keeley A, Faulkner BR. Influence of land use and watershed characteristics on protozoa contamination in a potential drinking water resources reservoir. Water Res2008; 42:2803-2813.
  • 7
    Mons C, Dumetre A, Gosselin S, Galliot C, Moulin L. Monitoring of Cryptosporidium and Giardia River contamination in Paris area. Water Res2009; 43:211-217.
  • 8
    Plutzer J, Tako MH, Marialigeti K, Torokne A, Karanis P. First investigations into the prevalence of Cryptosporidium and Giardia spp. in Hungarian drinking water. J Water Health 2007;5:573-584.
  • 9
    Xiao G, Qiu Z, Qi J, Chen Ji-Na, Liu F, Liu W, et al. Occurrence and potential health risk of Cryptosporidium and Giardia in the Three Gorges Reservoir, China. Water Res2013; 47:2431-2445.
  • 10
    Ministério da Saúde. Portaria MS n° 2914 de 12/12/2011. Dispõe sobre os procedimentos de controle e de vigilância da qualidade da água para consumo humano e seu padrão de potabilidade. Brasília: Ministério da Saúde; 2011.
  • 11
    Machado ECL, Stamford TLM, Machado EHL, Soares DS. Albuquerque MNL. Ocorrência de oocistos de Cryptosporidium spp. em águas superficiais na região metropolitana de Recife-PE. Arq Bras Med Vet Zootec 2009; 61:1459-1462.
  • 12
    Companhia Pernambucana de Saneamento (COMPESA). Sistemas de Abastecimento - Sistema Alto de Ceu. Recife: COMPESA; 2012. [Cited 2013 December 15]. Available at: http://www.compesa.com.br/saneamento/abastecimentodeagua
    » http://www.compesa.com.br/saneamento/abastecimentodeagua
  • 13
    American Public Health Association (APHA). Standard Methods for the Examination of Water and Wastewater. 21th ed. Washington: APHA; 2005.
  • 14
    Ajeagah GA, Cioroi M, Praisler M, Constantin O, Palela M, Bahrim G. An Ecological Assessment of the Pollution Status of the Danube River Basin in the Galati Region-Romania. J Water Resource Prot 2013; 5:876-886.
  • 15
    Onichandran S, Kumar T, Lim YAL, Sawangjaroen N, Andiappan H, Salibay CC. et al. Waterborne parasites and physico-chemical assessment of selected lakes in Malaysia. Parasitol Res 2013; 112:4185-4191.
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), the Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco (FACEPE) and the Companhia Pernambucana de Saneamento (COMPESA).

Publication Dates

  • Publication in this collection
    mar-apr 2015

History

  • Received
    24 July 2014
  • Accepted
    23 Feb 2015
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