Literature DB >> 29718924

Socioenvironmental factors associated with Schistosoma mansoni infection and intermediate hosts in an urban area of northeastern Brazil.

Taíssa Alice Soledade Calasans1,2, Geza Thais Rangel Souza3, Claudia Moura Melo1,2, Rubens Riscala Madi2,3, Verónica de Lourdes Sierpe Jeraldo1,2.   

Abstract

Schistosomiasis, which is caused by trematodes of the genus Schistosoma and by the species Schistosoma mansoni in Brazil, is transmitted primarily by Biomphalaria glabrata mollusks. Infections occur in humans and mollusks in freshwater environments contaminated with feces from infected humans. This study aimed to evaluate potential foci of schistosomiasis based on the identification of infection sites for the snails, factors that increased the human infection probability of S. mansoni infection, and the relationship of the disease with abiotic, biotic, and sociocultural factors. The study was conducted in an urban area on the northeast coast of Brazil; this location was chosen based on the following factors: the presence of B. glabrata, nearby freshwater, and the absence of sewer treatment. A parasitological analysis was performed to evaluate infections of the mollusks and residents inside the perimeter defined by the collection points. Questionnaires were applied to obtain demographic data and to identify behaviors that led to human infection. To verify the contamination of freshwater by human feces, a microbiological analysis of the water was performed at the mollusk collection points to determine the rate of contamination with fecal coliforms. A total of 10,270 B. glabrata mollusks were collected between August 2013 and August 2014, of which 8.8% were positive for S. mansoni; the prevalence ranged from 0 to 34.5% over the study period. A total of 232 coprological samples from the residents were analyzed. The S. mansoni infection prevalence rate was 16.4%, and the S. mansoni parasitic load in the infected residents was 54.9 eggs per gram of feces on average. Males were more affected by the parasite, especially in the 8-17-year-old age range. Thermotolerant coliforms were observed at the mollusk collection sites, which indicated that freshwater and sewage were in continuous contact. This contamination indicated poor sanitary conditions, as was previously observed, which could be combined with detrimental behavior due to the residents' habits. These conditions cause a predisposition for both intermediate and definitive infections of the hosts by creating a socioenvironmental scenario that is conducive to the formation and maintenance of potential schistosomiasis foci. This and similar areas deserve special attention from the government with an aim of improving sanitation services and local resident knowledge to prevent future contamination.

Entities:  

Mesh:

Year:  2018        PMID: 29718924      PMCID: PMC5931446          DOI: 10.1371/journal.pone.0195519

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Introduction

Schistosomiasis is considered a neglected parasitic disease and affects over 200 million people worldwide.This disease is caused by trematodes of the genus Schistosoma (Weiland, 1858) [1] and by the species Schistosoma mansoni in Brazil (Sambon 1907). In Brazil, Biomphalaria glabrata (Say, 1818) is one of the most important intermediate host species of S. mansoni due to its wide geographic distribution and high infection rates. The occurrence and spread of schistosomiasis are related to poor environmental conditions, with a high prevalence of human cases usually found in people live in unfavorable socioeconomic conditions [2,3,4]. Human and mollusk infections occur in freshwater bodies contaminated with the feces of people infected with schistosomes. Absent or inadequate sanitation, human cultural habits, and the presence of the Biomphalaria mollusk contribute to the persistence of the parasite's life cycle and consequently to the disease's geographic spread [5,6,7]. In Brazil, S. mansoni infection is considered a public health problem in 19 states. As a result, Brazil is considered the Latin American country with the greatest transmission foci, with approximately 30 million people at risk of contracting the disease and approximately 4–6 million people already infected [8,9,10]. Initially, schistosomiasis was typically endemic in rural areas; however, due to human migration, transmission also occurs in large Brazilian urban centers, with the northeast of the country having the highest prevalence rates [9, 11]. For instance, the state of Sergipe had a prevalence of 13.6% (14,471 positive cases/106,287 people analyzed) in 2005, 11.2% (16,196/145,069) in 2006, 11.8% (10,220/86,824) in 2007, and 10.6% (8,329/78,859) in 2008 based on parasitological examinations performed by the Brazilian Schistosomiasis Combat Program (Programa de Combate a Esquistossomose–PCE). In each year, 100% of the municipalities analyzed tested positive for S. mansoni infections [12]. Moreover, the tropical climate contributes to the establishment of schistosomiasis in this region because it provides conditions suitable for the presence of the mollusks that encourage the transmission of this endemic disease when associated with poor sanitary conditions [13]. Neglected tropical diseases, such as schistosomiasis, require prevention and control measures and elimination efforts; therefore, an understanding of the transmission factors in a particular area should be obtained [14,15]. These factors include the characteristics of the environment and the sociocultural processes that influence the transmission process. Moreover, implementation of health education interventions, preventive chemotherapy directed at the entire community, and access to sanitation and safe water are essential to interrupt the transmission and control cycle of schistosomiasis [16]. Furthermore, identifying the breeding grounds of the S. mansoni mollusk intermediate host and performing an evaluation of its ecological and biological aspects are critical for investigations of the transmission risk rates and the implementation of control strategies in locations where the disease is established [17,18]. The aim of this study was to evaluate potential schistosomiasis foci based on studies on the prevalence of S. mansoni infection in mollusks and individuals who lived near these foci, the influence of rainfall and environmental contamination due to the lack of a proper sanitation system, and sociocultural aspects of this endemic disease’s transmission process in an urban community in northeastern Brazil.

Materials and methods

Study site and population

The study was conducted in a community in the city of Nossa Senhora do Socorro, which is located in the state of Sergipe. The city has approximately 155,334 inhabitants and a land area of 158 km2 in northeastern Brazil. The community named Parque dos Farois has a population of approximately 15,000 according to local health service information. The study area has a biome characterized by Atlantic forest and a hot and humid tropical climate and is located on the shores of the sub-basin of the Poxim River (Fig 1). The main environmental issues affecting the study area are riparian deforestation, trash in the open, disordered urban occupation, and deficiencies in the water supply and sanitary network [19].
Fig 1

Location of the state of Sergipe and the Nossa Senhora do Socorro municipality showing the traveled perimeter in northeastern Brazil (Source: Atlas Digital- Quantum Gis 1.7.0).

Ethical aspects

The study received institutional approval from the Ethics Committee on Human Research from Tiradentes University under protocol log number 28689514.4.0000.5371. All participants were invited to sign the free and informed consent term. In this document, participants must have the freedom to leave the study at any time. All questions are clarified to ensure that there is no doubt about your participation without study. In cases of illiteracy, a thumbprint and a signature of a witness were collected. The parents or guardians signed the consent form authorizing the participation of minors under 18 years of age. By signing the form, the participants agreed to participate in the interview through questionnaires and to provide a fecal sample for the parasitological analysis. Participants under 18 years of age were assisted by parents or guardians during the interview. The results were communicated to the participants, and adults and children under 18 years of age infected with any type of helminth were referred to the local health unit for treatment with 50 mg/kg body weight of praziquantel (Farmanguinhos® 600 mg; manufactured by the Institute of Technology in Pharmaceuticals/Farmanguinhos with registration by the Oswaldo Cruz Foundation). The treatment accordance with according to the Brazilian guidelines of the Control Program of Schistosomiasis (PCE).

Rainfall data

The data related to rainfall were obtained from the Department of Water Resources of the State of Sergipe (Secretaria de Recursos Hídricos do Estado de Sergipe—SRH-SE) for monthly correlations with the prevalence and abundance of the collected mollusks.

Mollusk collection and cercarial emission

Mollusks were collected at five georeferenced points identified as P1 (10°55′230′′S 37°8′161′′W), P2 (10°55′231′′S 37°8′135′′W), P3 (10°55′326′′S 37°8′00′′W), P4 (10°55′18.37′′S 37°7′56.98′′W), and P5 (10°55′16.04′′S 37°7′51.80′′W), which were distributed in streams located near residences. The points were selected based on work that developed for the identification of mollusk transmitters of schistosomiasis by health workers operating in the Schistosomiasis Control Program (PCE) operated by the state government. Mollusks were collected with the aid of sieves and tongs. Each person conducted collections for a 1-hour period monthly between August 2013 and August 2014. S. mansoni infection was evaluated by individual exposure of the mollusks to artificial light at a distance of 30 cm for 4 hours. This procedure provided a temperature between 28 and 30°C, which was capable of stimulating cercarial emission [20, 21].

Questionnaire survey

To evaluate human infection with S. mansoni, a non-probabilistic, cross-sectional study was performed for accessibility in a 0.64-km2 area where mollusk collections were conducted concomitantly during the study period. The residents of all households located approximately 4.5 km from this area were visited and invited to participate in the study regardless of their ages gender, and whether or not they had a diagnosis of S. mansoni infection. A questionnaire was used to interview the participants face to face. The questionnaire consisted of multiple choice questions or binary answers, such as affirmation and negation questions (yes or no), and was used to obtain information about individual patterns divided into the following categories: family identification data (address, age, gender, place of birth, and residence time in the area), economic data (family income), and environmental/cultural aspects (water supply, garbage disposal, sewage, and forms of contact with the river/stream water, among other information) (S1 Appendix).

Human parasitological diagnosis

Following the principles of non-probabilistic sampling for convenience, all individuals who participated in the interviews received a plastic container for the collection of feces. The containers were collected, identified, and transferred to the laboratory for the parasitological analysis. One sample was collected from each individual in the morning in 2014. Two slides were prepared using the qualitative spontaneous sedimentation technique and the quantitative Kato-Katz technique. The Kato-Katz technique was also used to determine the parasitic load of the individuals for S. mansoni. The parasite load was defined by the number of eggs found on the slides and multiplied by the constant 24 and thus the number of eggs per gram of faeces (opg) was obtained, and was categorized as low light (1–99 epg), moderate (100–399 epg), or heavy (≥400 epg) [16, 22]. Individuals who had S. mansoni eggs on at least one of the two analyzed slides were considered positive. Other parasites found in the analyses were also included in this study.

Microbiological analysis

To determine the presence of total and thermotolerant coliforms, 100 ml of water was collected from points P1, P2, P3, P4, and P5 in both the dry and rainy seasons of 2014. The multiple-tube quantitative method was applied for the microbiological evaluation to determine the “most probable number” (NMP) of target microorganisms in the sample through the distribution of aliquots in a series of tubes containing differential culture media for the growth of the target microorganisms [23]. The sodium lauryl sulfate, Brilliant Green, and EC broths were used for the analysis. In the sodium lauryl sulfate broth, the presumed presence of coliforms was evidenced by the formation of gas in the Durham tubes, which was produced by the fermentation of lactose present in the environment. The Brilliant Green broth was used for confirmative evidence of total coliforms in the confirmed positive tubes inoculated in the sodium lauryl sulfate broth [24]. The total and thermotolerant coliform levels were analyzed and compared to the limits set by resolution 357 of the National Environmental Council (Conselho Nacional do Meio Ambiente—CONAMA) from March 2005, which provided the designation "Class 3 fresh water" to designate water suitable for human consumption.

Statistical analysis

The software STATISTICA 7.1 was used to perform the Spearman test correlation (rs) was used between two quantitative variables. This test was applied between the average of the monthly rainfall and the abundance and infection of mollusks. O software BioEstat 5.3 was used to perform the for the analysis of the independent variables and their associations with people with or without schistosomiasis, odds ratios were calculated (OR) with 95% confidence intervals (CIs) to verify the influence on the occurrence of a certain event between the parasitized and non-parasitized groups and Student’s paired t-test was used to compare the microbiological parameters of the NMP to the values established by the CONAMA resolution. A 5% level of significance was adopted for all analyses [25].

Results

Malacological study

Fig 2 shows the distribution of the collected mollusks. A total of 10,270 B. glabrata mollusks were collected during the study period. There was a negative correlation [(rs) = -0.03, n = 10.270, p> 0.05] between a monthly average rainfall and an abundance of B. glabrata occurring in the previous season (one month before). Mollusks were collected 2,487 (IC 95%: 0.024–0.038) in the year 2013 and in the year 2014 7,883 (95% CI: 0,101–0,115).
Fig 2

Distribution of Biomphalaria glabrata snails collected in urban areas and the monthly precipitation index.

Nossa Senhora do Socorro municipality, Sergipe, Brazil.

Distribution of Biomphalaria glabrata snails collected in urban areas and the monthly precipitation index.

Nossa Senhora do Socorro municipality, Sergipe, Brazil. After exposure to the light stimulus to release the cercariae, 8.8% (n = 912) (95% CI: 0.083–0.094) of the mollusks were found to be positive for S. mansoni. However, the prevalence varied between 0 and 34.5% during the study period. No positive mollusks were found between November 2013 and March 2014 (with the exception of December); however, starting in April, mollusks positive for S. mansoni infection were found coinciding with the rainy season (Fig 3). A correlation was observed between rainfall and B. glabrata infection during the study period [(rs) = 0.042, n = 10.270 p<0.05].
Fig 3

Correlation between B. glabrata infection and monthly rainfall (mm3) during the period from August 2013 to August 2014.

Human infection

Of the 232 stool samples collected from individuals living close to the mollusk collection points, 66.4% had at least one intestinal parasite. Schistosoma mansoni infection had the second highest prevalence at 16.4% when the spontaneous sedimentation and Kato-Katz techniques were combined (Table 1). The S. mansoni parasitic load of the infected population was 54.9, with a range from 24 to 144 eggs per gram (epg) of feces.
Table 1

Prevalence of S. mansoni and intestinal parasitic infections determined by the spontaneous sedimentation and Kato-Katz methods.

Infeccion byNumber (%)
Spontaneous SedimentationKato—KatzCombined results*
method (n = 232)method (n = 232)Men (n = 89)Women (n = 65)boths sexes (n = 232)95.0% C.I.# for OR
S. mansoni31 (13.4)7 (3.1)22 (24.7)16 (24.6)38 (16.4)0.12–0.22
A. lumbricoides30 (12.9)34 (14.6)40 (44.9)24 (36.9)64 (27.6)0.22–0.24
T. trichiura10 (4.3)11 (4.7)13 (14.6)8 (13.3)21 (9.1)0.06–0.13
Hookworm10 (4.3)0 (0)7 (7.8)3 (4.6)10 (4.3)0.02–0.08
E. vermicularis2 (0.8)4 (1.7)3 (3.4)3 (4.6)6 (2.6)0.01–0.06
H. nana2 (0.8)0 (0)0 (0)2 (3.1)2 (0.8)0.00–0.03
E. coli10 (4.3)-3 (3.4)7 (10.7)10 (4.3)0.02–0.08
E. histolytica/dispar1 (0.4)-1 (1.2)0 (0)1 (0.4)0.00–0.02
G. lamblia2 (0.8)-0 (0)2 (3.1)2 (0.8)0.00–0.03

*Combined result indicates any people that was positive either by Spontaneus Sedimentation or Kato-Katz.

#Confidence Intervals 95.0% (C.I.95%).

*Combined result indicates any people that was positive either by Spontaneus Sedimentation or Kato-Katz. #Confidence Intervals 95.0% (C.I.95%). Individuals infected with other helminths were encountered, particularly Ascaris lumbricoides with a prevalence of 27.6%. The commensal Entamoeba coli was among the most prevalent protozoans (Table 1). Regarding the age group, the majority of individuals infected with S. mansoni were children and adolescents in the 8- to 17-year-old age group and were represented by both genders (18.4% males and 23.7% females) (95% CI: 0.279–0.578). No differences were observed in the prevalence rates between men (10.5%) and women (7.9%) in the 29- to 49-year-old age group (95% CI: 0.191–0.475). Only males were infected in the age group of 18–28 years (18.4%) (95% CI: 0.092–0.334). However, only males were infected (7.9%) in the 50 years and above age group (95% CI: 0.027–0.208). Generally, S. mansoni infection was more prevalent in males, with the exception of the 40- to 49-year-old age group (95% CI: 0.058–0.273) (Fig 4).
Fig 4

Age group distribution of S. mansoni infection, 2014.

Demographic and socioeconomic variables

Regarding provenance, 65.8% of the residents infected with S. mansoni came from the state of Sergipe, 13.1% from Alagoas, and 7.9% from Pernambuco. In Table 2 it is possible to check the residence time of infected residents, and 50% reported living in place of 2 to 10 years and 36.8% live 11 to 20 years. The level of education of individuals infected with S. mansoni stood basically on incomplete primary education, with 78.9% of the population that low education level. The socioeconomic approach showed that 89.5% of the population had a low wage band to a minimum income.
Table 2

Residence time of individuals infected with Schistosoma mansoni in a community of Nossa Senhora do Socorro municipality, Sergipe, Brazil—2014.

Residence timeIndividuals
*N%
2 a 10 years1950
11 a 20 years1436.8
> 20 years513.2
Total38100

*N = Number

*N = Number

Risk factors for S. mansoni infection

The odds ratio analysis for each of the variables tested showed that male residents were 3.86 times more likely to be infected with S. mansoni. The remaining analyzed variables showed no significant risk of infection (Table 3). However, the area has poor sanitation, with residential waste dumped directly onto the streets through plumbing pipes improvised by the residents themselves, leading to the presence of open sewers with streams and puddles formed by both rainwater and residential sewage. These streams and puddles contained mollusks infected with S. mansoni.
Table 3

Association of environmental and demographic factors with Schistosoma mansoni infection in residents of the Nossa Senhora do Socorro municipality, 2014.

Risk FactorsS. mansoniOR*95.0% C.I.# for ORP-Value
PositiveNegative
Potable waterYes10810.840.35–2.000.873
No1496
Garbage collectionYes221530.620.16–2.360.7534
No313
SewerageYes13920.930.40–2.150.9633
No1279
Rudimentary cesspoolYes151220.720.27–1.880.6816
No741
Contact (water streams)Yes13791.220.51–2.890.8048
No1182
Contact (river water)Yes15931.190.50–2.810.8500
No1074
Habit (Barefoot)Yes14860.960.41–2.250.8975
No1165
SexM291313.861.76–8.44<0.0007
F9157

*OR = Odds Ratio

#Confidence Intervals 95.0% (C.I.95%)

*OR = Odds Ratio #Confidence Intervals 95.0% (C.I.95%)

Microbiological water analysis

The microbiological analysis results revealed different levels of contamination by total and thermotolerant coliforms in the samples from the five mollusk collection points. During the dry season, the total coliforms ranged from 2.1 x 104 to 7.5 x 104, and the fecal coliforms/thermotolerant coliforms ranged from 1.4 x 103 and 4.6 x 103. During the rainy season, the total coliforms ranged from 1.7 x 104 to 4.7 x 104, and the fecal coliforms/thermotolerant coliforms ranged from 1.4 x 103 to 5.4 x 103. During both the dry and rainy seasons, the thermotolerant coliform concentration was in accordance with the CONAMA resolution and showed no significant differences when the total mean was compared with the limits set by CONAMA. Conversely, the total coliform levels were above the allowed limit, and the paired t-test revealed total mean values significantly above those set by CONAMA in both evaluation periods: dry season—p < 0.0322, mean 3.54, and standard deviation ± 2.24; rainy season—p < 0.0094, mean 3.12, and standard deviation ± 1.24.

Discussion

Epidemiological studies of schistosomiasis are important for elucidating the dynamics of transmission in endemic areas because each site has biological, ecological, social, and economic characteristics that may affect this process [26]. The urban area studied presents a social and environmental scenario that is conducive to the formation/maintenance of potential schistosomiasis transmission foci. The presence of mollusks in the water bodies, the individual cultural habits of each resident, and the precarious nature of the basic sanitation are essential for understanding the results obtained in this study. In the scenario of schistosomiasis transmission in Brazil, B. glabrata mollusks are important actors because of their wide geographic distribution and the high rates of S. mansoni infection reported by other authors [11,12]. In the study area, the parasitological analysis revealed the presence of B. glabrata mollusks releasing S. mansoni cercariae, (8.8%), which can be considered as a sign of the presence of transmission focus ([27]) in view of the fact that infected residents were also found (16.4%). On the other hand, the Schistosoma transmission has an important seasonal component that is related to the distribution and density of the intermediate host and determined in the rainy periods by the increase of the rivers flow and the temporary water pools [28]. Although this study revealed no significant association between the mollusk density and rainfall, the latter factor appeared to influence these parameters; indeed, the density of the mollusks present and the mollusks shedding eliminating S. mansoni cercariae increased as the rainfall time increased. This correlation has been reported in other studies conducted in Brazil, which is the main endemic area for mansonic schistosomiasis in the Americas because the hot and humid tropical climate is conducive to the reproduction and maintenance of the host mollusks [8,29,30]. Before the rainy season, an important measure for the control of schistosomiasis is to maintain the cleanliness of the urban environment, as this can promote a significant reduction in the number of mollusks and their potential dispersion during the rainy season. The identification of schistosomiasis transmission foci is crucial for the development of control and health management plans in these communities [31]. Based on the location of mollusks infected with S. mansoni, we performed a parasitic evaluation of the community close to the mollusk collection sites. The results showed prevalence greater than 15%; thus, the area can be considered highly prevalent even though the intensity of the infections was low, with less than 100 eggs per gram of stool [16]. Similar to reports in other studies [32], this fall in the infection rate is the result of control measures based only on treatment without the implementation of any other major interventions in the health infrastructure [33]. A cross-sectional study conducted in the same area but based on data from the Schistosomiasis Control Program (Programa de Controle da Esquistossomose—PCE) from 2003–2008 found that the municipality of Nossa Senhora do Socorro was considered to have medium endemicity, with a mean prevalence of 13.98% [31]. These results show that the epidemiological status of schistosomiasis has undergone no major changes in improvements in the population over the last 10 years despite the efforts of government control programs. Other soil-borne parasitic infections were also identified in the residents of the study area, showing that the population was exposed to various infectious agents probably due to the poor sanitary conditions in the area. The highest prevalence encountered in this study occurred in children and adolescents, which corroborated the results from other studies that identified these age groups as the most affected due to the lack of hygiene, more frequent contact of young people with contaminated water, and their recreational activities. The greatest number of positive cases in Brazil has been found in the 6- to 20-year-old age group [6, 33, 34]. Together with the state of Sergipe, other states of the Brazilian Northeast are considered endemic for schistosomiasis, which reinforces the attention to the spread of the disease in the region and also to other regions of Brazil and the world as a result of migratory processes [6,9,32,33]. Many of the individuals infected with S. mansoni in this study were born in other Northeastern states such as Alagoas and Pernambuco which may also contribute to the spread and establishment of endemic disease in the study area. Notably, all positive individuals had a low education level and family income, reinforcing the fact that schistosomiasis is strongly linked to a low socioeconomic status. Several studies have reported that schistosomiasis is a disease that affects males more frequently [35, 36], which was also observed in our study, which showed that these have a significantly higher chance of acquiring the infection. This result may be related to the greater involvement of men in activities in rivers and streams near the community, such as fishing, river bathing for leisure and other activities. Similar results were found in the literature for studies conducted in the northeastern region of Brazil that showed higher prevalence rates for S. mansoni in males; the studies also suggested that the reason for these higher prevalence rates was possibly because males attended health services less frequently [37, 38, 39]. Although there was no significant association between schistosomiasis and demographic, social, environmental and cultural variables, certainly constant contact in areas with poor sanitation and in which infected intermediary hosts were detected may have contributed to the transmission of S. mansoni in the locality. Additionally, contact with contaminated water can also be accidental in the rainy season, when floods and overflowing streams facilitate human contact with the parasite [40, 41]. The same variables, sewage destination and water supply were analyzed in a study carried out in the State of Alagoas/ razil, in which no significant associations with S. mansoni infection were found [6]. Microbiological water quality evaluation is an essential tool for the prevention of waterborne infections. In addition to indicating the fecal contamination rate, this analysis is relevant because it focuses on confirming the presence of human waste in the water from which B. glabrata was collected. This finding is of interest because mollusk and human infections are strongly linked to contamination of the aquatic environment by coliforms [42]. The results obtained in this research revealed that the freshwater bodies were contaminated with total and thermotolerant coliforms, which certainly confirmed sewage discharge in that area and increased the likelihood that the S. mansoni eggs came from infected individuals in the community. Coliform bacteria have been extensively used as fecal pollution indicators in the evaluation of the sanitary conditions of water bodies because these microorganisms are specific to the human intestinal tract [32]. This study reveals worrying data regarding schistosomiasis in the community, including high prevalence of infection, presence of S. mansoni infected mollusks in streams located in front of residents' homes. These findings point to the need to implement comprehensive control measures aimed at controlling the population of mollusks because residents share the urban space with the residents, associated with improved sanitation conditions so that the sewage is not dumped directly into the environment. The situation of the urban community under study shows a new epidemiological situation observed in many Brazilian cities, the disorderly growth of cities often caused by rural migration, which gives rise to pockets of poverty in which residents live without adequate sanitation conditions being exposed to diverse diseases such as schistosomiasis. The Government's program of disease control in Brazil has worked and undoubtedly achieved good overall results, however this new urban transmission profile must be investigated and recognized in its particularities since each place has different socioenvironmental characteristics. In conclusion, the prevalence of schistosomiasis in the studied community is related to the aforementioned conditions that contribute to the maintenance of the endemic cycle. These results indicate that understanding the peculiarities of endemic areas is important for defining specific prevention and control strategies. Government intervention is necessary in the actions of improvements in sanitation and the treatment of infected residents with an aim of disrupting the biological cycle of S. mansoni to attempt to minimize the risks of transmission and the emergence of new cases. On the other hand, the recognition by the population of the need for health care is fundamental to reverse situations such as the one observed in the present research and that certainly go through the implementation of educational actions. Individuals infected with S. mansoni and/or other parasites were referred to the local health clinic for treatment, which does not guarantee that they will be reinfected in the same place. Finally, the data presented in this research show the reality of several urban communities concentrated in the periphery of many Brazilian cities and which clearly show that schistosomiasis in addition to other health situations could be minimized in a relevant way if, for example, adequate basic sanitation was offered to these populations.

Questionnaire used in interviews with residents to obtain the results of socioeconomic and demographic variables.

In addition to risk factors for S. mansoni infection. (PDF) Click here for additional data file.
  24 in total

1.  [Epidemiological characteristics and geographical distribution of schistosomiasis and geohelminths, in the State of Sergipe, according to data from the Schistosomiasis Control Program in Sergipe].

Authors:  Carla Virginia Vieira Rollemberg; Cybele Maria Bomfim Santos; Marília Matos Bezerra Lemos Silva; Acacia Maria Barros Souza; Angela Maria da Silva; José Antônio Pacheco de Almeida; Roque Pacheco de Almeida; Amélia Ribeiro de Jesus
Journal:  Rev Soc Bras Med Trop       Date:  2011 Jan-Feb       Impact factor: 1.581

2.  [Geographic distribution of Schistosoma mansoni transmitter snail species in State of São Paulo].

Authors:  Horacio Manuel Santana Teles
Journal:  Rev Soc Bras Med Trop       Date:  2005-09-12       Impact factor: 1.581

3.  [Ecoepidemiology of urban schistosomiasis in Itamaracá Island, Pernambuco, Brazil].

Authors:  C S Barbosa; O S Pieri; C B da Silva; F S Barbosa
Journal:  Rev Saude Publica       Date:  2000-08       Impact factor: 2.106

4.  [Urban transmission of schistosomiasis in children from a neighborhood of Salvador, Bahia].

Authors:  Isabel C S Guimarães; José Tavares-Neto
Journal:  Rev Soc Bras Med Trop       Date:  2006 Sep-Oct       Impact factor: 1.581

5.  [Schistosomiasis mansoni in Bahia, Brazil: historical trends and control measures].

Authors:  E H Carmo; M L Barreto
Journal:  Cad Saude Publica       Date:  2003-12-15       Impact factor: 1.632

6.  The Pampulha reservoir remains a potential urban focus of schistosomiasis mansoni in Brazil: changes in the occurrence patterns of Biomphalaria species and a new record of the parasite.

Authors:  Hudson Alves Pinto; Vitor Luís Tenório Mati; Alan Lane de Melo
Journal:  Rev Soc Bras Med Trop       Date:  2013 Jul-Aug       Impact factor: 1.581

7.  Evaluation of a 25-year-program for the control of schistosomiasis mansoni in an endemic area in Brazil.

Authors:  Ana K Sarvel; Aureo A Oliveira; Alexandre R Silva; Anna C L Lima; Naftale Katz
Journal:  PLoS Negl Trop Dis       Date:  2011-03-15

Review 8.  A research agenda for helminth diseases of humans: social ecology, environmental determinants, and health systems.

Authors:  Andrea Gazzinelli; Rodrigo Correa-Oliveira; Guo-Jing Yang; Boakye A Boatin; Helmut Kloos
Journal:  PLoS Negl Trop Dis       Date:  2012-04-24

9.  Schistosoma mansoni among pre-school children in Musozi village, Ukerewe Island, North-Western-Tanzania: prevalence and associated risk factors.

Authors:  Deodatus M Ruganuza; Humphrey D Mazigo; Rebecca Waihenya; Domenica Morona; Gerald M Mkoji
Journal:  Parasit Vectors       Date:  2015-07-16       Impact factor: 3.876

Review 10.  Epidemiology and control of human schistosomiasis in Tanzania.

Authors:  Humphrey D Mazigo; Fred Nuwaha; Safari M Kinung'hi; Domenica Morona; Angela Pinot de Moira; Shona Wilson; Jorg Heukelbach; David W Dunne
Journal:  Parasit Vectors       Date:  2012-11-28       Impact factor: 3.876

View more
  7 in total

Review 1.  Population Structure and Dynamics of Helminthic Infection: Schistosomiasis.

Authors:  Ronald E Blanton
Journal:  Microbiol Spectr       Date:  2019-07

Review 2.  Prevalence of Schistosoma mansoni and S. haematobium in Snail Intermediate Hosts in Africa: A Systematic Review and Meta-analysis.

Authors:  Tamirat Hailegebriel; Endalkachew Nibret; Abaineh Munshea
Journal:  J Trop Med       Date:  2020-09-07

3.  The changing profile of schistosomiasis in a changing urban landscape.

Authors:  Luciano K Silva; Lúcio M Barbosa; Jeffrey D Kovach; Rogério Dos Santos Teixeira; Ênio Silva Soares; Cristiane Wanderley Cardoso; Rosângela Vasconcelos Martins Marques; Tatiane Pereira Dos Santos; Mitermayer G Reis; Ronald E Blanton
Journal:  Int J Parasitol       Date:  2019-11-27       Impact factor: 3.981

4.  Association between Schistosoma mansoni infection and access to improved water and sanitation facilities in Mwea, Kirinyaga County, Kenya.

Authors:  Paul M Gichuki; Stella Kepha; Damaris Mulewa; Janet Masaku; Celestine Kwoba; Gabriel Mbugua; Humphrey D Mazigo; Charles Mwandawiro
Journal:  BMC Infect Dis       Date:  2019-06-07       Impact factor: 3.090

Review 5.  A systematic literature review of schistosomiasis in urban and peri-urban settings.

Authors:  Katharina Klohe; Benjamin G Koudou; Alan Fenwick; Fiona Fleming; Amadou Garba; Anouk Gouvras; Emma M Harding-Esch; Stefanie Knopp; David Molyneux; Susan D'Souza; Jürg Utzinger; Penelope Vounatsou; Johannes Waltz; Yaobi Zhang; David Rollinson
Journal:  PLoS Negl Trop Dis       Date:  2021-02-25

6.  Knowledge, attitudes, and practices regarding schistosomiasis infection and prevention: A mixed-methods study among endemic communities of western Uganda.

Authors:  Maxson Kenneth Anyolitho; Karolien Poels; Tine Huyse; Julius Tumusiime; Faith Mugabi; Casim Umba Tolo; Caroline Masquillier; Viola Nilah Nyakato
Journal:  PLoS Negl Trop Dis       Date:  2022-02-23

7.  A loop-mediated isothermal amplification assay for Schistosoma mansoni detection in Biomphalaria spp. from schistosomiasis-endemic areas in Minas Gerais, Brazil.

Authors:  Silvia Gonçalves Mesquita; Floria Gabriela Dos Santos Neves; Ronaldo Guilherme Carvalho Scholte; Omar Dos Santos Carvalho; Cristina Toscano Fonseca; Roberta Lima Caldeira
Journal:  Parasit Vectors       Date:  2021-08-06       Impact factor: 3.876

  7 in total

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