Abstract
Background
There are a number of conflicting studies on the prevalence of intestinal parasitic infections in HIV infection with regards to different seasons. This study was conducted to determine seasonal influence on the prevalence of intestinal parasitic infections in HIV-positive persons in Benin City, Nigeria.
Methods
Stool specimens from 2000 HIV-positive patients and 500 controls (HIV-negative individuals) were examined for ova, cysts or parasites using standard procedures.
Results
More intestinal parasitic infections were observed in the rainy season (17.6%) than the dry season (12.3%) (OR = 1.526, 95% CI = 1.184, 1.967, p = 0.0013). Male patients (18.3) had more episodes of intestinal parasitic infections than their female (13.7) counterparts (OR = 1.403, 95% CI = 1.092, 1.803, p = 0.0096).
Conclusion
Cryptosporidium species and Strongyloides stercoralis were the only parasitic agents that were associated with rainy season.
Keywords: Season, Intestinal Parasites, HIV
Introduction
Despite the worldwide efforts at controlling the menace of acquired immunodeficiency syndrome (AIDS), the number of infected persons is growing as well the number of deaths. In 2008, Nigeria recorded 0.28 million deaths resulting from HIV disease and the infection rate was put at 4.6 million (1). Superimposed infections due to defective immunity are a major health problem among HIV-positive persons. Intestinal infection, which is also one of the basic health problems in tropical regions, is common in these patients (2). Intestinal parasitic infections in HIV-infected patients are common in many regions and populations across Nigeria and represent a lasting public health challenge (3). The spectrum of opportunistic infections among HIV-infected persons varies from one region to another (4). Amongst these opportunistic infections, opportunistic protozoan infections are the most serious ones causing severe morbidity and mortality (5). There are a number of conflicting studies on the prevalence of intestinal parasitic infections in HIV infection with regards to different seasons. Some authors observed seasonal variations in the prevalence of intestinal parasitic infections in HIV persons (5, 6), while Kurniawan et al. (7) reported no seasonal influence. There is paucity of information on seasonal influence on the prevalence of parasitic infections in HIVpositive persons in Benin City. Hence, this study was conducted to determine seasonal influence on the prevalence of intestinal parasitic infections among HIV-positive persons in Benin City, Nigeria.
Materials and Methods
The cross sectional study was carried out at the University of Benin Teaching Hospital, Benin City - a teaching hospital with a referral status and center for United States President's Emergency Plan for AIDS Relief (PEPFAR). A total of 2,500 subjects consisting of 2,000 HIV-positive patients attending HIV clinics and 500 apparently healthy HIV non-infected individuals that served as controls were included in this study. Verbal informed consent was obtained prior to specimen collection.
Specimen collection and processing: Single stool specimen was collected from each patient in a clean wide-mouthed container. Freshly voided stool specimens were processed using formolether concentration technique and examined microscopically for ova, cysts or parasites using saline and iodine mounts on grease free slides (8). Part of the stool specimen was preserved in 10% formal-saline and from this a concentrated smear was made on a grease-free slide, fixed with methanol and stained by a modified Ziehl-Neelsen stain as described by Akinbo et al. (3). This was used to detect oocyst of Crystosporidium species, Isospora belli, Cyclospora cayetanensis.
The rainy season was defined as the period between the months of April and September and the dry season between October and March.
Statistical analysis: The frequency of data was analyzed using chi square (x2) test and odd ratio (OR) was calculated for each potential risk factor using the statistical software INSTAT® (GraphPad Software Inc., La Jolla, CA, USA).
Before the study was conducted, the Ethical Committee of the University of Benin Teaching Hospital, Benin City, Nigeria, had approved the protocol of this study.
Results
Generally, more intestinal parasitic infections were observed in the rainy season (17.6%) than the dry season (12.3%) (OR = 1.526, 95% CI = 1.184, 1.967, p = 0.0013). In the same vein, male patients (18.3) had more episodes of intestinal parasitic infections than their female (13.7) counterparts (OR = 1.403, 95% CI = 1.092, 1.803, p = 0.0096). The effect of gender on the prevalence of intestinal parasitic infections was observed only in the dry season where males had significantly higher prevalence of intestinal parasitic infections (p = 0.031). Among the intestinal parasitic agents, Crptosporidium species and Strongyloides stercoralis were associated with higher prevalence in the rainy season (Table 1).
Table 1.
Effect of gender and season on the prevalence of intestinal parasitic infections among HIV patients.
Season | Male | Female | |||||
Number tested |
Number positive |
Number tested |
Number positive |
OR | 95% CI | P value | |
HIV patients | |||||||
Rainy | 415 | 81 | 712 | 117 | 1.233 | 0.901,1.687 | 0.218 |
Dry | 253 | 41 | 620 | 66 | 1.623 | 1.066,2.473 | 0.031* |
Non-HIV Patients | |||||||
Rainy | 126 | 6 | 139 | 11 | 0.568 | 0.204,1.582 | 0.713 |
Dry | 83 | 8 | 152 | 6 | 2.561 | 0.857,7.652 | 2.098 |
On the other hand, intestinal parasitic infection was not associated with seasonal variation among HIV non-infected persons (OR = 0.703, 95% CI = 0.338, 1.462, p = 0.450), although the prevalence is higher (7.53%) in the dry season compared to the rainy season (5.41%) (Fig 1). Only Ascaris lumbricoides and hookworm were recovered from non-HIV patients and neither were significantly associated with seasonal variations (OR = 0.821 95%CI = 0.357, 1.889; p = 0.805 and OR = 0.439 95% CI = 0.097, 1.984; p = 0.480 respectively) (Table 2).
Figure 1.
Effect of seasonal variation on prevalence of intestinal parasites
Table 2.
Effect of season on the prevalence of parasitic infections in HIV-infected patients
Organism | Rainy | Dry | OR | 95% CI | P value |
E. histolytica | 8 | 4 | 1.560 | 0.4679, 5.198 | 0.662 |
G. intestinalis | 0 | 2 | 0.155 | 0.007, 3.240 | 0.373 |
Isospora belli | 19 | 9 | 1.653 | 0.744, 3.672 | 0.291 |
Cryptosporidium | 62 | 18 | 2.777 | 1.630, 4.730 | 0.0001* |
A. lumbricoides | 71 | 48 | 1.161 | 0.796, 1.693 | 0.5 |
Hookworm | 42 | 32 | 1.022 | 0.639, 1.633 | 0.929 |
S. stercoralis | 20 | 3 | 5.261 | 1.558, 17.767 | 0.006* |
T. trichiuris | 8 | 10 | 0.620 | 0.243, 1.577 | 0.438 |
Taenia spp | 1 | 3 | 0.259 | 0.027, 2.492 | 0.449 |
Discussion
Seasonal variations are known to affect the prevalence of a number of infections (9). With the advent of HIV a number of opportunistic intestinal parasitic infections have been reported (3). Although, a recent report (5) relates intestinal coccidian infection to seasonal variations, there is paucity of reports on effect of seasonal variations on the prevalence of intestinal parasitic infections among HIV patients. Intestinal parasitic infection is significantly associated with rainy season among HIV patients. Furthermore, rainy season may facilitate conditions and risk factors that predisposed to intestinal parasitic infections. Indeed, other parasitic infections such as malaria parasitaemia have been reported to have higher prevalence in the rainy season (10). Male HIV patients are significantly at risk of acquiring intestinal parasitic infections and the reason for this association may be adduced to more males being exposed than females based on occupational grounds. Surprisingly, the association of gender and intestinal parasitic infections was observed only in the dry season and the reason for this observation is unclear.
Considering the parasitic agents in relation to seasons, Cryptosporidium species and Strongyloides stercorlis were the only parasitic agents that were associated with rainy season. The finding of Cryptosporidium in association with rainy season had been noted (5) and its transmission is via different routes such as water, person-to person, contact with animal, and etc (11). During the rainy season cattle are seen roaming and grazing freely and as a result defaecate on soil. These faeces are washed into nearby streams, and rivers by flood of rain. Consumption of this contaminated water can lead to cryptosporidial infection and indeed, prevalence of cryptosporidial infection has been reported to be higher among HIV patients that used streams and rivers as a source of water (11).
In resource poor settings such as Nigeria, many people walk and play in open field barefooted, especially in the rainy season and these habits increase the chances of Strongyloides stercoralis infection. This may explain the association of S. stercoralis with rainy season in this study. Although, a similar mechanism of infection is also utilized by hookworm, the reason for the lack of association between hookworm and season is unclear.
There was no significant association between intestinal parasitic infection and seasonal variation among the non-HIV patients and the reason for this finding is unclear. Ascaris lumbricoides and hookworm infections were the only intestinal parasites recovered from the non- HIV patients.
Conclusively, intestinal parasitic infections are associated with rainy season among HIV patients. Cryptosporidium species and S. stercoralis were the parasitic agents associated with rainy season. This data will be useful in the epidemiology of intestinal parasitic infections in HIV patients as well as in their management.
Acknowledgements
We thank the Management of University of Benin Teaching Hospital for providing specimens to carry out this study and we equally acknowledge Professor A.N. Onunu of the Department of Internal Medicine, University of Benin Teaching Hospital for his expertise.
References
- 1.UNAIDS, author. Report on the Global AIDS epidemic. unaids.org/en/.../GlobalReport/2008.asp.
- 2.Kumar SS, Ananthan S, Saravanan P. Role of coccidian parasites in causation of diarrhea in infected patients in Chennai. Indian J Med Res. 2002;116:85–89. [PubMed] [Google Scholar]
- 3.Akinbo FO, Okaka CE, Omoregie R. Prevalence of intestinal parasitic infections among HIV patients in Benin City, Nigeria. Libyan J Med. 2010;5:5506. doi: 10.3402/ljm.v5i0.5506. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Vajpayee N, Kanswal S, Seth P, Wig N. Spectrum of opportunistic infections and profile of CD4 counts among AIDS patients in North India. Infection. 2003;31:336–340. doi: 10.1007/s15010-003-3198-y. [DOI] [PubMed] [Google Scholar]
- 5.Tuli L, Gulati AK, Sundar S, Mohapatra TM. Correlation between CD4 counts of HIV patients and enteric protozoan in different seasons - An experience of the tertiary care hospital in Varanasi (India) Biomed Centr Gastroenterol. 2008;8:36. doi: 10.1186/1471-230X-8-36. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Omar MA. Seasonal prevalence of intestinal parasites in the United States during 2000. Am J Trop Med Hyg. 2002;66(6):799–803. doi: 10.4269/ajtmh.2002.66.799. [DOI] [PubMed] [Google Scholar]
- 7.Kurniawan A, karyadi T, Dwintasari SW, et al. Intestinal parasitic infections in HIV/AIDS patients presenting with diarrhea in Jakarta in Indonesia. Trans R Soc Trop Med Hyg. 2009;103(9):892–898. doi: 10.1016/j.trstmh.2009.02.017. [DOI] [PubMed] [Google Scholar]
- 8.Cheesbrough M. Parasitological tests. Cambridge University Press; 1999. pp. 178–309. [Google Scholar]
- 9.Hall A, Crompton DWT, Stephenson LS, Wolgemuth JC. Intestinal parasitic infections of men in four regions of rural Kenya. Trans Royal Soc Trop Hyg. 1982;76(6):728–733. doi: 10.1016/0035-9203(82)90092-x. [DOI] [PubMed] [Google Scholar]
- 10.Nkuo-Akenji T, Menang ON. Prevalence of falciparum malaria together with acute diarrhea in children residing in a malaria endemic zone. African J Health Sc. 2005;12:26–30. doi: 10.4314/ajhs.v12i1.30797. [DOI] [PubMed] [Google Scholar]
- 11.Akinbo FO, Okaka CE, Omoregie R, Dearen T, Leon D, Xiao L. Molecular characterization of Cryptosporidium spp. in HIV-infected persons in Benin City, Edo State, Nigeria. Fooyin Journal of Health Sciences. 2010b;2(3–4):85–89. [Google Scholar]