Chapter 4 EGG PRODUCTION OF OESOPHAGOSTOMUM BIFURCUM, A LOCALLY COMMON PARASITE OF HUMANS IN TOGO. H.P. Krepel and A.M. Polderman

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Chapter 4 EGG PRODUCTION OF OESOPHAGOSTOMUM BIFURCUM, A LOCALLY COMMON PARASITE OF HUMANS IN TOGO H.P. Krepel and A.M. Polderman Published in the American Journal of Tropical Medicine and Hygiene 1992;46:469-472

48 Summary In northern Togo and northeastern Ghana, Oesophagostomum bifurcum is a common parasite in humans. Diagnosis is based on coproculture because the eggs of hookworm and Oesophagostomum are indistinguishable. To determine the level of egg production, 12 subjects were treated with 2 x 10 mg/kg of pyrantel pamoate and the worms they evacuated were then counted. Pretreatment and post-treatment species-specific egg counts were calculated on the basis of larval and total egg counts. The median worm burden was 81 (range 12-300) per person. The calculated median egg production was 33.7 egg/gram of feces per female worm. Assuming a total daily stool production of 150 g/day, this amounts to 5 055 eggs/day, which is comparable with the production of other nematodes of the same superfamily.

Egg production 49 Introduction In animals, oesophagostomiasis is a common infection that causes serious pathology. It is caused by Oesophagostomum species, which are nematodes of the same superfamily as hookworm. Some examples are O. colombianum, O. radiatum and O. dentatum. It has been established only recently that in northern Togo and northeastern Ghana, it is also a common infection in humans. Using a coproculture method, third-stage Oesophagostomum larvae were found in 30% of the population [1]. Use of a coproculture method is essential, since the eggs of Oesophagostomum cannot be distinguished from those of hookworm by size or by morphological criteria [2]. In contrast, the third-stage, infective larvae are very different [3]. The level of egg production of the species involved, O. bifurcum, is not known. The egg production of O. radiatum is 5 000/worm/day [4]. Hookworm produces between 10 000 and 30 000/worm/day in humans, depending on the species and the worm burden [2,5].Ternidens deminutus, another species belonging to the same order as hookworm and Oesophagostomum, produces between 3 500 and 7 000 eggs/day [6]. The purpose of this study was to estimate egg production of O. bifurcum in humans. Specific egg counts for Oesophagostomum before and after treatment were calculated using egg and larval counts. All adult worms excreted after treatment were counted. To avoid the possibility of quick degeneration of the adult worms after treatment, the participants were treated with pyrantel pamoate and a purgative. Materials and methods Trial population In the village of Lotogou, about 25 km west of the main town of Dapaong, several households were visited. The inhabitants were screened using one coproculture. Persons who were positive for Oesophagostomum could participate provided they were five years of age or older and had not received anthelmintic treatment in the recent past. Pregnant women and subjects suffering with major illnesses were excluded. Counting techniques One to three days before treatment, two stool samples were collected. From each sample, two egg counts (Kato smears, 25 mg) and three stool cultures (classic charcoal method[l]) were done. After seven days, the numbers of both hookworm and Oesophagostomum larvae in each culture were identified according to the key of Little [3]. and counted. One week after treatment, two egg counts and three coprocultures were performed on one stool sample.

50 Table 1. Egg production of Oesophagostomum bifurcum in 12 subjects in this study Pre-treatment Worms Egg production Subject/sex /age(years) epg Mwl Oel Oe-epg Total Female epg/worm epg/female worm l/f/9 2/F/10 3/F/25 4/F/40 5/M/8 6/M/8 7/M/8 8/M/8 9/M/8 10/M/9 ll/m/12 12/M/70 Median 4 360 2 160 1 840 10 180 2600 420 1 180 9 140 2 540 3440 4 580 9 120 3 020 17 37 64 391 249 16 17 164 62 63 107 217 89 56 117 28 28 19 23 241 221 61 173 12 3674 1304 1193 669 266 226 672 5443 1984 1697 2833 479 1 199 90 81 87 38 12 24 49 300 227 81 151 12 58 47 52 15 6 11 28 175 127 45 78 7 40,8 16,1 13,7 17,6 22,2 9,4 13,7 18,1 8,7 20,9 18,8 39,9 20,0 63,4 27,7 22,9 44,6 44,3 20,5 24,0 31,1 15,6 37,7 36,3 68,4 36,4 * Epg = epg/gram of feces; Hwl = hookworm larval counts; Oel = Oesophagostomum larval counts. Treatment and isolation of adult worms A purgative was given the day before treatment (do) at 6:00 PM. The next day (dl) at 7:00 AM, participants were treated with 10 mg/kg pyrantel pamoate. Two hours after treatment, a purgative was given again. Treatment and purgation were repeated on the second day (d2) at the same times. All stools produced during day 1 and day 2 were collected. The stools were washed and sieved with 1-mm and 300-/xm mesh sieves, and the adult worms were identified and counted. Calculation methods For the calculation of the worm's level of egg production, only data from those patients were included on whom Kato smears, stool cultures, and treatment were successfully performed. Moreover, very light infections (< 10 worms evacuated) were excluded. Of the 12 cases meeting the above criteria, the arithmetric means of the pre-treatment egg counts (eggs/gram of feces [epg] in Table 1) were calculated for each individual. Using the larval counts for both hookworm (Hwl) and Oesophagostomum (Oel), it was calculated which part of the egg output was attributed to Oesophagostomum (Oe-epg) and hookworm, respectively. These

Egg production 51 species-specific egg counts were then divided by the total number of adult worms to determine egg production per worm per gram of feces (epg/w), or by the number of adult female worms only to determine egg production per female worm per gram of feces (epg/fw). Results Pretreatment counts The median larval counts were 59 (range 12-241) per culture for Oesophagostomum, and 64 (range 16-391) for hookworm. The median total egg count was 3 020 epg (range: 420-10 180), while the median for Oesophagostomum was calculated at 1 199 (range 226-5 443) epg (Table 1). Recovery of adult worms A total of 703 female and 562 male Oesophagostomum worms were counted. The number of worms per participant varied from 12 to 300 (Table 1). Calculation of egg production The calculated median level of egg production for one Oesophagostomum worm was 17.9 epg per worm, while for female worms, this figure was 33.7 epg per female worm (Table 1). Assuming a total stool production of 150 g/day, this would mean that the total daily egg output is 2 685 eggs/worm, and 5 055 eggs/female worm. The pretreatment species-specific egg counts as well as the larval counts of Oesophagostomum showed a good correlation with the observed worm burden (Figure 1). Discussion It has only recently been established that human infections with O. bifurcum are common in northern Togo and northeastern Ghana [1]. Many biological and medical aspects still have to be examined, one of them being the the level of egg production. Knowing the level of egg production of the parasite provides also a means of estimating the worm burden. The morphological similarity of Oesophagostomum and hookworm eggs makes specific egg counts difficult to achieve. We used the proportion of Oesophagostomum versus hookworm larvae found in the coprocultures to calculate the number of Oesophagostomum eggs in the total egg counts.

52 (a) number of adult worms 100 number of larvae (b) number of adult worms 100 100 1.000 specific egg counts Figure 1. Relationship between Oesophagostomum worm burden and larval counts (a) (R = 0.91. P < 0.01) and specific egg counts (b) (R = 0.94, P < 0.01).

Egg production 53 The median level of egg production was calculated to be 33.7 epg/female worm. Assuming a total daily stool production of 150 g, this comes to 5 055 eggs/day. These levels are consistent with those of hookworm and Ternidens deminutus [2,5,6]. It must be stressed that the calculations are based on the assumption that the development of hookworm and Oesophagostomum larvae in coprocultures is equally successful. The linear relationship between worm burden and larval counts, and worm burden and species-specific egg counts would indicate that this parity was probably the case in our study. The mean egg excretion per female worm was calculated for 12 cases of an initial series of 30. Of the remaining 18 subjects, four were not included because live Oesophagostomum larvae were cultured following treatment. In five cases, there were indications that the pretreatment cultures were unreliable (few larvae cultured in patients excretin many eggs), while in nine cases, less than 10 adult worms were evacuated after treatment. In seven of the latter patients, very few eggs were found; these patients apparently had very light infections. In the remaining two, only a minor proportion of the feces produced after treatment was submitted for examination. It cannot be excluded that there is a bias in the resulting calculations of egg production; in very light infections, the level of egg produciton might be different. After treatment with pyrantel pamoate 2 x 10 mg/kg, few adult specimens of Necator americanus were recovered. One week after treatment, Oesophagostomum-positive cultures (excluded from the analysis in this report) were observed in only four of 30 persons. Hookworm larvae, however, were found in 28 cases. Thus, treatment with pyrantel pamoate was not sufficiently effective against hookworm. Therefore, it was therefore not possible to calculate the level of hookworm egg production, as was done for O.bifurcum.

54 Acknowledgements We thank the Ministers of Health and Education for support and assistance with the research in Togo. We also thank Mr. K.D. Amouzou, administrative director of Dapaong Hospital, for valuable advice, and Ms Lamboni Assibi for technical assistance. Financial support: This research was funded by the Netherlands Foundation for the Advancement of Tropcial Research (WOTRO).

Egg production 55 References 1. Polderman AM, Krepel HP, Baeta S, Blotkamp J, Gigase P, 1991. Oesophagostomiasis, a common infection of man in northern Togo and Ghana. American Journal of Tropical Medicine and Hygiene 44:336-344. 2. Beaver PC, Jung RC, Cupp EW, 1984. The strongylida: hookworms and other bursate nematodes, in Beaver and other, eds., 1987. Clinical Parasitology. : Lea & Febiger, 269-301. 3. Little MD, 1981. Differentiation of nematode larvae in coprocultures: guidelines for routine practice in medical laboratories. WHO Technical Report Series No 666: 144-150. 4. Rosenberger G, 1970. Krankheiten dürch Rundwürmer. in Rosenberger, ed., 1970. Krankheiten des Rindes. : Verlag Paul Parey, 920-932. 5. Warren KS, Mahmoud AAF, 1985. Hookworms, in Warren and others, eds., 1985. Tropical and Geopgrahical Medicine. : McGraw-Hill, 359-371. 6. Goldsmid JM, 1971. Studies on the Life Cycle and Biology of Ternidens Deminutus (Railliet & Henry, 1905) (Nematoda: Strongylidae). Journal of Helminthology 45:341-352.