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Comparative Parasitology 67(2) 2000 - Peru State College

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198 uuMKAKAiIVt, rAKAsuOLOuY, 6/(2), JULY <strong>2000</strong><br />

Table 1. Results of cage sampling for Hymenolepis nana using fecal flotation.<br />

Host species<br />

Domestic spiny mouse (Heteromyidae)<br />

Long-tailed chinchilla (Chinchilla lanigcra Molina, 1782)<br />

Black-tailed prairie dog (Cynomys ludovicianus Ord, 1815)<br />

Guinea pig (Cavia porcellus Linnaeus, 1758)<br />

Domestic mouse (Mus tnusculus Linnaeus, 1758)<br />

Ferret (Mustelaputoriusfa.ro Linnaeus, 1758)<br />

Mongolian gerbil (Meriones unguiculatus Milne-Edwards, 18<strong>67</strong>)<br />

European rabbit (Oryctolagux cuniculus Linnaeus, 1758)<br />

Siberian hamster (Phodopus sungorus Pallus, 1773)<br />

Norway rat (Rattus norvegicus Berkenhout, 1769)<br />

:i: Overall prevalence of infected cages was 9.1%.<br />

t A total of 5 individual prairie dogs was surveyed from the 2 cage samples.<br />

:i: Hymenolepis dirninuta eggs were also detected in the cage sample.<br />

sters showed prevalences of 66% and 44% respectively.<br />

Pet stores are traditionally implicated as potential<br />

sources of human parasite infections, but<br />

emphasis is centered upon feline, canine, or avian<br />

species rather than rodents. However, H.<br />

nana is a common zoonosis of pet rodents (Chomel,<br />

1992), and in 1969 infection was detected<br />

in Mongolian gerbils purchased as pets from a<br />

department store (Lussier and Loew, 1970). Given<br />

that children have less than optimal hygiene<br />

habits, and immune-compromised individuals,<br />

such as those with the acquired immunodeficiency<br />

syndrome (AIDS) or undergoing cancer<br />

treatment, are at greater risk for disease (Gerba<br />

et al., 1996), pet rodent infections raise obvious<br />

public health concerns. Additionally, there is a<br />

lack of survey data addressing the assumption<br />

that golden hamsters are more often parasitized<br />

with H. nana than are other rodents (Chomel,<br />

1992; Teclaw et al., 1992). The purpose of this<br />

study was to assess health risks associated with<br />

human and rodent interaction as they pertain to<br />

H. nana, through a survey of small animals sold<br />

by pet stores in southern Connecticut.<br />

Materials and Methods<br />

Once a week for 4 weeks beginning in July 1999, a<br />

fecal survey was conducted on all small animal cages<br />

from 3 pet stores. Samples of 5-10 fecal pellets were<br />

collected from the bedding of cages housing grouped<br />

animals and analyzed by fecal flotation (Hendrix,<br />

1998). A total of 110 cage samples was obtained from<br />

representatives of 11 domesticated small animal species<br />

(Table 1).<br />

Based on the findings from fecal analysis of small<br />

No. of cage<br />

samples<br />

3<br />

6<br />

2<br />

19<br />

18<br />

30<br />

3<br />

7<br />

11<br />

1<br />

22$<br />

Copyright © 2011, The Helminthological Society of Washington<br />

Samples ( + )<br />

for H. nana<br />

0<br />

0<br />

1<br />

0<br />

0<br />

6<br />

0<br />

0<br />

0<br />

0<br />

3<br />

Cage<br />

prevalence<br />

(%)*<br />

0<br />

0<br />

sot<br />

0<br />

0<br />

20<br />

0<br />

0<br />

0<br />

0<br />

14<br />

animal cages, individual rodents were purchased from<br />

9 different pet stores not included in the fecal survey,<br />

and a postmortem examination of the intestinal tract<br />

of each rodent was performed. Necropsy was conducted<br />

on a total of 38 rats, 39 golden hamsters, and<br />

72 domestic mice. Animals were killed by CO2 narcosis,<br />

and the small intestine, from the pyloric sphincter<br />

to the ileocecal juncture, was removed, placed in a<br />

Petri dish of tap water, and opened longitudinally.<br />

Worms were removed and counted. Representative<br />

specimens were stained, mounted, and deposited in the<br />

United <strong>State</strong>s National Museum Parasite Collection in<br />

Beltsville, Maryland, U.S.A. (USNPC No. 089330.00).<br />

Results<br />

Fecal analysis showed that 9.1% of cages<br />

housed infected animals, with animals from 1<br />

pet store testing positive for 3 of 4 weeks. Domestic<br />

mice and Norway rats exhibited prevalences<br />

of 30.0% and 13.6%, respectively. One<br />

of 2 black-tailed prairie dog cage samples revealed<br />

H. nana. All other species, including<br />

golden hamsters, were negative by fecal flotation<br />

analysis (Table 1).<br />

Necropsy results of purchased animals revealed<br />

that 7 of 9 pet stores were selling infected<br />

rats, domestic mice, and/or golden hamsters.<br />

Prevalence was highest in rats (31.6%), with<br />

mean intensity (MI) of 66 worms per host.<br />

Mouse prevalence was lower at 22.2% (MI =<br />

15), and only 4 golden hamsters (10.3%) were<br />

infected (MI = 15). One rat was infected with<br />

Hymenolepis dirninuta Rudolphi, 1819 (Table 2).<br />

Discussion<br />

Rodents typically remained in pet stores approximately<br />

7-10 days. The prepatent period for

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