Author/Authors :
Sadat Makki, Mahsa Department of Medical Parasitology and Mycology - School of Public Health, Tehran University of Medical Sciences, Tehran, Iran , Mowlavi, Gholamreza Department of Medical Parasitology and Mycology - School of Public Health, Tehran University of Medical Sciences, Tehran, Iran , Shahbazi, Farideh Department of Medical Parasitology and Mycology - School of Public Health, Tehran University of Medical Sciences, Tehran, Iran , Abai, Mohammad Reza Department of Medical Entomology - School of Public Health - Tehran University of Medical Sciences, Tehran, Iran , Najafi, Faezeh Department of Medical Parasitology and Mycology - School of Public Health, Tehran University of Medical Sciences, Tehran, Iran , Hosseini-Farash, Bibi Razieh Department of Parasitology and Mycology - Research Center for Skin Disease and Cutaneous Leishmaniasis - School of Medicin - Mashhad University of Medical Sciences, Mashhad, Iran , Teimoori, Salma Department of Medical Parasitology and Mycology - School of Public Health, Tehran University of Medical Sciences, Tehran, Iran , Hasanpour, Hamid Department of Medical Parasitology and Mycology - School of Public Health, Tehran University of Medical Sciences, Tehran, Iran , Naddaf, Saied Reza Department of Parasitology - Pasteur Institute of Iran, Tehran, Iran
Abstract :
Background: Hymenolepis diminuta is a cestod of rodents and rarely infects humans. Infection in humans is via
ingestion of infected insects. This study was aimed to detect H. diminuta cysticercoids in red flour beetles, Tribolium
castaneum, and cockroaches originated from different regions of Iran.
Methods: The red flour beetles and cockroaches were collected from local bakeries in five cities including Tehran,
Ahvaz, Kazerun, and Sabzevar during 2010–2011. Some beetles and cockroaches were colonized in insectary and
adults from F1 generation were fed on H. diminuta eggs. Both laboratory-infected and field-collected samples were
dissected and examined for cysticercoids. Detection of H. diminuta DNA in T. castaneum beetles was performed by
targeting a partial sequence of Ribosomal gene.
Results: Except the beetles from Ahvaz, all specimens were negative for cysticercoid by microscopy. Of the four
dissected beetles from Ahvaz, one harbored 12 cysticercoids. Also, 110 (52%) of laboratory-infected beetles showed
infection with an average of 12–14 larvae. None of the cockroaches was infected. Two beetles from Ahvaz, including
the remainder of the microscopic positive specimen, yielded the expected amplicon in PCR assay. The H.
diminuta DNA sequences generated in this study were identical and matched 97–100% with similar sequences from
GenBank database.
Conclusion: Lack of infection in the majority of beetles may reflect a low rat infestation rate in those areas, alternatively,
the examined specimens might not have been the representative samples of the T. castaneum populations.
Keywords :
Hymenolepis diminuta , Cysticercoid , Tribolium castaneum , Iran