Vector and rodent surveillance for Orientia tsutsugamushi in north India

• Published in: Journal of vector borne diseases 2022-10, Vol.59 (4), p.348-355
• Main Authors: Kaura, Taruna, Kaur, Jasleen, Bisht, Kamlesh, Goel, Shriya, Lakshmi, PVM, Grover, Gagandeep, Mewara, Abhishek, Biswal, Manisha
• Format: Article
• Language: English
• Subjects: Animals; Disease transmission; Epidemiology; Health aspects; Humans; India - epidemiology; Orientia tsutsugamushi - genetics; Polymerase chain reaction; Real-Time Polymerase Chain Reaction; Rodentia - parasitology; Rodents; Scrub Typhus - epidemiology; scrub typhus; o. tsutsugamushi; rodent vector; chigger mite; surveillance; north india; Surveillance; Trombiculidae - genetics; Typhus
• ISSN: 0972-9062
• DOI: 10.4103/0972-9062.355958

Background & objectives: Scrub typhus or chigger borne typhus, caused by Orientia tsutsugamushi is an emerging vector-borne disease as large numbers of cases have been reported in various tropical countries. It is transmitted to humans through bites of infected chiggers (larval mites). The knowledge about the vector, its distribution, density and habitat are important so as to understand the epidemiology of scrub typhus in a given area. To control rickettsial infections, regular rodent-vector surveillance should be planned in areas where the disease transmission is occurring and it will also help to strengthen the existing entomological data related to the vector of scrub typhus in northern India. Methods: In the present study, rodent-vector surveillance was planned for one whole year, covering both mite active and non-active seasons (October 2019-December 2020) in selected areas of Chandigarh and Punjab in north India. Rodent tissues and mites were also examined for the presence of O. tsutsugamushi by nested PCR for 56 kDa gene and real-time PCR for 47 kDa outer membrane protein gene. 18S gene PCR was performed for molecular identification of mites. Results: In the surveillance, three types of ectoparasite, viz. mites, fleas and ticks were obtained in rodents. All mites found were of Laelapidae family. None of the pooled rodent tissue samples as well as mite samples were found positive for O. tsutsugamushi by nested PCR for rickettsial DNA. Interpretation & conclusion: In the present study, we did not get any evidence of carriage of O. tsutsugamushi in either mites or rodents collected and sampled in selected regions in Chandigarh and Punjab. We need to strengthen the entomological surveillance over a broader region and increase the frequency of trapping rodents to increase clarity on vector-reservoir dynamics in this geographical region.