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J Parasit Dis Diagn Ther 2017 | Volume 2 Issue 4

International Conference on

Zoology, Microbiology & Medical Parasitology

October 30-November 01, 2017 | Chicago, USA

Prevalence and diversity of

Bartonella species

in ectoparasites fromwild-caught rodents and domestic

animals in the Northern and Northeastern regions of Thailand

Ratree Takhampunya

Armed Forces Research Institute of Medical Sciences, Thailand

E

ctoparasites are thought to be the important vectors

of Bartonella transmission among animals, including

humans. The Bartonella prevalence and species diversity in

several types of ectoparasites (ticks, fleas, chiggers, and lice)

collected from rodents and domestic animals (cats, dogs,

cattle, and chickens) were investigated in this study. The

surveillance study was conducted in 2 regions, 4 provinces;

2 provinces from the Northern region (Nan and Mae Hong

Son) and 2 provinces from the Northeastern region (Loei

and Nong Bua Lam Phu) during September 2013 to October

2014. Overall, a total of 539 pooled ectoparasites (102 fleas

pools, 80 ticks pools, 6 lice pools, and 351 chiggers pools)

were collected from wild-caught rodents and a total of 650

pooled ectoparasites (384 fleas pools, 213 ticks pools and

53 lice pools) were collected form domestic animals. Real-

time PCR assay with TaqMan probe targeting Bartonella-

specific ssrA gene was used for Bartonella DNA detection.

Amplification of Bartonella gltA gene was confirmed using

published primers, CS443f and CS1210r. Fleas were the

major ectoparasites collected from domestic animals

(59.0%), followed by ticks (32.8%), and lice (8.2%). Chiggers

were the most common ectoparasites collected from

rodents (65.1%), followed by fleas (18.9%), ticks (14.9%) and

lice (1.1%). Bartonella DNA was detected in all ectoparasites

types. Among ectoparasites collected from rodents, the

highest prevalence of Bartonella DNA was found in fleas

pools (24.5%, 25/102), then in lice pools (16.7%, 1/6) and

ticks pools (12.5%, 10/80), respectively. However, low

prevalence of Bartonella DNA was found in chiggers pools

(2.8%, 10/351). Likewise, high prevalence of Bartonella

DNA was also found in fleas pools collected from domestic

animals (14.1%, 54/381), while low prevalence was found

in lice pools (5.7%, 3/53) and tick pools (6.6%, 14/213).

Phylogenetic analysis of Bartonella gltA sequences (638 bp)

presented the diverse range of Bartonella species found in

ectoparasites collected from rodents including 4 Bartonella

species in B. elizabethae species complex (B. elizabethae,

B. tribocorum B. rattimassiliensis, and B. queenslandensis),

B. rochalimae and Candidatus B. thailandensis. However,

only 2 species (B. clarridgeiae and B. tamiae) was detected

in ectoparasites collected from domestic animals. Our data

showed an important role of ectoparasites as potential

vectors for Bartonella transmission among rodents and

domestic animals residing in close association with humans.

Speaker Biography

Ratree Takhampunya is currently working as an Research Associate in the Armed Forces

Research Institute of Medical Sciences-U.S. Army Medical Directorate in Thailand.

e:

Ratreet.fsn@afrims.org