• 제목/요약/키워드: Bartonella

검색결과 15건 처리시간 0.03초

Nested PCR법을 이용한 Cat Scratch Disease의 원인체인 Bartonella Henselae와 Bartonella Clarridgeiae균의 동물병원 수의사의 감염 실태조사 (Prevalence of Bartonella Henselae and Bartonella Clarridgeiae in Veterinarian Working at the Veterinary Teaching Hospital (by nested PCR))

  • 최은화;이종화;윤화영
    • 한국임상수의학회지
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    • 제27권4호
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    • pp.374-377
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    • 2010
  • Cat scratch disease is a zoonotic disease usually caused by the gram-negative bacterium Bartonella henselae. It is transmitted commonly by scratch or bite from cats or kitten. Cat scratch disease typically affects children and young adults, who develop regional lymphadenopathy. In contrast, in immunocompromised hosts, bacteremia may occur, bacillary angiomatosis and bacillary peliosis hepatitis or splenitis are the most common manifestations. Bartonella henselae was detected in three of thirty veterinarians and Bartonella clarridgeiae was detected in one of thirty veterinarians by a novel nested polymerase chain reaction. Cat scratch disease will not be neglected, and it needs continuous studies as well as observation and prevention of this disease.

Profiling Bartonella infection and its associated risk factors in shelter cats in Malaysia

  • Nurul Najwa Ainaa Alias;Sharina Omar;Nur Indah Ahmad;Malaika Watanabe;Sun Tee Tay;Nor Azlina Aziz;Farina Mustaffa-Kamal
    • Journal of Veterinary Science
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    • 제24권3호
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    • pp.38.1-38.12
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    • 2023
  • Background: Poor disease management and irregular vector control could predispose sheltered animals to disease such as feline Bartonella infection, a vector-borne zoonotic disease primarily caused by Bartonella henselae. Objectives: This study investigated the status of Bartonella infection in cats from eight (n = 8) shelters by molecular and serological approaches, profiling the CD4:CD8 ratio and the risk factors associated with Bartonella infection in shelter cats. Methods: Bartonella deoxyribonucleic acid (DNA) was detected through polymerase chain reaction (PCR) targeting 16S-23S rRNA internal transcribed spacer gene, followed by DNA sequencing. Bartonella IgM and IgG antibody titre, CD4 and CD8 profiles were detected using indirect immunofluorescence assay and flow cytometric analysis, respectively. Results: B. henselae was detected through PCR and sequencing in 1.0% (1/101) oral swab and 2.0% (1/50) cat fleas, while another 3/50 cat fleas carried B. clarridgeiae. Only 18/101 cats were seronegative against B. henselae, whereas 30.7% (31/101) cats were positive for both IgM and IgG, 8% (18/101) cats had IgM, and 33.7% (34/101) cats had IgG antibody only. None of the eight shelters sampled had Bartonella antibody-free cats. Although abnormal CD4:CD8 ratio was observed in 48/83 seropositive cats, flea infestation was the only significant risk factor observed in this study. Conclusions: The present study provides the first comparison on the Bartonella spp. antigen, antibody status and CD4:CD8 ratio among shelter cats. The high B. henselae seropositivity among shelter cats presumably due to significant flea infestation triggers an alarm of whether the infection could go undetectable and its potential transmission to humans.

Molecular Identification of Bartonella melophagi and Wolbachia Supergroup F from Sheep Keds in Xinjiang, China

  • Liu, Yonghong;He, Bo;Li, Fei;Li, Kairui;Zhang, Luyao;Li, Xianqiang;Zhao, Li
    • Parasites, Hosts and Diseases
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    • 제56권4호
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    • pp.365-370
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    • 2018
  • To confirm that Bartonella and Wolbachia were carried by sheep keds (Melophagus ovinus) in southern Xinjiang of China, 17 M. ovinus samples, which were collected in Aksu Prefecture, Xinjiang, were randomly selected. In this study, the Bartonella gltA and Wolbachia 16S rRNA gene were amplified through conventional PCR and the sequence of those amplified products, were analyzed. The results demonstrated that Bartonella was carried by all of the 17 sheep keds and Wolbachia was carried by 15 out of them. Bartonella was identified as B. melophagi. Three strains of Wolbachia were supergroup F and 1 strain has not been confirmed yet. It is the first report about Wolbachia supergroup F was found in sheep keds and provided the molecular evidence that B. melophagi and Wolbachia supergroup F were carried by sheep keds in Aksu Prefecture of southern Xinjiang, China. The 2 pathogens were found in sheep keds around Taklimakan Desert for the first time.

C-ANCA-positive glomerulonephritis associated with subacute infective endocarditis caused by Bartonella infection

  • Kim, Min Jeong;Jang, Ha Nee;Lee, Tae Won;Cho, Hyun Seop;Chang, Se-Ho;Kim, Hyun-Jung
    • Journal of Yeungnam Medical Science
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    • 제34권1호
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    • pp.140-145
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    • 2017
  • Glomerulonephritis (GN) is sometimes associated with infective endocarditis (IE). Bartonella endocarditis is difficult to diagnose because it is rare and cannot be detected by blood culture. This is the first report of cytoplasmic anti-neutrophil cytoplasmic antibody-positive subacute endocarditis-associated GN caused by Bartonella infection in South Korea. A 67-year-old man was hospitalized due to azotemia. He complained of weight loss and anorexia for 6 months. A diagnosis of IE was made based upon echocardiographic detection of vegetations on the mitral and aortic valves and a Bartonella antibody titer of 1:2,048. Renal histology identified focal crescentic GN. Azotemia and proteinuria improved after doxycycline and rifampin treatment combining with steroid therapy.

Bartonella rochalimae, B. grahamii, B. elizabethae, and Wolbachia spp. in Fleas from Wild Rodents near the China-Kazakhstan Border

  • Yin, Xiaoping;Zhao, Shanshan;Yan, Bin;Tian, Yanhe;Ba, Teer;Zhang, Jiangguo;Wang, Yuanzhi
    • Parasites, Hosts and Diseases
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    • 제57권5호
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    • pp.553-559
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    • 2019
  • The Alataw Pass, near the Ebinur Lake Wetland (northwest of China) and Taldykorgan (east of Kazakhstan), is a natural habitat for wild rodents. To date, little has been done on the surveillance of Bartonella spp. and Wolbachia spp. from fleas in the region. Here we molecularly detected Bartonella spp. and Wolbachia spp. in wild rodent fleas during January and October of 2016 along the Alataw Pass-Kazakhstan border. A total of 1,706 fleas belonging to 10 species were collected from 6 rodent species. Among the 10 flea species, 4 were found to be positive for Wolbachia, and 5 flea species were positive for Bartonella. Molecular analysis indicated that i) B. rochalimae was firstly identified in Xenopsylla gerbilli minax and X. conforms conforms, ii) B. grahamii was firstly identified in X. gerbilli minax, and iii) B. elizabethae was firstly detected in Coptopsylla lamellifer ardua, Paradoxopsyllus repandus, and Nosopsyllus laeviceps laeviceps. Additionally, 3 Wolbachia endosymbionts were firstly found in X. gerbilli minax, X. conforms conforms, P. repandus, and N. laeviceps laeviceps. BLASTn analysis indicated 3 Bartonella species showed genotypic variation. Phylogenetic analysis revealed 3 Wolbachia endosymbionts were clustered into the non-Siphonaptera Wolbachia group. These findings extend our knowledge of the geographical distribution and carriers of B. rochalimae, B. grahamii, B. elizabethae, and Wolbachia spp. In the future, there is a need for China-Kazakhstan cooperation to strengthen the surveillance of flea-borne pathogens in wildlife.

Bartonella Henselae 감염 후의 개 말초혈액단핵구에서의 사이토카인 양상 (Cytokine Production in Canine PBMC after Bartonella Henselae Infection)

  • 최은화;이종화;구혜정;박용호;윤화영
    • 한국임상수의학회지
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    • 제27권4호
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    • pp.311-314
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    • 2010
  • Bartonella henselae 는 고양이할큄병의 원인체이다. 고양이가 Bartonella spp.의 주된 보유숙주이기는 하지만, 최근 애완견의 할큄에 의한 고양이할큄병 발생이 보고되었다. 8두의 개에 1 ml의 인산완충식염수에 부유한 $2{\times}10^8CFU$의 B. henselae Houston-1을 0일에 피내주사하고, 동량을 21, 28, 36, 58, 64일째에 추가로 피내주사 하였다. B. henselae 감염을 nested PCR을 통해 확인하였다. B. henselae-PCR 양성군이 음성군에 비해 B. henselae로 말초혈액단 핵구를 자극한 후 얻은 배양상청액에서의 IFN-$\gamma$ 농도가 유의성 있게 높았다. B. henselae자극시, Th1활성을 보이는 개 말초혈액단핵구의 면역양상은 Th2활성을 보인다고 알려진 고양이와는 다른 것으로 보인다.

개에서 추출된 벼룩에서 분자생물학적 방법에 의한 Bartonella henselae DNA의 검출 (Molecular detection of Bartonella henselae DNA from fleas obtained from dogs, Korea)

  • 한태희;정주영;성희경;김상우
    • Clinical and Experimental Pediatrics
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    • 제49권9호
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    • pp.983-986
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    • 2006
  • 목 적 : 소아 임파선염의 흔한 원인균의 하나로 잘 알려진 Bartonella henselae는 주로 고양이 벼룩에 감염된 고양이와의 접촉을 통하여 병을 일으키는 것으로 알려졌지만, 최근에는 개도 보유 숙주임이 확인되었다. 국내의 CSD증례 보고들에서는 고양이보다 개와 접촉한 경우가 더 많은 것으로 보고되었다. 하지만 국내에서는 개나 고양이 또는 매개체인 고양이 벼룩 등에서 B. henselae가 확인된 경우가 아직 없었다. 이에 저자들은 개에게서 얻은 벼룩을 대상으로 B. henselae DNA가 존재하는지 알아보기 위하여 본 연구를 시행하였다. 방 법 : 전체 22마리의 개에서 얻은 총 42마리의 벼룩을 대상으로 연구를 시행하였다. 각각의 벼룩에서 DNA를 추출한 다음 B. henselae의 pap31 부위 유전자를 이용한 시발체를 사용하여 seminested PCR을 시행하였다. 결 과 : B. henselae DNA는 전체 22마리 중 4마리의 개(18.2%)에서 추출되었던 벼룩 42마리 중 7마리(16.7%)에서 확인되었다. PCR 결과를 확인하기 위하여 7개의 PCR 산물에 대한 염기서열 분석을 시행하였다. 염기서열 분석에 의하면 6개는 Huston-1 유전자형이었으며, 한 개는 Marseille 유전자형이었다. 결 론 : 국내 개에서 추출된 벼룩에서 Houston-1유전자형과 Marseille 유전자형을 포함한 B. henselae DNA가 존재하는 것으로 확인할 수 있었다. 국내에서 개가 CSD의 중요한 감염 경로일 가능성을 제시한 점에 의의가 있지만, 충분한 수의 고양이 및 개에서 얻은 혈청과 벼룩을 대상으로 한 추가적인 연구가 필요할 것으로 생각된다.

Seroprevalence of Toxoplasma gondii and Bartonella henselase infection in stray cats of the Daejeon City, Korea

  • Park, Hyung-Jin;Lee, Sang-Eun;Hong, Sung-Hee;Lee, Won-Ja;Seo, Kyoung-Won;Song, Kun-Ho
    • 대한수의학회지
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    • 제54권2호
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    • pp.87-89
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    • 2014
  • In this study, the seroprevalence of Toxoplasma (T.) gondii and Bartonella (B.) henselae infection among stray cats in Daejeon City, Korea was surveyed. A total of seven samples were positive (7/118, 5.93%) for T. gondii including three samples from female cats (3/58, 5.2%) and four samples from male cats (4/60, 6.7%). There was no significant difference between the genders. A total 22 samples (22/118, 18.6%) were positive for B. henselae; nine were from females and 13 were from males. There was no significant difference between genders. Nineteen samples had a titer of 1 : 50, two samples had a titer of 1 : 100, and one sample had a titer of 1 : 200. The present study is the first to use serological tests to analyze B. henselae prevalence among stray cats in Korea.

Prevalence of Anaplasma and Bartonella spp. in Ticks Collected from Korean Water Deer (Hydropotes inermis argyropus)

  • Kang, Jun-Gu;Ko, Sungjin;Kim, Heung-Chul;Chong, Sung-Tae;Klein, Terry A.;Chae, Jeong-Byoung;Jo, Yong-Sun;Choi, Kyoung-Seong;Yu, Do-Hyeon;Park, Bae-Keun;Park, Jinho;Chae, Joon-Seok
    • Parasites, Hosts and Diseases
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    • 제54권1호
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    • pp.87-91
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    • 2016
  • Deer serve as reservoirs of tick-borne pathogens that impact on medical and veterinary health worldwide. In the Republic of Korea, the population of Korean water deer (KWD, Hydropotes inermis argyropus) has greatly increased from 1982 to 2011, in part, as a result of reforestation programs established following the Korean War when much of the land was barren of trees. Eighty seven Haemaphysalis flava, 228 Haemaphysalis longicornis, 8 Ixodes nipponensis, and 40 Ixodes persulcatus (21 larvae, 114 nymphs, and 228 adults) were collected from 27 out of 70 KWD. A total of 89/363 ticks (266 pools, 24.5% minimum infection rate) and 5 (1.4%) fed ticks were positive for Anaplasma phagocytophilum using nested PCR targeting the 16S rRNA and groEL genes, respectively. The 16S rRNA gene fragment sequences of 88/89 (98.9%) of positive samples for A. phagocytophilum corresponded to previously described gene sequences from KWD spleen tissues. The 16S rRNA gene fragment sequences of 20/363 (5.5%) of the ticks were positive for A. bovis and were identical to previously reported sequences. Using the ITS specific nested PCR, 11/363 (3.0%) of the ticks were positive for Bartonella spp. This is the first report of Anaplasma and Bartonella spp. detected in ticks collected from KWD, suggesting that ticks are vectors of Anaplasma and Bartonella spp. between reservoir hosts in natural surroundings.