Three cases of cat scratch disease diagnosed by indirect immunofluorescence antibody assay and/or polymerase chain reaction of 16S rRNA gene of Bartonella henselae

被引:12
|
作者
Maruyama, S
Kabeya, H
Nogami, S
Sakai, H
Suzuki, J
Suzuki, H
Sugita, H
Katsube, Y
机构
[1] Nihon Univ, Coll Bioresource Sci, Dept Vet Med, Lab Vet Publ Hlth, Kanagawa 2528510, Japan
[2] Nihon Univ, Coll Bioresource Sci, Dept Vet Med, Lab Med Zool, Kanagawa 2528510, Japan
[3] Fukushima Prefectural Aizu Gen Hosp, Dept Pediat, Fukushima 9658555, Japan
[4] Fukushima Med Univ, Sch Med, Dept Pediat, Fukushima 9601295, Japan
[5] Sugita Surg Clin, Kanagawa 2520813, Japan
来源
JOURNAL OF VETERINARY MEDICAL SCIENCE | 2000年 / 62卷 / 12期
关键词
Bartonella henselae; cat scratch disease; PCR;
D O I
10.1292/jvms.62.1321
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Three suspected cases of cat scratch disease were diagnosed by indirect immunofluorescence antibody assay and/or polymerase chain reaction. Patient 1 was a 10-year-old female who presented swelling of the right axial lymph nodes with pain and fever. She kept a kitten, and many scratches were observed on her both legs and dorsum manus. Antibody titers against Bartonella (B.) henselae were 1:32 for IgM 3 weeks after the onset of the symptoms and 1:61 for IgG 8 weeks after the onset. The DNA for 16S rRNA type I of B. henselae was detected from the blood sample obtained 3 weeks after the onset of symptoms by polymerase chain reaction for the first time in Japan. Patient 2 was a 22-year-old female veterinary student with a cat scratch at the bottom of her neck by a male kitten. She developed a papule at the scratch, slight fever, and neck pain. Although both Bartonella-specific IgG and IgM antibodies were negative before the scratch, the IgG antibody titer rose to 1:512 14 weeks after the onset. B. henselae was isolated from the kitten and its DNA found to be for 16S rRNA type I by PCR. Patient 3 was a 23-year-old female veterinary student with a cat scratch on her left forearm. A small reddish papule developed on the scratch, and she experienced swelling of the left axial lymph node and pain. Both the IgG and IgM antibodies against B. henselae were negative before the cat scratch, and the IgG titer rose significantly to 1:128 and 1.1,024 in 2 and 5 weeks, respectively, after the onset of the symptoms.
引用
收藏
页码:1321 / 1324
页数:4
相关论文
共 50 条
  • [31] Rapid diagnosis of bacterial meningitis in children with fluorescence quantitative polymerase chain reaction amplification in the bacterial 16S rRNA gene
    Duan, Qun-Jun
    Shang, Shi-Qiang
    Wu, Yi-Dong
    EUROPEAN JOURNAL OF PEDIATRICS, 2009, 168 (02) : 211 - 216
  • [32] Rapid diagnosis of bacterial meningitis in children with fluorescence quantitative polymerase chain reaction amplification in the bacterial 16S rRNA gene
    Qun-Jun Duan
    Shi-Qiang Shang
    Yi-Dong Wu
    European Journal of Pediatrics, 2009, 168 : 211 - 216
  • [33] Broad-Range 16S rRNA Gene Polymerase Chain Reaction for Diagnosis of Culture-Negative Bacterial Infections
    Rampini, Silvana K.
    Bloemberg, Guido V.
    Keller, Peter M.
    Buechler, Andrea C.
    Dollenmaier, Guenter
    Speck, Roberto F.
    Boettger, Erik C.
    CLINICAL INFECTIOUS DISEASES, 2011, 53 (12) : 1245 - 1251
  • [34] Evaluation of an internally controlled real-time polymerase chain reaction assay targeting the groEL gene for the detection of Bartonella spp. DNA in patients with suspected cat-scratch disease
    Diederen, B. M. W.
    Vermeulen, M. J.
    Verbakel, H.
    van der Zee, A.
    Bergmans, A.
    Peeters, M. F.
    EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2007, 26 (09) : 629 - 633
  • [35] Evaluation of an internally controlled real-time polymerase chain reaction assay targeting the groEL gene for the detection of Bartonella spp. DNA in patients with suspected cat-scratch disease
    B. M. W. Diederen
    M. J. Vermeulen
    H. Verbakel
    A. van der Zee
    A. Bergmans
    M. F. Peeters
    European Journal of Clinical Microbiology & Infectious Diseases, 2007, 26 : 629 - 633
  • [36] Increased Pathogen Identification in Vascular Graft Infections by the Combined Use of Tissue Cultures and 16S rRNA Gene Polymerase Chain Reaction
    Ajdler-Schaeffler, Evelyne
    Scherrer, Alexandra U.
    Keller, Peter M.
    Anagnostopoulos, Alexia
    Hofmann, Michael
    Rancic, Zoran
    Zinkernagel, Annelies S.
    Bloemberg, Guido, V
    Hasse, Barbara K.
    FRONTIERS IN MEDICINE, 2018, 5
  • [37] A reverse transcriptase-polymerase chain reaction assay of Borrelia burgdorferi 16S rRNA for highly sensitive quantification of pathogen load in a vector
    Ornstein, K
    Barbour, AG
    VECTOR-BORNE AND ZOONOTIC DISEASES, 2006, 6 (01) : 103 - 112
  • [38] Detection of the Legionnaires' Disease Agent in Patients With Respiratory Symptoms by Culture, Detection of Urinary Antigen and Polymerase Chain Reaction of the 16S rRNA Gene in Ahvaz, Iran
    Moosavian, Mojtaba
    Sima, Mahtab Khoshkholgh
    Shoushtari, Maryam Haddadzadeh
    Alavi, Seyed Mohammad
    Naserabad, Mohammad Amin Fazeli
    Montazeri, Effat Abbasi
    JUNDISHAPUR JOURNAL OF MICROBIOLOGY, 2017, 10 (04)
  • [39] Detection of bacteremia in emergency department patients at risk for infective endocarditis using universal 16S rRNA primers in a decontaminated polymerase chain reaction assay
    Rothman, RE
    Majmudar, MD
    Kelen, GD
    Madico, G
    Gaydos, CA
    Walker, T
    Quinn, TC
    JOURNAL OF INFECTIOUS DISEASES, 2002, 186 (11): : 1677 - 1681
  • [40] Detection of bacteremia in neonates with systemic inflammatory response syndrome (SIRS) using 16S rRNA gene amplification by polymerase chain reaction (PCR)
    Rossini, M
    Innocenti, I
    D'Ambrosio, E
    Rossini, N
    Papoff, P
    Auriti, C
    Seganti, G
    Orzalesi, M
    Bucci, G
    PEDIATRIC RESEARCH, 1999, 45 (04) : 273A - 273A