Rapid Detection of Salmonella enterica Serovar typhi from Humans

被引:0
作者
Ganeshkumar, A. [1 ]
Shalini, U. [1 ]
Vaishnavi, K. [1 ]
Ismail, Remya [1 ]
Lakshmanaswamy, A. [1 ]
Vasanthi, N. S. [1 ]
Das, Arunava [1 ]
机构
[1] Bannari Amman Inst Technol, Dept Biotechnol, Sathyamangalam 638401, India
关键词
Salmonella enterica Serovar Typhi; PCR; Typhoid; Virulence; POLYMERASE-CHAIN-REACTION; MULTIPLEX PCR; SELECTIVE AMPLIFICATION; IDENTIFICATION; GENES; FEVER; VIAB; SEQUENCE; BLOOD; INVA;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Present study was carried out to investigate Salmonella enterica serovar Typhi associated with Typhoid fever in humans. A total of six blood samples were collected from six patients (4 males and 2 females) and processed for the isolation and identification of the causative agents and their virulence determinants. Microbial investigation revealed the causative agents Salmonella enterica Serovar Typhi in all the six clinical cases. In polymerase chain reaction (PCR) assay, all the six isolates were found positive for the Invasion gene (invA; 244bp fragment), Tyvelose epimerase gene (tyv; 615bp fragment), phage-1 flagellin gene for d-antigen (fliC-d; 750bp fragment) and Vi antigen genes (viaB; 439bp fragment). This study confirms the association of virulent strains of Salmonella enterica Typhi in occurrence of the Typhoid fever in humans. Present study suggested that PCR can be a useful, high throughput diagnostic tool for the rapid detection of Salmonella enterica Serovar Typhi.
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页码:837 / 841
页数:5
相关论文
共 12 条
[1]  
Agarwal S. C., 1962, B WORLD HEALTH ORGAN, V17, P331
[2]   Rapid identification of Salmonella serovars in feces by specific detection of virulence genes, invA and spvC, by an enrichment broth culture-multiplex PCR combination assay [J].
Chiu, CH ;
Ou, JT .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (10) :2619-2622
[3]   DEVELOPMENT OF NESTED PCR BASED ON THE VIAB SEQUENCE TO DETECT SALMONELLA-TYPHI [J].
HASHIMOTO, Y ;
ITHO, Y ;
FUJINAGA, Y ;
KHAN, AQ ;
SULTANA, F ;
MIYAKE, M ;
HIROSE, K ;
YAMAMOTO, H ;
EZAKI, T .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (03) :775-777
[4]   Selective amplification of tyv (rfbE), prt (rfbS), viaB, and fliC genes by multiplex PCR for identification of Salmonella enterica [J].
Hirose, K ;
Itoh, K ;
Nakajima, H ;
Kurazono, T ;
Yamaguchi, M ;
Moriya, K ;
Ezaki, T ;
Kawamura, Y ;
Tamura, K ;
Watanabe, H .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (02) :633-636
[5]   Antibiotic susceptibilities of Salmonella enterica serovar Typhi and S-enterica serovar Paratyphi A isolated from patients in Japan [J].
Hirose, K ;
Tamura, K ;
Sagara, H ;
Watanabe, H .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (03) :956-958
[6]  
Holt J. C., 1994, BERGEYS MANUAL DETER, P764
[7]  
Karami A, 2007, IRAN J PUBLIC HEALTH, V36, P38
[8]   Detection of Salmonella enterica serovar Typhi (S. Typhi) by selective amplification of invA, viaB, fliC-d and prt genes by polymerase chain reaction in mutiplex format [J].
Kumar, S ;
Balakrishna, K ;
Batra, HV .
LETTERS IN APPLIED MICROBIOLOGY, 2006, 42 (02) :149-154
[9]   Typhoid fever - important issues still remain [J].
Pang, T ;
Levine, MM ;
Ivanoff, B ;
Wain, J ;
Finlay, BB .
TRENDS IN MICROBIOLOGY, 1998, 6 (04) :131-133
[10]   DETECTION OF SALMONELLA-TYPHI IN THE BLOOD OF PATIENTS WITH TYPHOID-FEVER BY POLYMERASE CHAIN-REACTION [J].
SONG, JH ;
CHO, H ;
PARK, MY ;
NA, DS ;
MOON, HB ;
PAI, CH .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (06) :1439-1443