Literature DB >> 23343623

Streptococcus suis and porcine reproductive and respiratory syndrome, Vietnam.

Ngo Thi Hoa, Tran Thi Bich Chieu, Sam Do Dung, Ngo Thanh Long, Thai Quoc Hieu, Nguyen Tien Luc, Pham Thanh Nhuong, Vu Thi Lan Huong, Dao Tuyet Trinh, Heiman F L Wertheim, Nguyen Van Kinh, James I Campbell, Jeremy Farrar, Nguyen Van Vinh Chau, Stephen Baker, Juliet E Bryant.   

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Year:  2013        PMID: 23343623      PMCID: PMC3559037          DOI: 10.3201/eid1902.120470

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


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To the Editor: Streptococcus suis, an opportunistic pathogen of swine, is an emerging zoonotic pathogen among humans (). In Vietnam, S. suis is the leading cause of human acute bacterial meningitis (). Infection in humans is associated with direct exposure to infected pigs or infected raw or undercooked pork products (). Of the 35 S. suis serotypes, only a limited number are pathogenic for pigs, and clinical cases in humans have most frequently been attributed to serotype 2 (SS2) (). In Vietnam during September 2006–November 2007, the carrier rate of S. suis among slaughterhouse pigs was 41% (222/542); SS2 was the most frequently identified serotype in 14% (45/317) of S. suis isolations (). Porcine respiratory and reproductive syndrome (PRRS) is a major disease affecting the swine industry globally; the severity of PRRS in pigs can be increased by co-infection with S. suis (). In 2010, PRRS outbreaks in swine were reported in 49 of 63 Vietnamese provinces (Technical Appendix Figure) (). To understand the potential implications of swine PRRS outbreaks for human S. suis disease, we investigated co-infections of S. suis and PRRS virus (PRRSV) in sick pigs in 3 provinces of Vietnam during the PRRS outbreaks in 2010 (Technical Appendix Figure). We sampled 108 farms reporting pigs that had a clinical syndrome consistent with PRRSV infections in the provinces of Thai Binh (May), Tien Giang (July), and Soc Trang (July). Samples were blood from sick febrile pigs and postmortem tissue from freshly culled pigs. To confirm swine PRRS outbreaks, we performed reverse transcription real-time PCR on 1 randomly selected plasma sample from each farm (). A total of 103 (95%) plasma samples from 103 farms tested positive for PRRSV (Chinese genotype). We additionally selected 3 PRRSV-positive farms per province for comprehensive PRRSV screening of all 42 sampled pigs; 100% of samples from the 9 farms were PRRSV positive. After swine outbreaks ended, blood samples from 52 healthy pigs from 10 farms that had no recent history of PRRS were collected from Tien Giang Province (March 2011). None of the 52 plasma samples from the 10 control farms tested positive for PRRSV. We investigated the presence of SS2 in blood and tissue samples from pigs on PRRS- and non-PRRS–affected farms by bacterial culture (Technical Appendix Table). A total of 534 specimens from sick pigs yielded 9 (1.7%) SS2 isolates. One (2%) of 52 specimens from the healthy control pigs yielded a non-SS2 S. suis isolate. S. suis has been proposed to contribute to the spread of antimicrobial resistance genes to other human pathogenic streptococci (). The antimicrobial susceptibility results of 9 SS2 isolates by disk diffusion () revealed a high prevalence (6/9, 66%) of resistance to tetracycline, tobramycin, enrofloxacin, and either marbofloxacin or chloramphenicol. PCR amplification of the 16SrDNA gene () and the cps2J gene () was performed on all blood samples to detect S. suis and SS2, respectively. Ninety-two (18%) of 521 sick pigs from PRRSV outbreak farms were systemically infected with S. suis. In contrast, no healthy pigs from control farms were positive for S. suis by PCR (Technical Appendix Table). The SS2-cps2J–specific PCR was positive for 58 (11%) of 521 samples, and the S. suis-16SrDNA PCR was positive for 55 (11%). Twenty-one of the 16SrDNA-positive samples also were positive for cps2J-PCR, which indicated that 34 (7%) sick pigs were infected with non-SS2 strains. Therefore, SS2 accounted for most (58 [63%] of 92) S. suis–positive detections. The bacterial load of SS2 in blood ranged from 1 × 103 CFU/mL–1 to 8.3 × 106 CFU/mL–1 (median 9.2 × 103 CFU/mL–1). Overall, SS2 was found in 58 (11%) sick pigs and on 33 (32%) PRRS outbreak farms. The higher prevalence (92 [18%]) of systemic infections of S. suis and SS2 with high bacterial load in pigs from PRRS outbreak farms compared with prevalence on nonoutbreak farms (1 [2%] of 52) suggests increased systemic S. suis infections during swine PRRS outbreaks (p = 0.001, Fisher exact test). We investigated the possible association between swine PRRS outbreaks and human S. suis infection. Case reports of confirmed human infections during 2007–2010 at the 2 tertiary referral hospitals in Hanoi and Ho Chi Minh City were reviewed. The number of human S. suis infection cases increased in August 2010 in southern Vietnam and doubled in northern Vietnam during May–August and October–November 2010 (Figure). Swine PRRS outbreaks were reported during June–September and March–December 2010 in southern and northern provinces, respectively () (Technical Appendix Figure). Most patients with S. suis infection during these periods resided in provinces reporting swine PRRS outbreaks. Our data suggest a possible temporal association between swine PRRS outbreaks and human S. suis infections.
Figure

Monthly distribution of human Streptococcus suis infections in 2 referral hospitals, Vietnam, 2007–2010. Humans infected with S. suis during 2007–2009 are presented as mean total cases per month. Dark gray and black bars represent the number of S. suis case-patients at the Hospital for Tropical Diseases in Ho Chi Minh City during 2007–2009 and 2010, respectively. Light gray and white bars represent human S. suis cases at the National Hospital for Tropical Diseases in Hanoi during 2007–2009 and 2010, respectively.

Monthly distribution of human Streptococcus suis infections in 2 referral hospitals, Vietnam, 2007–2010. Humans infected with S. suis during 2007–2009 are presented as mean total cases per month. Dark gray and black bars represent the number of S. suis case-patients at the Hospital for Tropical Diseases in Ho Chi Minh City during 2007–2009 and 2010, respectively. Light gray and white bars represent human S. suis cases at the National Hospital for Tropical Diseases in Hanoi during 2007–2009 and 2010, respectively. We demonstrated increased prevalence of systemic S. suis and SS2 infection in pigs co-infected with PRRSV during the 2010 swine outbreaks in Vietnam. The results indicate an increased risk for potential zoonotic transmission of S. suis to humans during outbreaks of PRRS in swine.

Technical Appendix

Systemic Streptococcus suis infections in sick pigs from farms with confirmed porcine reproductive and respiratory syndrome and temporal distribution of outbreaks of porcine reproductive and respiratory syndrome in swine, 3 provinces, Vietnam, 2010.
  8 in total

1.  Streptococcus suis meningitis in adults in Vietnam.

Authors:  Nguyen Thi Hoang Mai; Ngo Thi Hoa; Tran Vu Thieu Nga; Le Dieu Linh; Tran Thi Hong Chau; Dinh Xuan Sinh; Nguyen Hoan Phu; Ly Van Chuong; To Song Diep; James Campbell; Ho Dang Trung Nghia; Tran Ngoc Minh; Nguyen Van Vinh Chau; Menno D de Jong; Nguyen Tran Chinh; Tran Tinh Hien; Jeremy Farrar; Constance Schultsz
Journal:  Clin Infect Dis       Date:  2008-03-01       Impact factor: 9.079

Review 2.  Streptococcus suis: a new emerging or an old neglected zoonotic pathogen?

Authors:  Marcelo Gottschalk; Jianguo Xu; Cynthia Calzas; Mariela Segura
Journal:  Future Microbiol       Date:  2010-03       Impact factor: 3.165

3.  Secondary infection with Streptococcus suis serotype 7 increases the virulence of highly pathogenic porcine reproductive and respiratory syndrome virus in pigs.

Authors:  Min Xu; Shujie Wang; Linxi Li; Liancheng Lei; Yonggang Liu; Wenda Shi; Jiabin Wu; Liqin Li; Fulong Rong; Mingming Xu; Guangli Sun; Hua Xiang; Xuehui Cai
Journal:  Virol J       Date:  2010-08-09       Impact factor: 4.099

4.  Multiplex PCR assay for detection of Streptococcus suis species and serotypes 2 and 1/2 in tonsils of live and dead pigs.

Authors:  C Marois; S Bougeard; M Gottschalk; M Kobisch
Journal:  J Clin Microbiol       Date:  2004-07       Impact factor: 5.948

5.  Slaughterhouse pigs are a major reservoir of Streptococcus suis serotype 2 capable of causing human infection in southern Vietnam.

Authors:  Thi Hoa Ngo; Thi Bich Chieu Tran; Thi Thu Nga Tran; Van Dung Nguyen; James Campbell; Hong Anh Pham; Huu Tho Huynh; Van Vinh Chau Nguyen; Juliet E Bryant; Tinh Hien Tran; Jeremy Farrar; Constance Schultsz
Journal:  PLoS One       Date:  2011-03-28       Impact factor: 3.240

6.  Risk factors of Streptococcus suis infection in Vietnam. A case-control study.

Authors:  Ho Dang Trung Nghia; Dang Trung Nghia Ho; Le Thi Phuong Tu; Thi Phuong Tu Le; Marcel Wolbers; Cao Quang Thai; Quang Thai Cao; Nguyen Van Minh Hoang; Van Minh Hoang Nguyen; Tran Vu Thieu Nga; Vu Thieu Nga Tran; Le Thi Phuong Thao; Thi Phuong Thao Le; Nguyen Hoan Phu; Hoan Phu Nguyen; Tran Thi Hong Chau; Thi Hong Chau Tran; Dinh Xuan Sinh; Xuan Sinh Dinh; To Song Diep; Song Diep To; Hoang Thi Thanh Hang; Thi Thanh Hang Hoang; Hoang Truong; James Campbell; Nguyen Van Vinh Chau; Van Vinh Chau Nguyen; Nguyen Tran Chinh; Tran Chinh Nguyen; Nguyen Van Dung; Van Dung Nguyen; Ngo Thi Hoa; Thi Hoa Ngo; Brian G Spratt; Tran Tinh Hien; Tinh Hien Tran; Jeremy Farrar; Constance Schultsz
Journal:  PLoS One       Date:  2011-03-08       Impact factor: 3.240

7.  Streptococcus suis, an Emerging Drug-Resistant Animal and Human Pathogen.

Authors:  Claudio Palmieri; Pietro E Varaldo; Bruna Facinelli
Journal:  Front Microbiol       Date:  2011-11-25       Impact factor: 5.640

8.  Rapid detection of a highly virulent Chinese-type isolate of Porcine Reproductive and Respiratory Syndrome Virus by real-time reverse transcriptase PCR.

Authors:  Xing-Long Xiao; Hui Wu; Yi-Gang Yu; Bang-Zhao Cheng; Xiao-Quan Yang; Gu Chen; Dong-Mei Liu; Xiao-Feng Li
Journal:  J Virol Methods       Date:  2008-03-03       Impact factor: 2.014

  8 in total
  11 in total

1.  Investigations of selected pathogens among village pigs in Central Papua, Indonesia.

Authors:  Widi Nugroho; Colin Frank Cargill; I Made Putra; Roy Neville Kirkwood; Darren John Trott; Siti Isrina Oktavia Salasia; Mitra Slipranata; Michael Philipp Reichel
Journal:  Trop Anim Health Prod       Date:  2015-09-17       Impact factor: 1.559

2.  Temporal and spatial association of Streptococcus suis infection in humans and porcine reproductive and respiratory syndrome outbreaks in pigs in northern Vietnam.

Authors:  V T L Huong; L V Thanh; V D Phu; D T Trinh; K Inui; N Tung; N T K Oanh; N V Trung; N T Hoa; J E Bryant; P W Horby; N V Kinh; H F L Wertheim
Journal:  Epidemiol Infect       Date:  2015-05-22       Impact factor: 2.451

Review 3.  Streptococcus suis, an important pig pathogen and emerging zoonotic agent-an update on the worldwide distribution based on serotyping and sequence typing.

Authors:  Guillaume Goyette-Desjardins; Jean-Philippe Auger; Jianguo Xu; Mariela Segura; Marcelo Gottschalk
Journal:  Emerg Microbes Infect       Date:  2014-06-18       Impact factor: 7.163

Review 4.  Streptococcus suis - The "Two Faces" of a Pathobiont in the Porcine Respiratory Tract.

Authors:  Désirée Vötsch; Maren Willenborg; Yenehiwot B Weldearegay; Peter Valentin-Weigand
Journal:  Front Microbiol       Date:  2018-03-15       Impact factor: 5.640

5.  Seasonal patterns and space-time clustering of porcine reproductive and respiratory syndrome (PRRS) cases from 2008 to 2016 in Vietnam.

Authors:  Hu Suk Lee; Thanh Long Pham; Tien Ngoc Nguyen; Mihye Lee; Barbara Wieland
Journal:  Transbound Emerg Dis       Date:  2019-01-30       Impact factor: 5.005

6.  Binding of Plasminogen to Streptococcus suis Protein Endopeptidase O Facilitates Evasion of Innate Immunity in Streptococcus suis.

Authors:  Yang Zhou; Kang Yan; Chengfeng Sun; Feng Liu; Wei Peng; Huanchun Chen; Fangyan Yuan; Weicheng Bei; Jinquan Li
Journal:  Front Microbiol       Date:  2021-07-08       Impact factor: 5.640

7.  Interaction of fibrinogen and muramidase-released protein promotes the development of Streptococcus suis meningitis.

Authors:  Junping Wang; Decong Kong; Shengwei Zhang; Hua Jiang; Yuling Zheng; Yating Zang; Huaijie Hao; Yongqiang Jiang
Journal:  Front Microbiol       Date:  2015-09-24       Impact factor: 5.640

Review 8.  A review of foodborne bacterial and parasitic zoonoses in Vietnam.

Authors:  Juan J Carrique-Mas; J E Bryant
Journal:  Ecohealth       Date:  2013-10-26       Impact factor: 3.184

Review 9.  Prospects for emerging infections in East and southeast Asia 10 years after severe acute respiratory syndrome.

Authors:  Peter W Horby; Dirk Pfeiffer; Hitoshi Oshitani
Journal:  Emerg Infect Dis       Date:  2013-06       Impact factor: 6.883

10.  EGFR transactivation contributes to neuroinflammation in Streptococcus suis meningitis.

Authors:  Xiao-Pei Yang; Ji-Yang Fu; Rui-Cheng Yang; Wen-Tong Liu; Tao Zhang; Bo Yang; Ling Miao; Bei-Bei Dou; Chen Tan; Huan-Chun Chen; Xiang-Ru Wang
Journal:  J Neuroinflammation       Date:  2016-10-19       Impact factor: 8.322

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