Literature DB >> 28673019

Gastrointestinal tract involvement in melioidosis.

Prapit Teparrukkul1, Worrarat Kongkasame1, Songla Chitsaeng1, Gumphol Wongsuwan2, Vanaporn Wuthiekanun2, Sharon J Peacock2,3,4, Direk Limmathurotsakul2,5,6.   

Abstract

Background: Little is known about the involvement of the human gut in carriage and disease associated with Burkholderia pseudomallei, the cause of melioidosis.
Methods: A hospital-based study was conducted in Northeast Thailand to culture stools or rectal swabs from patients with melioidosis, stools from controls with non-infectious diseases, and gastric biopsies from patients undergoing routine endoscopic investigation. Results and
Conclusion: B. pseudomallei was isolated from 9/83 (11%) stools and 9/58 (16%) rectal swabs from 141 patients with melioidosis. All stools from 244 control patients and 799 gastric biopsies from 395 patients with no evidence of melioidosis were culture negative for B. pseudomallei. It is not uncommon for melioidosis patients to shed B. pseudomallei in stool. Colonization of the gut of individuals without signs and symptoms of melioidosis may be rare.
© The Author 2017. Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene.

Entities:  

Keywords:  Burkholderia pseudomallei; Gastrointestinal tract; Melioidosis

Mesh:

Year:  2017        PMID: 28673019      PMCID: PMC6092629          DOI: 10.1093/trstmh/trx031

Source DB:  PubMed          Journal:  Trans R Soc Trop Med Hyg        ISSN: 0035-9203            Impact factor:   2.184


Introduction

Melioidosis is an often fatal infectious disease caused by the Gram-negative bacillus Burkholderia pseudomallei, which is commonly found in soil and water in tropical countries.[1] The disease is highly endemic in Southeast Asia and Northern Australia, and is increasingly reported from many other tropical regions, including South Asia, Africa, and Central and South America.[1] A recent modeling study estimated that there are about 165 000 human melioidosis cases per year worldwide, of whom 89 000 (54%) die.[1] Skin inoculation is considered to be the main route of infection, although there is increasing evidence to suggest that ingestion is an important route of human infection.[2,3] In experimental mouse models, B. pseudomallei ingestion produces an effective infection, is associated with colonization of the stomach, results in acute or chronic disease depending on inoculating dose, and may lead to gut carriage and shedding in the stool for weeks after inoculation.[4,5]B. pseudomallei can be isolated from rectal swabs during acute human infection,[6,7] which are routinely collected from patients with suspected melioidosis in Australia.[8] However, it is not known whether humans with melioidosis develop gut colonization and shed B. pseudomallei in the stool. Furthermore, B. pseudomallei is likely to be frequently consumed in water and food in settings where the organism is present in the environment,[2,3] and could colonize the gastrointestinal tract without clinical features or prior to the clinical presentation of melioidosis. A recent study conducted in Malaysia reported the isolation of B. pseudomallei from gastric biopsy samples in 15 of 215 (7%) patients who had gastric biopsy samples tested for Helicobacter pylori.[9] We previously conducted a prospective hospital-based 1:2 matched case-control study to investigate the activities of daily living associated with acquisition of melioidosis in Northeast Thailand.[2] Here, we reported the prevalence of B. pseudomallei in feces and rectal swabs taken from patients with melioidosis and in feces of control patients. In addition, we investigated whether B. pseudomallei colonizes the stomach in humans without clinical signs and symptoms of melioidosis by culturing gastric biopsies taken from patients in Northeast Thailand.

Materials and methods

A total of 83 stools and 58 rectal swabs were obtained from 141 culture-confirmed melioidosis cases presenting to Sunpasitthiprasong Hospital, Ubon Ratchathani, Northeast Thailand, between July 2010 and December 2011.[2] A single sample was taken from each case, with rectal swabs collected in cases who were critically ill. In parallel, 244 stool samples were collected from 244 patients who were admitted to the study hospital with non-infectious conditions during the same period (controls).[2] We also collected 799 gastric biopsy samples from 395 patients who underwent endoscopy and gastric biopsy at the study hospital between June 2014 and December 2015. The majority (n=390, 99%) had two gastric samples, the remaining cases having either one sample (1 patient), three samples (4 patients) or six samples (1 patient). Rectal swabs were inoculated onto Ashdown selective agar and then placed into CVC50 broth (trypticase soy broth with crystal violet at 5 mg/liter plus colistin at 50 mg/liter).[8] For each stool sample, an applicator swab was used to collect a small amount of stool from the container and directly inoculated onto Ashdown agar, and around 5 g of stool was added to CVC50 broth. Gastric biopsy samples were inoculated into CVC50 broth. All broths were incubated at 37°C in air for 48 hours, after which 10 μl was sub-cultured onto Ashdown agar. All agar plates were incubated at 37°C in air and inspected visually for 4 days. Presumptive B. pseudomallei colonies were identified using established methodologies.[8]

Results and Discussion

B. pseudomallei was isolated from 9/83 (11%) stools and 9/58 (16%) rectal swabs from 141 patients with melioidosis, confirming that it is not uncommon for these patients to shed B. pseudomallei in stool. The median age of patients was 53 years (range 18–78 years), 91 (65%) were men, 123 (87%) were considered acute (defined as symptoms present for less than 2 months), and 28 (20%) died within 28 days of the admission date. B. pseudomallei was also isolated from blood (n=67; 48%), respiratory specimens (61; 43%), urine (n=25; 18%), pus (n=47; 33%), throat swab (n=55; 39%), swabs from skin lesioins (n=10; 7%) and synovial fluid (n=7; 5%). This observation highlights an important possible reservoir for the introduction of B. pseudomallei into non-endemic areas, and may explain the mechanism by which this bacterium became globally disseminated between 1650 and 1850.[10] Duration of carriage is unknown, and it is not clear whether B. pseudomallei in stool and the rectal mucosa originated from primary gastrointestinal infection following ingestion or from secondary dissemination following inoculation or inhalation. It is also possible that B. pseudomallei simply passed through the gastrointestinal tract after patients swallowed sputum or drank contaminated water. All stools from 244 controls with non-infectious diseases and 799 gastric biopsies from 395 patients with no clinical evidence of melioidosis were culture negative for B. pseudomallei. This fails to replicate previous findings of positive gastric biopsies in people residing in a region where melioidosis is endemic,[9] and indicates that B. pseudomallei colonization of the gut of individuals without signs and symptoms of melioidosis is rare in Northeast Thailand despite frequent ingestion.[2,3] Further studies are needed to evaluate the presence of B. pseudomallei in drinking water, food and the human stomach in Kuala Lumpur and elsewhere in Malaysia.
  8 in total

1.  The use of selective media for the isolation of Pseudomonas pseudomallei in clinical practice.

Authors:  V Wuthiekanun; D A Dance; Y Wattanagoon; Y Supputtamongkol; W Chaowagul; N J White
Journal:  J Med Microbiol       Date:  1990-10       Impact factor: 2.472

2.  Pathogenicity of high-dose enteral inoculation of Burkholderia pseudomallei to mice.

Authors:  T Eoin West; Nicolle D Myers; Direk Limmathurotsakul; H Denny Liggitt; Narisara Chantratita; Sharon J Peacock; Shawn J Skerrett
Journal:  Am J Trop Med Hyg       Date:  2010-11       Impact factor: 2.345

3.  Selective broths for the isolation of Pseudomonas pseudomallei from clinical samples.

Authors:  A L Walsh; V Wuthiekanun; M D Smith; Y Suputtamongkol; N J White
Journal:  Trans R Soc Trop Med Hyg       Date:  1995 Jan-Feb       Impact factor: 2.184

4.  Global and regional dissemination and evolution of Burkholderia pseudomallei.

Authors:  Claire Chewapreecha; Matthew T G Holden; Minna Vehkala; Niko Välimäki; Zhirong Yang; Simon R Harris; Alison E Mather; Apichai Tuanyok; Birgit De Smet; Simon Le Hello; Chantal Bizet; Mark Mayo; Vanaporn Wuthiekanun; Direk Limmathurotsakul; Rattanaphone Phetsouvanh; Brian G Spratt; Jukka Corander; Paul Keim; Gordon Dougan; David A B Dance; Bart J Currie; Julian Parkhill; Sharon J Peacock
Journal:  Nat Microbiol       Date:  2017-01-23       Impact factor: 17.745

5.  Activities of daily living associated with acquisition of melioidosis in northeast Thailand: a matched case-control study.

Authors:  Direk Limmathurotsakul; Manas Kanoksil; Vanaporn Wuthiekanun; Rungrueng Kitphati; Bianca deStavola; Nicholas P J Day; Sharon J Peacock
Journal:  PLoS Negl Trop Dis       Date:  2013-02-21

6.  Persistent gastric colonization with Burkholderia pseudomallei and dissemination from the gastrointestinal tract following mucosal inoculation of mice.

Authors:  Andrew Goodyear; Helle Bielefeldt-Ohmann; Herbert Schweizer; Steven Dow
Journal:  PLoS One       Date:  2012-05-18       Impact factor: 3.240

7.  Melioidosis caused by Burkholderia pseudomallei in drinking water, Thailand, 2012.

Authors:  Direk Limmathurotsakul; Gumphol Wongsuvan; David Aanensen; Sujittra Ngamwilai; Natnaree Saiprom; Patpong Rongkard; Janjira Thaipadungpanit; Manas Kanoksil; Narisara Chantratita; Nicholas P J Day; Sharon J Peacock
Journal:  Emerg Infect Dis       Date:  2014-02       Impact factor: 6.883

8.  Culturable bacterial microbiota of the stomach of Helicobacter pylori positive and negative gastric disease patients.

Authors:  Yalda Khosravi; Yakhya Dieye; Bee Hoon Poh; Chow Goon Ng; Mun Fai Loke; Khean Lee Goh; Jamuna Vadivelu
Journal:  ScientificWorldJournal       Date:  2014-07-03
  8 in total
  3 in total

1.  Burkholderia pseudomallei as an Enteric Pathogen: Identification of Virulence Factors Mediating Gastrointestinal Infection.

Authors:  Javier I Sanchez-Villamil; Daniel Tapia; Grace I Borlee; Bradley R Borlee; David H Walker; Alfredo G Torres
Journal:  Infect Immun       Date:  2020-12-15       Impact factor: 3.441

2.  Disseminated melioidosis in early pregnancy - an unproven cause of foetal loss.

Authors:  Chee Yik Chang; Nina Lee Jing Lau; Bart J Currie; Yuwana Podin
Journal:  BMC Infect Dis       Date:  2020-03-06       Impact factor: 3.090

3.  Genetic variation associated with infection and the environment in the accidental pathogen Burkholderia pseudomallei.

Authors:  Julian Parkhill; Sharon J Peacock; Claire Chewapreecha; Alison E Mather; Simon R Harris; Martin Hunt; Matthew T G Holden; Chutima Chaichana; Vanaporn Wuthiekanun; Gordon Dougan; Nicholas P J Day; Direk Limmathurotsakul
Journal:  Commun Biol       Date:  2019-11-22
  3 in total

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