Shigella as a Cause of Diarrhea Hospitalization in Children Under Five: Evaluation by Conventional and Molecular Methods

被引:2
作者
Bansal, Pallavi [1 ]
Shah, Dheeraj [1 ]
Meena, Rajesh Kumar [1 ]
Rai, Gargi [2 ]
Das, Shukla [3 ]
Narang, Manish [1 ]
Gupta, Piyush [1 ]
机构
[1] Univ Coll Med Sci, Pediat, Delhi, India
[2] Univ Coll Med Sci, Microbiol, Delhi, India
[3] Univ Coll Med Sci, Microbiol, New Delhi, India
关键词
under-five children; under-five diarrhea; acute infectious diarrhea; shigella; stool culture; polymerase chain reaction; dysentery; diagnosis; children; ENTEROINVASIVE ESCHERICHIA-COLI; PREVALENCE; PCR; INFECTION; CULTURE; GEMS;
D O I
10.7759/cureus.50546
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and objectives: Shigella is an important cause of diarrhea in children under five, often missed by conventional laboratory methods. Blood in stools has always been a syndromic indicator for Shigella diarrhea, but most cases present with watery diarrhea without blood. This study aimed to determine the frequency of Shigella detected by molecular and conventional methods in children under five. Additionally, we aimed to study the clinical profile and outcome of children with Shigella diarrhea managed as per current diarrhea treatment guidelines. Methods: In this hospital-based prospective observational study, stool samples from 150 children (age range: one month to five years) with acute diarrhea (duration < seven days) were subjected to routine microscopic examination, stool culture, and DNA extraction. The extracted DNA from stored stool samples was subjected to polymerase chain reaction (PCR) amplification using a specific primer for the invasion plasmid antigen H gene sequence (ipaH) gene at 424 bp. Results were interpreted in the context of the percentage of isolation of Shigella by molecular (PCR) and conventional methods (stool microscopy and culture) and the follow-up outcome in terms of recurrence of diarrhea or dysentery and growth faltering over three months after discharge. Results: Shigella infection was diagnosed in stool samples by PCR from 13 (8.7%) children, whereas it was isolated by conventional stool culture in only one (0.7%) child. The sensitivity of culture was only 7.7% against PCR for the diagnosis of Shigella infection, whereas blood in stools had a sensitivity of 15.4%. The majority of Shigella PCR-positive cases (11 out of 13) presented with non-bloody diarrhea. None of the evaluated clinical predictors had a significant association with the Shigella infection. No statistically significant difference was found between PCR-positive and PCR-negative children at the end of follow-up (P>0.05). Conclusion: The majority of children with Shigella infection present with watery diarrhea rather than bloody diarrhea, and a history of blood in stools is a poor marker for the diagnosis of shigellosis. The diagnostic performance of stool culture is also very low compared to stool PCR for the diagnosis of Shigella diarrhea.
引用
收藏
页数:10
相关论文
共 22 条
  • [1] Aggarwal P, 2016, J RES HEALTH SCI, V16, P11
  • [2] [Anonymous], 2019, Levels Trends in Child Mortality, Report 2019
  • [3] [Anonymous], 2017, Diarrhoeal disease
  • [4] [Anonymous], 2018, Diarrhoea
  • [5] Ashworth A., 2003, Guidelines for the inpatient treatment of severely malnourished children
  • [6] Clinical and Laboratory Standards Institute, 2011, PERFORMANCE STANDARD
  • [7] Sensitivity and performance characteristics of a direct PCR with stool samples in comparison to conventional techniques for diagnosis of Shigella and enteroinvasive Escherichia coli infection in children with acute diarrhoea in Calcutta, India
    Dutta, S
    Chatterjee, A
    Dutta, P
    Rajendran, K
    Roy, S
    Pramanik, KC
    Bhattacharya, SK
    [J]. JOURNAL OF MEDICAL MICROBIOLOGY, 2001, 50 (08) : 667 - 674
  • [8] Islam MS, 1998, J DIARRHOEAL DIS RES, V16, P248
  • [9] Burden and aetiology of diarrhoeal disease in infants and young children in developing countries (the Global Enteric Multicenter Study, GEMS): a prospective, case-control study
    Kotloff, Karen L.
    Nataro, James P.
    Blackwelder, William C.
    Nasrin, Dilruba
    Farag, Tamer H.
    Panchalingam, Sandra
    Wu, Yukun
    Sow, Samba O.
    Sur, Dipika
    Breiman, Robert F.
    Faruque, Abu S. G.
    Zaidi, Anita K. M.
    Saha, Debasish
    Alonso, Pedro L.
    Tamboura, Boubou
    Sanogo, Doh
    Onwuchekwa, Uma
    Manna, Byomkesh
    Ramamurthy, Thandavarayan
    Kanungo, Suman
    Ochieng, John B.
    Omore, Richard
    Oundo, Joseph O.
    Hossain, Anowar
    Das, Sumon K.
    Ahmed, Shahnawaz
    Qureshi, Shahida
    Quadri, Farheen
    Adegbola, Richard A.
    Antonio, Martin
    Hossain, M. Jahangir
    Akinsola, Adebayo
    Mandomando, Inacio
    Nhampossa, Tacilta
    Acacio, Sozinho
    Biswas, Kousick
    O'Reilly, Ciara E.
    Mintz, Eric D.
    Berkeley, Lynette Y.
    Muhsen, Khitam
    Sommerfelt, Halvor
    Robins-Browne, Roy M.
    Levine, Myron M.
    [J]. LANCET, 2013, 382 (9888) : 209 - 222
  • [10] Use of quantitative molecular diagnostic methods to identify causes of diarrhoea in children: a reanalysis of the GEMS case-control study
    Liu, Jie
    Platts-Mills, James A.
    Juma, Jane
    Kabir, Furqan
    Nkeze, Joseph
    Okoi, Catherine
    Operario, Darwin J.
    Uddin, Jashim
    Ahmed, Shahnawaz
    Alonso, Pedro L.
    Antonio, Martin
    Becker, Stephen M.
    Blackwelder, William C.
    Breiman, Robert F.
    Faruque, Abu S. G.
    Fields, Barry
    Gratz, Jean
    Haque, Rashidul
    Hossain, Anowar
    Hossain, M. Jahangir
    Jarju, Sheikh
    Qamar, Farah
    Iqbal, Najeeha Talat
    Kwambana, Brenda
    Mandomando, Inacio
    McMurry, Timothy L.
    Ochieng, Caroline
    Ochieng, John B.
    Ochieng, Melvin
    Onyango, Clayton
    Panchalingam, Sandra
    Kalam, Adil
    Aziz, Fatima
    Qureshi, Shahida
    Ramamurthy, Thandavarayan
    Roberts, James H.
    Saha, Debasish
    Sow, Samba O.
    Stroup, Suzanne E.
    Sur, Dipika
    Tamboura, Boubou
    Taniuchi, Mami
    Tennant, Sharon M.
    Toema, Deanna
    Wu, Yukun
    Zaidi, Anita
    Nataro, James P.
    Kotloff, Karen L.
    Levine, Myron M.
    Houpt, Eric R.
    [J]. LANCET, 2016, 388 (10051) : 1291 - 1301