Skip to main content

Burden of laboratory-confirmed shigellosis infections in Guatemala 2007-2012: results from a population-based surveillance system



We describe the epidemiology and antimicrobial susceptibility patterns of culture-confirmed Shigella infections in facility-based surveillance sites in Guatemala. Current studies using quantitative molecular diagnostics suggest Shigella may contribute most to the global diarrheal disease burden. Since identification of Shigella requires culturing techniques using stool specimens and few laboratories in Guatemala routinely culture for this pathogen, little is known about the true burden of Shigella in Guatemala or, importantly, the antimicrobial resistance patterns.


Clinical, epidemiological, and laboratory data were collected on 5399 patients with acute diarrhea (≥3 loose stools in 24 h) from June 2007–August 2012. Multidrug resistance (MDR) was defined as resistance to ampicillin and trimethoprim/sulfamethoxazole.


Five percent (261) of stool specimens yielded Shigella spp. The annual incidence of laboratory-confirmed infections ranged from 5.0 to 24.1 per 100,000 persons in Santa Rosa and 0.3 to 6.2 per 100,000 in Quetzaltenango; 58% of cases occurred in children < 5 years of age. Thirty patients were hospitalized; one patient died. Oral rehydration or intravenous solution was used to treat 72% of hospitalized and 15% of ambulatory cases. Fifty-nine percent of cases were S. flexneri and 51% of cases were MDR.


Shigella is an important cause of bacterial diarrhea in children and prevalence of MDR highlights the importance of appropriate treatment regimens. This study demonstrates that strengthening laboratory capacity in Guatemala can help determine causes which can lead to prevention of diarrheal diseases, particularly in children. Such capacity building is also critical for rapid detection and control of public health threats at their source and therefore for global health security.


Globally, diarrheal infections resulted in an estimated 688 million illnesses in 2015, and 499,000 deaths in children under 5 years of age [1, 2]. Despite dramatic reductions in childhood mortality in the past decade, diarrhea remains a major cause of preventable childhood deaths worldwide [3, 4], and still leads to higher risk of growth faltering and other health effects in those children that survive [5]. Shigella is one of four primary pathogens that substantially contributes to moderate and severe diarrhea globally [6, 7]. Indeed, quantitative molecular diagnostics suggest Shigella may contribute most to the global diarrheal disease burden [8]. While case fatalities have significantly decreased over time, morbidity from shigelloses remains an important problem and warrants investments in surveillance to better understand antibiotic resistance, treatment options, and preventive measures, including vaccine development [9].

Characterized by fever, abdominal pain, tenesmus, and loose stools, Shigella is usually acquired by ingestion of contaminated food or water [10]. In addition to the high mortality [11], sequelae of shigellosis can include encephalopathy, hemolytic uremic syndrome, bacteremia, dysentery, rectal prolapse [12], hypoglycemia, hyponatremia [13], and reactive arthritis [10, 14]. Children may experience high fever with convulsions [12]. Though previous studies have demonstrated the effectiveness of certain antimicrobials as treatment, resistance to commonly used antimicrobials such as trimethoprim/sulfamethoxazole, ampicillin, third generation cephalosporins, quinolones and macrolides [15,16,17,18] complicates treatment for those with severe disease [12, 19]. Additionally, fluoroquinolones, which may be effective, are not recommended for children and pregnant women [19]. Shigellosis may also be confused with acute amoebic dysentery, leading to inappropriate treatment with metronidazole or tinidazole [19]. Lastly, the diversity of Shigella serotypes has historically rendered vaccine development difficult [15].

In Guatemala, diarrhea remains the second most common cause of morbidity and mortality in children < 5 years of age [20], and small, community-based studies implicate Shigella as a common cause of diarrhea [21, 22]. However, since identification of Shigella requires culturing techniques using stool specimens [10] and few laboratories in Guatemala routinely culture for this pathogen, little is known about the true burden of Shigella in Guatemala or the antimicrobial resistance patterns. Limited laboratory capacity in Guatemala also results in delays in detecting, or an inability to recognize, outbreaks of Shigella infections, in addition to illnesses caused by other pathogens. Thus, controlling such outbreaks at their source is difficult, thereby threatening global health security. In this report, we characterize cases of laboratory-confirmed shigellosis enrolled in a healthcare facility-based surveillance system in Guatemala from 2007 through 2012 in order to inform prevention and treatment guidelines in Guatemala and the Central America region.


Study sites

In July 2007, the U.S. Centers for Disease Control and Prevention International Emerging Infections Program (CDC IEIP), the Guatemalan Ministry of Public Health and Welfare (MSPAS), and the Center for Health Studies of the Universidad del Valle de Guatemala (UVG) initiated an active facility-based surveillance system for diarrheal, respiratory, acute neurologic infections, and non-differentiated febrile illnesses in the department of Santa Rosa [23]. The surveillance system, Vigilancia Integrada Comunitaria (VICo), captured patients in both ambulatory and hospital settings. An additional site was added in February 2009 in the department of Quetzaltenango. Santa Rosa is located in the southern part of the country with a population of 346,590 in 2002, and Quetzaltenango is in the western highlands with a population of 789,358 [24]. Compared with Quetzaltenango, Santa Rosa has a lower elevation (1219 m vs. 2438 m at the hospitals), higher average temperature, higher average rainfall, and a smaller proportion of the population is Amerindian indigenous (15% versus 62%).

In Santa Rosa, the facility-based surveillance system included the Cuilapa Regional Hospital, one health center staffed by a physician and nurses, and five health posts, each staffed by a nurse. The Cuilapa Regional Hospital is a 176-bed referral hospital that provides care for residents of Santa Rosa and the neighboring departments of Jutiapa and Jalapa. In Quetzaltenango, the surveillance system included the Western Regional Hospital, three health centers, and one health post. The Western Regional Hospital is a 425-bed referral hospital that provides care for Quetzaltenango and the neighboring departments of Huehuetenango, San Marcos, Totonicapan, among other departments in Guatemala and Mexico. Health centers and health posts in both departments were considered ambulatory care. Private clinics, small private hospitals, pharmacies, traditional healers, and one public hospital in coastal Quetzaltenango make up the other sources of healthcare in the two departments.

Case detection and data collection

A case of diarrhea was defined as ≥3 loose or liquid stools in a 24-h period with onset of illness within seven days before presenting to any participating facility. Inclusion criteria included residence in one of the municipalities included in the surveillance system. Cases with other diarrheal episodes within one week prior to the start of the current episode were excluded to avoid capturing illnesses due to chronic diarrhea. Surveillance nurses screened patients by reviewing logbook entries and assessed chief complaints for diarrhea-related visits and admissions. Detailed clinical, epidemiologic, demographic, and socioeconomic data were obtained from structured patient interviews and medical chart abstractions [25].

Laboratory methods

All consenting patients were requested to provide bulk stool specimen. Rectal swabs were performed on children < 5 years of age who were unable to provide a specimen. Stool samples from the ambulatory facilities were then stored in Cary-Blair transport media at 4 °C and transported at 4 °C within 48 h to one of the two regional hospitals for initial processing and testing. Samples were subsequently streaked by direct plating onto selective agars, MacConkey and Xylose-lysine-desoxycholate (XLD) [26]. After incubation, colonies suggestive of Shigella (lactose negative colonies) were tested biochemically with Triple Sugar Iron (TSI), lysine iron (LIA), Sulfide-indole-motility (SIM) medium, Motility-indole-ornithine (MIO) medium, citrate, and urea. If the result of the biochemical test then suggested the colony examined was Shigella positive, the isolate was then tested with antisera for the different Shigella species.

At the hospital laboratories, antimicrobial susceptibility testing was performed on Shigella isolates using the disk diffusion method with the following antibiotics: ampicillin, amoxicillin, ceftriaxone, gentamicin, kanamycin, streptomycin, ciprofloxacin, nalidixic acid, chloramphenicol, trimethoprim/sulfamethoxazole and tetracycline, using Clinical Laboratory Standards Institute (CLSI) breakpoints [27]. Multidrug-resistance (MDR) was defined as resistance to at least ampicillin and trimethoprim/sulfamethoxazole, an important MDR phenotype for Shigella [11]. Samples were later sent to serotyping. The isolates were serotyped by slide agglutination tests using specific antisera at UVG laboratories (Denka Seiken Co, Ltd.).

Data analysis

We examined the number of laboratory-confirmed Shigella cases identified in the surveillance system from July 2007 to August 2012 in Santa Rosa and from February 2009 to August 2012 in Quetzaltenango. We described the temperature and rainfall in each department during this period. Population-based annual crude incidence rates for Shigella were calculated by using the detected number of cases and catchment area population of the surveillance health facilities. Incidence rates were calculated from 2008 to 2012 for Santa Rosa, due to surveillance starting mid-year in 2007 in Santa Rosa. Incidence rates were calculated from 2009 to 2012 for Quetzaltenango. Population by municipality and age were obtained from the Guatemala National Institute of Statistics [24]. Population estimates for 2011 and 2012 were extrapolated from 2010 population data. As the catchment area for each surveillance site did not include all municipalities within a department, we used population estimates for only municipalities in our catchment area for the incidence denominator. The catchment area for the Cuilapa Regional Hospital included 11 municipalities in Santa Rosa Department, excluding the three coastal municipalities. The catchment area in Quetzaltenango included 10 municipalities, including Quetzaltenango city. Crude incidence rates were calculated across all ages and for children < 5 years of age. Poisson-based 95% confidence intervals were calculated for the annual rates of Shigella. The last year of surveillance was adjusted to account for eight months of observation. We also calculated adjusted incidence rates to account for differences in healthcare seeking behavior between hospitals and ambulatory care; we calculated different estimates of incidence based on cases that were detected at a hospital versus health center or post.

We described the demographic characteristics, symptoms, co-infections, and treatment of Shigella cases stratified by ambulatory and hospital settings for both Santa Rosa and Quetzaltenango. Chi-square or Fisher’s exact test were used to determine differences in characteristics between ambulatory and hospital settings. T-tests or analysis of variance (ANOVA) was used to test differences in means for continuous variables. We examined the number of days hospitalized patients spent in the intensive care unit, total length of hospital stay, and case fatality.

We characterized Shigella cases by serotype. Within each serotype, we counted the number of cases that were hospitalized and that reported bloody stool. Chi-square tests of proportions were used to determine differences across serotypes. Without comparative data from the underlying population at risk, we only assessed the proportion of Shigella cases according to potential risk factors, including education, safe water use, breastfeeding, refrigerator use, and large household size. Lastly, we reported the percent resistant to the antimicrobial classes and those with MDR. We also evaluated differences in antibiotic resistance between the surveillance sites and across time.


From 2007 to 2012, stool samples from 5399 patients yielded 261 cases of Shigellosis, of which 91% were reported from the Santa Rosa department. Sixty-two percent of Shigella infections occurred from May to October (Fig. 1). Greater than half of all Shigella cases (58%) occurred in children < 5 years of age with a median age of 3 years (range: 1 month to 91 years); 149 (57%) were female (Table 1). Thirty (12%) patients with Shigellosis were hospitalized; 25 (83%) of the hospitalized patients were <  5 years of age and 4 (13%) were aged ≥60 years. Among ambulatory cases, 126 (55%) were <  5 years of age and 7 (3%) were aged ≥60 years. Hospitalized patients were significantly younger than ambulatory patients (p < 0.001). A greater proportion of hospitalized patients reported vomiting (p < 0.0001) and had convulsions and lethargy (p < 0.05). Parasites were observed in stool samples of 30% of patients with Shigella. Eighteen (72%) hospitalized cases were treated with oral rehydration salts or intravenous solution. Among hospitalized cases, the median hospital stay was 4 days. Six cases (20%) were admitted to the intensive care unit and one case died. The case that died was a one-year old child in Santa Rosa with S. flexneri; no co-morbidities or treatment regimen was reported for this case.

Fig. 1
figure 1

Seasonality of Shigella cases relative to average temperatures and monthly rainfall, 2007–2012 in Santa Rosa and Quetzaltenango Departments, Guatemala. *Peak season of cases and rainfall is from May to October. †This peak is largely from an outbreak at a single birthday party. ‡Surveillance started in February 2009 in Quetzaltenango.

Table 1 Descriptive statistics of Shigella cases stratified by healthcare facility in Santa Rosa and Quetzaltenango Departments, Guatemala 2007–2012

The education level of the parents of children < 5 years of age was low with 94% having no or only basic education (up to 9th grade). Overall, 67% of families reported monthly income of under $130/month. Only 37% of all cases reported having a refrigerator at home and over 60% of cases came from households of more than five people. In both the hospital and ambulatory setting, 78% of cases < 2 years were breastfed. A majority of cases reported using the public and municipal water sources, and also home storage of water.

The crude annual incidence rate of Shigella cases ranged from 13.8 to 24.1 per 100,000 from 2008 to 2012 in the Santa Rosa Department for all ages, and 52.3 to 91.9 per 100,000 persons for children < 5 years for both hospital and ambulatory cases (Table 2). Ambulatory care incidence estimates are higher for both children < 5 years and all ages than hospital care in Santa Rosa; the annual incidence rate of Shigella cases ranged from 348.2 to 594.5 cases for children < 5 years and 108.1 to 174.0 cases for all ages (Additional file 1). In Quetzaltenango, the crude annual incidence rates ranged from 0.3 to 6.2 per 100,000 persons from 2009 to 2012 for all ages, and 0 to 31.1 per 100,000 persons for children < 5 years (Table 2). The adjusted annual incidence in ambulatory care was as high as 92.5 cases for children < 5 years and 22.1 cases for all ages in Quetzaltenango (Additional file 1). In Quetzaltenango, there are more cases in 2012 than in previous years.

Table 2 Crude incidence rates of Shigella by site and age group in Santa Rosa and Quetzaltenango Departments, Guatemala, 2008–2012

The most frequently isolated serotypes were Shigella flexneri (59%) and Shigella sonnei (36%). Among 30 hospitalized patients, 25 (83%) were infected with S. flexneri compared to 4 with S. sonnei (13%) and one with S. boydii. Among those cases with S. flexneri, 36% reported having bloody stool; 20% of S. sonnei cases reported having bloody stool.

Antimicrobial susceptibility testing was performed on 254 of the 261 laboratory-confirmed Shigella cases (Table 3). Resistance to ampicillin was detected in 61% of the isolates and resistance to trimethoprim/sulfamethoxazole in 83%; 120 (51%) cases were resistant to both (MDR). Sixty-three percent of cases in Santa Rosa were resistant to ampicillin as compared to 35% in Quetzaltenango, and 86% of cases in Santa Rosa were resistant to trimethoprim/sulfamethoxazole as compared to 52% in Quetzaltenango (Additional file 2). Fifty-five percent of cases were resistant to both ampicillin and trimethoprim/sulfamethoxazole (SMX/TMP) in Santa Rosa versus 13% in Quetzaltenango. Both resistance to ampicillin and MDR increased over the surveillance time period from 2007 to 2012 (Additional file 3). All isolates were resistant to at least one antimicrobial class tested; none were resistant to ciprofloxacin. Eighty percent of all isolates were resistant to at least three antimicrobial classes. There were no remarkable differences in antimicrobial resistance between hospital and ambulatory cases.

Table 3 Antimicrobial resistance by Shigella serotypes in Guatemala, 2007–2012


We characterized laboratory-confirmed Shigella cases captured by a facility-based surveillance system in Santa Rosa and Quetzaltenango, Guatemala. There are five characteristics among our findings that are pertinent to prevention and treatment of Shigellosis in Guatemala: age of infection, seasonality and region, species of Shigella, antimicrobial resistance, and antibiotic and rehydration treatments.

Most patients with Shigella presented to ambulatory care centers for treatment, and consistent with the known epidemiology of Shigella, we found the greatest burden of disease among young children [15]. Compared to the United States, the annual incidence of Shigella was higher for all ages and children < 5 years of age in Santa Rosa but not in Quetzaltenango [28, 29]. Incidence rates from active surveillance in Santa Rosa were 23.4–91.1 cases per 100,000 in children aged < 5 years compared with 16.9 cases per 100,000 reported in the U.S. [29]. Though higher than those of the U.S., rates in Guatemala were lower than those of Africa and Asia [30]. Still, the adjusted incidence estimates in this study revealed children < 5 years as an important age group, particularly in the ambulatory setting. Though children under 5 years comprised 58% of all cases and 80% of those hospitalized, 13% of those hospitalized were ≥ 60 years of age. Prevention of this food and waterborne infection must be targeted to protect the most vulnerable populations, that is, children and the elderly. Prevention measures like breastfeeding should be encouraged for children < 2 years, as recommended by the World Health Organization (WHO) [31].

There were large differences in the crude annual incidence rates of Shigella and antibiotic resistance patterns by department. Since higher temperatures allow bacteria to reproduce at a higher rate, the warm climate of Santa Rosa department may have contributed to the higher rate of food and waterborne disease [32, 33]. Moreover, most cases occurred during the warm, rainy season from May–October, indicating that special care must be taken in high-risk areas during this time to prevent transmission. Studies from China and Israel and the United States, as reported by the National Antimicrobial Resistance Monitoring System for Enteric Bacteria (NARMS) or other CDC surveillance, also found a seasonally higher rate of Shigella during periods of higher temperatures [33,34,35]. Such prevention tactics may include safe water and hygiene practices at the individual and household level, which for decades has been proven as an effective preventive measure for diarrheal disease [36, 37]. Special care in human feces disposal and prevention of transmission by hands, fomites and insects is essential. Low levels of education, however, and crowding at the household level may be obstacles to implementing prevention measures as these factors have been shown to increase diarrheal disease risk [38, 39]. Of note, the rates in Santa Rosa increased in 2012 as a result of an outbreak at a children’s birthday party involving 17 persons.

Similar to the rest of the world, the observed percentage of S. flexneri was approximately 60%; S. flexneri predominates in low-income countries [15]. However, S. sonnei (35%) is twice as high in our study as compared to global estimates for low-income countries (15%) [15]. Interestingly, in industrialized countries, S. sonnei is closer to 77% of Shigella infections while S. flexneri is 16% of Shigella infections, suggesting that Guatemala is in a developmental transition [15]. Fortunately, the epidemic of Shigella dysenteriae that affected much of Central America in the 1960s [40] and Guatemala in the 1990’s has abated [41]. Only one isolate of S. dysenteriae was detected in our surveillance.

Among isolates tested in our surveillance system in Guatemala, antimicrobial resistance to commonly used antimicrobials was high, as was the proportion that was resistant to at least three antimicrobial classes. The proportion of isolates that were resistant to at least ampicillin and SMX/TMP (51%) in Guatemala is markedly higher than in the United States (16%), as reported by NARMS in 2012 [11]. Because a majority of isolates of Shigella were resistant to accessible and inexpensive oral treatments like trimethoprim/sulfamethoxazole (83% resistant) and ampicillin (61% resistant), antimicrobial treatment options are limited in Guatemala. Though quinolones are effective and no resistance to ciprofloxacin was found in our study, quinolones have side effects such as joint and tendon injury, and are not generally used in children. In Bangladesh, there have been marked increases in resistance to ciprofloxacin [42]. This trend has also been noted in China, Canada, and the United States [11, 30, 43, 44]. Of note, resistance of Shigella to commonly used antibiotics in Guatemala, while greater than reported in the U.S. [11], is similar to that reported in other American countries including Mexico and Chile [43, 45].

While azithromycin is a first-line antibiotic treatment in the U.S. [16] and could be considered for treatment in Guatemala, it is important to note that resistance of Shigella to ampicillin and amoxicillin, both penem beta-lactam antibiotics, increased over the course of the surveillance period from 2007 to 2012. MDR resistance, resistance to both ampicillin and SMX/TMP, also increased over the surveillance period, limiting their therapeutic utility, especially in Santa Rosa. Continued surveillance of these dynamics is critical for understanding both prevention and treatment.

In addition to treatment with effective antibiotics, rehydration with oral rehydration solutions is a critical form of treatment [46]. Our findings, however, suggest that a substantial number of patients with Shigellosis were not treated with oral rehydration solution. Oral rehydration is an inexpensive and effective method that should be emphasized through education and policy.

Our findings are subject to limitations. These data apply only to the Departments of Santa Rosa and Quetzaltenango and therefore are not generalizable to all of Guatemala. However, they are the most comprehensive description of Shigella in Guatemala and Central America in the healthcare setting. As treatments are self-reported, information bias is a limitation of the reported use of rehydration therapies. Such bias, however, would indicate there are systematic differences among all cases and would neither over- or under-estimate treatment use. Furthermore, Shigella testing was done by standard cultures and not quantitative real-time polymerase chain reaction (PCR) due to resource constraints, suggesting the burden of disease estimates in this analysis are likely an underestimate of the true value [9]. By re-analyzing samples or subscribing to a quantitative real-time PCR detection method, the detection capability of Shigella would improve significantly and additionally aid in the current development of a vaccine against Shigella spp. The high detection rate of these species in samples should be prioritized as vaccination of children in early life could be greatly beneficial [3, 47].

Additionally, although healthcare utilization surveys in the same region in Guatemala demonstrated that a majority of patients sought care for their illness outside the home, less than a quarter of all cases and only 51% of children sought care at a government health facility [23, 48]. This indicates again that our estimates of Shigella cases are likely an underestimate of the true burden of disease in the population. Also, though the surveillance platform included the main hospital in each department, the ambulatory facilities were limited in Santa Rosa to five clinics in one municipality (Nueva Santa Rosa) and in Quetzaltenango to three municipalities. Not all patients sought care in those facilities. Patients seen in the emergency department but not admitted to the hospital were not captured by the surveillance system. As a result, our crude and adjusted disease rates may further be an underestimate of the true rates of Shigella disease.


This study demonstrates that Shigella is an important cause of enteric infections in Santa Rosa and Quetzaltenango, Guatemala, especially in children < 5 years of age. Shigella flexneri and S. sonnei were the most common species while S. dysenteriae was rare. Antibiotic resistance to commonly used antibiotics was prevalent and complicates treatment. This study demonstrates the importance of strengthening laboratory capacity in Guatemala for determining causes that can lead to prevention of diarrheal diseases, particularly in children. Such capacity building is also critical for rapid detection and control of public health threats at their source, and therefore for global health security. Future steps should include strengthening laboratory surveillance for antibiotic resistance patterns in the region, implementation of common preventive measures, and optimization of oral rehydration therapy.


(MIO) medium:


(SIM) medium:



Analysis of variance


U.S. Centers for Disease Control and Prevention International Emerging Infections Program


U.S. Centers for Disease Control and Prevention


Clinical Laboratory Standards Institute


Lysine iron


Multidrug resistance


Guatemalan Ministry of Public Health and Welfare


National Antimicrobial Resistance Monitoring System for Enteric Bacteria


Polymerase chain reaction




Triple Sugar Iron


Center for Health Studies of the Universidad del Valle de Guatemala


Vigilancia Integrada Comunitaria


World Health Organization


MacConkey and Xylose-lysine-desoxycholate


  1. Walker CL, Rudan I, Liu L, Nair H, Theodoratou E, Bhutta ZA, et al. Global burden of childhood pneumonia and diarrhoea. Lancet. 2013;381:1405–16.

    Article  Google Scholar 

  2. GBD 2015 Disease and Injury Incidence and Prevalence Collaborators. Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990–2015: a systematic analysis for the Global Burden of Disease Study 2015. Lancet. 2016;388:1545–602.

    Article  Google Scholar 

  3. Liu L, Johnson HL, Cousens S, Perin J, Scott S, Lawn JE, et al. Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000. Lancet [Internet]. Elsevier Ltd; 2012 [cited 2014 Jul 10];379:2151–61. Available from:

  4. Bay G, Miller T, Faijer DJ. Level & Trends in childhood mortality: estimates developed by the UN inter-agency Group for Child Mortality Estimation; 2012.

    Google Scholar 

  5. Kotloff KL, Nataro JP, Blackwelder WC, Nasrin D, Farag TH, et al. 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. Lancet. 2013;10(1016):60844–2.

    Google Scholar 

  6. Kotloff KL, Nataro JP, Blackwelder WC, Nasrin D, Farag TH, Panchalingam S, et al. 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. Lancet [Internet]. 2013 [cited 2014 Dec 24];382:209–22. Available from:

  7. Kotloff KL, Platts-Mills JA, Nasrin D, Roose A, Blackwelder WC, Levine MM. Global burden of diarrheal diseases among children in developing countries: Incidence, etiology, and insights from new molecular diagnostic techniques. Vaccine. 2017;35(49 Pt A):6783-9. Epub 2017 Jul 29.

    Article  Google Scholar 

  8. Liu J, Platts-Mills JA, Juma J, Kabir F, Nkeze J, Okoi C, et al. Use of quantitative molecular diagnostic methods to identify causes of diarrhoea in children: a reanalysis of the GEMS case-control study. Lancet [Internet]. Elsevier Ltd; 2016;388:1291–1301. Available from:

    Article  CAS  Google Scholar 

  9. Livio S, Strockbine NA, Panchalingam S, Tennant SM, Barry EM, Marohn ME, et al. Shigella isolates from the global enteric multicenter study inform vaccine development. Clin Infect Dis. 2014;59:933–41.

    Article  CAS  Google Scholar 

  10. Hale TL, Keusch GT. Shigella. In: Baron S, editor. Med. Microbiol. Galveston (TX): The University of Texas Medical Branch at Galveston; 1996.

  11. Centers for Disease Control and Prevention (CDC). National Antimicrobial Resistance Monitoring System for enteric Bacteria (NARMS): human isolates final report, vol. 2012; 2012.

    Google Scholar 

  12. Sur D, Ramamurthy T, Deen J, Bhattacharya SK. Shigellosis : challenges & management issues. Indian J Med Res. 2004;120:454–62.

    PubMed  Google Scholar 

  13. Cook GC, Zumla A. Manson’s tropical diseases [internet]. Elsevier Health Sciences; 2008 [cited 2015 Apr 25]. Available from:

  14. Hannu T, Mattila L, Siitonen A, Leirisalo-Repo M. Reactive arthritis attributable to Shigella infection: a clinical and epidemiological nationwide study. Ann. Rheum. Dis. [Internet]. 2005 [cited 2015 Apr 3];64:594–598. Available from:

  15. Kotloff KL, Winickoff JP, Ivanoff B, Clemens JD, Swerdlow DL, Sansonetti PJ, et al. Global burden of Shigella infections: implications for vaccine development and implementation of control strategies. Bull World Health Organ. 1999;77:651–66.

    CAS  PubMed  PubMed Central  Google Scholar 

  16. Centers for Disease Control and Prevention (CDC). National Antimicrobial Resistance Monitoring System for enteric Bacteria (NARMS): human isolates final report, vol. 2012; 2010.

    Google Scholar 

  17. European Center for Disease Control and Prevention. Annual epidemiological report on communicable disease in Europe, 2010. [Internet]. 2012. Available from:

  18. Heiman KE, Karlsson M, Grass J, Howie B, Kirkcaldy RD, Mahon B, et al. Notes from the field: Shigella with decreased susceptibility to azithromycin among men who have sex with men - United States, 2002-2013. MMWRMorbidity Mortal Wkly Rep. 2014;63:132–3.

    Google Scholar 

  19. Bhattacharya SK, Sur D. An evaluation of current shigellosis treatment. Expert Opin Pharmacother. 2003;4:1315–20.

    Article  CAS  Google Scholar 

  20. PAHO. Pan American health organization (PAHO), health in the Americas, 2007. Washington, D.C.: World Health Organization (WHO); 2007.

  21. Ramiro Cruz J, Cano F, Bartlett AV, Mendez H. Infection, diarrhea, and dysentery caused by Shigella species and campylobacter jejuni among Guatemalan rural children. Pediatr Infect Dis J. 1994;13:216–23.

    Article  CAS  Google Scholar 

  22. Pan American Health Organization (PAHO), Salud en Las Americas, 2012. 2012; Available from:

  23. Arvelo W et al. Incidence and etiology of infectious diarrhea from a facility-based surveillance system in Guatemala, 2008–2012. 2017;[in review.

  24. Instituto Nacional de Estadistica [Internet]. Available from:

  25. Reyes L, Arvelo W, Estevez A, Gray J, Moir JC, Gordillo B, et al. Population-based surveillance for 2009 pandemic influenza a (H1N1) virus in Guatemala, 2009. Influenza Other Respir Viruses. 2010;4:129–40.

    Article  Google Scholar 

  26. Dehydrated Culture Media, X.L.D. Agar. Oxoid Microbiology Products, Thermo Scientific. Basingstoke, UK.

  27. Clinical and Laboratory Standards Institute (CLSI). Performance standards for antimicrobial disk susceptibility tests (M02-A12). 2015.

    Google Scholar 

  28. Replogle ML, Fleming DW, Cieslak PR. Emergence of antimicrobial-resistant shigellosis in Oregon. Clin Infect Dis. 2000;30:515–9.

    Article  CAS  Google Scholar 

  29. Centers for Disease Control and Prevention (CDC). Incidence and trends of infection with pathogens transmitted commonly through food - foodborne diseases active surveillance network, 10 U.S. sites, 1996–2012. MMWR. Morb. Mortal. Wkly. Rep. [Internet]. 2013 [cited 2015 Mar 25];62:283–7. Available from:

  30. Lamberti LM, Bourgeois AL, Walker CLF, Black RE, Sack D. Estimating diarrheal illness and deaths attributable to Shigellae and enterotoxigenic Escherichia coli among older children, adolescents, and adults in South Asia and Africa. PLoS Negl Trop Dis. 2014;8:e2705.

    Article  Google Scholar 

  31. WHO. Infant and Young child feeding [internet]. World heal. Organ. 2011. Available from:

  32. Lake IR, Gillespie IA, Bentham G, Nichols GL, Lane C, Adak GK, et al. A re-evaluation of the impact of temperature and climate change on foodborne illness. Epidemiol Infect. 2009;137:1538–47.

    Article  CAS  Google Scholar 

  33. Gao L, Zhang Y, Ding G, Liu Q, Zhou M, Li X, et al. Meteorological variables and bacillary dysentery cases in Changsha city, China. Am J Trop Med Hyg. 2014;90:697–704.

    Article  Google Scholar 

  34. Cohen D, Bassal R, Goren S, Rouach T, Taran D, Schemberg B, et al. Recent trends in the epidemiology of shigellosis in Israel. Epidemiol Infect. 2014:1–12.

  35. Li Z, Wang L, Sun W, Hou X, Yang H, Sun L, et al. Identifying high-risk areas of bacillary dysentery and associated meteorological factors in Wuhan, China. Sci Rep. 2013;3:3239.

    Article  Google Scholar 

  36. Esrey SA, Feachem RG, Hughes JM. Interventions for the control of diarrhoeal diseases among young children: improving water supplies and excreta disposal facilities. Bull World Health Organ. 1985;63(4):757–72. Available from: PMCID: PMC2536385, PMID: 3878742.

  37. Fewtrell L, Kaufmann RB, Kay D, Enanoria W, Haller L, Colford JM. Water, sanitation, and hygiene interventions to reduce diarrhoea in less developed countries: a systematic review and meta-analysis. Lancet. Infect. Dis. [Internet]. 2005 [cited 2015 Jan 26];5:42–52. Available from:

    Article  Google Scholar 

  38. Colombara D V, Faruque ASG, Cowgill KD, Mayer JD. Risk factors for diarrhea hospitalization in Bangladesh, 2000-2008: a case-case study of cholera and shigellosis. BMC Infect Dis [Internet] 2014 [cited 2015 Aug 24];14:440. Available from:

  39. Khan M, Zanuzdana A, Burkart K, Krämer A. Determinants of Diarrhoea in “Urban” Slums of Dhaka and Adjacent Rural Areas: a Household-level Analysis. Popul. Space Place [Internet]. 2014 [cited 2015 Aug 24];20:498–511. Available from:

    Article  Google Scholar 

  40. Mata LJ, Gangarosa EJ, Cáceres A, Perera DR, Mejicanos ML. Epidemic Shiga bacillus dysentery in Central America. I. Etiologic investigations in Guatemala, 1969. J Infect Dis [Internet] 1970 [cited 2015 Aug 24];122:170–80. Available from:

  41. Centers for Disease Control and Prevention. International Notes Shigella dysenteriae Type 1 -- Guatemala, 1991 [Internet]. Morb. Mortal. Wkly. Rep. 1991 [cited 2015 Aug 24]. p. 427–8. Available from:

  42. Rahman M, Shoma S, Rashid H, El AS, Baqui AH, Siddique AK, et al. Increasing spectrum in antimicrobial resistance of Shigella isolates in Bangladesh: resistance to azithromycin and ceftriaxone and decreased susceptibility to ciprofloxacin. J Health Popul Nutr. 2007;25:158–67.

    PubMed  Google Scholar 

  43. Marcoleta A, Toro C, Prado V, Serrano M, Fernandez P, Benadof D, et al. Antibiotic susceptibility patterns among Shigella sonnei, isolated during three different periods in region Metropolitana. Chile Rev Chilena Infectol. 2013;30:616–21.

    Article  Google Scholar 

  44. Adefurin A, Sammons H, Jacqz-Aigrain E, Choonara I. Ciprofloxacin safety in paediatrics: a systematic review. Arch Dis Child. 2011;96:874–80.

    Article  Google Scholar 

  45. Zaidi MB, Estrada-Garcia T, Campos FD, Chim R, Arjona F, Leon M, et al. Incidence, clinical presentation, and antimicrobial resistance trends in Salmonella and Shigella infections from children in Yucatan, Mexico. Front Microbiol. 2013;4:288.

    Article  Google Scholar 

  46. Desjeux J-F, Briend A, Butzner JD. Oral rehydration solution in the year 2000: pathophysiology, efficacy and effectiveness. Baillieres. Clin. Gastroenterol. [Internet]. 1997 [cited 2015 Apr 28];11:509–27. Available from:

    Article  CAS  Google Scholar 

  47. Keddy KH, Smith AM, Page NA. GEMS extend understanding of childhood diarrhoea. Lancet [internet]. Elsevier Ltd; 2016;388:1252–1254. Available from:

    Article  Google Scholar 

  48. Lindblade KA, Johnson AJ, Arvelo W, Zhang X, Jordan HT, Reyes L, et al. Low usage of government healthcare facilities for acute respiratory infections in guatemala: implications for influenza surveillance. BMC Public Health [Internet]. 2011 [cited 2015 Apr 27];11:885. Available from:

Download references


We would like to thank the Guatemala National Epidemiology Center, the Health Areas of Santa Rosa and Quetzaltenango, and the surveillance hospitals, health centers, and health posts for their cooperation. We are grateful to Lesbia Arevalo, Liliana de Alvarez, for their laboratory support and Gerard Lopez, Fredy Muñoz and their team of programmers for the development of the Questionnaire Mobile program for data entry on PDAs. We also thank Dr. Fabiola Moscoso and the VICo surveillance nurses and field staff for their administrative and scientific support. We are very thankful for the active participation of the residents of Santa Rosa and Quetzaltenango.


This study was funded by the Global Health Protection Branch of the U.S. Centers for Disease Control and Prevention (CDC), and by Cooperative Agreement Number UO1 GH000028–02 from the CDC. Publication costs are funded by CDC.

Availability of data and materials

The datasets generated and analyzed during the current study are available from the corresponding author on reasonable request.

About this supplement

This article has been published as part of BMC Public Health Volume 19 Supplement 3, 2019: 10th anniversary of the Centers for Disease Control and Prevention - Global Disease Detection program. The full contents of the supplement are available online at

Author information

Authors and Affiliations



SH analyzed, interpreted, and was the primary author of the manuscript. SB help conceptualize the study, interpret data and write the manuscript. WA and KL designed the surveillance system and oversaw the data collection for the first few waves of data collection, helped interpret data, and edit the manuscript. BL and AR performed all the laboratory analysis on stool samples, helped write the methods and interpret data. JM and CB oversaw the surveillance system and data collection for the last few waves of data collection, helped interpret data, retrieve the data, and edit the manuscript. JM is the principal investigator at the partnering institution in Guatemala and helped oversee the lab analysis and surveillance, as well as data interpretation. JB is the principal investigator of the VICo study for CDC and oversaw the conceptualization of the manuscript, interpretation and helped guide edits of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Sonia Hegde.

Ethics declarations

Ethics approval and consent to participate

The surveillance protocol was approved by the institutional review boards of UVG (Guatemala City, Guatemala) and CDC (Atlanta, GA) (CDC IRB #5150). Verbal consent was requested of patients in order to screen them for eligibility. Written, informed consent was obtained from eligible patients willing to participate. For patients < 18 years of age, parents or guardians were asked to provide written, informed consent for the participation of the patient. Children aged seven through 17 were asked for written informed assent.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests’.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Additional files

Additional file 1:

Adjusted crude incidence rates of Shigella by age and type of healthcare facility in Santa Rosa and Quetzaltenango Departments, Guatemala, 2008–2012. (JPG 206 kb)

Additional file 2:

Antimicrobial resistance by site, 2007–2012. (JPG 159 kb)

Additional file 3:

Antimicrobial resistance by year from 2007 to 2012. (JPG 197 kb)

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hegde, S., Benoit, S.R., Arvelo, W. et al. Burden of laboratory-confirmed shigellosis infections in Guatemala 2007-2012: results from a population-based surveillance system. BMC Public Health 19 (Suppl 3), 474 (2019).

Download citation

  • Published:

  • DOI: