Invasive Salmonella infections result in significant morbidity and mortality in developing countries. In Asia, typhoid and paratyphoid fever are reported to be the major invasive Salmonella infections, while invasive non-typhoidal Salmonella (iNTS) infections are believed to be uncommon. Data from Sarawak, in Malaysian Borneo, are limited.
Methods
A retrospective study identifying all children aged < 15 years with invasive Salmonella infections from 2011 to 2016 was conducted in Bintulu Hospital in Sarawak. Population incidences, clinical and bacterial characteristics were examined.
Results
Forty-four patients were identified during the 6-year study period: 43 had iNTS infection and 1 had typhoid fever. The average annual iNTS incidence was 32.4 per 100,000 children aged < 5 years. None of the children had malaria or HIV infection, and only 7% were severely malnourished. Salmonella Enteritidis and Salmonella Java were the commonest NTS serovars identified. Pneumonia was the most common manifestation of iNTS disease, present in 20 (47%) children. Other manifestations included gastroenteritis, fever without a source, septic arthritis and meningitis. Salmonella Enteritidis was identified in 76% of those with pneumonia, significantly more frequently than in children with other manifestations. Over 25% of children with iNTS developed severe disease and nearly 10% suffered long term morbidity or mortality. While 78% of Salmonella Java isolates were multi-drug resistant, nearly all other isolates were susceptible to most antimicrobials, including ampicillin.
Conclusions
Bintulu Division in Sarawak observed a very high incidence of childhood iNTS infections. Enteric fever was uncommon. The epidemiology of invasive Salmonella infections in Malaysian Borneo differs considerably from that of neighbouring countries in Asia.
Abkürzungen
CI
Confidence interval
CSF
Cerebrospinal fluid
HIV
Human immunodeficiency virus
iNTS
Invasive non-typhoidal Salmonella
IQR
Interquartile range
NTS
Non-typhoidal Salmonella
OR
Odds ratio
SGI1
Salmonella genomic island 1
WHO
World Health Organization
Background
Invasive Salmonella infections, caused by the various serovars of Salmonella enterica subspecies enterica, result in significant morbidity and mortality in developing countries [1, 2]. Salmonella enterica serovars Typhi and Paratyphi, known as typhoidal Salmonella, typically cause the well-known manifestations of enteric fever (typhoid or paratyphoid fever) [1]. Other Salmonella enterica serovars, collectively termed non-typhoidal Salmonella (NTS), are important causes of gastro-intestinal infections, but may also cause severe invasive infections including bacteraemia and meningitis, with high fatality rates [3, 4]. These invasive NTS (iNTS) infections have mainly been reported in sub-Saharan Africa, predominantly among children with malnutrition or malaria and in adults living with human immunodeficiency virus (HIV) infection [5]. NTS have now emerged as a leading cause of bacterial bloodstream infection among children with fever in the sub-Saharan region, with population incidences as high as 742 per 100,000 person-years of observation [6].
The increasing iNTS burden seen in African children has not been mirrored in Asia. A large multicentre prospective study involving 5 Asian countries reported only 5 paediatric iNTS cases in its 12 month surveillance period [7]. The same study confirmed that typhoid and paratyphoid fever remain the predominant invasive Salmonella infections in Asian children, with annual incidences in Indonesia, India and Pakistan ranging from 149 to 573 per 100,000 children aged 2–5 years [8]. Recently however, a study in Kuala Lumpur in peninsular Malaysia reported that 16% of childhood community-acquired bacteraemia cases were caused by NTS, whereas only 2% were due to typhoidal Salmonella [9]. Unfortunately, unlike in Africa, little is known regarding the characteristics of these iNTS infections.
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The burden of both typhoidal and iNTS infections among children in Sarawak, Malaysian Borneo is not known. Similarly, the prevailing NTS serovars, risk factors for infection, clinical manifestations and outcomes, and the anti-microbial susceptibility of serovars in the region have never been documented. To answer these questions, we conducted a retrospective chart review to determine the population incidence, the clinical and the bacterial characteristics of invasive Salmonella infections among children in Bintulu, Sarawak.
Methods
Study site
The study was conducted at Bintulu Hospital, a 294 bed district hospital which provides medical, surgical and intensive care services to adults and children living in Bintulu Division and Belaga district of Kapit Division in Sarawak, Malaysian Borneo. This 32,000km2 area located within the central region of the state has a total population of approximately 256,000, including 72,000 children < 15 years. A large proportion of this population resides in Bintulu town, the largest town in the region. The region has a tropical climate with monsoon rains occurring between November and February each year. Malaysia has low HIV infection and malaria disease burdens, with incidence rates of 10.7 and 7.3 per 100,000 population reported in 2016 respectively [10].
Case definitions
An invasive Salmonella infection case was defined as a child < 15 years with a positive culture of Salmonella enterica species from any normally sterile site sample obtained within 48 h of admission. We retrospectively identified all cases admitted from January 2011 to December 2016 through a manual search of the microbiology laboratory logbooks and electronic database. Medical records of identified cases were then retrieved and details on demography, underlying medical conditions, symptoms, physical findings, laboratory results, case management, outcome and bacterial antimicrobial susceptibility and serotype were collected using standardized case report forms.
NTS included all Salmonella enterica subspecies enterica serotypes other than Typhi and Paratyphi A. In children aged < 10 years, severe malnutrition was defined as weight for age z-score ≤ − 3 based on the World Health Organization (WHO) child growth standards and the WHO growth reference data [11, 12]. Children aged > 10 years were excluded from this analysis. A clinical diagnosis of pneumonia was made when fever, cough and tachypnoea were present. Meningitis was confirmed when culture of cerebrospinal fluid (CSF) yielded S. enterica or when CSF examination revealed pleocytosis (≥10 white blood cells/μL in a non-traumatic lumbar puncture) in the presence of Salmonella bacteraemia. Tachycardia and tachypnoea were defined based on WHO definitions [13]. Severe anaemia was defined as a haemoglobin level < 7 g/dL. Multi-drug resistance was defined as non-susceptibility to 3 or more unrelated antimicrobial agents. Intermediate resistant isolates were considered non-susceptible. An appropriate antibiotic was defined as the use of an antimicrobial with good intracellular activity, namely amoxicillin, ampicillin, cotrimoxazole, chloramphenicol, ciprofloxacin or a 3rd generation cephalosporin, to which the Salmonella isolate was susceptible. A recurrent infection was defined as a culture-confirmed Salmonella infection occurring after the completion of an appropriate antibiotic for a previous invasive Salmonella infection.
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Microbiological methods
As part of routine clinical practice in Bintulu Hospital, blood for bacterial culture was collected in all children suspected to have severe bacterial infections and in those requiring parenteral antibiotics, based on the discretion of admitting clinicians. Between 1 and 3 ml of whole blood was collected and immediately inoculated into paediatric bottles (BACTEC Peds Plus/F Medium; Becton Dickinson, USA) and incubated in an automated blood culture system (BACTEC FX; Becton Dickinson, USA) for a maximum of 5 days. Positive growth was subcultured onto blood agar, chocolate agar and MacConkey agar. CSF and endotracheal secretions were cultured directly on blood agar, chocolate agar and MacConkey agar, while urine samples were cultured on blood agar and cystine lactose electrolyte deficient agar. Salmonella enterica was identified with either API®20E (BioMérieux, France) or BBL™ Crystal™ Identification Systems (Becton Dickinson, USA).
Antibiotic susceptibility were determined by Kirby-Bauer disk diffusion test (Becton Dickinson, USA) according to the Clinical and Laboratory Standard Institute (CLSI) guidelines. Breakpoints were based on the 2008 guidelines for isolates obtained prior to September 2013, and on the 2011 guidelines for isolates obtained subsequently.
Serotyping of the Salmonella isolates were performed in the national reference laboratory (Institute for Medical Research, Kuala Lumpur) according to the Kauffman-White scheme. Slide agglutination tests using commercially available mono- and poly-O groups Salmonella A, B, C, D and E antisera (Remel, Europe Ltd., UK) and polyvalent Salmonella antisera phase 1 and phase 2 flagellar H antigens (Remel, Europe Ltd., UK) were performed as described previously [14]. Salmonella enterica serovar Paratyphi B var. Java was distinguished from classical Salmonella Paratyphi B using a multiplex PCR targeting the common region for Salmonella and the ATG start codon for the STM 3356 gene of d-tartrate fermenting strains, as described previously [15].
HIV and malaria screening were only performed if clinically suspected.
Statistical analysis
Statistical analysis was performed using SPSS Statistics 21. The Kruskal-Wallis H test was used for numerical variables and either the χ2 test or Fisher’s exact test was used for categorical variables. The correlation between the number of cases and average monthly rainfall was examined using Spearman’s rank co-efficient test. Population data were obtained from the Malaysian Census Data 2010. Meteorological data were obtained from the Malaysian Meteorological Department.
Ethics statement
The study was approved by the Malaysian Medical Research Ethics Committee (NMRR-17-2438-37563). All data analyzed were anonymized.
Results
Bacterial isolation and typing
Forty-four children with invasive Salmonella infections were identified during the 6-year study period (3 in 2011, 4 in 2012, 9 in 2013, 7 in 2014, 13 in 2015 and 8 in 2016). Medical records of all identified cases were available for analysis. All cases had Salmonella isolated from blood. Salmonella was not isolated in any other specimen, including CSF.
NTS was isolated in 43 (98%) children while Salmonella enterica serovar Typhi was isolated in only 1 (2%) child. Of the 38 (88%) NTS isolates that were serotyped, Salmonella enterica serovar Enteritidis and Salmonella enterica serovar Paratyphi B var. Java (Salmonella Java) were the most common serovars identified (Table 1). Salmonella Java infections were only noted from 2014 (Fig. 1).
Table 1
Distribution of non-typhoidal Salmonella serovars in Bintulu
Serovar
Number
Percent
Salmonella Enteritidis
17
45
Salmonella Java
9
24
Salmonella Corvallis
6
16
Salmonella Ohio
1
3
Salmonella Kentucky
1
3
Salmonella Poona
1
3
Salmonella Derby
1
3
Salmonella Agona
1
3
Salmonella Hvittingfoss
1
3
Total
38
100
Fig. 1
Distribution of the 44 invasive Salmonella cases by year of admission and serovar. The bar chart shows the number of invasive Salmonella cases diagnosed in Bintulu in each year from 2011 to 2016, according to serovar
×
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Patient demographics and population incidence
Twenty-eight (64%) of the 44 children with invasive Salmonella infections were male. The median age of children with iNTS was 8 months (interquartile range [IQR], 4–11 months; range 8 days-11.8 years). Seven (16%) were aged < 2 months. The child with typhoid was 54 months old.
The average annual incidence of iNTS was 10.0 per 100,000 children aged < 15 years, with the highest incidence recorded in 2015 (18.1 per 100,000 children per year). The average annual incidence was 32.4 per 100,000 in children aged < 5 years and 135.1 per 100,000 in those aged < 1 year. In contrast, the average annual incidence of Salmonella Typhi infection was only 0.2 per 100,000 children < 15 years.
Although more invasive Salmonella cases occurred during the dryer months of the year (Fig. 2), no significant correlation was found between the monthly incidence and average monthly rainfall (rs = − 0.3, P = 0.3).
Fig. 2
Distribution of the 44 invasive Salmonella cases and average rainfall by month. The bar chart shows the distribution of the 44 invasive Salmonella cases according to the month of admission. The average monthly rainfall over the 6-year period (January 2011–December 2016) in Bintulu is shown in the line graph
×
Risk factors and clinical manifestations
Thirteen (30%) children had underlying medical conditions (Table 2), including 1 child who was diagnosed to have acute leukemia at presentation. None were suspected or diagnosed to have malaria or HIV infection. Severe malnutrition was present in only 3 (7%) of the 43 children aged < 10 years. Of these, 2 had Salmonella Enteritidis and 1 had Salmonella Java infection. Severe anemia was present in only 2 (5%) of the 43 children with data available. Both had Salmonella Enteritidis infection.
Table 2
Underlying medical conditions among children with invasive Salmonella infections in Bintulu
Medical condition
Number
% of all cases
NTS serovar isolated (number of cases)
Episodic viral wheeze/ multi-trigger wheeze
5
11
Salmonella Enteritidis (2), Salmonella Corvallis (1), Not serotyped (2)
Down syndrome
2
5
Salmonella Enteritidis (2)
Acute leukaemia
2
5
Salmonella Enteritidis (2)
Eczema
2
5
Salmonella Java (1), Salmonella Corvallis (1)
West syndrome
1
2
Salmonella Ohio (1)
Neonatal hepatitis syndrome
1
2
Salmonella Enteritidis (1)
Total
13
30
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Pneumonia was the most common clinical manifestation (Fig. 3), present in 20 (47%) of the 43 children with iNTS. Among those with pneumonia, Salmonella Enteritidis was identified in 13 (76%) of 17 children whose NTS isolates were serotyped, significantly more frequently than in children with other clinical manifestations (13/17 [76%] vs 4/21 [19%], P = 0.001, OR 13.9, 95%CI 2.9–66.7). Children with Salmonella Enteritidis infection presented predominantly with fever and respiratory symptoms and signs; gastro-intestinal symptoms and signs were uncommon (Table 3). Among 17 (85%) children with pneumonia whose chest radiograph findings were recorded, 12 (71%) had unilateral or bilateral peri-hilar interstitial haziness, 2 (12%) had unilateral or bilateral alveolar opacities while the remaining 3 (18%) had clear lung fields.
Fig. 3
Distribution of invasive Salmonella infections among children in Bintulu according to clinical manifestation and serovar. The bar chart depicts the distribution of the 44 invasive Salmonella cases identified in the study, according to the clinical manifestation at presentation, with the number of cases attributed to the various serovars shown
Table 3
Presentation of children with invasive non-typhoidal Salmonella infections by serovar in the 38 children whose isolates were serotyped
Characteristic
All serovars
Salmonella Enteritidis
Salmonella Java
Other NTS serovars
P
No. of patients
38
17
9
12
–
Presenting symptoms
Time between onset and admission, days, median (IQR)
2 (2–5)
3 (2–6)
3 (2–8)
2 (1–4)
0.1
Fever
34 (89)
16 (94)
7 (78)
11 (92)
0.4
Poor appetite
26 (68)
12 (71)
5 (56)
9 (75)
0.7
Lethargy or irritability
23 (61)
9 (53)
5 (56)
9 (75)
0.5
Cough
20 (53)
13 (77)
3 (33)
4 (33)
0.03
URTI symptoms
17 (45)
10 (59)
3 (33)
4 (33)
0.4
Diarrhea
15 (40)
4 (24)
6 (67)
5 (42)
0.1
Vomiting
5 (13)
1 (6)
2 (22)
2 (17)
0.5
Presenting signs
Signs of respiratory distress
26 (68)
15 (88)
4 (44)
7 (58)
0.05
Tachycardia for age
24 (63)
13 (77)
6 (67)
5 (42)
0.2
Tachypnoea for age
20 (53)
13 (77)
5 (56)
2 (17)
0.007
Signs of dehydration
15 (40)
4 (24)
5 (56)
6 (50)
0.2
Abnormal lung findingsa
13 (34)
9 (53)
1 (11)
3 (25)
0.1
Hepatomegaly
9 (24)
7 (41)
0 (0)
2 (17)
0.08
Pallor
7 (18)
4 (24)
1 (11)
2 (17)
0.9
Poor perfusion
6 (16)
3 (18)
2 (22)
1 (8)
0.7
Splenomegaly
2 (5)
2 (12)
0 (0)
0 (0)
0.5
Investigationsb
Hemoglobin, g/dL, median (IQR)
11.4 (10.1–12.2)
11.5 (10.4–12.2)
11.4 (10.2–14.0)
10.5 (9.4–12.7)
0.5
WBC, X 109 cells/L, median (IQR)
13.3 (9.7–18.3)
13.3 (9.5–17.6)
17.2 (10.3–20.3)
13.2 (8.5–17.6)
0.5
Neut, X 109 cells/L, median (IQR)
5.7 (4.2–13.5)
5.7 (3.6–9.1)
6.4 (4.8–15.2)
6.2 (4.2–14.3)
0.7
Lymph, X 109 cells/L, median (IQR)
5.4 (3.8–7.5)
5.8 (4.7–9.3)
5.8 (3.8–10.7)
4.4 (2.7–6.9)
0.3
Platelet, X 109/L, median (IQR)
343 (251–463)
362 (185–459)
462 (313–492)
347 (238–487)
0.4
ESR, mm/hr., median (IQR)
32 (10–48)
32 (10–41)
50 (24–75)
23 (6–61)
0.6
Sodium, mmol/L, median (IQR)
136 (133–138)
137 (135–139)
134 (129–137)
135 (133–137)
0.1
Urea, mmol/L, median (IQR)
3.1 (2.3–4.3)
2.7 (2.3–3.6)
3.5 (2.8–7.3)
3.4 (2.3–5.1)
0.4
Albumin, g/L, median (IQR)
38 (35–44)
36 (34–44)
45 (43–46)
41 (34–46)
0.3
AST, U/L, median (IQR)
51 (40–108)
49 (40–244)
98 (88–108)
48 (34–58)
0.4
ALT, U/L median (IQR)
22 (16–90)
22 (16–82)
97 (85–109)
19 (15–94)
0.4
Data are No. (%) unless otherwise indicated
a All children with abnormal lung examination had bilateral findings: 6 had both rhonchi and crepitation, 6 only rhonchi and 1 only crepitation
bOnly investigations done on the day of admission were included: 37 children had Hemoglobin, WBC, Platelet (Enteritidis, n = 17; Java, n = 8; Other serovars, n = 12); 27 children had differential counts (Enteritidis, n = 12; Java, n = 7; Other serovars, n = 8); 13 children had ESR (Enteritidis, n = 7; Java, n = 2; Other serovars, n = 4); 37 children had Sodium, Urea (Enteritidis, n = 17; Java, n = 9; Other serovars, n = 11); 15 children had Albumin, AST, ALT (Enteritidis, n = 9; Java, n = 2; Other serovars, n = 4)
Twelve (28%) children with iNTS presented with gastroenteritis (Fig. 3). Of the 10 whose isolates were serotyped, Salmonella Java and Salmonella Corvallis were identified in 6 (60%) and 3 (30%) children respectively. Salmonella Java was identified more frequently in children with gastroenteritis than in those with other diagnoses (6/10 [60%] vs 3/28 [11%], P = 0.005, OR 12.5, 95%CI 2.2–71.4). Fever and watery diarrhea were the most common presenting features, noted in 11 (92%) and 10 (83%) of the 12 children respectively. Only 2 (17%) had blood in stools. Stool cultures were performed in only 4 (33%) of these children; all were negative.
Two (5%) children had NTS meningitis, one caused by Salmonella Enteritidis and the other by Salmonella Poona. Both infants were < 2 months of age. Meningitis was significantly more common in this age group than in older infants and children (2/7 [29%] vs 0/36 [0%], P = 0.02). Both infants presented with an abrupt onset of fever and lethargy and rapidly developed septicaemic shock on the same day. Lumbar puncture was only performed after 3 and 7 days of admission respectively, due to the unstable cardio-respiratory condition. Both had abnormal CSF examination: 558 white blood cells/mm3 (80% polymorphs) and 41 white blood cells/mm3 (5% polymorphs) respectively. Twenty-seven (66%) of the remaining 41 children with NTS infections (who presented primarily with respiratory or gastro-intestinal manifestations) had lumbar puncture; all except 1 (who had a traumatic procedure) had normal CSF examination.
Two (5%) children presented with septic arthritis, both due to Salmonella Enteritidis. Both had unilateral hip joint involvement: one was a 5-month old infant without any risk factor while the other was an 11-year old with relapsed acute leukaemia on palliative chemotherapy.
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A 16-month old girl with West syndrome and swallowing difficulty requiring nasogastric tube feeding had occult bacteraemia with Salmonella Ohio. She presented to hospital with increased oropharyngeal secretions but had no fever or other localizing symptoms or signs.
Antimicrobial susceptibility
Among NTS isolates, in vitro resistance to tetracycline, ampicillin, chloramphenicol and cotrimoxazole was noted in 61% (25/41), 21% (9/43), 21% (9/43) and 5% (2/43) respectively. All isolates were susceptible to ciprofloxacin and ceftriaxone. Sixteen (94%) of the 17 Salmonella Enteritidis isolates were susceptible to ampicillin, whereas only 2 (22%) of the 9 Salmonella Java isolates were susceptible to this antimicrobial agent (Table 4). Multi-drug resistance was observed more frequently in Salmonella Java isolates than in Salmonella Enteritidis isolates (7/9 [78%] vs 1/17 [6%], P < 0.001, OR 56, 95%CI 4.3–724).
Table 4
Antimicrobial resistance of non-typhoidal Salmonella isolates by serovar
Antimicrobial
All serovars
n/N (%)
Salmonella Enteritidisa
n/N (%)
Salmonella Javaa
n/N (%)
Other NTS serovarsa
n/N (%)
Tetracyclineb
22/37 (59)
5/16 (31)
7/9 (78)
10/12 (83)
Ampicillin
9/38 (24)
1/17 (6)
7/9 (78)
1/12 (8)
Chloramphenicol
9/38 (24)
1/17 (6)
7/9 (78)
1/12 (8)
Cotrimoxazole
2/38 (5)
1/17 (6)
0/9 (0)
1/12 (8)
Ciprofloxacin
0/38 (0)
0/17 (0)
0/9 (0)
0/12 (0)
Ceftriaxone
0/38 (0)
0/17 (0)
0/9 (0)
0/12 (0)
aMulti-drug resistance was found in 9 isolates (Salmonella Enteritidis, n = 1; Salmonella Java, n = 7; Salmonella Ohio, n = 1)
bTetracycline susceptibility was not recorded in 1 Salmonella Enteritidis isolate
The sole Salmonella Typhi isolate was susceptible to all antimicrobials tested, including tetracycline, ampicillin, chloramphenicol, cotrimoxazole, ciprofloxacin and ceftriaxone.
Case management and outcome
Eleven (26%) children with iNTS required intensive care: both (100%) children with meningitis, 8 (40%) of 20 with pneumonia and 1 (8%) of 12 with gastroenteritis. Reasons for intensive care included impending respiratory failure (n = 7) and septicaemic shock (n = 4). Salmonella Enteritidis was identified in 8 (73%) of these children. Forty-seven percent of all children with invasive Salmonella Enteritidis infection required intensive care.
Invasive NTS infections resulted in death or severe sequelae in 4 (9%) children. There were 2 fatalities: one was a 4-week old infant with meningitis who had severe neurological deficits, remained ventilator-dependent after 15 days in intensive care and died when respiratory support was withdrawn; the other was a 4-month old who had pneumonia complicated by hemophagocytic lymphohistiocytosis. The 2 children who survived with severe sequelae included a 6-week old infant with meningitis (microcephaly, global developmental delay, infantile spasms and cortical blindness present at discharge from hospital at age 3.5 months and persisting on follow up at age 2 years) and a 3-month old with pneumonia who had limb amputations associated with purpura fulminans. Of these 4 cases, 3 (75%) had Salmonella Enteritidis and 1 (the infant with meningitis surviving with severe sequelae) had Salmonella Poona infection.
All children received parenteral antibiotics. Ampicillin was the most common empiric antibiotic used, initiated in 24 (55%) children. Other initial antibiotics, given either empirically or upon detection of Gram negative bacteraemia, included ceftriaxone (n = 6), cefuroxime (n = 4), ceftazidime (n = 4), ampicillin-sulbactam (n = 4), cefotaxime (n = 1) and benzyl penicillin (n = 1). Of those given ampicillin empirically, 3 were found to have non-susceptible isolates, requiring a switch to ceftriaxone. Thirty-five (80%) children ultimately received ceftriaxone, mainly to facilitate ambulatory care. The median duration of parenteral treatment was 14 (IQR 6–18) days. In 27 children, treatment was further extended with an oral antibiotic, mainly amoxicillin or cotrimoxazole. The median total duration of antibiotics was 21 (IQR 12–43) days.
Among survivors, fever resolved rapidly (within a median of 1 [IQR 1–2] day) following initiation of an appropriate antibiotic. Only 1 recurrent infection was recorded. This was in a 6 month old with an invasive Salmonella Enteritidis infection (presenting with pneumonia), treated with a total of 13 days of antibiotics (5 days of parenteral, 8 days oral). Ten days after completion of antibiotics, fever recurred. Salmonella Enteritidis was again cultured from blood.
Discussion
To our knowledge, this study is the first detailed report of invasive Salmonella infections among children in Sarawak, Malaysian Borneo, and shows a striking and underappreciated burden of iNTS disease, and conversely, a rarity of typhoidal Salmonella infections in this population. It also highlights important and previously undescribed clinical and bacterial characteristics of iNTS infections in this region.
The incidence of childhood iNTS infections found in this study were among the highest recorded outside of sub-Saharan Africa. The average annual incidence of 32.4 per 100,000 children aged < 5 years and 135.1 per 100,000 aged < 1 year in Bintulu were markedly higher than the iNTS incidences recorded at sites in all 5 Asian countries included in the multicentre community-based prospective study, namely Pakistan (7.2 per 100,000 aged 2–15 years), India (1.8 per 100,000), Indonesia (1.0 per 100,000), China (0.0 per 100,000 aged 5–60 years) and Viet Nam (0.0 per 100,000 aged 5–18 years) [7]. In fact, the average annual iNTS incidence in Bintulu was only slightly lower than the incidences in some areas of sub-Saharan Africa, including Mozambique (217.7 per 100,000 children aged < 1 year) and Kenya (36.6 per 100,000 children aged < 5 years) [16, 17]. The higher incidence found in Bintulu in comparison to the Asian sites may be due to the fact that children under 2 years, who typically have a higher risk of iNTS infection, were included in only 2 of the 5 sites of the multicentre study [7]. However, other unknown epidemiological factors may also be contributing to the higher incidence in Bintulu. Importantly, the iNTS incidence reported in the present study likely remains an under-estimate of the true population incidence as this hospital based study has only identified severe cases that resulted in hospitalization. Our findings are however consistent with those of a study estimating the global burden of iNTS which predicted an incidence of 5–92 cases per 100,000 population in Southeast Asia, and lends support to the conclusions that iNTS is a major but under-recognized cause of bacteraemic illness globally [18].
Intriguingly, the high incidence of childhood iNTS disease recorded in this study occurred in a population not burdened by malnutrition, malaria or HIV infection, unlike the iNTS infections described in most other regions [5, 19, 20]. For example, 31% of children with iNTS in Mozambique were severely malnourished while 43% had malaria [16]. In Bintulu, only 7% of children with iNTS were severely malnourished, and none were diagnosed to have malaria or HIV infection. Although 30% did have an underlying medical condition, the significance of this finding is unknown as the medical conditions, with the exception of acute leukaemia, were not commonly known risk factors of NTS infection. None of the children were screened for the presence of underlying primary immunodeficiency conditions, and this remains a limitation of the study.
Salmonella Enteritidis and Salmonella Java were the most common NTS serovars identified in Bintulu, causing 45 and 24% of the iNTS infections respectively. In Africa, Salmonella Enteritidis has been implicated in around 20% of iNTS cases, including 36% of childhood cases in Mali [5, 21]. Similarly, in Asia, Salmonella Enteritidis was identified in > 40% of iNTS cases in Vietnam and Peninsular Malaysia, confirming the global distribution and importance of this serovar in causing invasive disease [20, 22]. This is in contrast to the distribution of Salmonella Typhimurium, the other major serovar implicated in iNTS infections, responsible for almost 70% of cases in Africa [5]. No Salmonella Typhimurium iNTS infections were noted in Bintulu. Similarly, very few Salmonella Typhimurium iNTS cases were found in previous studies in Peninsular Malaysia [22, 23]. The reasons for this geographical variation in serovar distribution are not known, and further epidemiological studies are required.
Invasive Salmonella Enteritidis infections in Bintulu manifested with a wide spectrum of clinical presentations, foremost of which was pneumonia, and almost half resulted in severe disease. Pneumonia was the primary presentation in 76% of children with Salmonella Enteritidis bacteraemia, with the remainder presenting with septic arthritis, meningitis or fever without a source. Studies of iNTS disease in children in Africa have also reported respiratory presentations in large proportions of cases [24, 25]. In Ghana, NTS was shown to be the predominant organism isolated in children with clinical pneumonia [26]. In Thailand, clinical pneumonia was diagnosed in 25% of children with iNTS disease [27]. Interestingly, 82% of these children had abnormal, predominantly interstitial, infiltrates on the chest radiograph; a finding similarly noted in the present study. Whether these pulmonary manifestation are due solely to NTS or is instead due to infection with other more typical but undiagnosed viral or bacterial respiratory pathogens, either singly or as a part of a co-infection with the NTS, remains unknown. In the present study, almost 50% of children with Salmonella Enteritidis bacteraemia had severe disease necessitating intensive care. Death or long-term morbidity occurred in 18%, highlighting the considerable burden of these infections. In addition, long-term pulmonary sequelae, not evaluated in this study, could also have occurred.
In contrast to the Salmonella Enteritidis infections, invasive Salmonella Java infections manifested primarily with gastro-intestinal disease. Salmonella Java, described as the d-tartrate fermenting biovar of S. enterica subspecies enterica serovar Paratyphi B, is thought to be less virulent compared to the non d-tartrate fermenting variant (classical Salmonella Paratyphi B), with infections typically localized to the gastro-intestinal tract [28]. Large outbreaks of these gastro-intestinal tract infections have been reported, resulting mainly from contaminated food products [29]. Although invasive infections have been documented, Salmonella Java has not previously been reported to be a major cause of invasive disease [30, 31]. It is unclear whether the frequent bacteraemia found in the present study is due to increased invasiveness or is in fact a reflection of a large, unrecognized burden of gastro-intestinal Salmonella Java infections as the epidemiology of acute gastro-enteral infections in this population has not been studied.
NTS meningitis occurred more frequently in very young infants and resulted in severe morbidity and mortality. Both infants in this study were < 2 months of age, with one having a fatal outcome and the other suffering severe neurological sequelae. Previous studies have documented similar findings. Among non-HIV infected individuals in South Africa, NTS meningitis occurred only in those aged < 5 years [32]. Of these, 41% were < 2 months of age. Children with NTS meningitis in Kuala Lumpur had a mortality of 18%, with a further 36% having severe long-term sequelae [33]. In the present study, 67% of all children had CSF examination, despite the majority presenting with respiratory or gastro-intestinal manifestations without overt symptoms or signs of meningitis. CSF findings were normal in all except the 2 infants described above. These findings support a recently published recommendation that CSF be examined in all infants aged < 3 months diagnosed with NTS bacteraemia, but only when clinically indicated in older infants [34].
In regions with a high prevalence of iNTS infection, Salmonella has been reported to be the leading cause of septic arthritis in children [35]. This is in stark contrast to data from regions with low iNTS prevalence, where Staphylococcus and Streptococcus (and some Gram negative bacilli in the neonatal period) are the predominant causes of childhood septic arthritis. In the present study, 2 cases of septic arthritis were identified, possibly indicating a similar importance of NTS in the etiology of septic arthritis in Bintulu Division.
Apart from Salmonella Java isolates, nearly all other NTS isolates in the study were susceptible to most antimicrobials, including ampicillin. Worldwide, an increasing prevalence of antimicrobial resistance in NTS has been reported [1]. In Southeast Asia, resistance to ampicillin was documented in 31 and 68% of NTS isolates in Penang (Malaysia) and Bangkok (Thailand), respectively [23, 27]. Multi-drug resistance was documented in 48% of isolates in sub-Saharan Africa [6]. In Bintulu, multi-drug resistance was found mainly in Salmonella Java, with 78% of isolates noted to be multi-drug resistant. These isolates, only detected since 2014, had identical resistance spectrums consisting of ampicillin, chloramphenicol and tetracycline. Although the susceptibility to streptomycin and sulfonamides are not known (resistance to these antimicrobials are not routinely screened for in Bintulu), it is possible that these Salmonella Java isolates contain Salmonella genomic island 1 (SGI1), which typically harbor genes that confer resistance to these antimicrobials [36]. Multi-drug resistant Salmonella Java containing SGI1, believed to be clonal in origin, has been reported globally [37, 38]. The high prevalence of multi-drug resistance among the Salmonella Java isolates in Bintulu suggests either the dominance of the drug-resistant strain in this region, an increased predisposition to severe human infections or the presence of a common epidemiological source of infection in the patients. Studies to determine the complete drug-resistance profile, molecular typing, and source of the Salmonella Java infections are urgently needed. As Salmonella Java was less likely to be associated with respiratory presentations than Salmonella Enteritidis, the continued use of amino-penicillins in the empiric treatment of pneumonia among children in Bintulu, as is recommended in most guidelines, remains appropriate [39].
Conclusions
Bintulu Division in Sarawak, Malaysian Borneo has an important yet under-appreciated burden of childhood iNTS infections. Severe disease occurred in over 25%, with long-term morbidity and mortality in nearly 10% of cases, despite most children having no commonly known risk for infection. Salmonella Enteritidis was the commonest NTS serovar identified, with affected children presenting primarily with pneumonia. Apart from Salmonella Java, nearly all isolates were susceptible to most antimicrobials, including ampicillin.
Acknowledgements
We thank the Director-General of Health (Malaysian Ministry of Health) for his approval and support of this work. We also thank all our medical and nursing colleagues in the Pediatric and Intensive Care wards, as well as our laboratory colleagues in the Microbiology Unit of Bintulu Hospital and Bacteriology Unit of the Institute for Medical Research in Kuala Lumpur, for their expertise in the diagnosis and management of the patients.
Funding
Not applicable.
Availability of data and materials
The datasets used and analysed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The study was approved by the Malaysian Medical Research Ethics Committee (NMRR-17-2438-37563). As all data analyzed in this retrospective chart review were anonymized, the need to obtain consent was formally waived by the ethics committee.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
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Invasive Salmonella infections among children in Bintulu, Sarawak, Malaysian Borneo: a 6-year retrospective review
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