Sei sulla pagina 1di 10

THE LIBYAN JOURNAL OF

Infectious Diseases
The Official Periodical of the Libyan National Center
for Infectious Diseases Prevention and Control
Review Article Vol. 2 No. 1 Jan. - 2008

Infectious acute diarrhea in Libyan children: causative


agents, clinical features, treatment and prevention

Khalifa Sifaw Ghenghesh1,


ABSTRACT Ezzadin A. Franka1,
Diarrhea remains one of the principle causes of morbidity and Khaled A. Tawil1,
mortality in children in the world. Although studies on causative Salah Abeid1,
agents of children diarrhea in Libya are few, the available data shows Mustafa Ben Ali2,
that rotavirus is the major cause of diarrhea in Libyan children. Ibrahim A. Taher3,
However, bacterial and parasitic pathogens also play an important Rajab Tobgi3.
role in the etiology of diarrhea in children in Libya with salmonellae 1
Faculty of Medicine, Al-Fateh University,
and Cryptosporidium as major agents, respectively. Fever and Tripoli,
severe dehydration are common clinical features among diarrheic 2
Faculty of Arts and Sciences, El-
children particularly those affected by rotavirus. The emergence of Khomes University,El-Khomes,
antimicrobial-resistant enteric bacterial pathogens in this population 3
Faculty of Medicine, Gharyounis
has been noted and may complicate treatment options. The ease
University, Benghazi, Libya
Vol. 2 No.1 Jan. 2008

by which antimicrobial agents can be obtained over the counter in


Libya may play a role in the emergence of this problem. A serious
educational program in the country on the benefits of breast feeding
is needed. Also, the introduction of a rotavirus vaccine into the Key words:
vaccination program in Libya to protect the pediatric population Children, diarrhea, rotavirus,
should be taken into consideration.. Salmonella, Cryptosporidium, Libya

INTRODUCTION which may or may not be of an infectious nature


The Official Periodical of the Libyan National Center for Infectious Diseases Prevention and Control
Infectious Diseases

(2). The causative agents of infective diarrhea


Diarrhea remains one of the principle include bacteria, viruses and parasites. This
causes of morbidity and mortality in children review is aimed at providing comprehensive
worldwide. Recently, the World Health information on the etiological agents, clinical
Organization (WHO) estimated that diarrhea features, treatment and prevention of diarrhea
accounts for 1.6 to 2.5 million deaths annually, in Libyan children. The data was obtained from
with children below five years of age in Highwire Press (including PubMed) search for
developing countries being most affected (1). the period 1980-2007 using the terms «Diarrhea
THE LIBYAN JOURNAL OF

Diarrhea can be a symptom of various diseases, in Libya» and «Libyan children», «Salmonella
in Libya», «Shigella in Libya» and so forth for
Correspondence and reprint request : Khalifa Sifaw Ghenghesh
Dept. of Microbiology and Immunology, Faculty of Medicine, other enteric pathogens. Also, papers published
Al-Fateh University. in local biomedical journals, and when available
Phone: (+218) 092 397 3908
P.O.Box: 80013 Tripoli - Libya abstracts presented in local and international
Email: ghenghesh_micro@yahoo.com, Website: www.dmi.ly meetings on the subject were included.
Received : 3/ 11/ 2007, Accepted : 5 / 12/ 2007

10 www.nidcc.org.ly
Infectious acute diarrhea in Libyan children
Causative Agents and Clinical Table 1. Agents of infective acute diarrhea in
Libyan children1
Features of Diarrhea in Libyan
Rate of
Children Agents
occurrence
In general, younger children with Bacterial
diarrhea (<2 years) are more likely to harbor
1. EPEC2 4 - 11 %
enteropathogens than older diarrheic children
2. EAEC 3
NK4
with no significant differences among the
3. Salmonella sp. 6 -11 %
sexes (3,4). Bacterial, parasitic and viral agents
4. Shigella sp. 4-6%
of acute infectious diarrhea in Libyan children
are shown in Table 1. 5. Yersinia enterocolitica <1 %
6. Campylobacter sp. 2-6%
I. Bacterial agents: 7. Aeromonas sp. 0 - 15 %
1. Diarrheagenic Escherichia coli: At least six Parasitic
different pathotypes are known up to date 1. Entamoeba histolyitca/disapr 12 %
that cause enteric disease, such as diarrhea 2. Giardia lamblia 1 - 18 %
or dysentery and these include entero- 3. Cryptosporidium 13 %
pathogenic E. coli (EPEC), enterotoxigenic Rotavirus 24 - 31 %
E. coli (ETEC), enteroinvasive E. coli
Multiple agents 12 - 14.5 %
(EIEC), enterohaemorrhagic E. coli
(EHEC), entero-aggregative E. coli (EAEC) 1
Data obtained from references 3,4,6,7,14,28,29,34.
2
Enteropathogenic Escherichia coli,
and diffusely adherent E. coli (DAEC) 3
Enteroaggregative E. coli,

Vol. 2 No.1 Jan. 2008


(5). Of these pathotypes only EPEC can 4
not known.

be detected by specific antisera. Others


require the use of animals (e.g. ETEC and (EAEC) strains. Significantly (P=0.001)
EIEC) tissue culture (e.g. EAEC, DAEC) or more EPEC strains were identified from
immunological techniques (ELISA, RIA) diarrheal children (n=8) than from healthy
(e.g. EHEC), however molecular procedures controls (n=1), six EAEC strains were
(e.g. PCR) can be used to detect all different identified from diarrheal and three from
pathotypes of E. coli. healthy control. Most of the EPEC strains
In the nineties of last century, a study belonged to serogroups O55, O114 and
The Official Periodical of the Libyan National Center for Infectious Diseases Prevention and Control
carried out in Tripoli reported EPEC from O127. No ETEC, EIEC, STEC or EHEC Infectious Diseases
11% of 157 Libyan children with diarrhea were detected in the above mentioned study.
and from 7% of 157 controls with O114 Although these findings indicate that EPEC
and O119 being among the serogroups and EAEC could be the main pathotypes
detected (6). In the same period a study of diarrheagenic E. coli in Libyan children
from Benghazi reported EPEC from 4% of more studies are needed on larger collections
356 diarrheic children and none from 100 of E. coli isolated from children with and
controls with different serogroups being without diarrhea and from different regions
THE LIBYAN JOURNAL OF

detected that included O111 and O127 (4). of the country to confirm this observation.
Recently, Dow et al (7) examined 50 E. EHEC, also known as verotoxin-
coli strains (20 from diarrheic and 30 from producing E. coli, produces a Shiga-
non-diarrheic Libyan children) for virulence like toxin (Stx). More than one hundred
genes using PCR. They detected nine eae- different serogroups were reported to
positive (EPEC) and nine aggR-positive produce Stx however, E.coli O157:H7 is

www.nidcc.org.ly 11
Ghenghesh et al.
the predominant serogroup associated with the predominant serotypes of Salmonella
diarrhea. Ghenghesh et al (6) using specific associated with diarrhea in Libyan children
antisera reported the detection of this from different cities. Ghanim et al. (4)
serogroup in 7% of diarrheic children and in reported that more 89%, 85% and 31%
4% of controls. Other types of diarrheagenic of Salmonella-positive children with
E. coli (i.e. ETEC, EIEC and DAEC) have diarrhea had vomiting, fever and tenesmus,
not been reported previously from Libyan respectively.
children with diarrhea. 3. Shigella: Diarrhea associated with Shigella
2. Salmonella: It is widely accepted at present, infections results in nearly one million
by microbial taxonomists, that almost all deaths each year, especially among children
of the Salmonella that infect mammals in developing countries (11). There are four
and birds to be one species (S. enterica) species (groups) of Shigella: S. dysenteriae
divided into six subspecies (8). Within (group A), S. flexneri (group B), S. boydii
these subspecies there are at least more than (group C) and S. sonnei (group D) with 49
2000 serotypes. Most serotypes cause only recognized serovars, represnting subtypes
gastroenteritis, while specific serotypes (S. from three of the four groups (12).
typhi and S.paratyphi) cause enteric fever S.sonnei is the major cause of shigellosis in
(9). developed countries, while in developing
As shown in Table 1, nontyphoid countries S. flexneri and S. dysenteriae
salmonellae are the major bacterial cause of predominate. Studies from Libya show
diarrhea in Libyan children. In industrialized S.flexneri (mainly subtypes 2 and 4) as the
countries S. typhimurium and S. enteriditis major cause of Shigella-associated diarrhea
are the predominant serotypes responsible in children (3,4,13,14). Ali et al (3) reported
Vol. 2 No.1 Jan. 2008

for Salmonella-associated diarrhea in that in Shigella-positive children with


children (10). In Libya, serotypes other than diarrhea 100%, 50% and 83% of them had
S. enteritidis predominated since 1970s to fever, convulsions and blood in the stool,
present. However, S. enteritidis has been respectively. Table 3 shows information
reported from diarrheic Libyan children about Libyan children with diarrhea in
during 21st century (3). Table 2 shows Tripoli and their Shigella isolates.

Table 2. Predominant Salmonella serotypes isolated from Libyan Children with Diarrhea
The Official Periodical of the Libyan National Center for Infectious Diseases Prevention and Control
Infectious Diseases

Years of Predominant
City Reference
isolation serotype
S. wein
Tripoli 1975-1980 S. muenchen 64
S. typhimurium
S. saintpaul
Tripoli 1992-1993 62
S. muenchen
THE LIBYAN JOURNAL OF

S. typhimurium
Benghazi 2000-2001 S. muenchen 63
S. paratyphi
S. Heidelberg
Zliten 2000-2001 3
S. enteritidis

12 www.nidcc.org.ly
Infectious acute diarrhea in Libyan children
Table 3. Information about Libyan Children with Diarrhea in Tripoli and their Shigella Isolates (14)

Age Month of Length of diarrhea Episodes Species and


Patient Sex
(Mo) occurrence (days) per day serotype of Shigella
1 F 11 Sep 1 5 S. sonnei
2 F 30 Sep 2 3 S. flexneri type 2
3 M 27 Oct 1 6 S. sonnei
4 F 18 Oct 1 8 S. flexneri type 2
5 F 36 Oct 2 5-7 S. flexneri type 2
6 M 7 Dec 7 7-8 S. flexneri type 1
7 M 7 Apr 1 10 S. flexneri type 2
8 M 13 Jun 10 6-7 S. flexneri type 3
9 M 32 Jul 1 4 S. sonnei

4. Yersinia enterocolitica: A gastrointestinal 1. diarrheic.


tract pathogen that causes acute enteritis 6. Aeromonas: At least 14 species hybrization
with fever and inflammatory, occasionally groups are known in this genus with
bloody, watery diarrhea is the most frequent A.hydrophila, A. sobria and A. caviae being
occurrence, particularly in children (15). the prevalent species involved in human
This organism has been reported only disease (19-21). In children, the common
once from Libyan children with diarrhea at clinical picture caused by Aeromonas is
less than one percent and it appears not to the acute onset of watery diarrhea with

Vol. 2 No.1 Jan. 2008


be an important cause of diarrhea in such slightly raised body temperature (20). In
a population (6). This view is supported developing countries the rate of occurrence
by a study carried out in Benghazi by of Aeromonas in diarrheal children ranges
Ghanim et al (4). They examined stools of between 4-22% (22-24) while in developed
diarrheic children and none was positive for countries it is usually less than 3% (25-
Y.enterocolitica. 27). The rate of occurrence of Aeromonas
5. Campylobacter: Campylobacter jejuni in Libyan children from different cities
and C. coli are the most important human ranges between 0-15% with A. caviae being
pathogens in this genus, with the former the predominant species. A study from
The Official Periodical of the Libyan National Center for Infectious Diseases Prevention and Control
usually responsible for the majority (80- Tripoli, reported that of the 23 diarrheal Infectious Diseases
90%) of enteric Campylobacter infections children with fecal Aeromonas, 43.5% had
(16). In developing countries, non- mucus, and 26.1% had blood in their stools;
inflammatory, watery diarrhea is seemingly 34.8% and 39.1% presenting with fever and
the most common clinical pattern of disease vomiting respectively (28).
seen with Campylobacter infection and
usually restricted to children (16,17). II. Parasitic agents:
Campylobacter was reported from Libyan These include the intestinal protozoa
THE LIBYAN JOURNAL OF

children with diarrhea for the first time in Entamoeba histolytica, Giardia lamblia and
1994 (18). Ghanim et al (3) reported that Cryptosporidium. These organisms are common
children infected with campylobacter are causes of diarrhea in children in developing
also presented with fever and vominting. countries and asymptomatic infection is also
The rate of occurrence of Campylobacter in common in this population. Published studies
diarrheic Libyan children is shown in Table on children diarrhea due to parasitic agents

www.nidcc.org.ly 13
Ghenghesh et al.
in Libya are few and lack the description of form urban areas (e.g. Tripoli) and low
clinical features associated with the causative rates from rural areas (e.g Zliten) in Libya.
agents. However, Alsirieti et al (29) reported the Pockets of high and low prevalence have
detection of intestinal protozoa in 532 (76%) been described previously, and they appear
of 700 Libyan children attending Out Patient to be more common in urban areas than in
Clinics in Sirt City complaining of diarrhea, rural areas (41).
nausea, fever, vomiting, and abdominal pain. 3. Cryptosporidium: This organism is a
1. Entamoeba histolytica: An important recognized cause of diarrhea among children
cause of diarrhea in children in developing (mostly less than one year) in developing
countries and is usually characterized by countries and is associated with malnutrition
presence of blood in the stool. E. histolytica (42,43). Studies have also shown that
is identical morphologically to the non- asymptomatic infection is common and
pathogenic E. dispar. The latter is the new although its effect on children is less severe,
species name for what was previously such infection may have a negative effect
called «non-invasive» or «non-pathogenic» on weight gain (44). Reported prevalence of
E.histolytica (30). Therefore, the prevalence Cryptosporidium in diarrheic children from
rates of E. histolytica in the literature, developing countres ranged between 4 to
particularly rates reported from developing 32% (38,45,46) and from Libya between
countries, should be interpreted carefully. In 1 to 13% (3,34). It should be noted that in
this paper, prevalence rates will be reported the above mentioned studies lower rates of
as E. histolytica/dispar. Rates of 5-34% from Cryptosporidium were mostly reported from
diarrheal children in developing countries populations in urban areas (e.g Tripoli)
(31-33) and 4-46% in Libya (3,29,34) have and higher rates from non-urban areas (e.g
Vol. 2 No.1 Jan. 2008

been reported previously for E. histolytica/ Zliten).


dispar. of 20 Libyan diarrheic children
positive for E. histolytica/dispar, 95% had III. Viral agents:
fever, 30% convulsions and 60% had blood Although different types of enteric viruses
in the stool (3). are known to cause diarrhea in children, only
2. Giardia lamblia (syn. G. intestinalis, G. rotaviruses have been reported from Libya.
duodenalis): The most commonly isolated Rotaviruses are considered the most common
intestinal parasite throughout the world cause of acute diarrhea in young children in
The Official Periodical of the Libyan National Center for Infectious Diseases Prevention and Control
Infectious Diseases

and is particularly prevalent in children developed and developing countries (47). In


in developing countries and it is the most the latter, it is estimated that 20% to 70% of
cause of waterborne outbreaks of diarrhea hospitalizations and around 900.000 children
in developed countries (35,36). Although below the age of 5 die annually as a result of
diarrhea is the most frequent symptom rotaviruses infection (48). Of the 7 groups (A-
associated with G. lamblia infection, G) of rotaviruses group A is usually the cause
prolonged diarrhea with malnutrition and of rotavirus-associated diarrhea. Rotaviruses
growth failure in infancy have been also infections occur via the fecal-oral route.
reported (37).
THE LIBYAN JOURNAL OF

Occurring rates are similar in developing and


Prevalence rates of G. lamblia amongst developed countries. In Libya, rotavirus is
diarrheic children in developing countries the leading cause of infectious diarrhea with
ranged between <1-38.5% (38-40) and in reported rates of 24% to 31% (3,4,6). There
Libya ranged between 1-18% (3,29,34). is no seasonal variation in the occurrence of
High rates of G. lamblia have been reported rotavirus infection, although it appears to peak

14 www.nidcc.org.ly
Infectious acute diarrhea in Libyan children
in winter. A study from Zliten (3) reported 98% to commonly used, cheap oral antibiotics
of rotavirus-positive children with diarrhea among enteric pathogens have been reported
were dehydrated and more than 84% with fever from several developing countries (54-56). The
and vomiting. same can be said for enteric bacterial pathogens
isolated in this country. High rates of resistance
IV. Multiple pathogens: to multiple antimicrobial agents by different
Although single enteric agents are enteric pathogenic bacteria have been reported
responsible for most cases of infectious from different cities in Libya (13,62,64). The
diarrhea, multiple agents (two agents or ease of which antimicrobial agents can be
more) may also play an important role in this obtained in these countries including Libya
syndrome in developing countries. Multiple has been blamed for this problem (3,57).
enteric pathogens may act synergistically to There is dearth of information on the treatment
produce diarrhea (49). Rates of 12-14.5% of acute infectious diarrhea in Libya. Sood
for multiple agents have been reported from et al. (58), in Benghazi, studied the in vivo
Libyan children with diarrhea (3,4). sensitivity of salmonellae in 38 children with
gastroenteritis. The children were treated for 7
V. Nosocomial (hospital-acquired) days with gentamicin, to which the organisms
diarrhea: were sensitive in vitro. Stool culture remained
positive in 30 of the 38 cases. The children
Within the hospital setting, pediatric
improved on supportive and symptomatic
wards face both community and nosocomial
therapy. Sood et al. (58) study shows that
(hospital-acquired) diarrhea. The latter may
antibiotics have no role in the management of
result in aggravating the underlying disease
acute Salmonella gastroenteritis in children.

Vol. 2 No.1 Jan. 2008


and delay hospital discharge (50). Nosocomial
Unfortunately, gentamicin and other broad-
transmission of non-typhoid Salmonella
spectrum antimicrobial agents are still used in
among children has been reported previously
general practice in Libya to treat acute infectious
from several cities in Libya (51,64). Although,
diarrhea in Libyan children. The use of up to 3
hand washing is considered the most important
different antimicrobial agents by pediatricians
method in preventing transmission of infection
in treatment of diarrhea in children aged less
by the fecal-oral route, compliance of
than one year has been observed in government
healthcare workers with standard precautions is
and private clinics in the last decade (K.S.
variable and often poor (52,53). In addition, the
The Official Periodical of the Libyan National Center for Infectious Diseases Prevention and Control
Infectious Diseases
Ghenghesh, unpublished observation). There
high rate of the Salmonella carrier state among
is a serious problem among pediatricians
health care workers in some Libyan hospitals
in Libya as far as the use of broad-spectrum
may contribute to this problem (64). Recently,
antimicrobial agents in treatment of infectious
Ali et al. (3), in Zliten, reported significantly
acute diarrhea in children for the following
higher rates of isolation of multiple agents
reasons: first, it is well established from the
(mainly rotavirus plus another agent) from
published studies in this country that rotavirus
children with nosocomial diarrhea than from
is the most common cause of diarrhea; second,
children with community acquired diarrhea.
THE LIBYAN JOURNAL OF

most of the enteric bacteria associated with


children diarrhea (i.e. Salmonella and Shigella)
Antimicrobial Resistance and are multiple resistant to antimicrobial agents;
Treatment third, a high rate of children diarrhea is caused
by intestinal protozoa. Because antimicrobials
In the last two decades, high rates of resistance have no role in the treatment of the three groups

www.nidcc.org.ly 15
Ghenghesh et al.
of diarrheagenic agents mentioned above, and breast feeding respectively. Ghenghesh
pediatricians should refrain from prescribing et al. (6), in Tripoli, reported similar findings.
antimicrobial agents to patients with diarrhea A strong program by the health authorities and
in this country. Furthermore, gastrointestinal other related agencies using the media and
infections with enteric pathogens are generally other venues including schools, universities
self-limiting. Although, treatment of patients and maternity clinics should be carried out
with symptoms of infectious diarrhea with throughout the year to promote the benefits of
antibiotics remains controversial, antimicrobial breast feeding among child bearing mothers
therapy should be initiated for those who are to reduce the incidence of diarrhea in children
severely ill and for patients with risk factors less than two years of age.
for extraintestinal spread of infection after Most of the bacterial enteric pathogens are
obtaining appropriate blood and fecal cultures zoonetic organisms and therefore, different
(59). The current accepted treatment of all acute types of meats (i.e. lamb, beef, chicken and
infectious diarrheal diseases is rehydration, fish) are major sources of such organisms.
antibiotic treatment (when indicated), and Animal products (i.e. eggs, raw milk) are
nutritional therapy (57). also major sources of enteric pathogens. The
problem arises when meats and animal products
are not handled in the kitchen properly and
Prevention cross contamination occurs. This in turn may
Providing clean treated water for drinking increase the exposure probability of children to
and for preparation of foods (e.g. bottled milk) enteric pathogens. Mothers should be educated
is the first step in preventing infectious acute on how to handle meats and foods properly
diarrhea in children. A strong association in the kitchen to prevent cross contamination.
Vol. 2 No.1 Jan. 2008

between isolation of enteric pathogens from When treated water is not available, mothers
diarrheic children and use of untreated water need to be advised to boil the water used for
has been reported previously from Libya preparation of bottled milk for their children.
(3,28). Ali et al. (3) reported that according Also, the community should be educated on
to type of water consumed, nearly 57% of the importance of hand washing and personnel
children with diarrhea had non-treated water hygiene
at home. Single pathogens, rotavirus, Shigella, The housefly is well known to carry enteric
Aeromonas, E. histolytica/dispar, and G. lamblia pathogens and reducing its population has been
The Official Periodical of the Libyan National Center for Infectious Diseases Prevention and Control
Infectious Diseases

were isolated at higher rates from children with shown to result in lowering the incidence of
non-treated than from children with treated diarrheal disease in the community. Rahuma
water at home. They also reported that nearly et al. (60) isolated EPEC, Salmonella, Shigella,
all parents of diarrheic children stated that on Y.enterocolitica and Aeromonas from houseflies
certain occasions, during shortages of water collected from different locations in Misurata
particularly in summer, they used water from City. The public needs to be informed of the role
other sources not known whether treated or of houseflies in transmitting human pathogens
not. and the need for the careful disposal of sewage
Ghanim et al. (4), in Benghazi, reported a (and the excreta of other mammals). Control of
THE LIBYAN JOURNAL OF

clear association between diarrhea and feeding houseflies by health and municipal authorities
practices. They found nearly 50% of children needs to be improved.
with diarrhea were bottle-fed compared with A very strong association of dehydrated
14% and 11% among exclusively breast fed children with rotavirus diarrhea has been
babies and those on a combination of bottle reported from Libya (3). This observation

16 www.nidcc.org.ly
Infectious acute diarrhea in Libyan children
supports the view that rotavirus may be Swerdlow DL, Sansonetti PJ, et. al.. Global burden
responsible for a large part of the morbidity of Shigella infections: implications for vaccine
development and implementation of control strategies.
and mortality associated with this syndrome Bull WHO 1999; 77:651-655.
in this country and gives more weight to the
12. Bopp CA, Brenner FW, Fields PI, Wells JG,
need of a rotavirus vaccine to protect the Strockbine NA. Escherichia, Shigella, and
pediatric population (61). However, a number Salmonella. In: Murray PR., Baron EJ., Jorgensen
of questions have to be answered before JH., Pfaller MA., and Yolken RH. (eds) Manual of
embarking on such a project that include, Clinical Microbiology (8th). ASM Press, Washington,
DC, 2003. pp. 654-671.
among others, what are the groups, serotypes,
13. El Nageh, MM. 1984. Shigella dysentery in Tripoli,
genotypes and electrophoretic types of the
Libya. J. Trop. Med. Hyg., 87, 1-5.
strains that circulate in Libya.
14. Ghenghesh K, Bara F, Bukris B, Abeid S. Shigella-
associated diarrhea in children in Tripoli-Libya.
REFERENCES Saudi Med J 1997; 18: 557-559.
15. Bottone EJ. Yersinia enterocolitica: the charisma
1. Kosek M, Bern C, Guerrant RL. The global burden of continues. Clin Microbiol Rev 1997; 10: 257-276.
diarrheal disease, as estimated from studies published
16. Ketley JM. Pathogenesis of enteric infections by
between 1992 and 2000. Bull WHO 2003; 81: 197-
Campylobacter. Microbiol 1997; 143: 5-21.
204.
17. Taylor DN. Campylobacter infections in developing
2. Hill-King L. Viral diarroea. Biomed Scientist, May
countries. In: Nachamkin I, Blaser MJ, Tompkins LS.
issue 2005; 462-466.
(eds) Campylobacter jejuni: current status and future
3. Ali MB, Ghenghesh KS, Aissa RB, Abuhelfaia A, trends. ASM Press, Washington, DC, 1992; pp 20-
Dufani M. Etiolgy of childhood diarrhea in Zliten, 30.
Libya. Saudi Med J 2005; 26: 1759-1765.
18. Ghenghesh KS, Bara F, Bukris B, El-Surmani A,
4. Ghanim MA, Taher IAA, Ahmaida AI, Tobgi RS. Abeid SS Daw MA. Isolation of Campylobacter

Vol. 2 No.1 Jan. 2008


Etiolgy of childhood diarrhea in Benghazi, Libya. species from Libyan children with diarrhea (Abstract).
Garyounis Med J 2003; 20: 22-34. Jamahiriya`s Second Conference on Medical
5. Kaper JB, Nataro JP, Mobley HL. Pathogenic Sciences, Benghazi 1994; May 8-11.
Escherichia coli. Nat Rev Microbiol 2004: 2: 123- 19. Abbot SL, Cheung WK, Janda JM. The genus
140. Aeromonas: biochemical characteristics, atypical
6. Ghenghesh KS, Abeid SS, Bara F, Bukris B. Aetiology reactions, and phenotypic identification schemes. J
of childhood diarrhoea in Tripoli – Libya. Jamahiriya Clin Microbiol 2003; 41: 2348-2357.
Med J 2001; 1 (2): 23-29. 20. Figueras MJ. Clinical relevance of Aeromonas. Rev
7. Dow MA, Toth I, Malik A, Herpay M, Nogrady N, Med Microbiology 2005; 16: 145-153.

The Official Periodical of the Libyan National Center for Infectious Diseases Prevention and Control
Infectious Diseases
Ghenghesh KS, Nagy B. Phenotypic and genetic 21. Janda JM, Abbot SL. Evolving concepts regarding the
characterization of enteropathogenic Escherichia genus Aeromonas: an expanding panorama of species,
coli (EPEC) and enteroaggregative E. coli (EAEC) disease presentations, and unanswered questions.
from diarrhoeal and non-diarrhoeal children in Libya. Clin Infect Dis 1998; 27: 332-344.
Comp Immunol Microbiol Infect Dis 2006; 29: 100-
22. Teka T, Faruque ASG, Hossain M I, Fuchs GJ.
113.
Aeromonas-associated diarrhoea in Bangladeshi
8. Le Minor L. Typing of Salmonella species. Eur J Clin children: clinical and epidemiological characteristics.
Microbiol Infect 1988; 7: 214-218. Ann Trop Pediatr 1999; 19: 15-20.
9. Blaser MJ, Feldman RA. Salmonella bacteremia: 23. Dallal MMS, Moezardalan K. Aeromonas spp
reports to the Centers for Disease Control, 1968-
THE LIBYAN JOURNAL OF

associated with children`s diarrhoea in Tehran: a


1979. J Infect Dis 1981; 143: 743-746. case-control study. Ann Trop Paediatr 2004; 24: 45-
10. Centers for Disease Control and Prevention. 51.
Salmonella surveillance: annual summary, 2000. U.S. 24. Komathi AG, Ananthan S, Alavandi SV. Incidence
Department of Health and Human Services, Public and enteropathogenicity of Aeromonas spp in children
Health Service, Atlanta, Ga., 2000. suffering from acute diarrhoea in Chennai. Indian J
11. Kotloff KL, Winickoff JP, Ivanoff B, Clemens JD, Med Res 1998; 107: 252-256.

www.nidcc.org.ly 17
Ghenghesh et al.
25. Leblanc M, Delage G, Rousseau E, Dobrescu O, diarrhoeic and asymptomatic children in Jeddah,
Bernard-Bonnin AC. Prevalence of Aeromonas spp. Saudi Arabia. Ann Trop Med Parasitol 2003; 97: 505-
pediatric gastroenteritis. Canadian Med Associat J 510.
1988; 138: 714-717. 39. Al-Saeed AT, Issa SH. Frequency of Giardia lamblia
26. Prere MF, Bacrie SC, Baron O, Fayet O. Bacterial among children in Dohuk, northern Iraq. East
aetiology of diarrhoea in young children: high Mediterr Health J 2006; 12: 555-561.
prevalence of enteropathogenic Escherichia coli 40. Moalla H, Fendri C. Etiology of acute diarrhea in
(EPEC) not belonging to the classical EPEC children. Tunis Med 1994; 72: 25-28.
serogroups. Pathol Biol (Paris) 2006; 54: 600-602.
41. Fraser D. Epidemiology of Giardia lamblia and
27. Wilcox MH, Cook AM, Eley A, Spencer RC. Cryptosporidium infections in childhood. Israel J
Aeromonas spp as a potential cause of diarrhoea in Med Sci 1994; 30: 356-361.
children. J Clin Pathol 1992; 45: 959-963.
42. Enriquez FJ, Avilla CR, Santos JI, Tanaka-Kido
28. Ghenghesh KS, Bara F, Bukris B, El-Surmani A, J, Vallejo O, Sterling CR. Cryptosporidium
Abeid SS. Characterization of virulence factors of infections in Mexican children: clinical, nutritional,
Aeromonas isolated from children with and without enteropathogenic, and diagnostic evaluations. Am J
diarrhoea in Tripoli, Libya. J Diarrhoeal Dis Res Trop Med Hyg 1997; 56: 254-257.
1999; 17: 75-80.
43. Molbak K, Andersen M, Aaby P, Hojlyng N, Jakobsen
29. Alsirieti SRA, Elahwel AM, Elamari A. Intestinal M, Sodemann M, daSilva APJ. Cryptosporidium
protozoa in Libyan patients in Sirt. Jamahiyria Med J infections in infancy as a cause of malnutrition: a
2006; 6 (1): 59-61. community study from Guinea-Bissau, West Africa.
30. Petri WA, Singh U. Diagnosis and management of Am J Clin Nutr 1997; 65: 149-152.
amebiasis. Clin Infect Dis 1999; 29: 1117-1125. 44. Checkley W, Gilman RH, Epstein LD, Suarez M, Diaz
31. Youssef M, Shurman A, Bougnoux M, Rawashdeh R, JF, Cabrera L, et al.. Asymptomatic and symptomatic
Bretagne S, Strockbine N. Bacterial, viral and parasitic cryptosporidiosis: their acute effect on weight gain in
enteric pathogens associated with acute diarrhea in Peruvian children. Am J Epidemiol 1997; 145: 156-
hospitalized children from northern Jordan. FEMS 163.
Vol. 2 No.1 Jan. 2008

Immunol Med Microbiol 2000; 28: 257-263. 45. Bhattacharya MK, Teka T, Faruque ASG, Fuchs
32. Al-Eissa YA, Assuhaimi SA, Abdullah AM, AboBakr GJ. Cryptosporidium infection in children in Urban
AM, Al-Husain MA, Al-Nasser MN, et al. Prevalnce Bangaladesh. J Trop Pediatr 1997; 43: 282-286.
of intestinal parasites in Saudi children: a community- 46. Hamedi Y, Safa O, Haidari M. Cryptosporidium
based study. J Trop Pediatr 1995; 41: 47-49. infection in diarrheic children in southern Iran.
33. Habbari K, Tifnouti A, Bitton G, Mandil A. Intestinal Pediatr Infect Dis J 2005; 24: 86-88.
parasitosis and environmental pollution: 1343 47. Kapikian AZ, Chanock RM. Rotaviruses. In:
pediatric cases in Beni-Mellal, Morocco. Tunis Med Fields, BN., Knipe, DM., Howley, PM., et al. (eds)
2000; 78: 109-114. Fields Virology (3rd ed., Vol 2). Lippincott-Raven,
The Official Periodical of the Libyan National Center for Infectious Diseases Prevention and Control
Infectious Diseases

34. Ben Rashed MB, Abulhassa M, Tabit A, Hawas A. Philadelphia, 1996; pp. 1657-1708.
Demographic features of intestinal parasitic infection 48. Parashar UD, Bresee JS, Gentsch JR, Glass RI.
in Libyan children. Jamahiriya Med J 2006; 6 (2): Rotavirus. Emerg Infect Dis 1998; 4: 561-570.
138-140.
49. Albert MJ, Ansaruzzaman M, Talukder KA, et al.
35. Barwick RS, Levy DA, Braun GF, Beach MJ, Prevalence of enterotoxin genes in Aeromonas spp.
Calderon RL. Surveillance for water-borne disease isolated from children diarrhea, healthy controls, and
outbreaks-United States, 1997-1998. MMWR 2000; environment. J Clin Microbiol 2000; 38: 3785-3790.
44: 1-36.
50. Ratner AJ, Neu N, Jakob K, Grumet S, Adachi
36. Bryan RT, Pinner RW, Berkelman RI. Emerging A, Della-Latta P, et al. Nosocomial rotavirus in a
infectious diseases in the United States. Ann N Y
THE LIBYAN JOURNAL OF

pediatric hospital. Infect Control Hosp Epidemiol


Acad Sci 1994; 740: 346-361. 2001; 22: 299-301.
37. Flanagan PA. Giardia-diagnosis, clinical course and 51. Taher IAA, Tobgi RS. Emergence of multi-drug
epidemiology: a review. Epidemiol Infect 1992; resistant salmonellae isolated from neonates in
109:1-22. Benghazi-Libya. J Bahrain Med Soc 1997; 9: 165-
38. Al-Braiken FA, Amin A, Beeching NJ, Hommel M, 167.
Hart CA. Detection of Cryptosporidium amongst 52. Pittet D, Hugonnet S, Harbarth S, Mourouga P, Sauvan

18 www.nidcc.org.ly
Infectious acute diarrhea in Libyan children
V, Touveneau S, et al. Effectiveness of a hospital- 59. Hohmann EL. 2001. Nontyphoidal salmonellosis.
wide programme to improve compliance with hand Clin Infect Dis; 32: 263-269.
hygiene. Infection control programme. Lancet 2000; 60. Rahuma N, Ghenghesh KS, Ben Aissa R, Elamaari
356: 1307- 1312. A. Carriage by the housefly (Musca domestica)
53. Ros SP, Cabrera-Ros BL. Poor compliance with of multiple-antibiotic-resistant bacteria that are
universal precautions: a universal phenomenon? potentially pathogenic to humans, in hospital and
Pediatr Emerg Care 1990; 6: 183-185. other urban environments in Misurata, Libya. Ann.
54. Urio EM, Collison EK, Gashe BA, Sebunya TK, Trop. Med. Parasitol 2005; 99: 795–802.
Mpuchane. S. Shigella and Salmonella strains isolated 61. Ghenghesh KS, Kreasta M, El-bakoush M, Tobgi
from children under 5 years in Gaborone, Botswana, R. Rotavirus-associated gastroenteritis. Jamahiriya.
and their antibiotic susceptibility patterns. Trop Med Med J 2002; 2: 12-17.
Int Health 2001; 6: 55-59. 62. El-Ghodban A, Ghenghesh KS, Marialigeti K,
55. Shapiro RL, Kumar L, Phillips-Howard P, Wells JG, Abeid S. Serotypes, virulence factors, antibiotic
Adcock P, Brooks J, et al. Antimicrobial-resistant susceptibility, betalactamase activity and plasmid
bacterial diarrhea in rural western Kenya. J Infect Dis analysis of Salmonella from children with diarrhea
2001; 183: 1701-1704. in Tripoli (Libya). Acta Microbiol Immunol Hung
56. Rahman M, Islam H, Ahmed D, Sack RB. Emergence 2002; 49: 433-444.
of multidrug-resistant Salmonella Gloucester and 63. Gerged AY, Baiu SH, Ahmaida AI. Serotypes and
Salmonella Typhimurium in Bangladesh. J Health frequency of multi-drug resistant Salmonella isolated
Popul Nutr 2001; 19: 191-198. from diarrheal children in Benghazi, Libya. Garyounis
57. Sack RB, Rahman M, Yunus M, Khan EH. Med J 2004; 21: 41-49.
Antimicrobial resistance in organisms causing 64. El Nageh MM. Salmonella isolations from human
diarrheal disease. Clin Infect Dis 1997; 24: 102-105. faces in Tripoli, Libya. Trans R Soc Trop Med Hyg
58. Sood, SC, Bilaziz M, Basbas N. Salmonella enteritis 1988; 82: 324-326.
in children in Libya: role of antibiotic therapy. Ann
Trop Paediatr 1986; 6: 93-94.

Vol. 2 No.1 Jan. 2008


The Official Periodical of the Libyan National Center for Infectious Diseases Prevention and Control
Infectious Diseases
THE LIBYAN JOURNAL OF

www.nidcc.org.ly 19

Potrebbero piacerti anche