Introduction
Cronobacter is a genus of Gram-negative, facultative-anaerobic, nonspore-forming, motile bacteria belonging to the Enterobacteriaceae family. At present, seven species are known: Cronobacter sakazakii, C. malonaticus, C. dublinensis, C. muytjensii, C. turicensis, C. condimenti, and C. universalis (Iversen et al. 2007; Iversen et al. 2008; Joseph et al. 2012; Stephan et al. 2014). Except for C. condimenti, all species of Cronobacter have been isolated from clinical specimens. The Cronobacter species of serious clinical significance are as follows: C. sakazakii, C. malonaticus, C. turicencis, and C. universalis. Other members of the genus (C. dublinensis, C. muytjensii, and C. condimenti) are primarily environmental commensals with low clinical significance (Iversen et al. 2007; Kucerova et al. 2010; Holy et al. 2011; Holy et al. 2014; Holy and Forsythe 2014; Forsythe 2018). Cronobacter spp. are opportunistic pathogens that cause rare but life-threatening diseases such as meningitis, necrotizing enterocolitis, and bloodstream infections in neonates and infants. The infections caused by these bacteria are often severe with fatal health consequences. The lethality rate of meningitis in infants was estimated to be 41.9% with death occurring within hours after the manifestation of symptoms (Willis et al. 1988; Friedemann 2009; Holy and Forsythe 2014). The surviving individuals usually develop irreversible sequelae including serious neurological complications such as quadriplegia and impaired mental development (Bowen and Braden 2006). Infants up to two months of age, premature with low birth weight or immunocompromised newborns are at the highest risk for infection. Cronobacter spp. have also been recognized as causative agents of various infections in elderly adults suffering from serious underlying disease or malignancy (Dennison and Morris 2002; See at al. 2007).
Cronobacter spp. are naturally resistant to all macrolides, lincomycin, clindamycin, streptogramins, rifampicin, fusidic acid, and fosfomycin. Infections caused by these bacteria are usually treated with various combinations of ampicillin, gentamicin, cefotaxime, and chloramphenicol (Muytjens et al. 1983; Biering et al. 1989; Bar-Oz et al. 2001; Block et al. 2002). Cronobacter spp. tend to be more sensitive to most antibiotics that are being used clinically to treat infections caused by Enterobacteriaceae, although resistance to ampicillin has developed (Muytjens and van der Ros-van de Repe 1986). In 1980, all tested strains were susceptible to ampicillin, whereas in 2001, five cases of Cronobacter infection in which one or more of the isolates were resistant to ampicillin and first- and second-generation cephalosporins were described (Farmer et al. 1980; Lai 2011). Similarly, Block et al. (2002) reported that all Cronobacter isolates tested were β-lactamase positive. Caubilla-Barron et al. (2007) previously reported two neonatal deaths from extended-spectrum β-lactamase (ESBL)-encoding C. sakazakii strains in a retrospective study of the Cronobacter necrotizing enterocolitis and meningitis outbreak in the neonatal intensive care unit. Then, Stock and Weidemann (2002) studied some Cronobacter strains and found that all strains were susceptible to the tested β-lactams.
The β-lactamase activity in Cronobacter has been frequently reported by others (Pitout et al. 1997; Caubilla-Barron et al. 2007; Baldwin et al. 2009). In 1997, a low-level β-lactamase production in Cronobacter was detected by Pitout et al. (1997). In addition, Lai (2001) also reported that Cronobacter strains were resistant to ampicillin, cefazolin, and extended-spectrum penicillin. Moreover, a recent study showed that about 10.2% of the Cronobacter strains were resistant to cefotaxime, which is one of the third-generation cephalosporins related to penicillin (Pan et al. 2014). Rising antimicrobial resistance is generally a public health concern, potentially leading to prolonged illness and a higher risk of mortality.
The aim of this study was to examine over time the changes in antibiotic resistance of different Cronobacter spp. strains and to determine the susceptibility of Cronobacter isolates from clinical samples to 17 types of antibiotics.
Experimental
Materials and Methods
Bacterial strains and cultivation. The 52 isolates were collected during a survey of Cronobacter spp. carriage in patients of two hospitals over the 6-year period from May 2007 to August 2013. All strains were isolated from clinical samples (Table I). Microorganisms were routinely cultivated on blood agar (Oxoid, UK) at temperature of 37°C overnight.
Table I
Identification and genotyping of Cronobacter spp. isolated from clinical samples.
| Strain | Strain No. | Log (score)* | Sequence type | Origin | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| C. sakazakii | 1836 | 2.354 | 4 | Wound swab | ||||||||||||||
| C. sakazakii | 1837 | 2.432 | 4 | Wound swab | ||||||||||||||
| C. sakazakii | 1839 | 2.503 | 4 | Smear from area of percutaneous endoscopic gastrostomy | ||||||||||||||
| C. sakazakii | 1840 | 2.452 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 1841 | 2.444 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 1842 | 2.409 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 1901 | 2.467 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 1902 | 2.421 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 1903 | 2.487 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 1915 | 2.509 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 1916 | 2.464 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 1996 | 2.484 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 1997 | 2.505 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 1998 | 2.485 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2000 | 2.479 | 4 | Rectal swab | ||||||||||||||
| C. sakazakii | 2001 | 2.473 | 4 | Swab of the oral cavity | ||||||||||||||
| C. sakazakii | 2002 | 2.476 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2003 | 2.423 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2005 | 2.457 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2006 | 2.357 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2007 | 2.438 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2008 | 2.416 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2009 | 2.459 | 4 | Tongue swab | ||||||||||||||
| C. sakazakii | 2010 | 2.388 | 4 | Throat swab | ||||||||||||||
| C. sakazakii | 2011 | 2.417 | 4 | Suction catheter | ||||||||||||||
| C. sakazakii | 2012 | 2.494 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2013 | 2.451 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2021 | 2.446 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2016 | 2.448 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2017 | 2.510 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2019 | 2.367 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 2022 | 2.426 | 4 | Sputum | ||||||||||||||
| C. sakazakii | 1995 | 2.508 | 64 | Sputum | ||||||||||||||
| C. malonaticus | 1826 | 2.313 | 7 | Cannula | ||||||||||||||
| C. malonaticus | 1827 | 2.293 | 7 | Cannula | ||||||||||||||
| C. malonaticus | 1828 | 2.419 | 7 | Nose swab | ||||||||||||||
| C. malonaticus | 1829 | 2.329 | 7 | Throat swab | ||||||||||||||
| C. malonaticus | 1830 | 2.429 | 7 | Throat swab | ||||||||||||||
| C. malonaticus | 1831 | 2.415 | 7 | Throat swab | ||||||||||||||
| C. malonaticus | 1832 | 2.373 | 7 | Throat swab | ||||||||||||||
| C. malonaticus | 1833 | 2.398 | 7 | Stool - dissection | ||||||||||||||
| C. malonaticus | 1834 | 2.345 | 7 | Throat swab | ||||||||||||||
| C. malonaticus | 1835 | 2.336 | 7 | Throat swab | ||||||||||||||
| C. malonaticus | 1914 | 2.426 | 7 | Sputum | ||||||||||||||
| C. malonaticus | 1917 | 2.387 | 7 | Throat swab | ||||||||||||||
| C. malonaticus | 1999 | 2.361 | 7 | Throat swab | ||||||||||||||
| C. malonaticus | 2004 | 2.343 | 7 | Throat swab | ||||||||||||||
| C. malonaticus | 2014 | 2.388 | 7 | Throat swab | ||||||||||||||
| C. malonaticus | 2015 | 2.353 | 7 | Throat swab | ||||||||||||||
| C. malonaticus | 2018 | 2.339 | 7 | Sputum | ||||||||||||||
| C. malonaticus | 2020 | 2.173 | 7 | Stool | ||||||||||||||
| P. agglomerans/C. muytjensii | 1838 | 2.358 | 28 | Sputum | ||||||||||||||
| Strain | Strain No. | Minimum inhibitory concentration – MIC (mg · l–1) | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AMP | AMS | PIP | PPT | CRX | CTX | CTZ | CPM | MER | AZT | GEN | TOB | AMI | CIP | TIG | COL | COT | ||
| C. sakazakii | 1836 | 1 | 2 | 1 | 1 | 4 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 0.5 | 1 |
| C. sakazakii | 1837 | 0.5 | 0.5 | 1 | 1 | 1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.5 | 2 | 0.1 | 0.06 | 0.5 | 1 |
| C. sakazakii | 1839 | 1 | 1 | 1 | 1 | 2 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 0.5 | 1 |
| C. sakazakii | 1840 | 1 | 1 | 1 | 1 | 4 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 1 | 1 |
| C. sakazakii | 1841 | 1 | 2 | 1 | 1 | 2 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 0.5 | 1 |
| C. sakazakii | 1842 | 1 | 2 | 1 | 1 | 4 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 0.5 | 1 |
| C. sakazakii | 1901 | 0.5 | 0.5 | 2 | 1 | 1 | 0.1 | 0.1 | 0.2 | 0.1 | 0.2 | 0.2 | 0.5 | 0.5 | 0.1 | 0.2 | 0.5 | 1 |
| C. sakazakii | 1902 | 0.5 | 0.5 | 2 | 1 | 1 | 0.1 | 0.1 | 0.2 | 0.1 | 0.2 | 0.2 | 0.5 | 0.5 | 0.1 | 0.1 | 0.5 | 1 |
| C. sakazakii | 1903 | 1 | 0.5 | 2 | 1 | 2 | 0.1 | 0.1 | 0.2 | 0.1 | 0.2 | 0.2 | 0.5 | 0.5 | 0.1 | 0.1 | 0.5 | 2 |
| C. sakazakii | 1915 | 0.5 | 0.5 | 2 | 1 | 0.5 | 0.1 | 0.1 | 0.2 | 0.1 | 0.2 | 0.2 | 0.5 | 0.5 | 0.1 | 0.1 | 0.5 | 1 |
| C. sakazakii | 1916 | 8 | 2 | 8 | 4 | 4 | 0.1 | 0.5 | 0.1 | 0.1 | 0.2 | 0.2 | 0.5 | 1 | 0.1 | 0.1 | 0.5 | 1 |
| C. sakazakii | 1996 | 4 | 1 | 4 | 1 | 1 | 0.1 | 0.1 | 0.1 | 0.5 | 0.2 | 0.2 | 0.5 | 2 | 0.06 | 0.2 | 0.5 | 1 |
| C. sakazakii | 1997 | 1 | 0.5 | 2 | 1 | 1 | 0.1 | 0.1 | 0.2 | 0.1 | 0.2 | 0.2 | 0.5 | 0.5 | 0.1 | 0.06 | 0.5 | 1 |
| C. sakazakii | 1998 | 0.5 | 0.5 | 2 | 1 | 1 | 0.1 | 0.1 | 0.2 | 0.1 | 0.2 | 0.2 | 0.5 | 0.5 | 0.1 | 0.1 | 0.5 | 1 |
| C. sakazakii | 2000 | 1 | 1 | 1 | 1 | 1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.5 | 2 | 0.2 | 0.06 | 0.5 | 0.2 |
| C. sakazakii | 2001 | 2 | 1 | 2 | 1 | 4 | 0.1 | 0.1 | 0.1 | 0.5 | 0.1 | 1 | 0.2 | 1 | 0.06 | 0.03 | 0.1 | 0.2 |
| C. sakazakii | 2002 | 1 | 1 | 1 | 1 | 0.5 | 0.1 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.5 | 2 | 0.2 | 0.06 | 0.5 | 0.2 |
| C. sakazakii | 2003 | 2 | 1 | 2 | 1 | 4 | 0.1 | 0.1 | 0.1 | 0.5 | 0.1 | 1 | 0.2 | 2 | 0.06 | 0.06 | 0.1 | 0.2 |
| C. sakazakii | 2005 | 2 | 1 | 2 | 1 | 4 | 0.1 | 0.1 | 0.1 | 0.5 | 0.1 | 1 | 0.2 | 1 | 0.06 | 0.03 | 0.1 | 0.2 |
| C. sakazakii | 2006 | 2 | 0.5 | 2 | 1 | 4 | 0.1 | 0.1 | 0.1 | 0.5 | 0.1 | 1 | 0.5 | 1 | 0.06 | 0.03 | 0.1 | 0.2 |
| C. sakazakii | 2007 | 2 | 1 | 2 | 1 | 4 | 0.1 | 0.1 | 0.1 | 0.5 | 0.1 | 1 | 0.2 | 1 | 0.06 | 0.03 | 0.1 | 0.5 |
| C. sakazakii | 2008 | 2 | 1 | 2 | 1 | 4 | 0.1 | 0.1 | 0.1 | 0.5 | 0.1 | 1 | 0.5 | 1 | 0.06 | 0.03 | 0.1 | 0.2 |
| C. sakazakii | 2009 | 0.5 | 0.5 | 2 | 1 | 1 | 0.1 | 0.1 | 0.2 | 0.1 | 0.2 | 0.2 | 0.5 | 0.5 | 0.1 | 0.1 | 0.5 | 0.2 |
| C. sakazakii | 2010 | 2 | 1 | 2 | 1 | 2 | 0.1 | 0.2 | 0.1 | 0.5 | 0.2 | 0.5 | 0.5 | 1 | 0.1 | 0.06 | 1 | 2 |
| C. sakazakii | 2011 | 2 | 1 | 2 | 1 | 2 | 0.1 | 0.2 | 0.1 | 0.5 | 0.2 | 0.5 | 0.5 | 1 | 0.1 | 0.06 | 0.2 | 2 |
| C. sakazakii | 2012 | 1 | 0.5 | 2 | 1 | 1 | 0.1 | 0.2 | 0.1 | 0.5 | 0.2 | 0.5 | 0.5 | 1 | 0.1 | 0.06 | 0.2 | 2 |
| C. sakazakii | 2013 | 1 | 1 | 2 | 1 | 2 | 0.1 | 0.2 | 0.1 | 0.5 | 0.2 | 0.5 | 0.5 | 1 | 0.1 | 0.06 | 0.5 | 2 |
| C. sakazakii | 2021 | 2 | 1 | 2 | 1 | 2 | 0.1 | 0.2 | 0.1 | 0.5 | 0.2 | 0.5 | 0.5 | 1 | 0.1 | 0.06 | 1 | 2 |
| C. sakazakii | 2016 | 2 | 1 | 2 | 1 | 1 | 0.1 | 0.2 | 0.1 | 0.5 | 0.2 | 0.5 | 0.5 | 1 | 0.1 | 0.06 | 0.5 | 2 |
| C. sakazakii | 2017 | 2 | 1 | 2 | 1 | 2 | 0.1 | 0.2 | 0.1 | 0.5 | 0.2 | 0.5 | 0.5 | 1 | 0.1 | 0.06 | 1 | 2 |
| C. sakazakii | 2019 | 2 | 1 | 2 | 1 | 2 | 0.1 | 0.2 | 0.1 | 0.5 | 0.2 | 0.5 | 0.5 | 1 | 0.1 | 0.06 | 1 | 2 |
| C. sakazakii | 2022 | 2 | 1 | 2 | 1 | 4 | 0.1 | 0.1 | 0.1 | 0.5 | 0.1 | 1 | 0.2 | 1 | 0.06 | 0.03 | 0.1 | 0.5 |
| C. sakazakii | 1995 | 4 | 2 | 2 | 1 | 4 | 0.1 | 0.1 | 0.1 | 0.5 | 0.2 | 0.2 | 0.5 | 1 | 0.06 | 0.2 | 1 | 1 |
| C. malonaticus | 1826 | 0.5 | 1 | 1 | 1 | 2 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 1 | 1 |
| C. malonaticus | 1827 | 0.5 | 1 | 1 | 1 | 2 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 1 | 1 |
| C. malonaticus | 1828 | 0.5 | 1 | 1 | 1 | 1 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 0.5 | 0.03 | 0.06 | 1 | 1 |
| C. malonaticus | 1829 | 0.5 | 1 | 1 | 1 | 2 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 1 | 1 |
| C. malonaticus | 1830 | 1 | 2 | 1 | 1 | 2 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 1 | 1 |
| C. malonaticus | 1831 | 1 | 1 | 1 | 1 | 2 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 0.1 | 1 |
| C. malonaticus | 1832 | 0.5 | 1 | 1 | 1 | 2 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 1 | 1 |
| C. malonaticus | 1833 | 0.5 | 1 | 1 | 1 | 2 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 1 | 1 |
| C. malonaticus | 1834 | 0.5 | 1 | 1 | 1 | 1 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 1 | 1 |
| C. malonaticus | 1835 | 0.2 | 1 | 1 | 1 | 1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 1 | 1 |
| C. malonaticus | 1914 | 2 | 2 | 1 | 1 | 4 | 0.1 | 0.1 | 0.1 | 0.5 | 0.1 | 0.2 | 0.5 | 1 | 0.06 | 0.5 | 0.2 | 1 |
| C. malonaticus | 1917 | 1 | 1 | 1 | 1 | 1 | 0.1 | 0.1 | 0.1 | 0.5 | 0.1 | 0.2 | 0.2 | 0.5 | 0.06 | 0.2 | 0.2 | 1 |
| C. malonaticus | 1999 | 1 | 0.5 | 2 | 1 | 1 | 0.1 | 0.1 | 0.1 | 0.5 | 0.2 | 0.2 | 0.2 | 1 | 0.06 | 0.2 | 1 | 1 |
| C. malonaticus | 2004 | 0.5 | 0.5 | 2 | 1 | 1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.5 | 0.5 | 0.1 | 0.1 | 0.5 | 0.2 |
| C. malonaticus | 2014 | 1 | 0.5 | 2 | 0.5 | 2 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.06 | 0.2 | 2 | 2 |
| C. malonaticus | 2015 | 1 | 0.5 | 2 | 1 | 1 | 0.1 | 0.2 | 0.1 | 0.5 | 0.2 | 0.5 | 0.5 | 1 | 0.1 | 0.06 | 1 | 2 |
| C. malonaticus | 2018 | 1 | 1 | 2 | 1 | 2 | 0.1 | 0.2 | 0.1 | 0.5 | 0.2 | 0.5 | 0.5 | 1 | 0.1 | 0.06 | 1 | 2 |
| C. malonaticus | 2020 | 1 | 0.5 | 2 | 1 | 0.5 | 0.1 | 0.2 | 0.1 | 0.5 | 0.2 | 0.5 | 0.5 | 1 | 0.1 | 0.06 | 1 | 2 |
| P. agglomerans/ C. muytjensii | 1838 | 1 | 2 | 1 | 1 | 1 | 0.1 | 0.1 | 0.1 | 0.2 | 0.2 | 0.2 | 0.2 | 1 | 0.03 | 0.06 | 0.2 | 1 |